Screen4Care
@screen4care
Accelerating Diagnosis for Rare Disease Patients Through Genetic Newborn Screening and Artificial Intelligence
ID: 1446116518182277249
https://screen4care.eu/ 07-10-2021 14:14:30
239 Tweet
337 Followers
124 Following
Ale Babetto
@babale84
Co-founder and owner of @puntoventi. Giornalista per @disabili_com, @OssMalattieRare e #DìSalute Chiedetemi di scrivere tutto tranne la mia biografia
Silvia Grünbaum
@silviagrunbaum
TIA-lo único relevante....
Rare Disease Day
@rarediseaseday
29 February 2024 is Rare Disease Day. Raising awareness for patients, families and carers around the world that are affected by rare diseases. #RareDiseaseDay
Unique
@unique_charity
Unique supports & informs anyone born w/a rare chromosome or gene disorder, their families & carers. Eurordis Patient Organisation Award winner. rarechromo.org
Siobhan F
@shivvyneato
EURORDIS-Rare Diseases Europe
@eurordis
An alliance of over 1,000 patient organisations working across borders and diseases to improve the lives of all people living with rare diseases.
PTC Therapeutics
@ptcbio
PTC is a patient-centered biopharmaceutical company focused on discovering, developing & commercializing medicine for patients with rare disease
uniamomalattierare
@uniamofimronlus
Con oltre 200 realtà federate, per una migliore qualità di vita e per la tutela dei diritti delle persone con #malattierare. Alleanza nazionale di @Eurordis.
EU Research Results
@cordis_eu
🇪🇺 News & information on #EUFunded #EUResearch projects @EU_Commission 👩🔬🔬👨🔬 | 🎧 Listen to our podcast #CORDIScovery 👉 spoti.fi/3ppKoLX
Dr. Anupoma Haque
@anupomahaque
Corporate training & learning dev, int. & ext. Communication, Health Service Design & Policy, Strategic leadership, HTA, Digital & Mental Health.
Centro CREER
@centrocreer
Centro de Referencia Estatal de Atención a Personas con Enfermedades Raras y sus Familias (CREER) del Imserso
Vanesa
@vanesa26_4
~ Amante de la fotografía ~ Narcolepsia Tipo 1~ Tec. Farmacia
Alström Syndrome UK
@as_uk
'Alström Syndrome is a rare genetic condition affecting every organ in the body. ASUK provides support & guidance for those affected.' Tweets by Catherine Lewis
TURPIN Jean-Marie
@jmarieturpin
Les opinions, commentaires et points de vue sont les miens et ne sont pas nécessairement partagés par mon employeur.
Marga Peralta
@mapeav75
Ingeniera informática un poco friki dando la lata para que se conozca el #ehlersdanlos. Colaborando con @ANSEDH.
franco cappai
@francocappai
Beacon for Rare Diseases
@rarebeacon
Beacon is a UK-based charity that is building a united rare disease community with patient groups at its heart. Previously known as Findacure.
Daniel Stobo
@stobocop91
Orphanet
@orphanet
The reference portal and knowledge base for information on rare diseases and orphan drugs. Orphanet nomenclature, ORPHA codes, Orphanet RD Ontology @inserm
Rebecca Middleton
@rebeccamiddle16
Founder & CEO, HBA Support | Vice Chair Participant Panel at Genomics England | Managing Director, Middleton Davies@middlet0ndavies, @hba_support | Views Own
Rare Patient Voice
@rarepatientvoic
We help clients find rare & non-rare disease patients & caregivers for research studies, & connect patients & caregivers with paid research opportunities.
Nizar Mahlaoui M.D., M.P.H., Ph.D.
@mahlaouinizar
#PrimaryImmunoDeficiencies #PID #ePIDemiology @CEREDIH @SCETIDE #NECKER & #Founder #Coordinator @LaSuiteNecker #Transition #AYA #RareDiseases #PrixGalien2019
EPNS
@epnsnews
European Paediatric Neurology Society (EPNS): a society for physicians, health professionals, scientists and students with an interest in Child Neurology.
46664
@inigo_rr
Se busca poeta. Buena remuneración. |HIP-HOP|
Patient Worthy
@patientworthy
We're a resource for engaging, informative content and rare patient news, well done.
Encarna Guillén
@encarna_guillen
Pediatra, Genetista Clínica @AreaUnoArrixaca @murciasalud @UMU @IMIB @CIBERER @AEGHgenetica #RareDiseases
dazzle4rare
@dazzle4rare
Est. 2016 | Signal boost RARE with #dazzle4rare every Aug | #Signalise is our #podcast | Our 🔗 linktr.ee/dazzle4rare
Julien Poulain
@julienrpoulain
Interested in health, housing, econ, basketball & absurd memes. Comms manager & #EurordisRareOnAir host. Brightonian, turned Londoner, turned novice Parisian.
