T. Baykal

Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population

Steven F. Dobrowolski, Caroline Heintz, Trent Miller et al. · Molecular Genetics and Metabolism · 2010 · 79 citations

Aldehyde Dehydrogenase, Cellular Enzymology, Turkish Pku Population +10

Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2

Ute Spiekerkoetter, G. Huener, T. Baykal et al. · Journal of Inherited Metabolic Disease · 2003 · 53 citations

Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases

T. Baykal, Gülden Gökçay, Yasemi̇n Gökdemi̇r et al. · Journal of Inherited Metabolic Disease · 2005 · 47 citations · Full text

Novel mutations cause biotinidase deficiency in Turkish children

Robert J. Pomponio, Turgay Coşkun, Mübeccel Demirkol et al. · Journal of Inherited Metabolic Disease · 2000 · 45 citations

Screening for tetrahydrobiopterin deficiencies using dried blood spots on filter paper

Marcel R. Zurflüh, Marcello Giovannini, Laura M. Fiori et al. · Molecular Genetics and Metabolism · 2005 · 38 citations

Dried Blood Spots, Medicine, Bioanalysis +5