195 Clinical Trials in Kazakhstan, Page 2 of 20

Hide Studies Not Open or Pending

12

Selective Screening of Children for Hereditary Metabolic Diseases by Tandem Mass Spectrometry in Kazakhstan

Condition(s):Propionic/Methylmalonic Acidemias; Maple Syrup Urine Disease; Citrullinemia; Argininosuccinic Aciduria; Ornithine Transcarbamylase Deficiency; Carbamoyl Phosphate Synthetase I Deficiency; N-acetylglutamate Synthase Deficiency; Nonketotic Hyperglycinemia; Tyrosinemia; Homocystinuria; Arginase Deficiency; Isovaleric Acidemia; Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency; Isobutyryl-CoA Dehydrogenase Deficiency; Glutaric Acidemia Type I; 3-methylcrotonyl-CoA Carboxylase Deficiency; Biotinidase Deficiency; Malonyl-CoA Decarboxylase Deficiency; Beta-ketothiolase Deficiency; 3-hydroxy-3-methylglutaryl-CoA Lyase Deficiency; 3-methylglutaconyl-CoA Hydratase Deficiency; Medium-chain Acyl-CoA Dehydrogenase Deficiency; Very Long-chain Acyl-CoA Dehydrogenase Deficiency; Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency; Glutaric Acidemia Type II; Primary Carnitine Deficiency; Carnitine Palmitoyltransferase I Deficiency; Carnitine Palmitoyltransferase II Deficiency; Carnitine-acylcarnitine Translocase DeficiencyLast Updated:June 18, 2023Recruiting

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.