Carla Isabel Ferreira Pinto de Moura


AuthID: R-000-2YS

Confirmed Publications: 54



41
TITLE: 25 Analysis of CFTR gene mutations in Portuguese patients with idiopathic bronchiectasis  Full Text
AUTHORS: Grangeia, A; Amorim, A; Carla Pinto Moura ; Fernandes, S; Barros, A; Carvalho, F;
PUBLISHED: 2013, SOURCE: Journal of Cystic Fibrosis, VOLUME: 12
INDEXED IN: CrossRef
IN MY: ORCID
42
TITLE: Inv21p12q22del21q22 and intellectual disability  Full Text
AUTHORS: Renata Oliveira; Sofia Doria ; Carmen Madureira; Vera Lima ; Carolina Almeida ; Maria J Pinho; Ramalho C ; Eunice Matoso; Alberto Barros ; Isabel M Carreira ; Carla Pinto Moura ;
PUBLISHED: 2013, SOURCE: GENE, VOLUME: 517, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
43
TITLE: Spectrum and frequency of GJB2 mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients
AUTHORS: Tiago Daniel Matos ; Helena Simoes Teixeira; Helena Caria ; Ana Claudia Goncalves; Joana Chora; Maria do Ceu Correia; Carla Pinto Moura ; Helena Rosa; Luisa Monteiro; Assuncao O'Neill; Oscar Dias; Mario Andrea ; Graca Fialho ;
PUBLISHED: 2013, SOURCE: INTERNATIONAL JOURNAL OF AUDIOLOGY, VOLUME: 52, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 16
IN MY: ORCID
44
TITLE: Temporal intradiploic dilative vasculopathy: An additional pathogenic factor for the hearing loss in fabry disease?
AUTHORS: Carla Pinto Moura ; Soares, C; Seixas, D; Ayres Bastos, M; Oliveira, JP ;
PUBLISHED: 2013, SOURCE: JIMD Reports, VOLUME: 7
INDEXED IN: Scopus CrossRef: 2
IN MY: ORCID
45
TITLE: 345 Study of the prevalence of CFTR gene mutations in the Portuguese population  Full Text
AUTHORS: Gregorio, I; Grangeia, A; Carla Pinto Moura ; Vaz, L; Barros, A; Carvalho, F;
PUBLISHED: 2012, SOURCE: Journal of Cystic Fibrosis, VOLUME: 11
INDEXED IN: CrossRef
IN MY: ORCID
46
TITLE: Down syndrome: otolaryngological effects of rapid maxillary expansion
AUTHORS: Carla Pinto Moura ; Andrade, David ; Cunha, LM ; Tavares, MJ; Cunha, MJ; Vaz, P; Barros, H ; Pueschel, SM; Pais P Clemente;
PUBLISHED: 2008, SOURCE: JOURNAL OF LARYNGOLOGY AND OTOLOGY, VOLUME: 122, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef: 38
IN MY: ORCID
47
TITLE: Genes, Children and paediatricians
AUTHORS: João Silva; Cristina Godinho; Carla Pinto Moura ; Gabriela Soares; Margarida Reis Lima;
PUBLISHED: 2008, SOURCE: Nascer e Crescer, VOLUME: 17, ISSUE: 1
INDEXED IN: Scopus
IN MY: ORCID
48
TITLE: Voice parameters in children with down syndrome  Full Text
AUTHORS: Carla Pinto Moura ; Luis Miguel Cunha ; Helena Vilarinho; Maria Joao Cunha; Diamantino Freitas ; Miguel Palha; Siegfried M Pueschel; Pais Clemente, M;
PUBLISHED: 2008, SOURCE: JOURNAL OF VOICE, VOLUME: 22, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 50
IN MY: ORCID
49
TITLE: P147: Down syndrome: Rapid Maxillary Expansion and ENT Evolution
AUTHORS: Carla Pinto Moura ; Andrade, David ; Luis Miguel Cunha ; Maria Joao Cunha; Manuel Antonio Caldeira Pais Clemente; Sigfried M Pueshel;
PUBLISHED: 2006, SOURCE: Otolaryngology-Head and Neck Surgery, VOLUME: 135, ISSUE: 2_suppl
INDEXED IN: CrossRef: 1
IN MY: ORCID
50
TITLE: Rapid maxillary expansion and nasal patency in children with Down syndrome
AUTHORS: Carla Pinto Moura ; Vales, F; Andrade, David ; Cunha, LM ; Barros, H ; Pueschel, SM; Clemente, MP;
PUBLISHED: 2005, SOURCE: RHINOLOGY, VOLUME: 43, ISSUE: 2
INDEXED IN: Scopus WOS
IN MY: ORCID
Page 5 of 6. Total results: 54.

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