Welcome to Mwmbl! Feel free to submit a site to crawl. Please read the guidelines before editing results.

To contribute to the index you can get our Firefox Extension here. For recent crawling activity see stats.

＋ Add new ↺ Revert

• 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

  Dravet syndrome Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic

• 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…

• http://dravet.org.uk/ — found via Mwmbl

  Home | Dravet Syndrome UK | UK Dravet Charity - Dravet Syndrome …

  Shop - Dravet Syndrome UK
  Sign In - Dravet Syndrome UK
  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…
  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…
  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…
  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…
  Basket - Dravet Syndrome UK
  Sitemap - Dravet Syndrome UK
  Order details - Dravet Syndrome UK

• 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…

• 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…

• 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…

  Shop - Restless Legs Syndrome Foundation Restless Legs Syndrome Foundation is a registered 501(c)(3) non-profit corporation (Tax ID #56-1784846). Donations are tax-deductible as permissible by l…
  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…

• http://alportsyndrome.org/ — found via Mwmbl

  Alport Syndrome Foundation - Hope, Action, Support

• 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…

• 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 …

• https://www.leafly.com/news/tags/dravet-syndrome — found via Mwmbl

  Dravet Syndrome Archive | Leafly

  * Statements made on this website have not been evaluated by the U.S. Food and Drug Administration. These products are not intended to diagnose, treat, c…

• https://www.statnews.com/2024/12/12/stoke-therapeutics-dravet-syndrome-epilepsy/ — found via Mwmbl

  Why Stoke Therapeutics' Dravet syndrome drug is worth watching

  The company is hoping to set its treatment apart from existing therapies This story first appeared in Adam’s Biotech Scorecard, a subscriber-only newslet…

• https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE112627 — found via Mwmbl

  GEO Accession viewer

  Dravet syndrome is a severe, early-onset epileptic encephalopathy frequently resulting from de novo mutations of SCN1A. Mice with heterozygous deletion o…

  GSM3074539: 13: P24_129_WT; Mus musculus; RNA-Seq - SRA - NCBI Dravet syndrome is a severe, early-onset epileptic encephalopathy frequently resulting from de novo mutations of SCN1A. Mice with heterozygous deletion o…
  GSM3074537: 11: P24_129_KO; Mus musculus; RNA-Seq - SRA - NCBI Dravet syndrome is a severe, early-onset epileptic encephalopathy frequently resulting from de novo mutations of SCN1A. Mice with heterozygous deletion o…
  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…
  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…
  Fine Mapping and Candidate Gene Analysis of Dravet Syndrome Modi… Abstract Dravet syndrome is a developmental and epileptic encephalopathy (DEE) characterized by intractable seizures, comorbidities related to developmen…

• 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…

• https://wikipathways.org/pathways/WP5200.html — found via Mwmbl

  Dravet syndrome (WP5200) - Homo sapiens | WikiPathways

  Homo sapiens Share this pathway Dravet syndrome is a rare form of epilepsy. Between 70% and 80% of patients carry sodium channel α1 subunit gene (SCN1A) …

• http://pubmed.ncbi.nlm.nih.gov/39045432/ — found via Mwmbl

  Vagus nerve stimulation for the therapy of Dravet syndrome: a sy…

  Abstract Objective: Dravet syndrome (DS) is a refractory developmental and epileptic encephalopathy characterized by seizures, developmental delay and co…

  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…
  From genotype to phenotype in Dravet disease - PubMed Abstract Dravet syndrome combines clonic generalized, focal or unilateral seizures, beginning within the first year of life, often triggered by hyperther…

• https://www.thecut.com/amp/article/false-memory-syndrome-controversy.html — found via Mwmbl

  The Controversy Behind the False Memory Syndrome Foundation

  The last time Jennifer Freyd saw her parents was in December 1990. At 33, Jennifer was a tenured professor of psychology at the University of Oregon and …

• 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…

  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 …
  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…
  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…
  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 …
  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…
  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.…
  My account – Down Syndrome Foundation of Orange County
  Contact Us – Down Syndrome Foundation of Orange County

• 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…

• 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 …

  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 …
  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…
  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…
  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…
  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…
  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…
  Women – Stevens-Johnson Syndrome Foundation
  Gallery – Stevens-Johnson Syndrome Foundation
  Videos – Stevens-Johnson Syndrome Foundation
  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…
  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…
  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 …

• http://www.the-scientist.com/defending-against-dravet-71298 — found via Mwmbl

  Defending against Dravet | The Scientist

  Dravet Syndrome is a rare genetic form of childhood epilepsy that affects less than 1 in 10,000 people in the United States. But, for affected children, …

  Dravet Syndrome | The Scientist

• 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 …

• 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 …

• 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…

• 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…

• 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…

• https://teamnoonan.org/ — found via Mwmbl

  Noonan Syndrome Foundation

• 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…

• 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 …

• 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…

• 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…

• 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…

• 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…

  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…
  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…
  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…
  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…

• https://news.vumc.org/tag/dravet-syndrome/ — found via Mwmbl

  Dravet Syndrome | VUMC Reporter | Vanderbilt University

• https://vaxopedia.org/tag/dravet-syndrome/ — found via Mwmbl

  Dravet syndrome Archives - VAXOPEDIA

• 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…

• 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…

• 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…