Zobrazeno 1 - 10
of 37
pro vyhledávání: '"B. P. Hauffa"'
Publikováno v:
Acta Paediatrica. 89:1302-1311
UNLABELLED Height and weight in children with Prader-Willi syndrome, diagnosed by standard clinical criteria, follow a specific developmental pattern resulting in early childhood obesity, absent pubertal growth spurt and adolescent short stature. New
Publikováno v:
International Journal of Obesity. 25:S22-S25
BACKGROUND: Morbid obesity develops as a result of hyperphagia and compulsive eating behavior in patients with Prader-Willi syndrome (PWS), if caloric intake is not rigorously controlled. PWS-specific centile curves for adiposity indices constructed
Autor:
Graziano Grugni, C. J. Partsch, A. L. Carrel, H. R. Mogul, M. Castro-Magana, Ora H. Pescovitz, C. Lammer, R. L. Hintz, R. G. Rosenfeld, Peter Davies, D. B. Allen, I. Sipila, Phillip D.K. Lee, Susan E. Myers, B. P. Hauffa, D. M. Wilson, E. M. Ritzen, Urs Eiholzer, M. A. Angulo, M. Cappa, G. Chiumello
Publikováno v:
The Endocrinologist. 10:71S-74S
Prader-Willi syndrome (PWS) is a disabling condition characterized by hypotonia, hyperphagia, obesity, short stature, delayed or absent puberty, and mental retardation. The syndrome complex was first described in 1956 by Dr. Andrea Prader and colleag
Publikováno v:
Klinische Pädiatrie. 211:394-398
Short stature is a common reason for presenting a child to the pediatrician. Emotional deprivation may cause short stature and may simulate growth hormone deficiency. Diagnosis of emotional deprivation as the cause of growth retardation is difficult
Publikováno v:
Journal of Pediatric Orthopaedics, Part B. 8:103-106
Hormonal imbalance in puberty and biomechanical overload due to obesity have been implied in the still unknown cause of slipped capital femoral epiphysis (SCFE). Local mediators of growth hormone (GH) action, such as insulin-like growth factor I (IGF
Publikováno v:
European Journal of Pediatrics. 151:821-826
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase (21-OHase) deficiency is inherited as an autosomal recessive trait. Patients can present with the salt wasting, simple virilizing or a non-classical form of the disease. The gene for P450C21,
Autor:
F. Jockenhövel, W. Reinhardt, Georg Benker, S. Lederbogen, D. Reinwein, Th. Olbricht, B. P. Hauffa, W. Kuck
Publikováno v:
Journal of Endocrinological Investigation. 15:331-337
Of 50 patients with incidentalomas (INC), 18 were adrenalectomized and in 18 patients the INC was left in place. For 14 patients clinical data were insufficient for evaluation. Follow-up investigation of the 18 unoperated subjects 11-101 months (medi
Publikováno v:
Deutsche medizinische Wochenschrift (1946). 134(50)
Discontinuation of growth hormone (GH) treatment upon attainment of final height has been associated with impaired somatic development and altered body composition. Therefore, optimal care of patients with GH deficiency (GHD) in the transition phase
Publikováno v:
Klinische Wochenschrift. 69:725-730
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2008, 93 (11), pp.4183-4197. ⟨10.1210/jc.2008-0649⟩
Journal of Clinical Endocrinology and Metabolism, 93(11), 4183-4197. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2008, 93 (11), pp.4183-4197. ⟨10.1210/jc.2008-0649⟩
Journal of Clinical Endocrinology and Metabolism, 93(11), 4183-4197. Endocrine Society
OBJECTIVE: The objective of the study was to provide recommendations for the diagnosis and management of Prader-Willi syndrome throughout the life span to guide clinical practice. PARTICIPANTS: An open international multidisciplinary expert meeting w