Curation by Binzy_Boi 1 year, 2 months ago for query Dravet Syndrome Foundation
Original results
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https://en.wikipedia.org/wiki/Dravet_syndrome — found via Wikipedia
Dravet syndrome
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic
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https://en.wikipedia.org/wiki/Dravet_Syndrome_Foundation — found via Wikipedia
Dravet Syndrome Foundation
The Dravet Syndrome Foundation (DSF) is a volunteer-run, non-profit organization based in the United States. The mission of the foundation is to raise
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https://en.wikipedia.org/wiki/Charlotte_Dravet — found via Wikipedia
Charlotte Dravet
received the Dravet Award from the Dravet Syndrome Foundation Spain for her contribution to the knowledge and research of Dravet syndrome. In 2011 she
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https://en.wikipedia.org/wiki/Lennox–Gastaut_syndrome — found via Wikipedia
Lennox–Gastaut syndrome
Doose syndrome Dravet syndrome pseudo-Lennox–Gastaut syndrome (atypical benign partial epilepsy) LGS is more easily distinguished from Doose syndrome by
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https://en.wikipedia.org/wiki/Generalized_epilepsy_with_febrile_seizures_plus — found via Wikipedia
Generalized epilepsy with febrile seizures plus
severe myoclonic epilepsy of infancy (SMEI), which is also known as Dravet's syndrome, borderline SMEI (SMEB), and intractable epilepsy of childhood (IEC)
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https://dravetfoundation.org/ — found via Mwmbl
Home - Dravet Syndrome Foundation
What is Dravet Syndrome? Dravet syndrome, also known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare form of intractable epilepsy that begins i…
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http://www.dsfoc.org/ — found via Mwmbl
Down Syndrome Foundation of Orange County
Reflecting on a year of milestones and growth! Thanks to your support, we’ve empowered hundreds through our Learning Programs and Social Boundaries Serie…
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https://www.dsfoc.org/blog/ — found via Mwmbl
Blog – Down Syndrome Foundation of Orange County
Resources Offline Ordering Reflecting on a year of milestones and growth! Thanks to your support, we’ve empowered hundreds through our Learning Programs …
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http://www.dsfoc.org/store/ — found via Mwmbl
Store – Down Syndrome Foundation of Orange County
Touch and WriteFIZZBRAIN LLC*LP Favorite* Kids love learning to write - especially when they can use shaving cream, paint, and jello! Developed by teache…
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https://www.dsfoc.org/our-team/ — found via Mwmbl
Our Team – Down Syndrome Foundation of Orange County
Who Are We Board Members and Officers William E. Halle Co-Founder/President, Down Syndrome Foundation of Orange County (2001 to present) Partner, O'Neil …
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https://www.dsfoc.org/families/ — found via Mwmbl
Families – Down Syndrome Foundation of Orange County
Family Resources From face-to-face educational opportunities to online courses, DSF provides a variety of services to help your learner succeed. Online C…
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https://www.dsfoc.org/educators/ — found via Mwmbl
Educators – Down Syndrome Foundation of Orange County
Educator Resources From online courses to free printable resources, DSF provides a variety of services to help educators support learners with Down syndr…
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https://www.dsfoc.org/lp-archive/ — found via Mwmbl
LP Archive – Down Syndrome Foundation of Orange County
LP Archive We have many more resources, including professionally-printed materials, number lines, online courses, and more available in our Online Store.…
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http://www.dsfoc.org/partnership/ — found via Mwmbl
Partner Organizations – Down Syndrome Foundation of Orange County
Partner with DSF DSF partners with other Down syndrome groups to help build educational programming to support families and educators. Frequently Asked Q…
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http://sjsupport.org — found via Mwmbl
Stevens-Johnson Syndrome Foundation – Educate before you medicate
Welcome The Stevens-Johnson Syndrome Foundation is a non-profit organization founded in 1996. The purpose of the foundation is to provide the public and …
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http://sjsupport.org/?cat=6 — found via Mwmbl
Education – Stevens-Johnson Syndrome Foundation
The Stevens – Johnson Syndrome Foundation is working with researchers to find causes, better treatment plans and genetic markers. We need your help. Plea…
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http://sjsupport.org/?cat=65 — found via Mwmbl
SJS/TEN – Stevens-Johnson Syndrome Foundation
The Stevens – Johnson Syndrome Foundation is working with researchers to find causes, better treatment plans and genetic markers. We need your help. Plea…
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http://sjsupport.org/?cat=11 — found via Mwmbl
Health – Stevens-Johnson Syndrome Foundation
Health The Stevens – Johnson Syndrome Foundation is working with researchers to find causes, better treatment plans and genetic markers. We need your hel…
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http://sjsupport.org/?cat=3 — found via Mwmbl
Blog – Stevens-Johnson Syndrome Foundation
Blog August is SJS Awareness Month! Please join us and pass the ribbon for SJS Awareness Pass the ribbon for Stevens Johnson Syndrome Awareness! Please p…
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http://sjsupport.org/?cat=9 — found via Mwmbl
