Strauss, Arnold W.

Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death

Ibdah, J. A., Paul, H., Zhao, Y., Binford, S., Salleng, K., Cline, M., Matern, D., Bennett, M. J., Rinaldo, P., & Strauss, A. W. (2001) · Journal of Clinical Investigation

Metabolism and Genetic DisordersMitochondrial Function and Pathology

Cited by 181

Diagnosis of Very Long Chain Acyl-Dehydrogenase Deficiency From an Infant's Newborn Screening Card

Wood, J. C., Magera, M. J., Rinaldo, P., Seashore, M. R., Strauss, A. W., & Friedman, A. (2001) · Pediatrics

Metabolism and Genetic DisordersGenomics and Rare Diseases

Cited by 62

Isolation and sequencing of a complementary deoxyribonucleic acid clone encoding human placental 173-estradiol dehydrogenase: Identification of the putative cofactor binding site

Gast, M. J., Sims, H. F., Murdock, G. L., Gast, P. M., & Strauss, A. W. (1989) · American Journal of Obstetrics and Gynecology

Estrogen and related hormone effectsSteroid Chemistry and Biochemistry

Cited by 45