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Ufundowane przez członka IRDiRC = 
Projekt badawczy
HOLANDIA
Gelderland
NIJMEGEN
TREATCilia: Novel Therapeutic Avenues for dynein-related Ciliopathies
Radboudumc - Radboud universitair medisch centrum
Afdeling Genetica
HOLANDIA
Zuid-Holland
ROTTERDAM
Obstructieve slaap apneu in syndromale craniosynostose
Erasmus MC - Erasmus Medisch Centrum
Afdeling Plastische, Reconstructieve en Handchirurgie
HOLANDIA
Zuid-Holland
ROTTERDAM
Hersenafwijkingen in syndromale craniosynostose
Erasmus MC - Erasmus Medisch Centrum
Afdeling Plastische, Reconstructieve en Handchirurgie
HOLANDIA
Zuid-Holland
ROTTERDAM
Genetische oorzaken van craniofaciale aandoeningen
Erasmus MC - Erasmus Medisch Centrum
Afdeling Plastische, Reconstructieve en Handchirurgie
HOLANDIA
Zuid-Holland
ROTTERDAM
Verstoorde ademhaling bij craniofaciale aandoeningen
Erasmus MC - Erasmus Medisch Centrum
Afdeling Plastische, Reconstructieve en Handchirurgie
HOLANDIA
Zuid-Holland
ROTTERDAM
Hersendoorbloeding in relatie tot hersendruk in craniosynostose
Erasmus MC - Erasmus Medisch Centrum
Afdeling Plastische, Reconstructieve en Handchirurgie
HISZPANIA
Murcia
MURCIA
Implementación de la secuenciación masiva en el diagnóstico e identificación de nuevos genes en la displasia ectodérmica
IMIB - Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca
Grupo de investigación en Pediatría
ZJEDNOCZONE KRÓLESTWO
Essex
LONDON
Natural history and management in Craniosynostoses syndromes
Great Ormond Street Hospital
Clinical Genetics
FRANCJA
AUVERGNE-RHONE-ALPES
LYON
DIVERCIL : Analyse de la diversité des cils et des flagelles - FR
Faculté de Médecine Lyon Est
Institut NeuroMyoGène (INMG) - CNRS UMR 5310 / INSERM U1217
WŁOCHY
LAZIO
ROMA
Analisi del profilo molecolare delle craniostenosi umane come modello paradigmatico di alterata osteogenesi: identificazione della patogenesi molecolare finalizzata alla scoperta alla scoperta di nuovi marcatori diagnostici e di nuovi bersagli terapeutici
Policlinico Universitario "A. Gemelli"
U.O.C. di Neurochirurgia Infantile
WŁOCHY
LAZIO
ROMA
Analisi del profilo molecolare delle craniostenosi umane come modello paradigmatico di alterata osteogenesi: identificazione della patogenesi molecolare finalizzata alla scoperta alla scoperta di nuovi marcatori diagnostici e di nuovi bersagli terapeutici
Università Cattolica del Sacro Cuore
Istituto di Anatomia Umana e Biologia Cellulare
STANY ZJEDNOCZONE AMERYKI
Washington
ADDRESS: NOT PROVIDED - US
Role of bcl11b in development of the craniofacial skeleton
Institution: Information not provided - US
BELGIA
ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS
GENODERM: Mise au point d'une méthode d'analyse génétique par mendéliomes et génomes dans le diagnostic des génodermatoses et des maladies génétiques rares à expression cutanée
Hôpital Universitaire des Enfants Reine Fabiola - HUDERF
Dermatologie
FRANCJA
ILE-DE-FRANCE
PARIS
STaHR : Stimulation de la Recombinaison Homologue pour la Thérapie Génique - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
FRANCJA
PAYS DE LA LOIRE
NANTES
FROGH : Etude Génétique de la Population Française - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
JAPONIA
JAPAN
AICHI
Management ofthe clinical diagnostic centre for rare intractable diseases with genome instability and development of potential therapeutic medicine
Research Institute of Environmental Medicine, Nagoya University
JAPONIA
JAPAN
AICHI
Establishment of the Next-generation Muti-omics Clinical Diagnostic Centre for rare intractable diseases with genome instability
Research Institute of Environmental Medicine, Nagoya University
JAPONIA
JAPAN
TOKYO
