1
TITLE: The Use of Simulators for Teaching Fine Needle Aspiration Cytology in Veterinary Medicine
AUTHORS: Pires, JL ; Payo, P ; Marcos, R ;
PUBLISHED: 2021, SOURCE: JOURNAL OF VETERINARY MEDICAL EDUCATION
INDEXED IN: WOS
2
TITLE: Usher syndrome and Nebulin-associated myopathy in a single patient due to variants in MYO7A and NEB
AUTHORS: Nuno Maia; Ana Rita Soares; Ana Maria Fortuna; Isabel Marques; Ana Goncalves; Rosario Santos; Manuel Melo Pires ; Arjan P M de Brouwer; Paula Jorge;
PUBLISHED: 2020, SOURCE: CLINICAL CASE REPORTS
INDEXED IN: Scopus WOS
4
TITLE: Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database  Full Text
AUTHORS: Jorge Oliveira; Marcia E Oliveira; Wolfram Kress; Ricardo Taipa; Manuel Melo Pires ; Pascale Hilbert; Peter Baxter; Manuela Santos; Henk Buermans; Johan T den Dunnen; Rosario Santos;
PUBLISHED: 2013, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 21, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
5
TITLE: Loss of WNK2 expression by promoter gene methylation occurs in adult gliomas and triggers Rac1-mediated tumour cell invasiveness
AUTHORS: Sonia Moniz; Olga Martinho ; Filipe Pinto; Barbara Sousa; Claudia Loureiro; Maria Jose Oliveira ; Luis Ferreira Moita ; Mrinalini Honavar; Celia Pinheiro; Manuel Pires ; Lopes, JM ; Chris Jones; Joseph F Costello; Joana Paredes ; Rui Manuel Reis ; Peter Jordan ;
PUBLISHED: 2013, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 22, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 42
IN MY: ORCID
8
TITLE: Multiple cerebral infarcts and intravascular central nervous system lymphoma: A rare but potentially treatable association  Full Text
AUTHORS: Catarina Cruto; Ricardo Taipa; Cecilia Monteiro; Isabel Moreira; Manuel Melo Pires ; Manuel Correia;
PUBLISHED: 2013, SOURCE: JOURNAL OF THE NEUROLOGICAL SCIENCES, VOLUME: 325, ISSUE: 1-2
INDEXED IN: Scopus WOS CrossRef: 4
IN MY: ORCID
9
TITLE: Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency  Full Text
AUTHORS: Celia Nogueira; Barros, José ; Maria Jose Sa ; Luisa Azevedo ; Ricardo Taipa; Alessandra Torraco; Maria Chiara Meschini; Daniela Verrigni; Claudia Nesti; Teresa Rizza; Joao Teixeira; Rosalba Carrozzo; Manuel Melo Pires ; Laura Vilarinho; Filippo M Santorelli;
PUBLISHED: 2013, SOURCE: NEUROGENETICS, VOLUME: 14, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 39
IN MY: ORCID
10
TITLE: Clinical, Neuropathological, and Genetic Characteristics of the Novel IVS9+1delG GRN Mutation in a Patient with Frontotemporal Dementia
AUTHORS: Ricardo Taipa; Assuncao Tuna; Joana Damasio; Pedro S Pinto; Sara Cavaco ; Sonia Pereira; Gabriel Milterberger Miltenyi; Daniela Galimberti; Manuel Melo Pires ;
PUBLISHED: 2012, SOURCE: JOURNAL OF ALZHEIMERS DISEASE, VOLUME: 30, ISSUE: 1
INDEXED IN: Scopus WOS
IN MY: ORCID
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