Events – Stevens-Johnson Syndrome Foundation
August is SJS Awareness Month! Please join us and pass the ribbon for SJS Awareness Pass the ribbon for Stevens Johnson Syndrome Awareness! Please print …
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http://sjsupport.org/?cat=7 — found via Mwmbl
Elderly – Stevens-Johnson Syndrome Foundation
Elderly We need your help! August is Stevens-Johnson Syndrome Awareness month. Won’t you please help us spread awareness by writing your governor request…
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http://sjsupport.org/?cat=12 — found via Mwmbl
Miscellaneous – Stevens-Johnson Syndrome Foundation
Miscellaneous Here’s how you can help the Stevens – Johnson Syndrome Foundation every time you shop on line through Amazon smiles campaign. It’s so easy …
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http://sjsupport.org/?cat=5 — found via Mwmbl
Disabled – Stevens-Johnson Syndrome Foundation
We need your help! August is Stevens-Johnson Syndrome Awareness month. Won’t you please help us spread awareness by writing your governor requesting a pro…
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http://sjsupport.org/?cat=4 — found via Mwmbl
Children – Stevens-Johnson Syndrome Foundation
We need your help! August is Stevens-Johnson Syndrome Awareness month. Won’t you please help us spread awareness by writing your governor requesting a pr…
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http://fmsfonline.org/ — found via Mwmbl
False Memory Syndrome Foundation
Welcome To MEMORY AND REALITY Website of the False Memory Syndrome Foundation Some of our memories are true, some are a mixture of fact and fantasy, and …
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http://www.angelman.org/ — found via Mwmbl
Angelman Syndrome Foundation – With you for the journey
“At the ASF Clinic, Emily benefitted from an entirely different level of knowledge and professionalism. She saw a team of doctors, therapists and other sp…
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https://www.loeysdietz.org/ — found via Mwmbl
Loeys-Dietz Syndrome Foundation
Loeys-Dietz Syndrome Foundation Healing Hearts. Inspiring Hope. Our purpose is to provide information about what Loeys-Dietz syndrome (LDS) is and to pro…
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http://www.loeysdietz.org/ask — found via Mwmbl
Help Center — Loeys-Dietz Syndrome Foundation
Have a question? We can help. The registered nurse in our help center answers your questions Monday-Friday 9:00 AM to 5:00 PM Eastern Time. We will respo…
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http://www.bardetbiedl.org — found via Mwmbl
Bardet Biedl Syndrome Foundation
The Bardet Biedl Syndrome Foundation and Family Association is dedicated to improving the lives of individuals and families affected by BBS. Our mission …
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http://www.rls.org — found via Mwmbl
Home - Restless Legs Syndrome Foundation
“I started dreading every day because I knew that by evening I would have this burning sensation in my legs that just wouldn’t quit. I couldn’t sleep. Fo…
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http://www.rls.org/login — found via Mwmbl
Login - Restless Legs Syndrome Foundation
Connect With Us Get Updates Restless Legs Syndrome Foundation is a registered 501(c)(3) non-profit corporation (Tax ID #56-1784846). Donations are tax-de…
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https://www.rls.org/about-us/board — found via Mwmbl
Board - Restless Legs Syndrome Foundation
Board RLS Foundation Board of Directors The Restless Legs Syndrome (RLS) Foundation Board of Directors is responsible for setting organizational goals an…
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https://www.rls.org/treatment — found via Mwmbl
Treatment - Restless Legs Syndrome Foundation
Treatment There is currently no cure for RLS, but many treatment options are available to help manage symptoms. Your doctor can help you explore ways to …
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https://www.rls.org/about-us/staff — found via Mwmbl
Staff - Restless Legs Syndrome Foundation
Staff Meet the team Karla Dzienkowski, RN, BSN Executive Director In January 2014, Karla accepted the position of executive director. Since then she has …
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http://barthsyndrome.org — found via Mwmbl
Home : Barth Syndrome Foundation
The only organization dedicated to saving lives around the world through education, advances in treatments, and finding a cure for Barth syndrome: a life…
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https://mowat-wilson.org/ — found via Mwmbl
Mowat-Wilson Syndrome Foundation | Official Website
FACES OF MOWAT-WILSON SYNDROME Thank you to all the families that have shared the photos of their loved ones. CONNECT WITH THE MOWAT-WILSON SYNDROME FOUN…
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https://www.edsrf.org/ — found via Mwmbl
Home - Ehlers-Danlos Syndrome Research Foundation
Ehlers-Danlos Syndrome Research Foundation What is Ehlers-Danlos Syndrome? People with EDS suffer from a range of systemic problems, including widespread…
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http://www.rtsplace.org/ — found via Mwmbl
Rothmund-Thomson Syndrome Foundation
Rothmund-Thomson Syndrome (RTS) is a rare genetic disorder that can affect people of all races and nationalities. Symptoms often first appear during infan…
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http://ptlsfoundation.org/ — found via Mwmbl
Potocki-Lupski Syndrome Foundation – The genetic key to a life f…
“Our mission is to increase public awareness, understanding and acceptance of Potocki-Lupski Syndrome (PTLS or Dup. 17p11.2) by providing information to f…
