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Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 30, 2002
McCune-Albright syndrome--the German experience
N Albers, S Jörgens, D Deiss, et al.
Lancet (London, England)
|
June 23, 1984
Dissociation between plasma adrenal androgens and cortisol in Cushing's disease and ectopic ACTH-producing tumour: relation to adrenarche
B P Hauffa, S L Kaplan, M M Grumbach
Klinische Padiatrie
|
November 26, 1999
[Psychosocially stunted growth masked as growth hormone deficiency]
B Doeker, Simić-Schleicher, B P Hauffa, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
February 1, 1992
Transient elevation of urinary catecholamine excretion and cholestatic liver disease in a neonate with hypopituitarism
J Krähe, B P Hauffa, H A Wollmann, et al.
European Journal of Pediatrics
|
November 1, 1992
Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 families
D Strumberg, B P Hauffa, B Horsthemke, et al.
Journal of Intellectual Disability Research : JIDR
|
December 17, 2003
Behavioural and emotional disturbances in people with Prader-Willi Syndrome
H-C Steinhausen, U Eiholzer, B P Hauffa, et al.
Hormone Research
|
January 30, 2002
Clinical and novel molecular findings in a 6.8-year-old Turkish boy with triple A syndrome
K Schmittmann-Ohters, A Huebner, A Richter-Unruh, et al.
Neuropsychobiology
|
April 5, 2001
Dehydroepiandrosterone sulphate and corticotropin levels are high in young male patients with conduct disorder: comparisons for growth factors, thyroid and gonadal hormones
T N Dmitrieva, R D Oades, B P Hauffa, et al.
Acta Endocrinologica
|
November 1, 1989
Discordant immune and growth response to pituitary and biosynthetic growth hormone in siblings with isolated growth hormone deficiency type IA
B P Hauffa, R Illig, T Torresani, et al.
BJU International
|
August 10, 2000
Long-term follow-up of female patients with congenital adrenal hyperplasia from 21-hydroxylase deficiency, with special emphasis on the results of vaginoplasty
S Krege, K H Walz, B P Hauffa, et al.
Page
of 6
Search research articles
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Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 30, 2002
McCune-Albright syndrome--the German experience
N Albers, S Jörgens, D Deiss, et al.
Lancet (London, England)
|
June 23, 1984
Dissociation between plasma adrenal androgens and cortisol in Cushing's disease and ectopic ACTH-producing tumour: relation to adrenarche
B P Hauffa, S L Kaplan, M M Grumbach
Klinische Padiatrie
|
November 26, 1999
[Psychosocially stunted growth masked as growth hormone deficiency]
B Doeker, Simić-Schleicher, B P Hauffa, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
February 1, 1992
Transient elevation of urinary catecholamine excretion and cholestatic liver disease in a neonate with hypopituitarism
J Krähe, B P Hauffa, H A Wollmann, et al.
European Journal of Pediatrics
|
November 1, 1992
Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 families
D Strumberg, B P Hauffa, B Horsthemke, et al.
Journal of Intellectual Disability Research : JIDR
|
December 17, 2003
Behavioural and emotional disturbances in people with Prader-Willi Syndrome
H-C Steinhausen, U Eiholzer, B P Hauffa, et al.
Hormone Research
|
January 30, 2002
Clinical and novel molecular findings in a 6.8-year-old Turkish boy with triple A syndrome
K Schmittmann-Ohters, A Huebner, A Richter-Unruh, et al.
Neuropsychobiology
|
April 5, 2001
Dehydroepiandrosterone sulphate and corticotropin levels are high in young male patients with conduct disorder: comparisons for growth factors, thyroid and gonadal hormones
T N Dmitrieva, R D Oades, B P Hauffa, et al.
Acta Endocrinologica
|
November 1, 1989
Discordant immune and growth response to pituitary and biosynthetic growth hormone in siblings with isolated growth hormone deficiency type IA
B P Hauffa, R Illig, T Torresani, et al.
BJU International
|
August 10, 2000
Long-term follow-up of female patients with congenital adrenal hyperplasia from 21-hydroxylase deficiency, with special emphasis on the results of vaginoplasty
S Krege, K H Walz, B P Hauffa, et al.
Page
of 6