FamilieSCN2A
@familiescn2a
Our vision is to find effective treatments and a cure for SCN2A disorders.
ID: 2878029249
http://www.scn2a.org 15-11-2014 14:06:33
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Philanthropy News Digest
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UT Physicians
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Prof Ingrid Scheffer
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Ethan Perlstein bio/acc
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Caitlin C. Clements
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Mike Graglia 🌻
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Beacon for Rare Diseases
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La Jolla Labs Inc.
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International League Against Epilepsy
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Scripps Research
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Alicia Ljungdahl
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Medical Student @bcmhouston | Assistant Specialist in the Sanders Lab @UCSFPsychiatry & @IdrmOxford | @UCBerkeley Alum
jennifer burke
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Jen Q Pan
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Bindley Bioscience Center
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Torie Robinson 🇺🇦
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Dad of two remarkable kids. Founder of KIF1A.org & Rescue7.org. Works with families affected by neurological diseases & cancer. Firefighter. Baseball & hockey.
Leah
@leahedscn2a
Founder, Executive Director and Former President of the FamilieSCN2A Foundation. Mom and rare disease advocate of epilepsy and autism, SCN2A-related disorders.
dazzle4rare
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Est. 2016 | Signal boost RARE with #dazzle4rare every Aug | #Signalise is our #podcast | Our 🔗 linktr.ee/dazzle4rare
Effie Parks
@onceuponagene
Rare Disease Advocate | Award Winning Podcaster | Speaker | Captain Connection | RareMama to my sweet, Ford, who lives with #CTNNB1 🦓
SynGAP Research Fund (SRF)
@curesyngap1
#SYNGAP1 🧬 = 🧠NDD DEE causing #Epilepsy #Autism #ID #Sleep #GI. Incidence = 6️⃣.1️⃣/💯k ICD10 syngap.fund/F78A1 syngap.fund/10 🎙
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Vivianna DeNittis
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TheRareFair
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Deanna Portero
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Dr. Lori L. Isom
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Jenny Downs
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Brain Ablaze
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CACNA1A Foundation
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Yasmin Salomón Otero
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UCI Epilepsy Research Center
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Oxford_IDRM
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Sarah Weckhuysen
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Farah Ladha
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Cure CLCN4
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AGE Program - Adult Genetic Epilespy
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Department of Paediatrics
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@UniofOxford, @OxfordMedSci, world leader in child health research, from early proof-of-concept fundamental science to clinical application.
Sarah Drislane
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Kristy Johnson
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Daniela Bezerra (Dra Dani)
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