Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Maria D. Urban"'
Publikováno v:
Hormone Research in Paediatrics. 59:205-210
Objective: We present the 1st case of prepubertal hyperandrogenism because of a defect in the conversion of cortisone (E) to cortisol (F) by hepatic11β-hydroxysteroid dehydrogenase type 1. Methods and Results: Clinical and anthropometric data were o
Publikováno v:
Hormone Research in Paediatrics. 49:46-50
We studied 2 subjects with a 45,X/46,X,ring(Y) karyotype. Both of them were evaluated because of short stature and a subnormal rate of linear growth. One patient had additional features of the Ullrich-Turner syndrome. Both subjects had normal male ex
Autor:
Claude J. Migeon, Majid Ghahremani, Maria D. Urban, Jerry Pelletier, John S. Fuqua, Terry R. Brown, Ellen S. Sher, Elizabeth J. Perlman, Gary D. Berkovitz
Publikováno v:
Human Genetics. 97:506-511
Among a group of patients with abnormal sexual differentiation, we have identified two subjects who had a 46,XY karyotype, ambiguous genitalia, and well-developed Müllerian structures, but normal appearing testes. The presence of ambiguous genitalia
Autor:
Penny A. Bard, Peter A. Lee, Kirby D. Smith, Vikram Jaswaney, James A. Amrhein, Gary D. Berkovitz, Patricia Y. Fechner, Peter N. Goodfellow, Sandra M. Marcantonio, Gail Stetten, Eva Tsalikian, Cheryl S. Reid, Claude J. Migeon, Maria D. Urban
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 76:690-695
The condition of 46,XX maleness is characterized by testicular development in subjects who have two X chromosomes but who lack a normal Y chromosome. Several etiologies have been proposed to explain 46,XX maleness: 1) translocation of the testis-dete
Autor:
Jörg Dötsch, Thomas Horbach, Tomasz Romer, Ellen Schoof, Ewa M. Małunowicz, T.J. Cole, M. Hermanussen, Umit Karayalcin, Maria D. Urban, Per Björntorp, Evangelia Charmandari, Jürgen Kratzsch, Mikael Knip, Gökhan Yazıcıoğlu, George P. Chrousos, Gulay Ozbilim, Roland Rosmond, Mustafa Kemal Balci, Hasan Altunbaş, Ender Semiz, Wolfgang Rascher, Artur Bossowski, Claude Bouchard, Monique Chagnon, Anja Stuppy, Hans K. Åkerblom, R. Carbon, Emmanuil Souvatzoglou, Frank Harig, Paula Vähäsalo, Tomoshige Kino, Vesa Eskola, Helmut Singer
Publikováno v:
Hormone Research in Paediatrics. 59:209-209
Publikováno v:
The Journal of Pediatrics. 94:823-827
Long-term, low-dosage androgen treatment of patients with Turner syndrome results in more rapid growth and significantly greater adult height than in control patients who receive only estrogen for pubertal development. Seventeen patients treated with
Publikováno v:
Hormone Research. 13:81-89
2 Cases of childhood Cushing's disease have been treated with bilateral adrenalectomy and autotransplantation of adrenal tissue. Transplantation was unsuccessful in 1 case. In the other patient, replacement therapy was discontinued without any sympto
Autor:
Melvin Ching, Antonello Sannia, Richard A. Jungmann, Maria D. Urban, Doriano Fabbro, J.C.M. Khoo, Zeev Hochberg, Otakar Koldovsky, K.H. Voigt, W. Kleinert, Robert A. Richman, Linda V. Oberkotter, Claude J. Migeon, E. Heinze, Sharon M. Ventura, Ermanno Rolandi, G. Magnani, Sally L. Dachtler, Catherine M. Vandenberg, Tommaso Barreca, C.H. Tan, Alfred Tenore, John S. Parks, Peter A. Lee, Urs Eppenberger
Publikováno v:
Hormone Research. 14:I-IV
Publikováno v:
Human Immunology. 2:139-145
Close linkage between HLA and the gene for 21-OH deficiency causing congenital virilizing adrenal hyperplasia (CVAH) has been well documented. HLA-A/B and HLA/GLO recombination data placed the CVAH gene within the HLA-A to GLO interval, with CVAH inv
Publikováno v:
New England Journal of Medicine. 299:1392-1396
The effects of congenital adrenal hyperplasia on adult height and fertility were studied in 30 afflicted men. The patients' heights ranged from 150.0 to 178.6 cm (mean ±1 S.D. of 164.0±7.6), which is significantly lower than both the mean adult hei