Clinical Trials on Mitochondrial Neurogastrointestinal Encephalopathy Syndrome

Total 8 results

    • NCT01694953
      Conditions: Mitochondrial NeuroGastroIntestinal Encephalopathy (MNGIE)
    • NCT02427178
      Conditions: Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE)
    • NCT04245917
      Conditions: Mitochondrial Neurogastrointestinal Encephalomyopathy
    • NCT03866954
      Not yet recruiting
      Conditions: Mitochondrial Diseases; Metabolic Disease; Inborn Errors of Metabolism
    • NCT01803906
      Conditions: Mitochondrial Disorders; Mitochondrial Disease; Melas; Kearns Sayer; NARP; MNGIE; LHON; Mitochondrial Depletion Syndrome; Leigh's Disease
    • NCT02473445
      Conditions: Mitochondrial Diseases
    • NCT02171104
      Conditions: Mucopolysaccharidosis Disorders; Hurler Syndrome; Hunter Syndrome; Maroteaux Lamy Syndrome; Sly Syndrome; Alpha-Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Glycoprotein Metabolic Disorders; Sphingolipidoses; Recessive Leukodystrophies; Globoid Cell Leukodystrophy; Metachromatic Leukodystrophy; Niemann-Pick B; Niemann-Pick C Subtype 2; Sphingomyelin Deficiency; Peroxisomal Disorders; Adrenoleukodystrophy With Cerebral Involvement; Zellweger Syndrome; Neonatal Adrenoleukodystrophy; Infantile Refsum Disease; Acyl-CoA Oxidase Deficiency; D-Bifunctional Enzyme Deficiency; Multifunctional Enzyme Deficiency; Alpha-methylacyl-CoA Racmase Deficiency; Mitochondrial Neurogastrointestingal Encephalopathy; Severe Osteopetrosis; Hereditary Leukoencephalopathy With Axonal Spheroids (HDLS; CSF1R Mutation); Inherited Metabolic Disorders
    • NCT01694940
      Conditions: Mitochondrial Disorders; Mitochondrial Genetic Disorders; Mitochondrial Diseases; Disorder of Mitochondrial Respiratory Chain Complexes; Deletion and Duplication of Mitochondrial DNA