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The Journal of Clinical Endocrinology and Metabolism
|
August 14, 2008
Recommendations for the diagnosis and management of Prader-Willi syndrome
A P Goldstone, A J Holland, B P Hauffa, et al.
Clinical Endocrinology
|
November 1, 1985
Congenital adrenal hyperplasia due to deficient cholesterol side-chain cleavage activity (20, 22-desmolase) in a patient treated for 18 years
B P Hauffa, W L Miller, M M Grumbach, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 14, 1999
Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XY female patient with a premature termination in the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia
E Korsch, M Peter, O Hiort, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 9, 2004
Leydig cell hypoplasia: absent luteinizing hormone receptor cell surface expression caused by a novel homozygous mutation in the extracellular domain
A Richter-Unruh, M Verhoef-Post, S Malak, et al.
European Journal of Pediatrics
|
January 1, 1991
Severe hypoaldosteronism due to corticosterone methyl oxidase type II deficiency in two boys: metabolic and gas chromatography-mass spectrometry studies
B P Hauffa, J Sólyom, E Gláz, et al.
Pediatric Research
|
April 1, 1989
Hormone ontogeny in the ovine fetus: XIX: The effect of a potent luteinizing hormone-releasing factor agonist on gonadotropin and testosterone release in the fetus and neonate
S J Clark, B P Hauffa, K P Rodens, et al.
European Journal of Endocrinology
|
February 10, 2012
Functional and total IGFBP3 for the assessment of disorders of the GH/IGF1 axis in children with chronic kidney disease, GH deficiency, or short stature after SGA status at birth
A K Büscher, R Büscher, L Pridzun, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 13, 2002
Male LH-independent sexual precocity in a 3.5-year-old boy caused by a somatic activating mutation of the LH receptor in a Leydig cell tumor
A Richter-Unruh, H T Wessels, U Menken, et al.
Hormone Research
|
August 20, 2009
Is the response to growth hormone in short children born small for gestational age dependent on genetic or maternal factors?
Otto Mehls, A Lindberg, M Bettendorf, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 1, 2000
Diagnosis and management of juvenile hyperthyroidism in Germany: a retrospective multicenter study
J Dötsch, T Siebler, B P Hauffa, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 53) with videos related to
Sort By:
Page
of 6
The Journal of Clinical Endocrinology and Metabolism
|
August 14, 2008
Recommendations for the diagnosis and management of Prader-Willi syndrome
A P Goldstone, A J Holland, B P Hauffa, et al.
Clinical Endocrinology
|
November 1, 1985
Congenital adrenal hyperplasia due to deficient cholesterol side-chain cleavage activity (20, 22-desmolase) in a patient treated for 18 years
B P Hauffa, W L Miller, M M Grumbach, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 14, 1999
Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XY female patient with a premature termination in the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia
E Korsch, M Peter, O Hiort, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 9, 2004
Leydig cell hypoplasia: absent luteinizing hormone receptor cell surface expression caused by a novel homozygous mutation in the extracellular domain
A Richter-Unruh, M Verhoef-Post, S Malak, et al.
European Journal of Pediatrics
|
January 1, 1991
Severe hypoaldosteronism due to corticosterone methyl oxidase type II deficiency in two boys: metabolic and gas chromatography-mass spectrometry studies
B P Hauffa, J Sólyom, E Gláz, et al.
Pediatric Research
|
April 1, 1989
Hormone ontogeny in the ovine fetus: XIX: The effect of a potent luteinizing hormone-releasing factor agonist on gonadotropin and testosterone release in the fetus and neonate
S J Clark, B P Hauffa, K P Rodens, et al.
European Journal of Endocrinology
|
February 10, 2012
Functional and total IGFBP3 for the assessment of disorders of the GH/IGF1 axis in children with chronic kidney disease, GH deficiency, or short stature after SGA status at birth
A K Büscher, R Büscher, L Pridzun, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 13, 2002
Male LH-independent sexual precocity in a 3.5-year-old boy caused by a somatic activating mutation of the LH receptor in a Leydig cell tumor
A Richter-Unruh, H T Wessels, U Menken, et al.
Hormone Research
|
August 20, 2009
Is the response to growth hormone in short children born small for gestational age dependent on genetic or maternal factors?
Otto Mehls, A Lindberg, M Bettendorf, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 1, 2000
Diagnosis and management of juvenile hyperthyroidism in Germany: a retrospective multicenter study
J Dötsch, T Siebler, B P Hauffa, et al.
Page
of 6