J. A. Völlmin

STEROID 17, 20‐DESMOLASE DEFICIENCY: A NEW CAUSE OF MALE PSEUDOHERMAPHRODITISM

M. Zachmann, J. A. Völlmin, William Hamilton et al. · Clinical Endocrinology · 1972 · 161 citations

Spermatogenesis, Fertility, Genetics +21

The use of deuterated phenylalanine for the elucidation of the phenylalanine-tyrosine metabolism

H.‐Ch. Curtius, J. A. Völlmin, K Baerlocher · Clinica Chimica Acta · 1972 · 72 citations

Biosynthesis, Phenylalanine-tyrosine Metabolism, Engineering +6

Unusual Type of Congenital Adrenal Hyperplasia Probably Due to Deficiency of 3β-Hydroxysteroid Dehydrogenase. Case Report of a Surviving Girl and Steroid Studies¹

M. Zachmann, J. A. Völlmin, G. Mürset et al. · The Journal of Clinical Endocrinology & Metabolism · 1970 · 63 citations · Full text

Unusual Type, Gynecology, External Genitalia +19

Pathogenesis of phenylketonuria: Inhibition of dopa and catecholamine synthesis in patients with phenylketonuria

H.‐Ch. Curtius, K Baerlocher, J. A. Völlmin · Clinica Chimica Acta · 1972 · 54 citations

Renal Function, Medicine, Renal Pathology +7

Structural elucidation with a thermal fragmentation—Gas chromatography—Mass spectrometry combination

J. A. Völlmin, P. Kriemler, Itiro Omura et al. · Microchemical Journal · 1966 · 53 citations

Structural Elucidation, Gas Chromatography, Natural Sciences +8