Zobrazeno 1 - 10
of 98
pro vyhledávání: '"R, Sandrini"'
Autor:
R.C. Ribeiro, E.L. Michalkiewicz, B.C. Figueiredo, L. DeLacerda, F. Sandrini, M.D. Pianovsky, G. Sampaio, R. Sandrini
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 33, Iss 10, Pp 1225-1234 (2000)
Childhood adrenocortical tumors (ACT) are rare. In the USA, only about 25 new cases occur each year. In Southern Brazil, however, approximately 10 times that many cases are diagnosed each year. Most cases occur in the contiguous states of São Paulo
Externí odkaz:
https://doaj.org/article/686989a23d4c4868811191e2df76d373
Publikováno v:
Proceedings of the Institution of Mechanical Engineers, Part A: Journal of Power and Energy. 225:1066-1075
This article investigates the possibility to enhance the performance of a biomass organic Rankine cycle (ORC) plant by adding an externally fired gas turbine (EFGT), yielding a combined EFGT + ORC system. A typical ORC configuration is first modelled
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17f87ecd4b4566e8b119bece7f3f77cf
https://doi.org/10.1177/0957650911415188
https://doi.org/10.1177/0957650911415188
Publikováno v:
Acta Paediatrica. 82:56-60
The dose of glucocorticoid was evaluated in the treatment of 19 patients with salt-losing congenital adrenal hyperplasia due to complete or nearly complete 21-hydroxylase deficiency. In most cases, follow-up was from infancy to puberty. The dose of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba160221f4d6fc1d8c31df5063fd5c99
https://doi.org/10.1111/j.1651-2227.1993.tb12844.x
https://doi.org/10.1111/j.1651-2227.1993.tb12844.x
Publikováno v:
One Century of the Discovery of Arsenicosis in Latin America (1914-2014) As2014: Proceedings of the 5th International Congress on Arsenic in the Environment, May 11-16, 2014, Buenos Aires, Argentina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8725b734141edd3bb4beec2a9ec34430
https://doi.org/10.1201/b16767-156
https://doi.org/10.1201/b16767-156
Autor:
R. Sandrini
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 82:2027-2031
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a68d367bfb8d51ee3c5a1ad0f9a79a53
https://doi.org/10.1210/jc.82.7.2027
https://doi.org/10.1210/jc.82.7.2027
Autor:
R. Sandrini, A.C. Mehl, Gibran Avelino Frandoloso, Pedro Henrique Isaacson Velho, B. Araujo, Maria Aparecida Pachaly, Mauricio Carvalho, G.B.G. Silva
Publikováno v:
QJM : monthly journal of the Association of Physicians. 108(1)
A 28-year-old patient was admitted because of painless, massive hematuria (Figure 1), accompanied by severe hypotension and hemodynamic instability. It was the fifth episode in the last 3 months. He has been previously treated for epilepsy, diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74d83017408d5be404aac29c9de19fff
https://pubmed.ncbi.nlm.nih.gov/22670062
https://pubmed.ncbi.nlm.nih.gov/22670062
Autor:
Pedro André Kowacs, M. R. Young Blood, Rogério Andrade Mulinari, R. Sandrini, Elcio Juliato Piovesan, Lineu Cesar Werneck
Publikováno v:
Cephalalgia : an international journal of headache. 27(4)
A randomized double-controlled trial involving 22 patients with Noonan syndrome (NS) and 22 normal individuals (control group) was carried out to determine the prevalence of migraine in patients with NS. The NS group consisted of 11 males aged 19.55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eefeb917451e4652546a9175c5a3e9b
https://pubmed.ncbi.nlm.nih.gov/17376109
https://pubmed.ncbi.nlm.nih.gov/17376109
Autor:
H T, Hooper, B C, Figueiredo, C C, Pavan-Senn, L, De Lacerda, R, Sandrini, J K, Mengarelli, K, Japp, L P, Karaviti
Publikováno v:
Clinical genetics. 65(3)
A 14-year-old female presented to the Pediatric Endocrine Clinic, Universidade Federal o Parana Curitiba, Brazil, for obesity. A few years later, despite normal breast development, the patient had failed to menstruate and lacked pubic and axillary ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef7b13f1dd5ecbd1d179b4fdcdd3003e
https://pubmed.ncbi.nlm.nih.gov/14756668
https://pubmed.ncbi.nlm.nih.gov/14756668
Publikováno v:
Minerva chirurgica. 55(12)
Broad is the spectrum of congenital chest wall deformities. Fortunately the severe life-threatening deformities (i.e. ectopia cordis and Jeune's disease) are rarer than the more frequent pectus excavatum and carinatum. Funnel chest is the most common
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3fa5cc4d8caec48e987b0235282fedb5
https://pubmed.ncbi.nlm.nih.gov/11310181
https://pubmed.ncbi.nlm.nih.gov/11310181
Autor:
B C, Figueiredo, C A, Stratakis, R, Sandrini, L, DeLacerda, M A, Pianovsky, C, Giatzakis, H M, Young, B R, Haddad
Publikováno v:
The Journal of clinical endocrinology and metabolism. 84(3)
Although several genes have been investigated in adrenal tumorigenesis, the genetic background of adrenocortical tumors (ACT) remains poorly characterized. In southern Brazil, the annual incidence of ACT is unusually high, ranging from 3.4-4.2/millio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d5d4b30d8b41ad584436736ac61ce093
https://pubmed.ncbi.nlm.nih.gov/10084604
https://pubmed.ncbi.nlm.nih.gov/10084604