Zobrazeno 1 - 10
of 264
pro vyhledávání: '"B L, WAJCHENBERG"'
Autor:
B. L. Wajchenberg
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 80:2791-2794
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffa58e0455113a6bcffd7847ffd8e33f
https://doi.org/10.1210/jc.80.9.2791
https://doi.org/10.1210/jc.80.9.2791
Publikováno v:
Journal of Radioanalytical and Nuclear Chemistry Letters. 200:337-349
This work reports the radioiodination of human thyrotropin (hTSH) in our laboratory (IPEN) and evaluates its quality in comparison with a commercial product. The radioiodination yield obtained in 20 experiments ranged from 18.5 to 56.3%, while the pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cec776c95faf3d25dbee13e69de5e8a
https://doi.org/10.1007/bf02163787
https://doi.org/10.1007/bf02163787
Autor:
B. L. Wajchenberg
Publikováno v:
Endocrine Reviews. 15:752-787
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d8747e33f7821050d52c2860bcd3a48
https://doi.org/10.1210/er.15.6.752
https://doi.org/10.1210/er.15.6.752
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
Autor:
B L Wajchenberg, Héctor M. Targovnik, Viviana Varela, Geraldo Medeiros-Neto, Gilbert Vassart, Jacques Emile Dumont, Gustavo Daniel Frechtel
Publikováno v:
Journal of Endocrinological Investigation. 16:415-419
Thyroid tissue total RNAs from multinodular goiter (G2) and from hereditary goiter with defective Tg synthesis (JNA) were hybridized with a 5'albumin cDNA probe (F-47), a 3' albumin cDNA probe (B-44) and a thyroglobulin cDNA probe (phTgM3). JNA refer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd47705cfec2e9d3f7aaded6202321b8
https://doi.org/10.1007/bf03348869
https://doi.org/10.1007/bf03348869
Autor:
Meyer Knobel, B L Wajchenberg, Ampica Mangklabruks, Ana-Elisa Correa Billerbeck, Geraldo Medeiros-Neto, Leslie J. DeGroot, Nancy J. Cox
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 72:471-476
We have conducted biochemical and genetic studies in five unrelated families (denoted A, C, R, P, and G), which included nine goitrous subjects (five borderline euthyroid and four hypothyroid) with complete (n = 6) or partial (n = 3) thyroid peroxida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d196b9cf1c63fbe3b5d722abb346754
https://doi.org/10.1210/jcem-72-2-471
https://doi.org/10.1210/jcem-72-2-471
Autor:
J. Cuba, W. El-Andere, A. Buescu, M. Vaisman, Mauro Tendrich, V. De Luca, A. A. Pereira, B. L. Wajchenberg, B. Wanke, E. K. Tourinho
Publikováno v:
The American Journal of Tropical Medicine and Hygiene. 44:83-92
Fifteen patients with proven disseminated paracoccidioidomycosis (PCM) had computed tomography (CT) and ultrasonography (US) performed to evaluate the form, shape, density and size of their adrenal glands. Plasma and urinary cortisol were determined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6ddb852fc3dd70e0aca50a4929a1452
https://doi.org/10.4269/ajtmh.1991.44.83
https://doi.org/10.4269/ajtmh.1991.44.83
Autor:
Viviana Varela, Carmen Abatangelo, Héctor M. Targovnik, Geraldo Medeiros-Neto, B L Wajchenberg
Publikováno v:
Thyroid. 1:339-345
We have studied a member (JBM) of a family MO previously described, with congenital goiter, hypothyroidism, and presence of hyposialylated Tg in the follicular lumen. Other congenital goiters (MA and JNA) with virtual absence of Tg were studied simil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f00de373bce34f60b74d29209188808f
https://doi.org/10.1089/thy.1991.1.339
https://doi.org/10.1089/thy.1991.1.339
Autor:
B L, Wajchenberg, M A, Albergaria Pereira, B B, Medonca, A C, Latronico, P, Campos Carneiro, V A, Alves, M C, Zerbini, B, Liberman, G, Carlos Gomes, M A, Kirschner
Publikováno v:
Cancer. 88(4)
The clinical features and natural history of adrenocortical carcinoma are highly dependent on the type of center reporting their experience. Observations from oncology services suggest a high incidence of nonfunctioning tumors, whereas reports from e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b6858e47f063d71666ad8181fa332f13
https://pubmed.ncbi.nlm.nih.gov/10679640
https://pubmed.ncbi.nlm.nih.gov/10679640
Autor:
M N, Nikiforova, Y E, Nikiforov, P, Biddinger, D R, Gnepp, L A, Grosembacher, B L, Wajchenberg, J A, Fagin, R M, Cohen
Publikováno v:
Clinical endocrinology. 51(1)
Pancreatic islet betacell tumours occur either sporadically or as part of inherited neoplastic syndromes, most commonly multiple endocrine neoplasia (MEN) type 1. Recently, a transgenic mouse model has been established in which the expression of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::59a93e23887a8a002a336ac792d185ba
https://pubmed.ncbi.nlm.nih.gov/10468960
https://pubmed.ncbi.nlm.nih.gov/10468960