Medical specialists from Kazakhstan tagged as investigators in clinical trials studying Multiple Acyl Coenzyme A Dehydrogenase 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 Multiple Acyl Coenzyme A Dehydrogenase Deficiency
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Rigshospitalet, DenmarkGroupe Hospitalier Pitie-SalpetriereCompletedCarnitine Palmitoyltransferase II Deficiency | Very Long Chain Acyl Coa Dehydrogenase DeficiencyDenmark
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Oregon Health and Science UniversityCompletedNormal Volunteers | Trifunctional Protein Deficiency | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Carnitine Palmitoyltransferase II Deficiency, MyopathicUnited States
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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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Oregon Health and Science UniversityCompletedTrifunctional Protein Deficiency | Carnitine Palmitoyltransferase 2 Deficiency | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
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Ultragenyx Pharmaceutical IncCompletedCarnitine Palmitoyltransferase (CPT I or CPT II) Deficiency | Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency | Long-chain 3-hydroxy-acyl-CoA Dehydrogenase (LCHAD) Deficiency | Trifunctional Protein (TFP) Deficiency | Carnitine-acylcarnitine Translocase (CACT) DeficiencyUnited States, United Kingdom
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Oregon Health and Science UniversityCompletedTrifunctional Protein Deficiency | Very Long Chain Acyl Coa Dehydrogenase Deficiency | Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Carnitine Palmitoyltransferase Deficiency 2United States
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University of PittsburghHorizon Pharma Ireland, Ltd., Dublin IrelandCompletedMedium-chain Acyl-CoA Dehydrogenase (MCAD) DeficiencyUnited States
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Ultragenyx Pharmaceutical IncCompletedLong-chain Fatty Acid Oxidation Disorders (LC-FAOD) | Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency | Trifunctional Protein (TFP) Deficiency | Carnitine Palmitoyltransferase (CPT II) Deficiency | Longchain 3-hydroxy-acyl-CoA Dehydrogenase (LCHAD) DeficiencyUnited States, United Kingdom
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Rigshospitalet, DenmarkUnknownCarbohydrate Metabolism, Inborn Errors | Metabolism, Inborn Errors | Lipid Metabolism, Inborn Errors | Glycogen Storage Disease Type II | Glycogen Storage Disease Type V | VLCAD Deficiency | Glycogen Storage Disease Type III | Phosphoglycerate Kinase Deficiency | Neutral Lipid Storage Disease | Carnitine... and other conditionsDenmark
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Jerry Vockley, MD, PhDAcer Therapeutics Inc.RecruitingMedium-chain Acyl-CoA Dehydrogenase DeficiencyUnited States