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J Homoki

Showing results (11-20 of 49) with videos related to

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Klinische Padiatrie|November 1, 1996
[Gas chromatography-mass spectrometry determination of plasma 5 alpha-androstane-3 alpha,17 beta-diol and 5 alpha-androstane-3 alpha,17 beta-diol glucuronide in children with premature and normal puberty ]S A Wudy, J Homoki, W M Teller
Steroids|April 1, 1987
A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiencyC H Shackleton, J Homoki, N F Taylor
Human Genetics|April 15, 1976
A test for heterozygocity of 21-hydroxylase deficiency: preliminary reportJ Homoki, W M Teller, A T Fazekas
The Journal of Pediatrics|March 4, 1999
Spontaneous growth and bone age development in a patient with 17alpha-hydroxylase deficiency: evidence of the role of sexual steroids in prepubertal bone maturationE I Mayer, J Homoki, M B Ranke
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|December 8, 2000
Hormonal and clinical effects of chronic gonadotropin-releasing hormone agonist treatment in polycystic ovary syndromeA Szilágyi, J Homoki, S Bellyei, et al.
Steroids|August 28, 2001
Determination of 17alpha-hydroxypregnenolone in human plasma by routine isotope dilution mass spectrometry using benchtop gas chromatography-mass selective detectionS A Wudy, M Hartmann, C Solleder, et al.
European Journal of Pediatrics|January 1, 1992
Urinary excretion of 17-hydroxypregnanolones in patients with different forms of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencyJ Homoki, J Sólyom, U Wachter, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1985
[Therapy of juvenile struma. Comparison between combination treatment and monotherapy]J Homoki, D Garbrecht, U Loos, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1996
Diagnosis and treatment of a child with the syndrome of apparent mineralocorticoid excess type 1J Müller-Berghaus, J Homoki, D V Michalk, et al.
The Journal of Endocrinology|August 1, 1975
Genetic differences in the cortisol concentration of the adrenal and other tissues of white and coloured guinea-pigsA T Fazekas, J Homoki, W M Teller, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Klinische Padiatrie|November 1, 1996
[Gas chromatography-mass spectrometry determination of plasma 5 alpha-androstane-3 alpha,17 beta-diol and 5 alpha-androstane-3 alpha,17 beta-diol glucuronide in children with premature and normal puberty ]S A Wudy, J Homoki, W M Teller
Steroids|April 1, 1987
A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiencyC H Shackleton, J Homoki, N F Taylor
Human Genetics|April 15, 1976
A test for heterozygocity of 21-hydroxylase deficiency: preliminary reportJ Homoki, W M Teller, A T Fazekas
The Journal of Pediatrics|March 4, 1999
Spontaneous growth and bone age development in a patient with 17alpha-hydroxylase deficiency: evidence of the role of sexual steroids in prepubertal bone maturationE I Mayer, J Homoki, M B Ranke
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|December 8, 2000
Hormonal and clinical effects of chronic gonadotropin-releasing hormone agonist treatment in polycystic ovary syndromeA Szilágyi, J Homoki, S Bellyei, et al.
Steroids|August 28, 2001
Determination of 17alpha-hydroxypregnenolone in human plasma by routine isotope dilution mass spectrometry using benchtop gas chromatography-mass selective detectionS A Wudy, M Hartmann, C Solleder, et al.
European Journal of Pediatrics|January 1, 1992
Urinary excretion of 17-hydroxypregnanolones in patients with different forms of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencyJ Homoki, J Sólyom, U Wachter, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1985
[Therapy of juvenile struma. Comparison between combination treatment and monotherapy]J Homoki, D Garbrecht, U Loos, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1996
Diagnosis and treatment of a child with the syndrome of apparent mineralocorticoid excess type 1J Müller-Berghaus, J Homoki, D V Michalk, et al.
The Journal of Endocrinology|August 1, 1975
Genetic differences in the cortisol concentration of the adrenal and other tissues of white and coloured guinea-pigsA T Fazekas, J Homoki, W M Teller, et al.
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