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M Zachmann

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Monatsschrift Fur Kinderheilkunde|April 1, 1978
[Diabetes insipidus, diabetes mellitus, optic nerve atrophy, and deafness--an autosomal recessive syndrome (didmoad-syndrome) (author's transl)]E Boltshauser, U Zellweger, M Zachmann
The Journal of Pediatrics|August 1, 1980
Gonadotropin deficiency and cryptorchidism in three prepubertal brothers with congenital adrenal hypoplasiaM Zachmann, R Illig, A Prader
Helvetica Paediatrica Acta|December 1, 1974
Skinfold thickness in infancy and adolescence. A longitudinal correlation study in normal childrenI Hernesniemi, M Zachmann, A Prader
Acta Endocrinologica|August 1, 1976
Urinary testosterone glucuronide and sulphate in newborns and young infantsH Krawczynska, M Zachmann, A Prader
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
A single amino acid substitution in the putative redox partner-binding site of P450c17 as cause of isolated 17,20-lyase deficiencyA Biason-Lauber, E Leiberman, M Zachmann
Acta Endocrinologica|October 1, 1974
Urinary steroid dynamics after a single dose of metyraponeM Zachmann, J A Völlmin, M Zagalak
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 26, 1999
Acute metabolic effects of human growth hormone on 15N-nitrogen balance in patients with thalassaemia as compared to patients with other types of short statureM Zachmann, B Kempken, V De Sanctis
European Journal of Pediatrics|June 1, 1994
Virilizing adrenal tumour mimicking congenital adrenal hyperplasia with P450c11 (11 beta-hydroxylase) deficiencyE A Werder, R Voutilainen, M Zachmann
The Journal of Pediatrics|December 1, 1976
Interrelation of the therapeutic effects of growth hormone and testosterone on growth in hypopituitarismA Aynsley-Green, M Zachmann, A Prader
The Journal of Clinical Endocrinology and Metabolism|September 1, 1982
Two types of male pseudohermaphroditism due to 17, 20-desmolase deficiencyM Zachmann, E A Werder, A Prader
Pageof 17

Showing results (51-60 of 165) with videos related to

Sort By:
Pageof 17
Monatsschrift Fur Kinderheilkunde|April 1, 1978
[Diabetes insipidus, diabetes mellitus, optic nerve atrophy, and deafness--an autosomal recessive syndrome (didmoad-syndrome) (author's transl)]E Boltshauser, U Zellweger, M Zachmann
The Journal of Pediatrics|August 1, 1980
Gonadotropin deficiency and cryptorchidism in three prepubertal brothers with congenital adrenal hypoplasiaM Zachmann, R Illig, A Prader
Helvetica Paediatrica Acta|December 1, 1974
Skinfold thickness in infancy and adolescence. A longitudinal correlation study in normal childrenI Hernesniemi, M Zachmann, A Prader
Acta Endocrinologica|August 1, 1976
Urinary testosterone glucuronide and sulphate in newborns and young infantsH Krawczynska, M Zachmann, A Prader
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
A single amino acid substitution in the putative redox partner-binding site of P450c17 as cause of isolated 17,20-lyase deficiencyA Biason-Lauber, E Leiberman, M Zachmann
Acta Endocrinologica|October 1, 1974
Urinary steroid dynamics after a single dose of metyraponeM Zachmann, J A Völlmin, M Zagalak
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 26, 1999
Acute metabolic effects of human growth hormone on 15N-nitrogen balance in patients with thalassaemia as compared to patients with other types of short statureM Zachmann, B Kempken, V De Sanctis
European Journal of Pediatrics|June 1, 1994
Virilizing adrenal tumour mimicking congenital adrenal hyperplasia with P450c11 (11 beta-hydroxylase) deficiencyE A Werder, R Voutilainen, M Zachmann
The Journal of Pediatrics|December 1, 1976
Interrelation of the therapeutic effects of growth hormone and testosterone on growth in hypopituitarismA Aynsley-Green, M Zachmann, A Prader
The Journal of Clinical Endocrinology and Metabolism|September 1, 1982
Two types of male pseudohermaphroditism due to 17, 20-desmolase deficiencyM Zachmann, E A Werder, A Prader
Pageof 17