M. Whyte

Metabolic fate of phenobarbital. A quantitative study of p-hydroxyphenobarbital elimination in man.

A. Dekaban, M. Whyte, 1977, Drug metabolism and disposition: the biological fate of chemicals.

Increased plasma pyridoxal-5′-phosphate levels before and after pyridoxine loading in carriers of perinatal/infantile hypophosphatasia

C. Greenberg, S. Coburn, B. Chodirker, 1990, Journal of Inherited Metabolic Disease.

Familial Cerebellar Degeneration with Slow Eye‐movements, Mental Deterioration and Incidental Nevus of Ota (Oculo‐dermal Melanoeytosis)

M. Whyte, A. Dekaban, M. Whyte, 1976, Developmental medicine and child neurology.

Idiopathic hypoparathyroidism presenting with seizures during infancy: X-linked recessive inheritance in a large Missouri kindred.

M. Whyte, M. Whyte, V. Weldon, 1981, The Journal of pediatrics.

Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndrome

A. Chines, W. Mcalister, G. Gottesman, 1997, Pediatric Radiology.

Increased serum pyridoxal-5'-phosphate in pseudohypophosphatasia.

D. Cole, S. Coburn, L. Ryan, 1986, The New England journal of medicine.

Severe hypophosphatemia in children with kwashiorkor is associated with increased mortality.

M. Manary, C. Hart, M. Whyte, 1998, The Journal of pediatrics.