Zobrazeno 1 - 10
of 16
pro vyhledávání: '"B B, Mendonça"'
Publikováno v:
Clinical genetics. 91(2)
Genetic studies in Disorders of Sex Development (DSD), representing a wide spectrum of developmental or functional conditions of the gonad, have mainly been oriented towards the coding genome. Application of genomic technologies, such as whole-exome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d55801bd52c3979b121a7caadbf93bb
https://pubmed.ncbi.nlm.nih.gov/27801941
https://pubmed.ncbi.nlm.nih.gov/27801941
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:
A L, Boehmer, A O, Brinkmann, L A, Sandkuijl, D J, Halley, M F, Niermeijer, S, Andersson, F H, de Jong, H, Kayserili, M A, de Vroede, B J, Otten, C W, Rouwé, B B, Mendonça, C, Rodrigues, H H, Bode, P E, de Ruiter, H A, Delemarre-van de Waal, S L, Drop
Publikováno v:
The Journal of clinical endocrinology and metabolism. 84(12)
17Beta-hydroxysteroid dehydrogenase-3 (17betaHSD3) deficiency is an autosomal recessive form of male pseudohermaphroditism caused by mutations in the HSD17B3 gene. In a nationwide study on male pseudohermaphroditism among all pediatric endocrinologis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96f4284f72aa41dd4ad0a211c7d1058b
https://pubmed.ncbi.nlm.nih.gov/10599740
https://pubmed.ncbi.nlm.nih.gov/10599740
Autor:
M A, Pereira, A, Halpern, L R, Salgado, B B, Mendonça, M, Nery, B, Liberman, D H, Streeten, B L, Wajchenberg
Publikováno v:
Clinical endocrinology. 49(4)
The prevalence of Nelson's syndrome has varied greatly, at least in part because of the variability of the diagnostic criteria employed by different authors. We define Nelson's syndrome as the presence of an enlarging pituitary tumour associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9bd9bd5a34ef32c4a4321b9d16e61841
https://pubmed.ncbi.nlm.nih.gov/9876353
https://pubmed.ncbi.nlm.nih.gov/9876353
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:
A C, Magalhães, K C, Uehara, D, Iezzi, L S, Lo, S C, Mathias, L R, Salgado, M A, Ramos, B B, Mendonça, B, Liberman, B L, Wajchenberg
Publikováno v:
Revista do Hospital das Clinicas. 50(4)
We compared 1.5 T magnetic resonance (MR) image findings in 193 patients with congenital pituitary insufficiency. One hundred and thirty nine of the MR studies were obtained in patients who had isolated growth hormone deficiency (GHD). Other fifty-fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c38342619929a01e8603416005b7b6f
https://pubmed.ncbi.nlm.nih.gov/8560145
https://pubmed.ncbi.nlm.nih.gov/8560145
Publikováno v:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas. 27(5)
1. Adrenal ectopic tissue has been detected in the paragonadal region of normal women. In patients with congenital adrenal hyperplasia due to 21-hydroxylase (21-OH) deficiency, the manifestation of hyperplasia of paragonadal accessory adrenal tissue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccd30b3b700361b43fe927f61065eb11
https://pubmed.ncbi.nlm.nih.gov/8000336
https://pubmed.ncbi.nlm.nih.gov/8000336
Publikováno v:
Pediatric Research. 41:301-301
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e350eb94f035382d3beb5d11d04865c2
https://doi.org/10.1203/00006450-199702000-00030
https://doi.org/10.1203/00006450-199702000-00030
Autor:
B B, Mendonça, G, Madureira, W, Bloise, A, Albergaria, A, Halpern, B, Liberman, S M, Villares, M C, Batista, V F, Avancini, C T, Nitterdorfi
Publikováno v:
Revista paulista de medicina. 107(1)
The authors studied 8 patients (4 males and 4 females) with Cushing's syndrome due to ectopic ACTH secretion. Chronological age ranged from 15 to 45 years and duration of the disease ranged from 3 to 48 months. All patients presented typical signs of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::633596f88cb3601e7635bfcb5130ff3d
https://pubmed.ncbi.nlm.nih.gov/2559451
https://pubmed.ncbi.nlm.nih.gov/2559451
Autor:
B B, Mendonça, M C, Batista, I J, Arnhold, W, Nicolau, G, Madureira, V S, Lando, M B, Kohek, D G, Carvalho, W, Bloise
Publikováno v:
Revista do Hospital das Clinicas. 42(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::84673394cec188cde9ba2fcb8a2f35fb
https://pubmed.ncbi.nlm.nih.gov/3441728
https://pubmed.ncbi.nlm.nih.gov/3441728