Rani H. Singh

Urine and plasma galactitol in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia.

S. Wehrli, L. Elsas, R. Singh, 1999, Metabolism: clinical and experimental.

A prevalent mutation for galactosemia among black Americans.

L. Elsas, S. Langley, K. Lai, 1996, The Journal of pediatrics.

In vivo oxidation of [13C]galactose in patients with galactose-1-phosphate uridyltransferase deficiency.

L. Elsas, P. Klein, G. Berry, 1995, Biochemical and molecular medicine.

Impaired growth in Rabson-Mendenhall syndrome: lack of effect of growth hormone and insulin-like growth factor-I.

L. Elsas, J. Parks, N. Longo, 1994, The Journal of clinical endocrinology and metabolism.