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TITLE: Collagen type IV-related nephropathies in Portugal: pathogenic COL4A5 mutations and clinical characterization of 22 families. COL4A5 -related nephropathies in Portugal   Full Text
AUTHORS: Sa, MJN; Sampaio, S ; Oliveira, A; Alves, S; Carla Pinto Moura ; Silva, SE; Castro, R; Araujo, JA; Rodrigues, M; Neves, F; Seabra, J; Soares, C; Gaspar, MA; Tavares, I ; Freitas, L; Sousa, TC; Henriques, AC; Costa, FT; Morgado, E; Sousa, FT; Sousa, JP; da Costa, AG; Filipe, R; Garrido, J; Montalban, J; Ponce, P; Alves, R; Faria, B; Carvalho, MF; Pestana, M ; Carvalho, F ; Oliveira, JP ; ...More
PUBLISHED: 2015, SOURCE: CLINICAL GENETICS, VOLUME: 88, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 6
32
TITLE: Individuals With Normal GLA Gene Sequence May Present Abnormally Spliced Alpha-Galactosidase mRNA Transcripts
AUTHORS: Susana Ferreira ; Miguel Viana-Baptista; Daniel Rodrigues; Oliveira, JP ;
PUBLISHED: 2015, SOURCE: Gene, Cell and Tissue, VOLUME: 3, ISSUE: 1
INDEXED IN: CrossRef
33
TITLE: More on noncompaction in Fabry's disease
AUTHORS: Elisabete Martins ; Oliveira, JP ;
PUBLISHED: 2015, SOURCE: REVISTA PORTUGUESA DE CARDIOLOGIA, VOLUME: 34, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 2
34
TITLE: Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document  Full Text
AUTHORS: Marieke Biegstraaten; Reynir Arngrimsson; Frederic Barbey; Lut Boks; Franco Cecchi; Patrick B Deegan; Ulla Feldt Rasmussen; Tarekegn Geberhiwot; Dominique P Germain; Chris Hendriksz; Derralynn A Hughes; Ilkka Kantola; Nesrin Karabul; Christine Lavery; Gabor E Linthorst; Atul Mehta; Erica van de Mheen; Oliveira, JP ; Rossella Parini; Uma Ramaswami; Michael Rudnicki; Andreas Serra; Claudia Sommer; Gere Sunder Plassmann; Einar Svarstad; Annelies Sweeb; Wim Terryn; Anna Tylki Szymanska; Camilla Tondel; Bojan Vujkovac; Frank Weidemann; Frits A Wijburg; Peter Woolfson; Carla E M Hollak; ...More
PUBLISHED: 2015, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 10, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 234
35
TITLE: The alpha-galactosidase A p.Arg118Cys variant does not cause a Fabry disease phenotype: Data from individual patients and family studies  Full Text
AUTHORS: Susana Ferreira ; Alberto Ortiz; Dominique P Germain; Miguel Viana Baptista; Antonio Caldeira Gomes; Marta Camprecios; Maria Fenollar Cortes; Angel Gallegos Villalobos; Diego Garcia; Jose A Antonio Garcia Robles; Jesus Egido; Eduardo Gutierrez Rivas; Jose A Antonio Herrero; Sebastian Mas; Raluca Oancea; Paloma Peres; Luis M Manuel Salazar Martin; Jesus Solera Garcia; Helena Alves; Scott C Garman; Oliveira, JP ; ...More
PUBLISHED: 2015, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 114, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 67
38
TITLE: A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia
AUTHORS: Seabra, CM; Quental, S; Neto, AP ; Carvalho, F ; Goncalves, J; Oliveira, JP ; Fernandes, S; Sousa, M ; Barros, A ; Amorim, Antonio ; Lopes, AM;
PUBLISHED: 2014, SOURCE: REPRODUCTIVE BIOMEDICINE ONLINE, VOLUME: 29, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 17 Handle
39
TITLE: Consensus recommendation on Fabry disease diagnosis in adult patients with kidney disease  Full Text
AUTHORS: van der Tol, L; Biegstraaten, M; Florquin, S; Vogt, L; Weerman, MAV; Hollak, CEM; Hughes, DA; Lachmann, RH; Oliveira, JP ; Ortiz, AA; Svarstad, E; Terryn, W; Tondel, C; Waldek, S; Wanner, C; West, ML; Linthorst, GE;
PUBLISHED: 2014, SOURCE: 10th Annual World Symposium of the Lysosomal-Disease-Network (LDN) in MOLECULAR GENETICS AND METABOLISM, VOLUME: 111, ISSUE: 2
INDEXED IN: WOS CrossRef
40
TITLE: Histopathological evidence of Fabry disease in a female patient with left ventricular noncompaction
AUTHORS: Martins, E ; Pinho, T; Carpenter, S; Leite, S; Garcia, R; Madureira, A; Oliveira, JP ;
PUBLISHED: 2014, SOURCE: Revista Portuguesa de Cardiologia, VOLUME: 33, ISSUE: 9
INDEXED IN: Scopus CrossRef: 16
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