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https://rls.org.statvoo.com — found via Mwmbl
Home - Restless Legs Syndrome Foundation Restless Legs Syndrom…
rls.org has global traffic rank of 249,280. rls.org has an estimated worth of US$ 28,081, based on its estimated Ads revenue. rls.org receives approximat…
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https://jotup.co/node/550404 — found via Mwmbl
Pri-Med and Sjögren's Syndrome Foundation Partner to Develop Aut…
BOSTON, Nov. 12, 2019 /PRNewswire/ -- Pri-Med, a leader in continuing medical education, is pleased to announce a new partnership with the Sjögren's Synd…
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http://www.shwachman-diamond.org/ — found via Mwmbl
Shwachman-Diamond Syndrome Foundation
Order SDSF Swag or Order One-of-A-Kind SDS Awareness Items What is Shwachman-Diamond Syndrome? Shwachman Diamond Syndrome Foundation About Us Shwachman D…
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https://clsf.info/ — found via Mwmbl
Home
Coffin-Lowry Syndrome Foundation Support for families affected by Coffin-Lowry Syndrome Welcome! The purpose of CLSF is to provide a clearinghouse for in…
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http://whale.to/b/west_q.html — found via Mwmbl
Dr. Louis Joyon "Jolly" West
False Memory Syndrome Foundation Shortly after he had entered University of Wisconsin, he enlisted in the U.S. Army. In the Army Specialized Training Pro…
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https://pubmed.ncbi.nlm.nih.gov/38737515/ — found via Mwmbl
Feeding Difficulties and Gastrostomy in Dravet Syndrome: A UK-Wi…
Abstract Background and objectives: Dravet syndrome (DS) is one of the most common monogenic epilepsies. Alongside the core seizure and developmental phe…
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https://dravetsyndromenews.com/ — found via Mwmbl
Dravet Syndrome News Home | Dravet Syndrome News
The National Institute of Drug and Food Surveillance (INVIMA) of Colombia has approved Trunerox as an add-on treatment for seizures in people with Dravet …
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http://hal.inria.fr/UP-SANTE/hal-04581736v1 — found via Mwmbl
Placebo response in patients with Dravet syndrome: Post-hoc anal…
Résumé Objective Dravet syndrome is a rare, early childhood-onset epileptic and developmental encephalopathy. Responses to placebo in clinical trials for…
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https://doi.org/10.7554/eLife.43387 — found via Mwmbl
Disordered breathing in a mouse model of Dravet syndrome | eLife
Abstract Dravet syndrome (DS) is a form of epilepsy with a high incidence of sudden unexpected death in epilepsy (SUDEP). Respiratory failure is a leadin…
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https://doi.org/10.15221/17.163 — found via Mwmbl
3DBODY.TECH Conference - Proceedings and Catalog of Abstracts an…
Dravet syndrome (DS) is a rare and severe form of epilepsy, associated with mutations of SCN1A gene, encoding for the sodium channel voltage-dependent Na…
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https://doi.org/10.1172/JCI159316 — found via Mwmbl
JCI - Viral vector–mediated expression of NaV1.1, after seizure …
Dravet syndrome (DS) is a rare and severe form of developmental epileptic encephalopathy. Infants with DS appear to develop normally during the first 6 mo…
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https://doi.org/10.1172/jci159316 — found via Mwmbl
JCI - Viral vector–mediated expression of NaV1.1, after seizure …
Dravet syndrome (DS), an intractable childhood epileptic encephalopathy with a high fatality rate, is typically caused by loss-of-function mutations in o…
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https://doi.org/10.1089/hum.2022.037 — found via Mwmbl
Cell-Selective Adeno-Associated Virus-Mediated SCN1A Gene Regula…
Abstract Dravet syndrome (DS) is a developmental and epileptic encephalopathy caused by monoallelic loss-of-function variants in the SCN1A gene. SCN1A en…
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http://dravet.org.uk/about-us/ — found via Mwmbl
About Us - Dravet Syndrome UK
About Us Dravet Syndrome UK was created in 2009 by a group of parents who came together looking for support, resources and information relating to a rare…
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http://dravet.org.uk/contact/ — found via Mwmbl
Contact - Dravet Syndrome UK
Contact Send us a message Get in touch Alternatively, you can contact the charity through our registered address: Dravet Syndrome UK PO Box 756 Chesterfi…
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http://dravet.org.uk/Research/ — found via Mwmbl
Our Research - Dravet Syndrome UK
Our Research Funding research is an essential part of our mission to bring hope to families living with Dravet Syndrome and improve their lives. Although…
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http://dravet.org.uk/families/ — found via Mwmbl
For Families - Dravet Syndrome UK
For Families Welcome to the area of our website that is dedicated to families. Here you can find useful information and get practical support in navigati…
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https://scite.ai/reports/23622210 — found via Mwmbl
Dravet syndrome (severe myoclonic epilepsy in infancy) - [scite …
Objective: To delineate the phenotype of early childhood epileptic encephalopathy due to de novo mutations of CHD2, which encodes the chromodomain helica…
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https://scite.ai/authors/han-zhou-VKWw3O — found via Mwmbl
Han Zhou scite author profile
Dravet syndrome (DS) is an intractable developmental and epileptic encephalopathy caused largely by de novo variants in the SCN1A gene, resulting in hapl…
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http://www.ncbi.nlm.nih.gov/pubmed/32848094 — found via Mwmbl
