SYNGAP1 Foundation
@syngap1fnd
SYNGAP1 Foundation is a legacy page dedicated to preserving the work and mission of our 100% charitable nonprofit in the USA, focused on #SYNGAP1
ID: 2954080201
http://www.syngap1foundation.org 31-12-2014 22:04:04
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SoulOTech
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I can only point you to water... The rest is up to you. Let's go.
Kristin Faulder
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Prof Ingrid Scheffer
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UHN Foundation
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Official foundation for @UHN Toronto General and Toronto Western hospitals, @TorontoRehab and @MichenerInst. Never been done is what we do.
Neurology Journal
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National Organization for Rare Disorders (NORD)
@rarediseases
National Organization for Rare Disorders (#NORD) is the voice of the U.S. #RareDisease community for 40+ years strong. Official U.S. sponsor of #RareDiseaseDay.
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Accessia Health
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McKesson Corporation
@mckesson
We're an impact-driven healthcare organization dedicated to “Advancing Health Outcomes For All.”
Ethan Perlstein bio/acc
@eperlste
ceo @PerlaraPBC (@ycombinator W16), ceo @epalrestat, ceo @endrarediseases, solo vc @AngelList, evo pharmacologist, mTOR worshipper, cofounder of K&L, $CURES
Stéphane Auvin
@stephane_auvin
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Ana Mingorance
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Dr Elin Haf Davies
@elinhafdavies
Founder / CSO @aparitohealth PhD, 1st Welsh woman to row across the Atlantic & Indian @acmedsci #FLIER #Cymraes 🏴 #ClinicalTrials
Emma Gordon
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American Epilepsy Society
@amepilepsysoc
We support research and education for professionals working towards a world without epilepsy. RTs ≠ endorsements. Also @amepilepsysoc.bsky.social.
Barbara Drake
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Stephanie Fischer
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#Raredisease patient advocate & #stroke survivor.🦓 Member of @PARareDisease. Opinions are my own.
Zack Williams, PhD
@quantpsychiatry
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International League Against Epilepsy
@ilaeweb
A preeminent association of healthcare professionals & scientists working toward a world where no person's life is limited by epilepsy. RTs are not endorsements
Baketashitanrou
@baketashitanrou
#pediatricneurologist #bioinformatics #iPSCs #RNAseq #Transcriptome #hypomyelination #raredisease #genetics #Englishlearner
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@aloktayi
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MGH Neurology
@mghneurology
On a mission to find new treatments and cures to eliminate the devastating impact of neurological disorders.
Tracy Dixon-Salazar
@tracydixonsalaz
Mom. Rare Disease & LGS Advocate. Neuroscientist. The largest most neglected healthcare resource, worldwide, is the patient. Executive Director @LGS_Foundation
Dennis Lal
@laldennis
Director of the Center for Neurogenetics; Associate Professor at UTH - Neurogenetics & Informatics - My opinions are my own & do not reflect my employer.
Institute of Medical Science
@uoftims
Advancing Health through Graduate Research @uoftmedicine
International SCN8A Alliance
@scn8aalliance
The International SCN8A Alliance is working collaboratively with families, clinicians and researchers to advance the understanding of and treatments for SCN8A.
FamilieSCN2A
@familiescn2a
Our vision is to find effective treatments and a cure for SCN2A disorders.
Hélène Le Borgne
@helenelborgne
European, bretonne. Public health & research at EU level, rare diseases, transplantation. Youth & Sports (RTs/follows ≠ endorsements, own views).
Torie Robinson 🇺🇦
@torierobinson10
@EpilepsySparks Insights Podcast Host & YouTuber 🧠🧬 | International Speaker | #Epilepsy & #MentalHealth Research fiend | @MaudsleyNHS Gvnr | All views my own
Child Neurology Society
@childneurosoc
Child Neurology Society's official twitter account for members. At the #CNS, every member counts because every child counts. Retweets ≠ endorsement.
Luke Rosen
@lukebrosen
Dad of two remarkable kids. Founder of KIF1A.org & Rescue7.org. Works with families affected by neurological diseases & cancer. Firefighter. Baseball & hockey.
Effie Parks
@onceuponagene
Rare Disease Advocate | Award Winning Podcaster | Speaker | Captain Connection | RareMama to my sweet, Ford, who lives with #CTNNB1 🦓
UCLA Tarjan Center
@ucla_tarjan
A University Center for Excellence in Disabilities Education, Research and Service. koji.to/k/8zjZ
Sandor Beniczky
@sbeniczky
Neurologist & clinical neurophysiologist, working mainly with #epilepsy & #EEG at the Danish Epilepsy Center and @AarhusUni. Editor-in-chief @EpiDisorders
Tika Tkemaladze
@tikatkemaladze
Clinical geneticist, Head of the Department of Molecular and Medical Genetics, at TSMU, passionate about rare and undiagnosed diseases
U of T Adult Neurology Residents
@uoftneurons
Interested medical students, please DM us!
