Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Mariano Castro-Magana"'
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 35(6)
Objectives Prader–Willi syndrome (PWS) is a complex genetic disorder with severe hypotonia, failure to thrive, childhood obesity, hypogonadism/hypogenitalism and learning/behavioral problems with endocrine-related growth and other hormone deficienc
Publikováno v:
Journal of bone and mineral metabolism. 40(1)
Publikováno v:
Journal of Bone and Mineral Metabolism. 40:175-175
Autor:
Moris Angulo, Mariano Castro-Magana
Publikováno v:
Journal of the Endocrine Society
Baseline a.m ACTH and Cortisol levels in Children with Prader-Willi-syndrome are no different from general population. Moris Angulo, MD1 & Mariano Castro-Magaña, MD1 1Dept of Peds, NYU-Winthrop Hospital, New York, NY Background Prader-Willi syndrome
Publikováno v:
Pediatric Research. 87:970-970
Publikováno v:
Journal of Bone and Mineral Metabolism. 38:139-139
The following corrections are found in the original publication of the article and corrected as below.
Publikováno v:
The Endocrinologist. 14:261-264
A 3-year and 11-months-old boy presented with a 9-month history of increasing penile enlargement, pubic hair, deepening of the voice, and rapid growth. The erect penile length was 14 cm with bilateral testicular volume of 3 mL. Laboratory evaluation
Autor:
Jodi F. Evans, Carmen D. Tapiador, Yaw Appiagyei-Dankah, James K. Yeh, John F. Aloia, Mariano Castro-Magana
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 284:E566-E573
The hypophysectomized rat has been used as a model to study the effects of growth hormone deficiency on bone. Here, we have investigated the influence of growth hormone administration to hypophysectomized rats (HX) for 6 wk on accumulation of triglyc
Autor:
Kenneth C. Copeland, Barry H. Rich, Chantal Lutfallah, Weihua Wang, Mariano Castro-Magana, Raphael David, Ying Tai Chang, J. Ian Mason, Anzar Haider, Songya Pang
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:2611-2622
To define the hormonal criteria via genotypic proof for 3beta-hydroxysteroid dehydrogenase (3beta-HSD) deficiency in the adrenals and gonads, we investigated the type II 3beta-HSD genotype in 55 patients with clinical and/or hormonal presentation sug
Autor:
Nicolle M. Siegart, Mariano Castro Magana, Joshua DeLeon, Siham Accacha, Jorge Mejia Corletto, Iryna Voloshyna, Lora J. Kasselman, Allison B. Reiss
Publikováno v:
Journal of the American College of Cardiology. 69:2067