Myasthenia gravis complicated with cryptococcal meningitis after thymectomy and long-term immunosuppressive therapy

Autor: Lorenzoni, P J, Scola, R H, Kay, C S K, Almeida, S M, Muro, M D, Búrigo, I P, Carraro Jr, H, Werneck, L C

Publikováno v: Arquivos de Neuro-Psiquiatria, Volume: 69, Issue: 2b, Pages: 410-411, Published: 2011

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______608::712a9c6380ce5672a1e9f0906165fc72
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2011000300031&lng=en&tlng=en

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Identification and Functional Characterization of a Novel Mutation in theNKX2-1Gene: Comparison with the Data in the Literature

Autor: Cláudia Suemi Kamoi Kay, Alfonso Massimiliano Ferrara, Domenico Salvatore, Immacolata Cristina Nettore, Paola Mirra, Paola Ungaro, Paolo Emidio Macchia, Paulo José Lorenzoni, Isac Bruck, Rosana Herminia Scola, Valentina Pagliara, Francesco Beguinot, Annarita Sibilio, Gianfranco Fenzi, Lineu Cesar Werneck, Lúcia Helena Coutinho dos Santos

Publikováno v: Thyroid (N.Y.N.Y.) (2013). doi:10.1089/thy.2012.0267
info:cnr-pdr/source/autori:Nettore IC, Ferrara AM, Mirra P, Sibilio A, Pagliara V, Kamoi Kay CS, Lorenzoni PJ, Werneck LC, Bruck I, Coutinho Dos Santos LH, Beguinot F, Salvatore D, Ungaro P, Fenzi G, Scola RH, Macchia PE./titolo:Identification and functional characterization of a novel mutation in the NKX2-1 gene: comparison with the data in the literature./doi:10.1089%2Fthy.2012.0267/rivista:Thyroid (N.Y.N.Y.)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume

Background: NKX2-1 mutations have been described in several patients with primary congenital hypothyroidism, respiratory distress, and benign hereditary chorea, which are classical manifestations of the brain-thyroid-lung syndrome (BTLS). Methods: Th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5281a61463200a7c66fc653b80a79329
http://hdl.handle.net/11588/565596