Antisense oligonucleotides increase Scn1a expression and reduce …
Abstract Dravet syndrome (DS) is an intractable developmental and epileptic encephalopathy caused largely by de novo variants in the SCN1A gene, resultin…
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http://www.ncbi.nlm.nih.gov/pubmed/21844054 — found via Mwmbl
Alleged cases of vaccine encephalopathy rediagnosed years later …
Abstract Dravet syndrome is a rare epileptic encephalopathy linked to mutations in SCN1A (neuronal sodium channel α1 subunit) and characterized by an ons…
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http://www.ncbi.nlm.nih.gov/pubmed/28538134 — found via Mwmbl
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet S…
Abstract Background: The Dravet syndrome is a complex childhood epilepsy disorder that is associated with drug-resistant seizures and a high mortality ra…
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https://www.sciencegate.app/keyword/99753 — found via Mwmbl
dravet syndrome Latest Research Papers | ScienceGate
Dravet Syndrome is a severe, drug-resistant, and rare epileptiform disorder that is typically presented in the first year of life in an otherwise healthy …
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https://www.sciencegate.app/keyword/59791 — found via Mwmbl
oral solution Latest Research Papers | ScienceGate
Dravet Syndrome is a severe, drug-resistant, and rare epileptiform disorder that is typically presented in the first year of life in an otherwise healthy…
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https://www.sciencegate.app/keyword/75773 — found via Mwmbl
behavioral phenotype Latest Research Papers | ScienceGate
Abstract Background Dravet Syndrome is a severe childhood pharmaco-resistant epileptic disorder mainly caused by mutations in the SCN1A gene, which encod…
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https://wikipedia.org/wiki/Dravet_syndrome — found via Mwmbl
Dravet syndrome - Wikipedia
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomaldominantgenetic disorder which causes a catastrophi…
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https://radiopaedia.org/articles/30521 — found via Mwmbl
Dravet syndrome | Radiology Reference Article | Radiopaedia.org
On this page: Clinical presentation The typical presentation occurs during the first six months to one year of life as tonic-clonic seizures (including s…
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https://norml.org/blog/tag/dravet-syndrome/ — found via Mwmbl
Dravet syndrome Archives - NORML
The administration of oral cannabis extracts is associated with the mitigation of seizures in adolescents with epilepsy, according to clinical data publi…
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http://www.kegg.jp/entry/H01818 — found via Mwmbl
KEGG DISEASE: Dravet syndrome
The Dravet syndrome is a rare form of epileptic encephalopathy, and is accompanied by impaired psychomotor and neurologic development, occurring in the f…
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http://www.kegg.jp/entry/ds_ja:H01818 — found via Mwmbl
KEGG DISEASE: ドラベ症候群
The Dravet syndrome is a rare form of epileptic encephalopathy, and is accompanied by impaired psychomotor and neurologic development, occurring in the f…
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https://www.medscape.com/viewarticle/880634 — found via Mwmbl
Cannabidiol Cuts Seizures in Dravet Syndrome
Cannabidiol Cuts Seizures in Dravet Syndrome The purified oral formulation of cannabidiol (CBD; Epidiolex, GW Pharmaceuticals) reduced seizure frequency …
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https://www.medscape.com/viewarticle/721291 — found via Mwmbl
Pertussis Vaccination Triggers Dravet Syndrome in Predisposed Ch…
May 5, 2010 — Pertussis vaccination may trigger an earlier onset of Dravet syndrome in children who are destined to develop the disease because they poss…
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http://www.drugbank.ca/articles/A155017 — found via Mwmbl
Sporadic infantile epileptic encephalopathy caused by mutations …
Dravet syndrome (DS) is a genetically determined epileptic encephalopathy mainly caused by de novo mutations in the SCN1A gene. Since 2003, we have perfo…
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http://www.pubmed.gov/30104343/ — found via Mwmbl
A Transient Developmental Window of Fast-Spiking Interneuron Dys…
Abstract Dravet syndrome is a severe, childhood-onset epilepsy largely due to heterozygous loss-of-function mutation of the gene SCN1A, which encodes the…
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http://www.pubmed.gov/34759881/ — found via Mwmbl
Treatment Guidelines for Rare, Early-Onset, Treatment-Resistant …
Abstract Background: Dravet syndrome (DS), Lennox-Gastaut syndrome (LGS) and CDKL5 deficiency disorder (CDD) are rare epileptic conditions, characterised…
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http://hdl.handle.net/2445/187140 — found via Mwmbl
Dipòsit Digital de la Universitat de Barcelona: The contribution…
Introduction: Dravet Syndrome (DS) is a severe, developmental epileptic encephalopathy (DEE) that begins in infancy and is characterized by pharmaco-resi…
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http://www.jneurosci.org/content/41/3/524 — found via Mwmbl
Impaired θ-γ Coupling Indicates Inhibitory Dysfunction and Seizu…
Abstract Dravet syndrome (DS) is an epileptic encephalopathy that still lacks biomarkers for epileptogenesis and its treatment. Dysfunction of NaV1.1 sod…
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https://centaur.reading.ac.uk/88389/ — found via Mwmbl
Cannabidiol (CBD) improves survival and behavioural comorbiditie…
Abstract/Summary Background and Purpose Dravet syndrome is a severe, genetic form of paediatric epilepsy associated with premature mortality and comorbid…
