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Kliniske forsøg sponsoreret af German Institute of Human Nutrition
I alt 3078 resultater
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Aktiv, ikke rekrutterende
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National Human Genome Research Institute (NHGRI)AfsluttetRheumatoid arthritisForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetHuntingtons sygdomForenede Stater
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National Human Genome Research Institute (NHGRI)Suspenderet
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National Human Genome Research Institute (NHGRI)AfsluttetIRB beslutningstagningForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetProteus syndromForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetBRAF V600E mutationForenede Stater
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)AfsluttetHjernelidelser | Holoprosencefali | HPE | Forsinkede udviklingsforstyrrelserForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetKraniosynostose | Muenke syndromForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetGenetik | Vækstforstyrrelse | PIK3CA-Relateret Overgrowth Spectrum (PROS)Forenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetOkulokutan albinismeForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetPodokoniose | Ikke-filariel elefantiasisEtiopien
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)AfsluttetPolydaktyli | Misdannelser | Flere abnormiteterForenede Stater, Kalkun
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National Human Genome Research Institute (NHGRI)AfsluttetArvelig Inclusion Body MyopatiForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetTelangiectasia, arvelig hæmoragisk | Osler-Rendu-Weber sygdom | Osler-Rendu sygdomForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetMedfødte abnormiteter | Fødselsdefekt | Medfødte defekterForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetKræft | Myelofibrose | Lungefibrose | Gauchers sygdom | Hermansky-Pudlak syndrom (HPS)Forenede Stater
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)AfsluttetDuchennes muskeldystrofiForenede Stater
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)AfsluttetLungekræft | Blod pårørende til patient m/lungekræft | CigaretrygereForenede Stater
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)Afsluttet
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National Human Genome Research Institute (NHGRI)AfsluttetLungefibrose | Metabolisk sygdom | Okulokutan albinisme | Hermansky-Pudlak syndrom (HPS) | Mangel på blodpladeopbevaringspoolForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetBrystneoplasmer | Ovariale neoplasmerForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetDværgvækst | AkondroplasiForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetMikrocefali | Ikke at trives | Abnormiteter | Mental retarderingForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetSmerte | Ehlers-Danlos syndromForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetArvelige sygdommeForenede Stater
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University of FloridaNational Human Genome Research Institute (NHGRI)Afsluttet
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University of FloridaNational Human Genome Research Institute (NHGRI)RekrutteringFarmakogenetisk test | Brug af receptpligtig medicinForenede Stater
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National Human Genome Research Institute (NHGRI)RekrutteringMetabolisk sygdom | Purin-pyrimidin metabolisme | AICDA, OMIM *605257, Immundefekt med Hyper-IgM, Type 2; HIGM2 | UNG, OMIM *191525, Hyper-IgM Syndrome 5 | NT5C3A, OMIM *606224, Anæmi, hæmolytisk, på grund af UMPH1-mangel | UMPS, OMIM *613891, Orotic Aciduria | DHODH, OMIM *126064, Millers syndrom... og andre forholdForenede Stater
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National Human Genome Research Institute (NHGRI)Rekruttering
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National Human Genome Research Institute (NHGRI)Rekruttering
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National Human Genome Research Institute (NHGRI)Rekruttering
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National Human Genome Research Institute (NHGRI)RekrutteringMitokondrielle lidelser | Leighs sygdom | Oxidativ phosphoryleringsmangel | Elektrontransportkædeforstyrrelser, mitokondrieForenede Stater
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National Human Genome Research Institute (NHGRI)RekrutteringLungefibrose | Sunde frivillige | Hermansky-Pudlak syndrom (HPS)Forenede Stater
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National Human Genome Research Institute (NHGRI)Rekruttering
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National Human Genome Research Institute (NHGRI)Aktiv, ikke rekrutterendeSunde frivillige | Aterosklerotisk hjertesygdomForenede Stater
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National Human Genome Research Institute (NHGRI)AfsluttetBrystkræft | TyktarmskræftForenede Stater
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National Human Genome Research Institute (NHGRI)Afsluttet