A healthcare claims analysis to identify and characterize patients with suspected X-Linked Myotubular Myopathy (XLMTM) in the Brazilian Healthcare System

Autor: Paulo Victor Sgobbi Souza, Tmirah Haselkorn, Jader Baima, Renato Watanabe Oliveira, Fabián Hernández, Marina G. Birck, Marcondes C. França

Publikováno v: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)

Abstract Background X-linked myotubular myopathy (XLMTM) is a rare, life-threatening congenital disease, which is not well-defined. To our knowledge, no studies characterizing the XLMTM disease burden have been conducted in Brazil. We identified and

Externí odkaz: https://doaj.org/article/9ca6438626e94bd9a4f211feb78cc9fc

Depression symptoms and hypothyroidism in a population-based study of middle-aged Brazilian women

Autor: Claudia S. Lopes, Joanna Miguez Nery Guimarães, Jader Baima, Rosely Sichieri

Publikováno v: Journal of Affective Disorders. 117:120-123

Background Overt hypothyroidism is often recognized as an important cause of depression, but in sub-clinical cases, results are inconsistent and most prior studies have involved small samples. Methods We evaluated the association between hypothyroidi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c062578c14d018a121d94281153eabc8
https://doi.org/10.1016/j.jad.2008.12.012

Hereditary corticosteroid-binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred

Autor: Jader Baima, Elisa Brunner, Julio Abucham, José Gilberto H. Vieira, Teresa C. Vieira

Publikováno v: Clinical Endocrinology. 58:756-762

Summary objective Abnormal corticosteroid-binding globulin (CBG) is an extremely rare condition and only three mutations have been described in four families. The molecular basis of an abnormal CBG in a Brazilian family was studied and correlations b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c14499f8a5be9ddaa4a9494c8884668d
https://doi.org/10.1046/j.1365-2265.2003.01783.x

Identification of a polymorphic glutamic acid stretch in the α2b-adrenergic receptor and lack of linkage with essential hypertension

Autor: Michael Burzstyn, Diane E. Handy, Lindsay A. Farrer, Haralambos Gavras, Anita L. DeStefano, Oscar Joost, Timothy Martel, Athanasios J. Manolis, Margaret Bresnahan, Michael Nicolaou, Jader Baima, Clinton T. Baldwin, Faina Schwartz, Irene Gavras

Publikováno v: American Journal of Hypertension. 12:853-857

Essential hypertension, a clinically significant elevation in blood pressure with no recognizable cause, is believed to be attributable to the collective effect of genetic predisposing factors in combination with specific environmental factors, such

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f2a9a33d1e743fbac815f5f7f068a48
https://doi.org/10.1016/s0895-7061(99)00070-9

Levosimendana em pacientes com insuficiência cardíaca descompensada: eficácia em uma coorte brasileira. Resultados do estudo BELIEF

Autor: Edimar Alcides Bocchi, Fábio Vilas-Boas, Salvador Rassi, Jorge Pinto Ribeiro, Silvia G. Lage, Maria da Consolação Vieira Moreira, Denilson Campos de Albuquerque, Antonio Carlos Pereira Barretto, Jader Baima

Publikováno v: Arquivos Brasileiros de Cardiologia v.90 n.3 2008
Arquivos Brasileiros de Cardiologia
Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS

Fundamento: A levosimendana é um novo agente inodilatador que aumenta a contratilidade cardíaca pela sensibilização ao Ca(2+) e induz vasodilatação por meio da ativação dos canais KATP/BKCa. Objetivo: Estudar a eficácia e segurança da levos

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b26a8232b421a1cf4be06f573c30997e
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2008000300008