New results
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https://en.wikipedia.org/wiki/Dravet_Syndrome_Foundation — found via Wikipedia
Dravet Syndrome Foundation
The Dravet Syndrome Foundation (DSF) is a volunteer-run, non-profit organization based in the United States. The mission of the foundation is to raise
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https://en.wikipedia.org/wiki/Dravet_syndrome — found via Wikipedia
Dravet syndrome
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic
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https://en.wikipedia.org/wiki/Charlotte_Dravet — found via Wikipedia
Charlotte Dravet
received the Dravet Award from the Dravet Syndrome Foundation Spain for her contribution to the knowledge and research of Dravet syndrome. In 2011 she
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https://en.wikipedia.org/wiki/Lennox–Gastaut_syndrome — found via Wikipedia
Lennox–Gastaut syndrome
Doose syndrome Dravet syndrome pseudo-Lennox–Gastaut syndrome (atypical benign partial epilepsy) LGS is more easily distinguished from Doose syndrome by
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https://en.wikipedia.org/wiki/Generalized_epilepsy_with_febrile_seizures_plus — found via Wikipedia
Generalized epilepsy with febrile seizures plus
severe myoclonic epilepsy of infancy (SMEI), which is also known as Dravet's syndrome, borderline SMEI (SMEB), and intractable epilepsy of childhood (IEC)
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https://dravetfoundation.org/ — found via Mwmbl
Home - Dravet Syndrome Foundation
What is Dravet Syndrome? Dravet syndrome, also known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare form of intractable epilepsy that begins i…
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http://www.dsfoc.org/ — found via Mwmbl
Down Syndrome Foundation of Orange County
Reflecting on a year of milestones and growth! Thanks to your support, we’ve empowered hundreds through our Learning Programs and Social Boundaries Serie…
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https://www.dsfoc.org/blog/ — found via Mwmbl
Blog – Down Syndrome Foundation of Orange County
Resources Offline Ordering Reflecting on a year of milestones and growth! Thanks to your support, we’ve empowered hundreds through our Learning Programs …
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http://www.dsfoc.org/store/ — found via Mwmbl
Store – Down Syndrome Foundation of Orange County
Touch and WriteFIZZBRAIN LLC*LP Favorite* Kids love learning to write - especially when they can use shaving cream, paint, and jello! Developed by teache…
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https://www.dsfoc.org/our-team/ — found via Mwmbl
Our Team – Down Syndrome Foundation of Orange County
Who Are We Board Members and Officers William E. Halle Co-Founder/President, Down Syndrome Foundation of Orange County (2001 to present) Partner, O'Neil …
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https://www.dsfoc.org/families/ — found via Mwmbl
Families – Down Syndrome Foundation of Orange County
Family Resources From face-to-face educational opportunities to online courses, DSF provides a variety of services to help your learner succeed. Online C…
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https://www.dsfoc.org/educators/ — found via Mwmbl
Educators – Down Syndrome Foundation of Orange County
Educator Resources From online courses to free printable resources, DSF provides a variety of services to help educators support learners with Down syndr…
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https://www.dsfoc.org/lp-archive/ — found via Mwmbl
LP Archive – Down Syndrome Foundation of Orange County
LP Archive We have many more resources, including professionally-printed materials, number lines, online courses, and more available in our Online Store.…
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http://www.dsfoc.org/partnership/ — found via Mwmbl
Partner Organizations – Down Syndrome Foundation of Orange County
Partner with DSF DSF partners with other Down syndrome groups to help build educational programming to support families and educators. Frequently Asked Q…
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http://sjsupport.org — found via Mwmbl
Stevens-Johnson Syndrome Foundation – Educate before you medicate
Welcome The Stevens-Johnson Syndrome Foundation is a non-profit organization founded in 1996. The purpose of the foundation is to provide the public and …
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http://sjsupport.org/?cat=6 — found via Mwmbl
Education – Stevens-Johnson Syndrome Foundation
The Stevens – Johnson Syndrome Foundation is working with researchers to find causes, better treatment plans and genetic markers. We need your help. Plea…
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http://sjsupport.org/?cat=65 — found via Mwmbl
SJS/TEN – Stevens-Johnson Syndrome Foundation
The Stevens – Johnson Syndrome Foundation is working with researchers to find causes, better treatment plans and genetic markers. We need your help. Plea…
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http://sjsupport.org/?cat=11 — found via Mwmbl
Health – Stevens-Johnson Syndrome Foundation
Health The Stevens – Johnson Syndrome Foundation is working with researchers to find causes, better treatment plans and genetic markers. We need your hel…
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http://sjsupport.org/?cat=3 — found via Mwmbl
Blog – Stevens-Johnson Syndrome Foundation
Blog August is SJS Awareness Month! Please join us and pass the ribbon for SJS Awareness Pass the ribbon for Stevens Johnson Syndrome Awareness! Please p…
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http://sjsupport.org/?cat=9 — found via Mwmbl
Events – Stevens-Johnson Syndrome Foundation
