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Kliniske forsøg med Aspartylglykosaminuri
I alt 5 resultater
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Neurogene Inc.AfsluttetLysosomale opbevaringssygdomme | Aspartylglucosaminuri | Aspartylglucosamidase (AGA) mangelForenede Stater
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Greenwood Genetic CenterAfsluttetGalactosialidose | Sialidose | Fucosidosis | Aspartylglucosaminuri | Alpha Mannosidose | Beta Mannosidose | Mucolipidose II | Mucolipidose III | Schindlers sygdomForenede Stater
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Masonic Cancer Center, University of MinnesotaAfsluttetMucopolysaccharidosis | Hurler syndrom | Sphingolipidoser | Peroxisomale lidelser | Krabbes sygdom | Adrenoleukodystrofi (ALD) | Hunters syndrom | Sly Syndrom | Fucosidosis | Aspartylglucosaminuri | Alpha Mannosidose | Metakromatisk leukodystrofi (MLD) | Maroteaux-Lamy syndromForenede Stater
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Masonic Cancer Center, University of MinnesotaAfsluttetSphingolipidoser | Niemann-Pick sygdom, type C | Krabbes sygdom | Sly Syndrom | Fucosidosis | Aspartylglucosaminuri | Alpha Mannosidose | Hurlers syndrom | Maroteaux-Lamy syndrom | Wolmans sygdom | Niemann-Pick sygdom type BForenede Stater
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Masonic Cancer Center, University of MinnesotaRekrutteringHurler syndrom | Sphingolipidoser | Peroxisomale lidelser | Metakromatisk leukodystrofi | Alpha-Mannosidose | Hunters syndrom | Mucopolysaccharidosis lidelser | Maroteaux Lamy syndrom | Sly Syndrom | Fucosidosis | Aspartylglucosaminuri | Glycoprotein metaboliske forstyrrelser | Recessive leukodystrofier | Globoidcelle... og andre forholdForenede Stater