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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://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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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://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.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://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://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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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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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://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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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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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://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…