Zobrazeno 1 - 10
of 111
pro vyhledávání: '"M L, Kottler"'
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 47, Iss 5, Pp 55-58 (2010)
We report a woman with primary amenorrhoea and infertility associated with an isolated deficiency of pituitary FSH that does not respond to GnRH administration. Serum inhibin B was undetectable and antimullerian hormone (AMH) was within the normal ra
Externí odkaz:
https://doaj.org/article/48590677aa7c4add8a013e8132d5eaec
Publikováno v:
Archives de Pédiatrie. 21:1115-1119
Resume L’intoxication a la vitamine D est une cause rare mais grave de l’hypercalcemie chez le nouveau-ne et le petit nourrisson. A travers neuf observations d’hypercalcemie chez des nouveau-nes ayant recu par voie orale 600 000 unites de la vi
Publikováno v:
Pathologie Biologie. 58:367-371
Parental imprinting and the type of the genetic alteration play a determinant role in the phenotype expression of GNAS locus associated to pseudohypoparathyroidism (PHP). This imprint is tissue-specific, mainly localized in the kidney and the thyroid
Akademický článek
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Autor:
H. Guillozo, C. Palix, T. M. Nguyen, Marthe Rizk-Rabin, F. Brouillard, P. Lagier, M. L. Kottler, J.M. Garnier, Michèle Garabédian, P. Adiceam
Publikováno v:
Journal of Bone and Mineral Research. 17:1728-1737
In this study, two related young children, brother and sister, exhibited severe vitamin D-resistant rickets without alopecia. Sequence analysis of the total vitamin D receptor (VDR) cDNA from skin fibroblasts revealed a substitution of the unique try
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 21(10)
Vitamin D intoxication with severe hypercalcemia is rare in the neonatal and infancy period. Through nine cases of hypercalcemia, secondary to taking 600,000 units of vitamin D (Sterogyl(®)), a review of vitamin D requirements and possible mechanism
Autor:
J. Blumberg-Tick, Mohieddine Moumni, Raymond Counis, M. L. Kottler, Yannick Lerrant, F. Bergametti
Publikováno v:
Endocrinology. 136:2803-2808
It was previously established that the administration of a potent GnRH agonist such as triptorelin (D-Trp6-GnRH) induced desensitization of pituitary gonadotropic cells, resulting in decreased expression of gonadotropin beta-subunit genes and the sup
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 79:1390-1394
We report the case of a patient with bilateral testicular tumors and congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Catheterization of the left testicular and adrenal veins was performed. The presence of 11 beta-hydroxylated steroid
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 140:S570-S571