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Cancer|January 12, 2000
Von Hippel-Lindau syndrome. A pleomorphic conditionC A Friedrich
Human Molecular Genetics|March 21, 2001
Genotype-phenotype correlation in von Hippel-Lindau syndromeC A Friedrich
Annals of Human Genetics|May 1, 1985
A population study of alpha-keto acid reductaseC A Friedrich, R E Ferrell
Rheumatic Diseases Clinics of North America|September 1, 1999
Management of lipid disordersC A Friedrich, D J Rader
Biochemical Genetics|October 1, 1987
The reduction of aromatic alpha-keto acids by cytoplasmic malate dehydrogenase and lactate dehydrogenaseC A Friedrich, D C Morizot, M J Siciliano, et al.
Annals of Human Genetics|January 1, 1988
Biochemical and genetic identity of alpha-keto acid reductase and cytoplasmic malate dehydrogenase from human erythrocytesC A Friedrich, R E Ferrell, M J Siciliano, et al.
Muscle & Nerve|February 17, 2001
Acute axonal neuropathy in maple syrup urine diseaseK A Kleopa, D M Raizen, C A Friedrich, et al.
Calcified Tissue International|December 1, 1990
Alpha 2-HS glycoprotein phenotypes and quantitative hormone and bone measures in postmenopausal womenJ E Eichner, C A Friedrich, J A Cauley, et al.
The American Journal of Cardiology|February 17, 2001
Safety and effectiveness of Niaspan when added sequentially to a statin for treatment of dyslipidemiaM L Wolfe, S F Vartanian, J L Ross, et al.
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