August is SJS Awareness Month! Please join us and pass the ribbon for SJS Awareness Pass the ribbon for Stevens Johnson Syndrome Awareness! Please print …
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http://sjsupport.org/?cat=7 — found via Mwmbl
Elderly – Stevens-Johnson Syndrome Foundation
Elderly We need your help! August is Stevens-Johnson Syndrome Awareness month. Won’t you please help us spread awareness by writing your governor request…
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http://sjsupport.org/?cat=12 — found via Mwmbl
Miscellaneous – Stevens-Johnson Syndrome Foundation
Miscellaneous Here’s how you can help the Stevens – Johnson Syndrome Foundation every time you shop on line through Amazon smiles campaign. It’s so easy …
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http://sjsupport.org/?cat=5 — found via Mwmbl
Disabled – Stevens-Johnson Syndrome Foundation
We need your help! August is Stevens-Johnson Syndrome Awareness month. Won’t you please help us spread awareness by writing your governor requesting a pro…
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http://sjsupport.org/?cat=4 — found via Mwmbl
Children – Stevens-Johnson Syndrome Foundation
We need your help! August is Stevens-Johnson Syndrome Awareness month. Won’t you please help us spread awareness by writing your governor requesting a pr…
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http://fmsfonline.org/ — found via Mwmbl
False Memory Syndrome Foundation
Welcome To MEMORY AND REALITY Website of the False Memory Syndrome Foundation Some of our memories are true, some are a mixture of fact and fantasy, and …
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http://www.angelman.org/ — found via Mwmbl
Angelman Syndrome Foundation – With you for the journey
“At the ASF Clinic, Emily benefitted from an entirely different level of knowledge and professionalism. She saw a team of doctors, therapists and other sp…
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https://www.loeysdietz.org/ — found via Mwmbl
Loeys-Dietz Syndrome Foundation
Loeys-Dietz Syndrome Foundation Healing Hearts. Inspiring Hope. Our purpose is to provide information about what Loeys-Dietz syndrome (LDS) is and to pro…
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http://www.loeysdietz.org/ask — found via Mwmbl
Help Center — Loeys-Dietz Syndrome Foundation
Have a question? We can help. The registered nurse in our help center answers your questions Monday-Friday 9:00 AM to 5:00 PM Eastern Time. We will respo…
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http://www.bardetbiedl.org — found via Mwmbl
Bardet Biedl Syndrome Foundation
The Bardet Biedl Syndrome Foundation and Family Association is dedicated to improving the lives of individuals and families affected by BBS. Our mission …
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http://www.rls.org — found via Mwmbl
Home - Restless Legs Syndrome Foundation
“I started dreading every day because I knew that by evening I would have this burning sensation in my legs that just wouldn’t quit. I couldn’t sleep. Fo…
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http://www.rls.org/login — found via Mwmbl
Login - Restless Legs Syndrome Foundation
Connect With Us Get Updates Restless Legs Syndrome Foundation is a registered 501(c)(3) non-profit corporation (Tax ID #56-1784846). Donations are tax-de…
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https://www.rls.org/about-us/board — found via Mwmbl
Board - Restless Legs Syndrome Foundation
Board RLS Foundation Board of Directors The Restless Legs Syndrome (RLS) Foundation Board of Directors is responsible for setting organizational goals an…
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https://www.rls.org/treatment — found via Mwmbl
Treatment - Restless Legs Syndrome Foundation
Treatment There is currently no cure for RLS, but many treatment options are available to help manage symptoms. Your doctor can help you explore ways to …
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https://www.rls.org/about-us/staff — found via Mwmbl
Staff - Restless Legs Syndrome Foundation
Staff Meet the team Karla Dzienkowski, RN, BSN Executive Director In January 2014, Karla accepted the position of executive director. Since then she has …
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http://barthsyndrome.org — found via Mwmbl
Home : Barth Syndrome Foundation
The only organization dedicated to saving lives around the world through education, advances in treatments, and finding a cure for Barth syndrome: a life…
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https://mowat-wilson.org/ — found via Mwmbl
Mowat-Wilson Syndrome Foundation | Official Website
FACES OF MOWAT-WILSON SYNDROME Thank you to all the families that have shared the photos of their loved ones. CONNECT WITH THE MOWAT-WILSON SYNDROME FOUN…
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https://www.edsrf.org/ — found via Mwmbl
Home - Ehlers-Danlos Syndrome Research Foundation
Ehlers-Danlos Syndrome Research Foundation What is Ehlers-Danlos Syndrome? People with EDS suffer from a range of systemic problems, including widespread…
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http://www.rtsplace.org/ — found via Mwmbl
Rothmund-Thomson Syndrome Foundation
Rothmund-Thomson Syndrome (RTS) is a rare genetic disorder that can affect people of all races and nationalities. Symptoms often first appear during infan…
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http://ptlsfoundation.org/ — found via Mwmbl
Potocki-Lupski Syndrome Foundation – The genetic key to a life f…
“Our mission is to increase public awareness, understanding and acceptance of Potocki-Lupski Syndrome (PTLS or Dup. 17p11.2) by providing information to f…
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https://rls.org.statvoo.com — found via Mwmbl
