Medical specialists from Belgium tagged as investigators in clinical trials studying Galactosemia
Total 1 results
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Francois Boemer, PhDSeen in:
- Wallonia, Liege, CRMN, Hôpital La Citadelle
Trials:- NCT05687474 (Sub-Investigator)
Conditions:- Congenital Adrenal Hyperplasia;
- Hemophilia A;
- Hemophilia B;
- Mucopolysaccharidosis I;
- Mucopolysaccharidosis II;
- Cystic Fibrosis;
- Alpha 1-Antitrypsin Deficiency;
- Sickle Cell Disease;
- Fanconi Anemia;
- Chronic Granulomatous Disease;
- Wilson Disease;
- Severe Congenital Neutropenia;
- Ornithine Transcarbamylase Deficiency;
- Mucopolysaccharidosis VI;
- Lysosomal Acid Lipase Deficiency;
- Wiskott-Aldrich Syndrome;
- Propionic Acidemia;
- Adrenoleukodystrophy;
- Glycogen Storage Disease;
- Metachromatic Leukodystrophy;
- Crigler-Najjar Syndrome;
- Galactosemias;
- Pompe Disease;
- Shwachman-Diamond Syndrome;
- Congenital Hypothyroidism;
- Alpha-Thalassemia;
- Biotinidase Deficiency;
- Diamond Blackfan Anemia;
- Chediak-Higashi Syndrome;
- Catecholaminergic Polymorphic Ventricular Tachycardia;
- Cystinosis;
- X Linked Hypophosphatemia;
- Aromatic L-amino Acid Decarboxylase Deficiency;
- Gaucher Disease, Type 1;
- Mucopolysaccharidosis IV A;
- Alport Syndrome;
- Smith-Lemli-Opitz Syndrome;
- Mucopolysaccharidosis VII;
- Primary Hyperoxaluria;
- Griscelli Syndrome;
- Dopamine Beta Hydroxylase Deficiency;
- Glut1 Deficiency Syndrome;
- Maple Syrup Urine Disease;
- Congenital Myasthenic Syndrome;
- Jervell-Lange Nielsen Syndrome;
- Menkes Disease;
- Homocystinuria;
- Progressive Familial Intrahepatic Cholestasis;
- Ataxia With Vitamin E Deficiency;
- Glycine Encephalopathy;
- Pseudohypoaldosteronism Type 1;
- Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency;
- Familial Chylomicronemia;
- Familial Hemophagocytic Lymphocytosis;
- Glucose 6 Phosphate Dehydrogenase Deficiency;
- Citrullinemia 1;
- Glutaric Acidemia I;
- Phosphoglucomutase 1 Deficiency;
- Tyrosinemia, Type I;
- Familial Hyperinsulinemic Hypoglycemia 1;
- Maturity Onset Diabetes of the Young;
- Hypophosphatasia, Infantile;
- Pituitary Hormone Deficiency, Combined;
- Inflammatory Bowel Disease 25, Autosomal Recessive;
- Thiamine-Responsive Megaloblastic Anemia;
- Thiamine Metabolism Dysfunction Syndrome 2;
- Cerebral Folate Transport Deficiency;
- Segawa Syndrome, Autosomal Recessive;
- Sepiapterin Reductase Deficiency;
- Late-Infantile Neuronal Ceroid Lipofuscinosis;
- Charcot-Marie-Tooth Disease, Type 6C;
- Hereditary Hyperekplexia;
- Brain Dopamine-Serotonin Vesicular Transport Disease;
- Very Long Chain Hydroxy Acyl Dehydrogenase Deficiency;
- Disaccharide Intolerance I;
- Beta Ketothiolase Deficiency;
- Phosphoglycerate Dehydrogenase Deficiency;
- Pyridoxine-5'-Phosphate Oxidase Deficiency;
- Pyridoxine-Dependent Epilepsy;
- Phenylalanine Hydroxylase Deficiency;
- Riboflavin Deficiency;
- Medium Chain Acyl CoA Dehydrogenase Deficiency;
- Malonic Acidemia;
- Isovaleric Acidemia;
- Phosphoserine Aminotransferase Deficiency;
- Phosphoserine Phosphatase Deficiency;
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria;
- S-Adenosylhomocysteine Hydrolase Deficiency;
- Transcobalamin Deficiency;
- Isolated Methylmalonic Acidemia;
- Cobalamin Deficiency;
- Holocarboxylase Synthetase Deficiency;
- Fanconi Bickel Syndrome;
- Glucose Galactose Malabsorption;
- Fructosemia;
- Fructose-1,6-Diphosphatase Deficiency;
- Carbamoyl Phosphate Synthase 1 Deficiency;
- Citrullinemia Type II;
- Creatine Deficiency Syndrome;
- Systemic Primary Carnitine Deficiency;
- Carnitine Palmitoyltransferase Deficiency 2;
- Carnitine Palmitoyltransferase Deficiency 1;
- Carnitine Acylcarnitine Translocase Deficiency;
- Riboflavin Transporter Deficiency;
- Branched-Chain Keto Acid Dehydrogenase Kinase Deficiency;
- Andersen Tawil Syndrome;
- Timothy Syndrome;
- Familial Hypertrophic Cardiomyopathy Type 4;
- Pseudohypoaldosteronism, Type II;
- Hereditary Nephrogenic Diabetes Insipidus;
- Congenital Nephrotic Syndrome, Finnish Type;
- Hereditary Retinoblastoma;
- Aciduria, Argininosuccinic;
- 3-Hydroxy 3-Methyl Glutaric Aciduria;
- 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency;
- Argininemia;
- Deficit in Anterior Pituitary Function and Variable Immunodeficiency;
- Severe Combined Immune Deficiency;
- Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type);
- Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type);
- Deficiency of GOT2;
- Succinyl-Coa:3-Ketoacid Coa-Transferase Deficiency;
- N Acetyl Glutamate Synthetase Deficiency;
- Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of
Clinical Trials on Galactosemia
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Applied Therapeutics, Inc.Active, not recruiting
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Applied Therapeutics, Inc.Active, not recruitingClassic GalactosemiaUnited States
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Applied Therapeutics, Inc.CompletedClassic GalactosemiaUnited States
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Academisch Ziekenhuis MaastrichtCompleted
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Emory UniversityPatient-Centered Outcomes Research InstituteCompleted
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Arizona State UniversityWashington State UniversityEnrolling by invitationLanguage Disorders in Children | Classic Galactosemia | Speech Disorders in ChildrenUnited States
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Children's University Hospital, IrelandUniversity College Dublin; Health Research Board, Ireland; Medical Research Charities...Completed
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University of MiamiHRSA/Maternal and Child Health BureauCompletedPhenylketonuria | Inborn Errors of Metabolism | GalactosemiaUnited States
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Maastricht University Medical CenterCompleted
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Maastricht University Medical CenterThe Dutch Galactosemia SocietyUnknown