Lizzienencinitas
@lizzienencinit1
Molecular diagnostics consultant. Lover of knowledge and growth. Views are my own.
EpiEpiNet - Epileptogenesis & Epilepsy Network
@epiepinet
We are an European Project to boost R&D in epilepsy and create a positive impact in patients, caregiving institutions and society in general.
CYSHCNet - Pediatric Health Systems Researchers
@cyshcnetwork
Our researchers & lived experience partners work to improve the health care system for children & youth with special health care needs and their families.
Rachel Marin de Carvalho
@rachel76151331
Neurologist | Epileptologist post-graduate student |
John George Bauer-Buis
@johngbauer_buis
JGBB (personal, private).
Abby Turnwald (she/her)
@pedsgcabby
Pediatric genetic counselor, neurogenetics, advocate for the rare disease community, let’s talk about sibling health
CEPCAL
@cepcal_latam
Colaborativa para Enfermedades Poco Frecuentes en el Caribe y América Latina (CEPCAL) is a regional initiative working towards improving the lives of patients
Kathleen
@kathleen46mcfar
rareparenting
@rareparenting
Mom-created resource for parents of children with #disabilities, #rarediseases and #specialneeds
David Anthony
@davidantho82777
eugeniaroza
@eugeniaroza1501
Raffaele Di Giacomo, PhD
@sciqst
Precise references in medicine. sciqst.com ByronInsight AG, Zurich, Switzerland
Rare-X
@rarex_2024
Rare-X 2024, Africa's leading conference on rare disease treatment and access, will be taking place at Indaba Hotel, Johannesburg from 14-17 February 2024
David Anthony
@davidantho72294
God first... Family.... Country music.... Sport... TV shows #TITANS #nahsville #GoPred
Amara Tris
@trisvany
Am blessed, loved, positive and highly favored
PagChapman
@mfca3bqko6kpe8
Major Gifts Ramp-Up
@majorgiftsramp
NONPROFITS WHO IMPLEMENT MAJOR GIFTS RAMP-UP fund programs from scratch that work and raise money!
Vineet 4B2B
@v4b2b
A Student of Collaborative Consumption Patterns in #Healthcare. Passionately inviting #Partnerships For Health ! ~40 years as student of Preventive healthcare!
Michael W. Young
@mwyoungrx
Life Sciences Strategist enabling people to live with better health, greater vision & more hope. Enjoy driving new ideas & old Alfa Romeos.
CLAE / LCCE
@clae_lcce
The Canadian League Against Epilepsy is an organization of advocates, medical & basic science professionals who aim to 📈the lives of those living with Epilepsy
Dr. Heather Mefford @hcmefford.bsky.social
@hcmefford
Physician, scientist, mom, wife #genetics #epilepsy #pediatrics #raredisease @StJude @StJudeResearch formerly @UWMedicine
Tracey Tracey
@traceytlc333
Mum who fights for her kids. ASD, Leukaemia, MYBPC3, BRCA2 Cardiomyopathy, Epileptic Encephalopathy, ESES, Graves’ disease +. Loves all Animals, especially Dogs
Heidi Grabenstatter
@patientintv
RDCA-DAP Scientific Director @CPathInstitute, patient advocate, neuroscientist, and proud mom. Opinions are my own.
Javier F Caceres
@javierfcaceres1
Head of Genome Regulation Section @mrc_hgu. Studying mechanisms of Gene expression and RNA biology. Co-Senior editor @RNAJournal
ClarityCo
@theclarityco
ClarityCo is a market insight and strategy group, disrupting the status quo of how companies derive and act upon customer insights.
Dr. Sher A. Khan
@sakmarwat79
As a Molecular biologist/Human geneticist I am always thinking that too many complexities are involved in the development of each creature.
Neuro Equilibrium
@neuroequilibri1
NeuroEquilibrium is India’s Largest & Most Advanced Chain of Vertigo Treatment Clinics.
Laura Louizos
@pspawareness
Advocate for Atypical Parkinsonism | Founder of Coleen Cunningham Foundation 🌿 | Author 📚 | Caregiver ❤️ | Sharing support and inspiration 💪
The Notorious EEG (M. Scott Perry MD)
@thenotoriouseeg
Epileptologist/Head of Neurosciences @cookchildrens, I 💜 #HailState, buffalo wings, art, music & foremost Becky & my daughters. Views are mine, not my employer
Brian Wallach
@bsw5020
Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease.
Dr. Kevin Smith
@kevinsmithuhn
President & CEO, University Health Network (@UHN). Professor, IHPME, Dept. of Medicine, Inst. of Medicine, RotmanSOM, University of Toronto