Home - Restless Legs Syndrome Foundation Restless Legs Syndrom…
rls.org has global traffic rank of 249,280. rls.org has an estimated worth of US$ 28,081, based on its estimated Ads revenue. rls.org receives approximat…
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https://jotup.co/node/550404 — found via Mwmbl
Pri-Med and Sjögren's Syndrome Foundation Partner to Develop Aut…
BOSTON, Nov. 12, 2019 /PRNewswire/ -- Pri-Med, a leader in continuing medical education, is pleased to announce a new partnership with the Sjögren's Synd…
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http://www.shwachman-diamond.org/ — found via Mwmbl
Shwachman-Diamond Syndrome Foundation
Order SDSF Swag or Order One-of-A-Kind SDS Awareness Items What is Shwachman-Diamond Syndrome? Shwachman Diamond Syndrome Foundation About Us Shwachman D…
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https://clsf.info/ — found via Mwmbl
Home
Coffin-Lowry Syndrome Foundation Support for families affected by Coffin-Lowry Syndrome Welcome! The purpose of CLSF is to provide a clearinghouse for in…
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http://whale.to/b/west_q.html — found via Mwmbl
Dr. Louis Joyon "Jolly" West
False Memory Syndrome Foundation Shortly after he had entered University of Wisconsin, he enlisted in the U.S. Army. In the Army Specialized Training Pro…
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https://pubmed.ncbi.nlm.nih.gov/38737515/ — found via Mwmbl
Feeding Difficulties and Gastrostomy in Dravet Syndrome: A UK-Wi…
Abstract Background and objectives: Dravet syndrome (DS) is one of the most common monogenic epilepsies. Alongside the core seizure and developmental phe…
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https://dravetsyndromenews.com/ — found via Mwmbl
Dravet Syndrome News Home | Dravet Syndrome News
The National Institute of Drug and Food Surveillance (INVIMA) of Colombia has approved Trunerox as an add-on treatment for seizures in people with Dravet …
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http://hal.inria.fr/UP-SANTE/hal-04581736v1 — found via Mwmbl
Placebo response in patients with Dravet syndrome: Post-hoc anal…
Résumé Objective Dravet syndrome is a rare, early childhood-onset epileptic and developmental encephalopathy. Responses to placebo in clinical trials for…
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https://doi.org/10.7554/eLife.43387 — found via Mwmbl
Disordered breathing in a mouse model of Dravet syndrome | eLife
Abstract Dravet syndrome (DS) is a form of epilepsy with a high incidence of sudden unexpected death in epilepsy (SUDEP). Respiratory failure is a leadin…
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https://doi.org/10.15221/17.163 — found via Mwmbl
3DBODY.TECH Conference - Proceedings and Catalog of Abstracts an…
Dravet syndrome (DS) is a rare and severe form of epilepsy, associated with mutations of SCN1A gene, encoding for the sodium channel voltage-dependent Na…
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https://doi.org/10.1172/JCI159316 — found via Mwmbl
JCI - Viral vector–mediated expression of NaV1.1, after seizure …
Dravet syndrome (DS) is a rare and severe form of developmental epileptic encephalopathy. Infants with DS appear to develop normally during the first 6 mo…
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https://doi.org/10.1172/jci159316 — found via Mwmbl
JCI - Viral vector–mediated expression of NaV1.1, after seizure …
Dravet syndrome (DS), an intractable childhood epileptic encephalopathy with a high fatality rate, is typically caused by loss-of-function mutations in o…
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https://doi.org/10.1089/hum.2022.037 — found via Mwmbl
Cell-Selective Adeno-Associated Virus-Mediated SCN1A Gene Regula…
Abstract Dravet syndrome (DS) is a developmental and epileptic encephalopathy caused by monoallelic loss-of-function variants in the SCN1A gene. SCN1A en…
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http://dravet.org.uk/about-us/ — found via Mwmbl
About Us - Dravet Syndrome UK
About Us Dravet Syndrome UK was created in 2009 by a group of parents who came together looking for support, resources and information relating to a rare…
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http://dravet.org.uk/contact/ — found via Mwmbl
Contact - Dravet Syndrome UK
Contact Send us a message Get in touch Alternatively, you can contact the charity through our registered address: Dravet Syndrome UK PO Box 756 Chesterfi…
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http://dravet.org.uk/Research/ — found via Mwmbl
Our Research - Dravet Syndrome UK
Our Research Funding research is an essential part of our mission to bring hope to families living with Dravet Syndrome and improve their lives. Although…
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http://dravet.org.uk/families/ — found via Mwmbl
For Families - Dravet Syndrome UK
For Families Welcome to the area of our website that is dedicated to families. Here you can find useful information and get practical support in navigati…
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https://scite.ai/reports/23622210 — found via Mwmbl
Dravet syndrome (severe myoclonic epilepsy in infancy) - [scite …
Objective: To delineate the phenotype of early childhood epileptic encephalopathy due to de novo mutations of CHD2, which encodes the chromodomain helica…
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https://scite.ai/authors/han-zhou-VKWw3O — found via Mwmbl
Han Zhou scite author profile
Dravet syndrome (DS) is an intractable developmental and epileptic encephalopathy caused largely by de novo variants in the SCN1A gene, resulting in hapl…
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http://www.ncbi.nlm.nih.gov/pubmed/32848094 — found via Mwmbl
