Medical specialists from Kazakhstan tagged as investigators in clinical trials studying Carbamoyl Phosphate Synthetase 1 Deficiency
Total 1 results
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Zhanna Zh Baibosynova, nurseSeen in:
- Aktobe Region, Aktobe, Regional perinatal center of Aktobe region
Trials:- NCT05910151 (Sub-Investigator)
Conditions:- Ornithine Transcarbamylase Deficiency;
- Biotinidase Deficiency;
- Citrullinemia;
- Glutaric Acidemia Type II;
- Argininosuccinic Aciduria;
- Maple Syrup Urine Disease;
- Primary Carnitine Deficiency;
- Homocystinuria;
- Carnitine Palmitoyltransferase II Deficiency;
- Arginase Deficiency;
- Very Long-chain Acyl-CoA Dehydrogenase Deficiency;
- Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency;
- N-acetylglutamate Synthase Deficiency;
- Medium-chain Acyl-CoA Dehydrogenase Deficiency;
- Tyrosinemia;
- Isovaleric Acidemia;
- Carnitine-acylcarnitine Translocase Deficiency;
- Glutaric Acidemia Type I;
- Propionic/Methylmalonic Acidemias;
- Carbamoyl Phosphate Synthetase I Deficiency;
- Nonketotic Hyperglycinemia;
- Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency;
- Isobutyryl-CoA Dehydrogenase Deficiency;
- 3-methylcrotonyl-CoA Carboxylase Deficiency;
- Malonyl-CoA Decarboxylase Deficiency;
- Beta-ketothiolase Deficiency;
- 3-hydroxy-3-methylglutaryl-CoA Lyase Deficiency;
- 3-methylglutaconyl-CoA Hydratase Deficiency;
- Carnitine Palmitoyltransferase I Deficiency
Clinical Trials on Carbamoyl Phosphate Synthetase 1 Deficiency
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Baylor College of MedicineChildren's National Research InstituteRecruitingOrnithine Transcarbamylase Deficiency | Urea Cycle Disorder | Carbamyl Phosphate Synthetase Deficiency | Argininosuccinic Aciduria | Hyperargininemia | Citrullinemia 1 | ARGI Deficiency | ASL Deficiency | ASS Deficiency | NAGS DeficiencyUnited States
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Children's Hospital of PhiladelphiaEunice Kennedy Shriver National Institute of Child Health and Human Development...WithdrawnUrea Cycle Disorders, Inborn | Inborn Errors of Metabolism | Propionic Acidemia | Methylmalonic Acidemia | Carbamyl Phosphate Synthetase Deficiency
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Cytonet GmbH & Co. KGCompletedOrnithine Transcarbamylase Deficiency | Urea Cycle Disorders | Citrullinemia | Carbamoylphosphate Synthetase I DeficiencyGermany
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West Kazakhstan Medical UniversityRecruitingOrnithine Transcarbamylase Deficiency | Biotinidase Deficiency | Citrullinemia | Glutaric Acidemia Type II | Argininosuccinic Aciduria | Maple Syrup Urine Disease | Primary Carnitine Deficiency | Homocystinuria | Carnitine Palmitoyltransferase II Deficiency | Arginase Deficiency | Very Long-chain Acyl-CoA... and other conditionsKazakhstan
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MedicureRecruitingPyridox(am)Ine 5'-Phosphate Oxidase DeficiencyUnited States, Australia
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University Hospital, Strasbourg, FranceUnknownThe Glutathione Synthetase DeficiencyFrance
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The First Hospital of Jilin UniversityNational Natural Science Foundation of ChinaUnknownGenetic Diseases, Inborn | Asparagine Synthetase DeficiencyChina
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National Human Genome Research Institute (NHGRI)TerminatedCitrullinemia | Argininosuccinic Aciduria | Hyperargininemia | Ornithine Carbamoyltransferase Deficiency | Carbamoyl-Phosphate Synthase I Deficiency | N-Acetylglutamate Synthase DeficiencyUnited States
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Mendel TuchmanChildren's Hospital of Philadelphia; University of California, Los Angeles; Icahn... and other collaboratorsCompletedMethylmalonic Acidemia | Carbamoyl-Phosphate Synthase I Deficiency Disease | Propionic Acidemia, Type I and/or Type II | Ornithine Carbamoyltransferase DeficiencyUnited States
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University of Mississippi, OxfordCompletedMalaria | Glucose 6 Phosphate Dehydrogenase DeficiencyUnited States