Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Human Molecular Genetics|March 21, 2001
Genotype-phenotype correlation in von Hippel-Lindau syndromeC A FriedrichAnnals of Human Genetics|May 1, 1985
A population study of alpha-keto acid reductaseC A Friedrich, R E FerrellRheumatic Diseases Clinics of North America|September 1, 1999
Management of lipid disordersC A Friedrich, D J RaderBiochemical 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.American Journal of Human Genetics|September 16, 1999
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.Pageof 1