Antisense oligonucleotides increase Scn1a expression and reduce …
Abstract Dravet syndrome (DS) is an intractable developmental and epileptic encephalopathy caused largely by de novo variants in the SCN1A gene, resultin…
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http://www.ncbi.nlm.nih.gov/pubmed/21844054 — found via Mwmbl
Alleged cases of vaccine encephalopathy rediagnosed years later …
Abstract Dravet syndrome is a rare epileptic encephalopathy linked to mutations in SCN1A (neuronal sodium channel α1 subunit) and characterized by an ons…
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http://www.ncbi.nlm.nih.gov/pubmed/28538134 — found via Mwmbl
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet S…
Abstract Background: The Dravet syndrome is a complex childhood epilepsy disorder that is associated with drug-resistant seizures and a high mortality ra…
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https://www.sciencegate.app/keyword/99753 — found via Mwmbl
dravet syndrome Latest Research Papers | ScienceGate
Dravet Syndrome is a severe, drug-resistant, and rare epileptiform disorder that is typically presented in the first year of life in an otherwise healthy …
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https://www.sciencegate.app/keyword/59791 — found via Mwmbl
oral solution Latest Research Papers | ScienceGate
Dravet Syndrome is a severe, drug-resistant, and rare epileptiform disorder that is typically presented in the first year of life in an otherwise healthy…
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https://www.sciencegate.app/keyword/75773 — found via Mwmbl
behavioral phenotype Latest Research Papers | ScienceGate
Abstract Background Dravet Syndrome is a severe childhood pharmaco-resistant epileptic disorder mainly caused by mutations in the SCN1A gene, which encod…
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https://wikipedia.org/wiki/Dravet_syndrome — found via Mwmbl
Dravet syndrome - Wikipedia
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomaldominantgenetic disorder which causes a catastrophi…
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https://radiopaedia.org/articles/30521 — found via Mwmbl
Dravet syndrome | Radiology Reference Article | Radiopaedia.org
On this page: Clinical presentation The typical presentation occurs during the first six months to one year of life as tonic-clonic seizures (including s…
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https://norml.org/blog/tag/dravet-syndrome/ — found via Mwmbl
Dravet syndrome Archives - NORML
The administration of oral cannabis extracts is associated with the mitigation of seizures in adolescents with epilepsy, according to clinical data publi…
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http://www.kegg.jp/entry/H01818 — found via Mwmbl
KEGG DISEASE: Dravet syndrome
The Dravet syndrome is a rare form of epileptic encephalopathy, and is accompanied by impaired psychomotor and neurologic development, occurring in the f…
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http://www.kegg.jp/entry/ds_ja:H01818 — found via Mwmbl
KEGG DISEASE: ドラベ症候群
The Dravet syndrome is a rare form of epileptic encephalopathy, and is accompanied by impaired psychomotor and neurologic development, occurring in the f…
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https://www.medscape.com/viewarticle/880634 — found via Mwmbl
Cannabidiol Cuts Seizures in Dravet Syndrome
Cannabidiol Cuts Seizures in Dravet Syndrome The purified oral formulation of cannabidiol (CBD; Epidiolex, GW Pharmaceuticals) reduced seizure frequency …
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https://www.medscape.com/viewarticle/721291 — found via Mwmbl
Pertussis Vaccination Triggers Dravet Syndrome in Predisposed Ch…
May 5, 2010 — Pertussis vaccination may trigger an earlier onset of Dravet syndrome in children who are destined to develop the disease because they poss…
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http://www.drugbank.ca/articles/A155017 — found via Mwmbl
Sporadic infantile epileptic encephalopathy caused by mutations …
Dravet syndrome (DS) is a genetically determined epileptic encephalopathy mainly caused by de novo mutations in the SCN1A gene. Since 2003, we have perfo…
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http://www.pubmed.gov/30104343/ — found via Mwmbl
A Transient Developmental Window of Fast-Spiking Interneuron Dys…
Abstract Dravet syndrome is a severe, childhood-onset epilepsy largely due to heterozygous loss-of-function mutation of the gene SCN1A, which encodes the…
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http://www.pubmed.gov/34759881/ — found via Mwmbl
Treatment Guidelines for Rare, Early-Onset, Treatment-Resistant …
Abstract Background: Dravet syndrome (DS), Lennox-Gastaut syndrome (LGS) and CDKL5 deficiency disorder (CDD) are rare epileptic conditions, characterised…
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http://hdl.handle.net/2445/187140 — found via Mwmbl
Dipòsit Digital de la Universitat de Barcelona: The contribution…
Introduction: Dravet Syndrome (DS) is a severe, developmental epileptic encephalopathy (DEE) that begins in infancy and is characterized by pharmaco-resi…
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http://www.jneurosci.org/content/41/3/524 — found via Mwmbl
Impaired θ-γ Coupling Indicates Inhibitory Dysfunction and Seizu…
Abstract Dravet syndrome (DS) is an epileptic encephalopathy that still lacks biomarkers for epileptogenesis and its treatment. Dysfunction of NaV1.1 sod…
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https://centaur.reading.ac.uk/88389/ — found via Mwmbl
Cannabidiol (CBD) improves survival and behavioural comorbiditie…
Abstract/Summary Background and Purpose Dravet syndrome is a severe, genetic form of paediatric epilepsy associated with premature mortality and comorbid…