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
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. #RareDiseaseDayUnique
@unique_charity
Unique supports & informs anyone born w/a rare chromosome or gene disorder, their families & carers. Eurordis Patient Organisation Award winner. rarechromo.orgEURORDIS-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.Ilaria Vacca
@vivosunamela
Editor in chief @OssMalattieRare, journalist, mum of 3. #Giornalismo e #scicomm con il cuore e con la testa. #malattierare ma non solo.EU Research Results
@cordis_eu
🇪🇺 News & information on #EUFunded #EUResearch projects @EU_Commission 👩🔬🔬👨🔬 | 🎧 Listen to our podcast #CORDIScovery 👉 spoti.fi/3ppKoLXSDU Science
@natsdu
Science news and tweets from the Faculty of Science, University of Southern Denmark. #dkvid #dkscience #dkforskProRaris
@proraris
ProRaris - Alliance des Maladies Rares en Suisse ProRaris - Allianz Seltener Krankheiten Schweiz ProRaris – Alleanza delle Malattie Rare in Svizzera ProRaris.chSyddansk Universitet
@syddanskuni
matcher #dkmedier med #dkforsk. #FindEnForsker på 65502700 eller vores presse-site herunder 👇The KATT Dazzle
@thekattdazzle
My curse **is** my gift. hEDS+PoTS Intellectual curiosity = my problem. Opinions = MINE. Retweet ≠ endorsements or represent #Dazzle4RareEuropean IP Helpdesk
@iprhelpdesk
Funded by the @EU_Commission and managed by @EU_EISMEA. Tweets by the social media team. Third-party content not necessarily endorsed.OMaR Malattie Rare
@ossmalattierare
Osservatorio Malattie Rare è la prima agenzia giornalistica dedicata al mondo delle #malattierare, dei #tumori rari e dei #farmaciorfani.APMARR ITALIA
@apmarr_italia
APMARR, Associazione Nazionale Persone con Malattie Reumatologiche e Rare, per la tutela del diritto alla salute dei pazienti reumaticiLeMalattieRare.Info
@malattierare
Il portale dedicato ai malati rari e alle loro famiglie. A cura di Margherita De BacPfizer Inc.
@pfizer_news
The official Twitter channel dedicated to media announcements & investor communications from Pfizer Inc. To see all of our Tweets, please follow @pfizer.European Patients' Forum
@eupatientsforum
We are the leading voice of patient organisations in Europe. #EuropeForPatientsDr. Aliya Shah
@aliya_hshah
#Health #Healthcare #Medical #HealthTech #medicine #surgery #diet #nutrition #wellbeing #mentalhealth #DigitalHealth #RoyalistMalattie Rare
@malattie_rare
Le #malattie rare colpiscono milioni di persone, ma sono spesso ignorate dalla popolazione e dalle aziende farma: ecco quindi la necessità di farle conoscere.UndiagnosedDay
@undiagnosedday
We want to make March 5 World #UndiagnosedDay to support #undiagnosedpatients, #diseasedetectives, and medical researchers advancing #diagnosticmedicine.Ilaria Ciancaleoni Bartoli
@ilariacbartoli
Giornalista, fondatrice e direttrice di Osservatorio Malattie Rare (OMaR), il megafono delle persone con malattia rara.Genomics England
@genomicsengland
We’re working to enable faster and deeper genomic research, to bring genomic healthcare to all who need it.22Q11 Ireland
@22q11_ireland
Parent group raising awareness of #22q Working toward integrated care for 22qDS & individually rare collectively common #RareDiseases. Tweets AnneL CHY 17647I Malati Invisibili
@malatinvisibili
Comitato I Malati Invisibili Onlus - Malattie Rare e Orfane di Diagnosi.Baebies
@baebiesinc
Our mission is to save lives and make lives better for all by bringing new technologies, new tests, and new hope. Everyone deserves a healthy start.Enrico Orzes
@sezro1
Biologist specialized in clinical pathology and scientific journalist.MaRaC
@malattierareco
Malattie Rare Empoli
@empoli_rare
Ambulatorio Malattie Rare della Neurologia di Empoli (FI)Master Malattie Rare
@mastermarare
Patient Worthy
@patientworthy
We're a resource for engaging, informative content and rare patient news, well done.Telefono Verde Malattie Rare
@tvmr_cnmr
Il Telefono Verde Malattie Rare (TVMR) è una helpline dedicata alle malattie rare, istituita presso il @cnmr_ISS, risponde al n. 800.89.69.49.Virginie Bros-Facer
@virginiebf31
Scientific Director @eurordis (European Organisation for #RareDisease). Views are my owndazzle4rare
