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TITLE: Intravenous Immunoglobulin in Lupus Panniculitis  Full Text
AUTHORS: Joao Espirito Santo; Gomes, MF; Gomes, MJ; Peixoto, L; Pereira, SC; Acabado, A; Freitas, J; Vinhas V de Sousa;
PUBLISHED: 2010, SOURCE: CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, VOLUME: 38, ISSUE: 2-3
INDEXED IN: Scopus WOS CrossRef: 26
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TITLE: Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations  Full Text
AUTHORS: Di Leo, E; Magnolo, L; Bertolotti, M; Bourbon, M ; Carmo C Pereira; Pirisi, M; Calandra, S; Tarugi, P;
PUBLISHED: 2008, SOURCE: CLINICAL GENETICS, VOLUME: 74, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
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TITLE: Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: Study of 19 heterozygous and 2 homozygous patients  Full Text
AUTHORS: Casals, T; Pacheco, P; Barreto, C; Gimenez, J; Ramos, MD; Pereira, S; Pinheiro, JA; Cobos, N; Curvelo, A; Vazquez, C; Rocha, H; Seculi, JL; Perez, E; Dapena, J; Carrilho, E; Duarte, A; Palacio, AM; Nunes, V; Lavinha, J; Estivill, X;
PUBLISHED: 1997, SOURCE: HUMAN MUTATION, VOLUME: 10, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef