Zobrazeno 1 - 10
of 132
pro vyhledávání: '"W, Bloise"'
Autor:
W Nicolau, Berenice B. Mendonca, R G Sutcliffe, Ivo J.P. Arnhold, B L Wajchenberg, A J Russell, M Vasconcelos-Leite, A M Wallace, W Bloise
Publikováno v:
Journal of Molecular Endocrinology. 12:119-122
A mutation (A82T) is described in the coding sequence of the gene for 3ß-hydroxysteroid dehydrogenase (3ß-HSD) type II that is associated with variable clinical consequences. Four homozygotes are described, all of which showed elevated levels of Δ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::180a8bd039c08e12819b962596160fe3
https://doi.org/10.1677/jme.0.0120119
https://doi.org/10.1677/jme.0.0120119
Publikováno v:
Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine. 12(4)
Previous in vitro studies have demonstrated zinc (Zn++) inhibition of basal and of potassium (K+) or thyrotropin-releasing hormone (TRH)-stimulated prolactin (PRL) secretion, in a selective, reversible, and dose-dependent manner. Thus, Zn++ may regul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb6db6570c80a892cc162ec6d0cfed58
https://pubmed.ncbi.nlm.nih.gov/10816735
https://pubmed.ncbi.nlm.nih.gov/10816735
Autor:
T A, Bachega, A E, Billerbeck, G, Madureira, I J, Arnhold, M A, Medeiros, J A, Marcondes, C A, Longui, W, Nicolau, W, Bloise, B B, Mendonca
Publikováno v:
Human heredity. 49(1)
The frequency of large mutations was determined in 131 Brazilian patients with different clinical forms of 21-hydroxylase deficiency, belonging to 116 families. DNA samples were examined by Southern blotting hybridization with genomic CYP21 and C4cDN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::32d0746dc5778d81627ab6abf241fddc
https://pubmed.ncbi.nlm.nih.gov/10189236
https://pubmed.ncbi.nlm.nih.gov/10189236
Publikováno v:
The Journal of clinical endocrinology and metabolism. 84(2)
In genetic males, mutation of the 17beta-hydroxysteroid dehydrogenase 3 (17HSD3)gene that is normally expressed in the testes impairs testosterone formation and causes development of male pseudohermaphroditism. We have ascertained seven women who are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8ec28ea4a1c5056b24c61bfe570398e
https://pubmed.ncbi.nlm.nih.gov/10022457
https://pubmed.ncbi.nlm.nih.gov/10022457
Publikováno v:
Revista do Hospital das Clinicas. 52(1)
Pheochromocytoma is a rare neoplasm, found in 0.1% of all hypertensive patients. Extraadrenal pheochromocytomas occur in 18% of all cases and 1% accurate in the bladder. In this study, we report a case of a vesical pheochromocytoma in a 40-year-old m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c927503206cba817d6d453c3ef24143
https://pubmed.ncbi.nlm.nih.gov/9334469
https://pubmed.ncbi.nlm.nih.gov/9334469
Autor:
S L Blethen, Berenice B. Mendonca, H P Schwarz, J D Wilson, D W Russel, W Bloise, Wayne M. Geissler, S F Witchel, Stefan Andersson, Ling Wu, J E Griffin, Melvin M. Grumbach, D L Davis, Maria I. New, Gordon B. Cutler
Publikováno v:
The Journal of clinical endocrinology and metabolism. 81(1)
Autosomal recessive mutations in the 17 beta-hydroxysteroid dehydrogenase 3 gene impair the formation of testosterone in the fetal testis and give rise to genetic males with female external genitalia. Such individuals are usually raised as females, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82f5319c142c7020332760c3de40ed2e
https://pubmed.ncbi.nlm.nih.gov/8550739
https://pubmed.ncbi.nlm.nih.gov/8550739
Publikováno v:
Revista do Hospital das Clinicas. 47(6)
The possibility of treatment of endocrine exophthalmos by resection of orbital fat has been discussed by Olivari. The orbital fat is located in two spaces: the outer space which surrounds the extraocular muscles the anterior extensions of which form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1d03ad52434dc6a85a653e7368c6155
https://pubmed.ncbi.nlm.nih.gov/1340614
https://pubmed.ncbi.nlm.nih.gov/1340614
Autor:
M A, Pereira, S M, Jugue, O M, Moura, K, Gross, A, Halpern, W, Nicolau, B, Liberman, W, Bloise, B, Mendonça, N D, Cabral
Publikováno v:
Revista da Associacao Medica Brasileira (1992). 38(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::268d5547be893a6a39a5c0422fccea7e
https://pubmed.ncbi.nlm.nih.gov/1307058
https://pubmed.ncbi.nlm.nih.gov/1307058
Publikováno v:
Pediatric Research. 36:678-678
Androgen receptor (AR) gene was studied in 8 patients with AIS diagnosed clinically and biochemically. All had 46,XY karyotype and bilateral testes. Four with complete form had normal female external genitalia and breast development at puberty. Four
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b93a750b9258ad7e6a28d74ad5b1a519
https://doi.org/10.1203/00006450-199411000-00062
https://doi.org/10.1203/00006450-199411000-00062
Publikováno v:
Revista do Hospital das Clinicas. 33(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::894637bf03c6d06a482f6248828cc89b
https://pubmed.ncbi.nlm.nih.gov/663512
https://pubmed.ncbi.nlm.nih.gov/663512