Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Renata C Scalco"'
Autor:
Renata C Scalco, Ericka B Trarbach, Edoarda V A Albuquerque, Thais K Homma, Thais H Inoue-Lima, Mirian Y Nishi, Berenice B Mendonca, Alexander A L Jorge
Publikováno v:
Endocrine Connections, Vol 8, Iss 11, Pp 1513-1519 (2019)
Most patients with Turner syndrome (TS) need hormone replacement therapy because of hypergonadotropic hypogonadism; individual outcomes, however, are highly variable. Our objective was to assess the influence of five estrogen recept or 1 gene (ESR1)
Externí odkaz:
https://doaj.org/article/b9f192b6f04846c2b4f2a7d8a3c6d9d8
Autor:
Renata C. Scalco, Fernanda T. Gonçalves, Hadassa C. Santos, Mari M. S. G. Cardena, Carlos A. Tonelli, Mariana F. A. Funari, Rosana M. Aracava, Alexandre C. Pereira, Cintia Fridman, Alexander A. L. Jorge
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 2, Pp 436-441 (2017)
ABSTRACT Homozygous STAT5B mutations causing growth hormone insensitivity with immune dysfunction were described in 10 patients since 2003, including two Brazilian brothers from the south of Brazil. Our objectives were to evaluate the prevalence of t
Externí odkaz:
https://doaj.org/article/d662dc41a14d4187960452232e373408
Autor:
Naiara C.B. Dantas, Mariana F.A. Funari, Gabriela A. Vasques, Nathalia L.M. Andrade, Raíssa C. Rezende, Vinicius Brito, Renata C. Scalco, Ivo J.P. Arnhold, Berenice B. Mendonca, Alexander A.L. Jorge
Publikováno v:
Hormone Research in Paediatrics. 95:264-274
Introduction: Isolated SHOX haploinsufficiency is a common monogenic cause of short stature. Few studies compare untreated and rhGH-treated patients up to adult height (AH). Our study highlights a growth pattern from childhood to AH in patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f725a4f22addf2ac734bc4e41a79381
https://doi.org/10.1159/000524374
https://doi.org/10.1159/000524374
Autor:
Sonir Roberto Rauber Antonini, Berenice B. Mendonca, Renata C. Scalco, Sofia Helena Valente de Lemos-Marini, Alexander A. L. Jorge, Ester R. Silveira, Ivo J.P. Arnhold, Naiara C.B. Dantas, Gil Guerra-Júnior, Adriana F. Braz, Alexsandra C. Malaquias
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Context: Treatment with growth hormone (GH) is considered effective in improving adult height (AH) in Turner syndrome (TS). However, there are few studies comparing AH between treated patients and a concurrent untreated group. Objective: To assess th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c447aa8bcef76e544a9417a2e5804f20
https://doi.org/10.1159/000516869
https://doi.org/10.1159/000516869
Disorders of the GH-IGF axis include a large heterogeneous group of conditions with distinct phenotypes. Each of the defects identified in this axis is responsible for a rare and specific condition that endocrinologists need to be familiar with. Trad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9aaac4cfe47424ac4217778271fa04c
https://doi.org/10.1093/med/9780198870197.003.0181
https://doi.org/10.1093/med/9780198870197.003.0181
Autor:
Thais Kataoka Homma, Thais H. Inoue-Lima, Mirian Yumie Nishi, Ericka B. Trarbach, Edoarda Vasco de Albuquerque Albuquerque, Alexander A. L. Jorge, Renata C. Scalco, Berenice B. Mendonca
Publikováno v:
Endocrine Connections, Vol 8, Iss 11, Pp 1513-1519 (2019)
Endocrine Connections
Endocrine Connections
Most patients with Turner syndrome (TS) need hormone replacement therapy because of hypergonadotropic hypogonadism; individual outcomes, however, are highly variable. Our objective was to assess the influence of five estrogen receptor 1 gene (ESR1) p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d2c49567efe43817bb1c69db2b40f2e
https://doi.org/10.1530/ec-19-0398
https://doi.org/10.1530/ec-19-0398
Autor:
Marilena Nakaguma, Thais H. Inoue-Lima, Alexander A. L. Jorge, Renata C. Scalco, Ivo J.P. Arnhold, Berenice B. Mendonca, Gabriela A Vasques
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 32:173-179
Background When evaluating peripubertal short stature patients, the interpretation of insulin-like growth factor 1 (IGF-1) levels based on chronological age (CA) can be inaccurate due to the influence of sex steroids and, presently, there is no evide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe3407c6024747199f24ba66bc794471
https://doi.org/10.1515/jpem-2018-0435
https://doi.org/10.1515/jpem-2018-0435
Autor:
Erika Bezerra Parente, Monica Fernandez, Jose Viana Lima, Carolina Croce Azuaga, Monica De Aguiar Medeiros, Luciana Mela Umeda, Nilza Maria Scalissi, Adriano Namo Cury, Marilia Tomiyoshi Asato, Erika Fukunaga, Thiago Fraga Napoli, Renata C. Scalco, João Eduardo Nunes Salles, Pedro Franco
Publikováno v:
Journal of the Endocrine Society
Background and aims: The physiopathology of hyperinsulinemic hypoglycemia (HH) after gastric bypass (GB) is not well understood, although it is a common adverse event after this procedure. The fast absorption of glucose after a meal, the high glucose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::650dc738547903e4e26e47ec17eff02c
http://europepmc.org/articles/PMC7209378
http://europepmc.org/articles/PMC7209378
Autor:
Berenice B. Mendonca, Alexander A. L. Jorge, Gil Guerra-Júnior, Adriana F. Braz, Alexsandra C. Malaquias, Sonir Roberto Rauber Antonini, Renata C. Scalco
Publikováno v:
Journal of the Endocrine Society
Background: Short stature is the most frequent clinical manifestation in Turner syndrome (TS), occurring in 98% of these patients. Growth hormone was shown to improve adult height in TS patients from diverse genetic backgrounds. However, there are fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce6e755c0107e9e60970df7c25cf9b19
https://doi.org/10.1210/jendso/bvaa046.1649
https://doi.org/10.1210/jendso/bvaa046.1649
Autor:
Renata C. Scalco, Cybelle A Louback, C. Bueno, Marcos A C Oliveira, Jose Viana Lima, Nilza Maria Scalissi, Gustavo Piech Ricardo
Publikováno v:
Journal of the Endocrine Society
Introduction Neuroendocrine Neoplasms are rare, with an incidence of 5 to 100,000 inhabitants, constituting 1% of all malignancies, presenting high survival rates in general, even in metastatic diseases. However, in those poorly differentiated, as in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31888e687af8b90936a4f60d0f200a62
https://doi.org/10.1210/jendso/bvaa046.1601
https://doi.org/10.1210/jendso/bvaa046.1601