Formation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute
KANADA
Ontario
OTTAWA, ONTARIO
Detection and simulation of femoroacetabular impingement
University of Ottawa
School of Electrical Engineering and Computer Science (EECS)
NIEMCY
Sachsen-Anhalt
MAGDEBURG
EUROlinkCAT: Europaweites Netzwerk zum Outcome von angeborenen Fehlbildungen (partner DE)
Universitätsklinikum Magdeburg A.ö.R
MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
ZJEDNOCZONE KRÓLESTWO
Cambridgeshire
HINXTON
The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER
ZJEDNOCZONE KRÓLESTWO
Tyne & Wear
NEWCASTLE UPON TYNE
ESDN: European Skeletal Dysplasia Network (coordination)
Newcastle upon Tyne Hospitals NHS Trust
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine
Wieloośrodkowy projekt badawczy
- Zentrum für Kinder- und Jugendmedizin Freiburg
- Sektion Pädiatrische Genetik der Klinik für Allgemeine Kinder- und Jugendmedizin
- TIGEM - Telethon Institute of Genetics and Medicine
- Laboratorio di Ricerca
- Radboudumc - Radboud universitair medisch centrum
- Afdeling Genetica
- Faculté de Médecine Lyon Est
- Institut NeuroMyoGène (INMG) - CNRS UMR 5310 / INSERM U1217
- Institut für Humangenetik der Universität Göttingen
- Institut für Humangenetik
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- Muséum National d'Histoire Naturelle
- Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
- Institut de Recherche en Santé - Université de Nantes
- L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
- IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
- Servizio Clinico di Consulenza Genetica
- Istituto Dermopatico dell'Immacolata - IRCCS
- Laboratorio di Biologia Molecolare e Cellulare
- Faculty of Medical and Human Sciences - University of Manchester
- Department of Dental Medicine and Surgery
- Med. Klinik und Poliklinik II des UKGM am Standort Gießen
- ECCPS: Excellence Cluster Cardio-Pulmonary System - Office
- Med. Klinik und Poliklinik II des UKGM am Standort Gießen
- Medizinische Klinik und Poliklinik II
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
- Faculty of Life Sciences - University of Manchester
- Wellcome Trust Centre for Cell Matrix Research - B.3016
NIEMCY
Baden-Württemberg
FREIBURG
FACE: Forschungsverbund ausgewählter craniofacialer Entwicklungsstörungen
WŁOCHY
CAMPANIA
NAPOLI
EUCILIA: Pathophysiology of rare diseases due to ciliary dysfunction: nephronophthisis, oral-facial-digital type 1 and bardet-biedl syndromes
HOLANDIA
Gelderland
NIJMEGEN
SYSCILIA: A systems biology approach to dissect cilia function and its disruption in human genetic disease
FRANCJA
AUVERGNE-RHONE-ALPES
LYON
DIVERCIL : Analyse de la diversité des cils et des flagelles
NIEMCY
Niedersachsen
GÖTTINGEN
CRANIRARE: An integrated clinical and scientific approach for craniofacial malformations
KANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
FRANCJA
ILE-DE-FRANCE
PARIS
STaHR : Stimulation de la Recombinaison Homologue pour la Thérapie Génique
FRANCJA
PAYS DE LA LOIRE
NANTES
FROGH : Etude Génétique de la Population Française
WŁOCHY
LAZIO
ROMA
UnRareNet: network multicentrico di ricerca per le malattie rare non diagnosticate (terminato)
WŁOCHY
LAZIO
ROMA
GENESKIN: European network on rare genetic skin diseases
ZJEDNOCZONE KRÓLESTWO
Greater Manchester
MANCHESTER
EUROCRAN: European collaboration on craniofacial anomalies - Eurocleft clinical network (TERMINATED)
NIEMCY
Hessen
GIEßEN
ECCPS: Exzellenzcluster 'Kardiopulmonales System'
NIEMCY
Hessen
GIEßEN
UGLC (University of Giessen Lung Center): Lungenzentrum Gießen
NIEMCY
Sachsen-Anhalt
MAGDEBURG
International Clearinghouse for Birth Defects Monitoring Systems
ZJEDNOCZONE KRÓLESTWO
Greater Manchester
MANCHESTER