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Citation: U. Eiholzer et al., TREATMENT WITH HUMAN GROWTH-HORMONE IN PATIENTS WITH PRADER-LABHART-WILLI-SYNDROME REDUCES BODY-FAT AND INCREASES MUSCLE MASS AND PHYSICAL PERFORMANCE, European journal of pediatrics, 157(5), 1998, pp. 368-377
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ZACHMANN M
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Citation: M. Vonaster et al., PSYCHIATRIC, NEUROPEDIATRIC, AND NEUROPSYCHOLOGICAL SYMPTOMS IN A CASE OF HYPOMELANOSIS OF ITO, European child & adolescent psychiatry, 6(4), 1997, pp. 227-233
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Citation: E. Leiberman et al., SUBNORMAL CORTISOL RESPONSE TO ADRENOCORTICOTROPIN IN ISOLATED PARTIAL 17,20-LYASE DEFICIENCY, Journal of pediatric endocrinology & metabolism, 10(4), 1997, pp. 387-390
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Citation: A. Schinzel et al., KALLMANN-SYNDROME IN A BOY WITH A T(1-10) TRANSLOCATION DETECTED BY REVERSE CHROMOSOME PAINTING, Journal of Medical Genetics, 32(12), 1995, pp. 957-961
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ZAPF J
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Citation: Ej. Schoenle et al., REPLACEMENT OF GROWTH-HORMONE (GH) IN NORMALLY GROWING GH-DEFICIENT PATIENTS OPERATED FOR CRANIOPHARYNGIOMA, The Journal of clinical endocrinology and metabolism, 80(2), 1995, pp. 374-378
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Citation: S. Schmitt et al., PITUITARY-STALK THICKENING WITH DIABETES-INSIPIDUS PRECEDING TYPICAL MANIFESTATIONS OF LANGERHANS CELL HISTIOCYTOSIS IN CHILDREN, European journal of pediatrics, 152(5), 1993, pp. 399-401
Citation: M. Zachmann, RECENT ASPECTS OF STEROID-BIOSYNTHESIS IN MALE SEX-DIFFERENTIATION - CLINICAL-STUDIES, Hormone research, 38(5-6), 1992, pp. 211-216