BIOTIN-RESPONSIVE ALOPECIA AND DEVELOPMENTAL REGRESSION

This publication has 12 references indexed in Scilit:

• Massive excretion of 2-oxoglutaric acid and 3-hydroxyisovaleric acid in a patient with a deficiency of 3-methylcrotonyl-CoA carboxylase
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1976
• COMBINED CARBOXYLASE DEFECT: BIOTIN-RESPONSIVENESS IN CULTURED FIBROBLASTS
  The Lancet, 1976
• Organic aciduria. Treatable cause of floppy infant syndrome.
  Archives of Disease in Childhood, 1976
• Studies on the urinary acidic metabolites excreted by patients with β-methylcrotonylglycinuria, propionic acidaemia and methylmalonic acidaemia, using gas-liquid chromatography and mass spectrometry
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1974
• Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria.
  Archives of Disease in Childhood, 1973
• BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIA
  The Lancet, 1971
• $beta;-HYDROXYISOVALERIC ACIDURIA AND $beta;-METHYLCROTONYLGLYCINURIA: A NEW INBORN ERROR OF METABOLISM
  The Lancet, 1970
• BIOTIN-RESPONSIVE PROPIONICACIDÆMIA
  The Lancet, 1970
• Clinical Biotin Deficiency (“Egg White Injury”).
  Acta Medica Scandinavica, 1958
• Seborrheic dermatitis of infants and Leiner's disease: A biotin deficiency
  The Journal of Pediatrics, 1957