Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Berenice B. de Mendonça"'
Autor:
Danilo Moretti-Ferreira, Célia P. Koiffmann, Anita Wajntal, Aron J. Diament, Berenice B. de Mendonça, Josefina Mattieli, P. H. Saldanha
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 49, Iss 2, Pp 164-171 (1991)
Crianças com síndrome de Sotos apresentam aceleração do crescimento, macrocrania, padrões acromagalóides e dificuldades iniciais no desenvolvimento neuropsicomotor. A delineação da síndrome e o diagnóstico diferencial estão baseados na ava
Externí odkaz:
https://doaj.org/article/6ef60812e94a4996bd05d3f82d87eb0c
Autor:
Milena Garcia, Abrão, Ana Elisa C, Billerbeck, Mirian Yumie, Nishi, Suemi, Marui, Berenice B de, Mendonça
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 49(6)
DNA extraction of peripheral leukocytes is the most broadly used technique to obtain DNA. However, cell collection from an oral swab, frequently used in forensics, is useful to obtain DNA samples, mainly in newborns, children and patients who live fa
Autor:
Alexander A de Lima, Jorge, Hamilton C de, Menezes Filho, Theresa S Soares, Lins, Dulce Rondini, Guedes, Durval, Damiani, Nuvarte, Setian, Ivo J Prado, Arnhold, Berenice B de, Mendonça
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 49(3)
We studied the growth hormone receptor (GHR) gene in 6 patients with Laron syndrome (LS) from 4 unrelated families. Exons 2 to 10 were amplified by PCR using specific intronic pairs of primers. The PCR products were directly sequenced. Our results sh
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 49(5)
The adrenocortical tumorigenesis is a complex process, which involves multiple genetic changes. A better knowledge on the mechanisms involved in tumor development would enable an early identification of malignant disease and also lead to the developm
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 48(5)
A high frequency of adrenocortical tumors has been observed in Brazilian children and adults from South and Southwestern regions. The valuable national experience in the management of these tumors have resulted in several and relevant basic and clini
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 48(4)
Carney complex (CNC) is a familial multiple neoplasia syndrome associated with abnormal skin and mucosal pigmentation, primary pigmented nodular adrenocortical disease (PPNAD), cardiac and cutaneous myxomas, GH and PRL pituitary adenoma, testicular t
Autor:
Tânia A S S, Bachega, Ana Elisa C, Billerbeck, Erica B, Parente, Sofia H V, Lemos-Marini, Maria Tereza M, Baptista, Maricilda P, Mello, Gil, Guerra, Hilton, Kuperman, Nuvarte, Setian, Durval, Damiani, Natália, Torres, Margaret de, Castro, Berenice B de, Mendonça
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 48(5)
We analyzed the clinical and molecular data of 205 patients with the three different clinical forms of 21-hydroxylase deficiency, in whom the clinical and molecular diagnosis were already defined. The most frequent mutations were I2 splice in the sal
Autor:
Maria Helena Palma Sircili, Berenice B. de Mendonca, Francisco Tibor Denes, Guiomar Madureira, Tânia Aparecida Sartori Sanchez Bachega, Frederico Arnaldo de Queiroz e Silva
Publikováno v:
Clinics, Vol 61, Iss 3, Pp 209-214 (2006)
The ideal surgical technique and appropriate age for performing feminizing genitoplasty are debatable, and few long-term outcome studies have been reported. PURPOSE: To report a retrospective study on anatomical and functional outcomes of feminizing
Externí odkaz:
https://doaj.org/article/4b11f7310ea34693aab662e3f43771fb