Louis J. Elsas

A prevalent mutation for galactosemia among black Americans.

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

ARHI: A new target of galactose toxicity in Classic Galactosemia.

K. Wierenga, M. Tang, K. Lai, 2008, Bioscience hypotheses.

A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase gene.

S. Pinnell, M. Marshall, H. Yeowell, 1994, Journal of Clinical Investigation.

Selective urinary screening for mucopolysaccharidoses.

L. Elsas, P. Dembure, J. Drumheller, 1990, Clinical biochemistry.

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.

Molecular and biochemical characterization of human galactokinase and its small molecule inhibitors.

K. Wierenga, K Lai, M Tang, 2010, Chemico-biological interactions.