Axel Olin
@axelolin2
Researcher at KTH working with developing technologies for immune monitoring and diagnostics. View are my own.
Emma Matthews 💙
@emmam_channels
Neurologist and Neuromuscular Specialist @StGeorgesTrust, Reader @StGeorgesUni, Director Genomics CAG, Rare Disease Lead @SEgenomics #neuromuscular #channels
ERDERA
@erdera_org
#ERDERA- The European Rare Diseases Research Alliance
Osservatorio Terapie Avanzate
@terapieavanzate
Informazione indipendente sulle nuove biotecnologie in ambito biomedico. #TerapiaGenica, #CRISPR, editing genomico, terapia cellulare, immunoterapia e #RNAi
Nazrul Raj
@nazrulraj5
I am website designer, developer, seo and blogger.
wocky slush
@subzeroyields
Different strokes (golf) for different folks!
robi (httpz)
@iam_robi_
CTO, founder @ tekkare.com and @ asweknow.com. Building open innovation programs in healthcare. zk, fhe & bcfl.
Mavi Lab
@mviclab
Gillian Sapia RN
@gillianhsapia
Rare Disease mom. Legislative Advocate and Activist. I post rare disease bills from Congress and Senate. Ask Congress to cosponsor current bills. Ask me how?!
SYNGAP Elternhilfe e.V.
@syngap1germany
Selbsthilfegruppe und Verein für Eltern von Kindern mit SYNGAP1 Syndrom (Gendefekt) Entwicklungsstörung, Epilepsie, Autismus Patient org. for SYNGAP1 families
commonancestor
@dnatriplethreat
Representing rare. Triple threat 🧬 of a 🦄, 🦓, and 👽
Baby's First Test
@babysfirsttest_
Baby's First Test is the nation's newborn screening education resource center for families and health professionals.
Elliott Williams
@e_j_r_williams
An account I use to observe Twitter. No content here. Move along, citizen.
Rare Disease Clinical Trial Network, Ireland
@rare_trial
HRB-funded clinical trial network aiming to increase the quantity and quality of rare disease clinical trials in Ireland, keeping the patient voice at our core
Ilaria Gasson
@ilargasso
Andria Abbasi
@abbasiandr41823
Merida Mckennan
@mckennanme58239
Paula Jofré Pacheco
@pejofrepa
Mariana Gameiro Silva
@marianacagsilva
The Med13L Foundation
@med13l_fdn
Supporting MED13L families through awareness, research, and community. Connecting hearts and minds to overcome challenges. #NDD #Epilepsy #Autism #ID 🧬💙🧠
Canadian Rare Disease Network (CRDN)
@canadianrdn
Pan-Canadian network uniting clinical, scientific and patient experts to improve the health and well-being of individuals affected by rare diseases.
Katarina Nedog
@katarinan2411
FriAnn
@annaacida
-Che si fa il giorno dopo della rivoluzione? -Sempre la rivoluzione. (cit.)
Kutand Alkım Bayer
@kutandalkim
IZTECH-Chemistry, this is my official account, opinions and views are my own, interested in science and technology.
Saume Paret Ruiz
@paretsaume
licenciada en Cultura Física y Deporte en el año 2007.
Francesca Ceradini
@franceradini
Molecular Biologist Science Writer #scicomm #Rarediseases #AdvancedTherapies #patients. Scientific Director @TerapieAvanzate @OssMalattieRare Views are my own
Johan Prevot
@johanprevot
Executive Director @ IPOPI All views strictly personal.
VASCERN
@vascern
Gathering the best expertise in Europe to provide accessible cross-border healthcare to patients with rare vascular diseases #ERNeu #RareDiseases
ern euro_nmd
@euro_nmd
Building bridges and breaking barriers in rare neuromuscular diseases.
Inmaculada González
@inmaggenet
laboratorio de genética bioquímica en HCUV Arrixaca Murcia . Detección y Prevención "Cribado Neonatal" Diagnostico de ECM .CARM
Association IRIS
@associationiris
IRIS reconnue d’Utilité Publique en 2007 -Soutenir les familles -Favoriser le diagnostic -Représenter les patients -Promouvoir le don -Soutenir la recherche
ERN ReCONNET 🇪🇺
@ern_reconnet
🔬🩺 European Reference Network on Rare and Complex Connective Tissue and Musculoskeletal Diseases #ERNReCONNET
Alessandra Renieri
@renieriale
MD-PhD leading one of the biggest Medical Genetics center in Italy at University Hospital in Siena for genetic counselling/test & gene editing in rare diseses.