@dazzle4rare
Est. 2016 | Signal boost RARE with #dazzle4rare every Aug | #Signalise is our #podcast | Our 🔗 linktr.ee/dazzle4rareOsservatorio Screening Neonatale
@oss_screening
Un progetto @ossmalattierare, #SIMMESN Società Italiana Malattie Metaboliche e Screening Neonatale e #MetabERN • #ScreeningNeonatale #NewbornScreeningNCBRS Worldwide Foundation - Nicolaides Baraitser
@ncbrsfoundation
Our aim is to help families by providing practical advice, annual conferences, raising awareness of #NCBRS and possibly help to fund any future research studiesCoordinamento Lazio Malattie Rare-CoLMaRe
@laziorare
[email protected]ERDERA
@erdera_org
#ERDERA- The European Rare Diseases Research AllianceRivista Italiana delle Malattie Rare
@rimalattierare
La #Rivista, un sito web dedicato: per fare cultura e colmare il gap di informazione su argomenti complessi come le #malattierare. #RareDiseaseOrphanet Italia
@orphanetit
Il portale delle malattie rare e dei farmaci orfaniLa Terra di Mezzo Associazione It Malattie Rare
@la_malattie
CeSER - Centrum für Seltene Erkrankungen Ruhr
@ceser_bochum
Das @CeSER_Bochum der #RuhrUniBochum vernetzt Ärzt:innen, Forscher:innen + Patient:innen mit #SeltenerErkrankung. Hier informieren wir zu News und Netzwerken.cmRNAbone
@cmrnabone
cmRNAbone is an EU-funded research project working on a novel gene therapy for bone regeneration. Funded under Horizon 2020 (GA-No 874790).Min Seo Kim, MD, MSs
@minseokim_md
Physician-scientist | Postdoc @MGHMedicine @BroadInstitute of MIT and Harvard | Genomics/Omics/Artificial intelligence | Former Public Health OfficialLeibniz-Institut für Analytische Wissenschaften
@isas_leibniz
Das ISAS entwickelt Analyseverfahren für die #Gesundheitsforschung. Unser Ziel ist es, die Prävention, Frühdiagnose & Therapie von Erkrankungen zu verbessern.ScreenPlus
@screenplusny
We are the largest newborn pilot screening program in the United States. Our goal is to identify babies with rare disorders earlier #2024NBS #rarediseasesEssener Zentrum für Seltene Erkrankungen (EZSE)
@ezse_de
Das EZSE liegt im Herzen der Metropole Ruhr und vereint Experteninnen und Experten mit langjähriger Erfahrung auf dem Gebiet seltener Erkrankungen.BAPEMED
@bapemed
Bulgarian Association for Personalized Medicine, for the benefit of patients and the health care system.Screen4Rare
@screen4rare
A multi-stakeholder platform launched by IPOPI, ISNS and ESID aiming to exchange knowledge and best practices on newborn screening for rare diseases.Institut für Humangenetik 🧬 | Uniklinik Leipzig
@hug_leipzig
Das Institut bietet genetische Diagnostik & ambulante Beratungen an. Zudem erfolgt Forschung zu seltenen Erkrankungen & studentische Lehre am @UKL_Leipzig.National Screening Service
@nsshse
Your official guide to what's happening at the National Screening Service. Not monitored 24/7. Twitter policy: bit.ly/NSS-twi-policy #ChooseScreeningRARE Revolution Magazine
@rarerevolutionm
Digital magazine giving a voice to those affected by rare conditions and the charities that support them. Contact us: [email protected]Rady Genomics
@radygenomics
🧬Mila's Miracle
@stopbatten
Mila fought hard against Batten disease, a rare fatal condition with no cure. Her story is now giving new hope to millions with genetic disease.22q11 Europe
@22q11europe
A European network of 22q11 Deletion Syndrome Support Groups actively promoting the wellbeing of people living with 22q11DSPakhi Rajesh Kumar Dixit
@pakhi_dixit
Social Media @FrancaFund @Genomes2People @ICoNSeqOrg & Comms @spinbylablacoKyle Lee
@kylej_lee
Ella Mercer (she/her)
@ella_mercer1
Research Involvement and Comms Officer @UKTSA. Passionate about amplifying patients and carers voices. All views are my own, retweets are not endorsements.Team Ca Testicolo-Pene-Uretra-Malattie Rare
@teamcatesticolo
La squadra specializzata sui tumori del testicolo, pene, uretra e patologie rare di @SIU_Italia, Società Italiana di Urologia #SIUASCOGU.Solve-RD
@solve_rd
Solve-RD is a H2020 funded flagship EU project. We will solve large numbers of rare diseases, for which a molecular cause is not known yet.