Clinical trial with Phenilbutirrate to reduce lactic acid in patients affected with Melas Syndrome and PHD deficency encephalopathy Clinical trial with Phenilbutirrate to reduce lactic acid in patients affected with Melas Syndrome a ...
Phenylbutyrate Therapy in Mitochondrial Disease with lactic acidosis: an opel label clinical trial in MELAS and PHD deficiency patients - PHEMI Phenylbutyrate Therapy in Mitochondrial Disease with lactic acidosis: an opel label clinical trial i ...
Melas Syndrome and PDH deficency enchephalopathy MedDRA version: 20.0;Level: PT;Classification code 10053872;Term: MELAS syndrome;System Organ Class: 10010331 - Congenital, familial and genetic disorders MedDRA version: 20.0;Level: LLT;Classification code 10062950;Term: Leigh syndrome;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Nutritional and Metabolic Diseases [C18] Melas Syndrome and PDH deficency enchephalopathy MedDRA version: 20.0;Level: PT;Classification code ...