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Carla Isabel Ferreira Pinto de Moura
AuthID:
R-000-2YS
Publications
Confirmed
To Validate
Document Source:
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Document Type:
All Document Types
Article (45)
Review (4)
Note (3)
Proceedings Paper (2)
Editorial Material (2)
Abstract (2)
Article in Press (2)
Book Chapter (1)
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Cit. WOS Dsc
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Cit. Scopus Dsc
IF Scopus Dsc
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Results:
10
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Confirmed Publications: 61
31
TITLE:
Acute pediatric pediatric neck infections: Outcomes in a seven-year series
Full Text
AUTHORS:
Corte, FC
; Firmino Machado, J;
Carla Pinto Moura
;
Spratley, J
; Santos, M;
PUBLISHED:
2017
,
SOURCE:
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY,
VOLUME:
99
INDEXED IN:
Scopus
WOS
CrossRef
:
28
IN MY:
ORCID
|
CIÊNCIAVITAE
32
TITLE:
Genetic Study of Primary Dystonias: Recommendations from the Centro Hospitalar Sao Joao Neurogenetics Group
Full Text
AUTHORS:
Monteiro, A
;
João Massano
; Leão, M; Garrett, C;
Carla Pinto Moura
;
Azevedo, E
; Guimarães, J;
Oliveira, JP
;
Castro, P
;
PUBLISHED:
2017
,
SOURCE:
ACTA MEDICA PORTUGUESA,
VOLUME:
30,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
33
TITLE:
Investigation of Genetic Aetiology in Neurodegenerative Ataxias: Recommendations from the Group of Neurogenetics of Centro Hospitalar Sao Joao, Portugal
Full Text
AUTHORS:
Gomes, T; Guimaraes, J; Leao, M;
Carla Pinto Moura
; Garrett, C;
Azevedo, E
;
João Massano
; Oliveira, JP;
Castro, P
;
PUBLISHED:
2017
,
SOURCE:
ACTA MEDICA PORTUGUESA,
VOLUME:
30,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
34
TITLE:
Why, how and when are patients with Chromosomal anomalies hospitalized?. PS034
AUTHORS:
Manuel Gonçalves-Pinho
; João Vasco Santos; Sílvia Fernández; Micaela Gregório;
Carla Pinto Moura
; Alberto Freitas;
PUBLISHED:
2017
,
SOURCE:
Porto Biomedical Journal,
VOLUME:
2,
ISSUE:
5
INDEXED IN:
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
35
TITLE:
Early results of next-gen cytogenetics implementation in Portugal
AUTHORS:
Dezső David; João Freixo; Bárbara Marques; Inês Carvalho; Natália Tkachenko; Natália Oliva Teles; Mariana Marques; Manuela Cardoso; Joana Fino; Cristina Alves; Ana Fortuna;
Dória Sófia
;
Carla Pinto Moura
; Hildeberto Correia; Isabel Marques Carreira; Joaquim Sá; Rui M Gonçalves; João Lavinha; Teresa Kay; Michael Talkowski;
Cynthia Morton;
...More
PUBLISHED:
2016
,
SOURCE:
European Journal Human Genetics Conference, 21-24 May 2016
INDEXED IN:
Handle
IN MY:
ORCID
36
TITLE:
Increased expression of alpha 7nAChR in chronic rhinosinusitis: The intranasal cholinergic anti-inflammatory hypothesis
Full Text
AUTHORS:
Rui Cerejeira;
Susana Fernandes
;
Carla Pinto Moura
;
PUBLISHED:
2016
,
SOURCE:
AURIS NASUS LARYNX,
VOLUME:
43,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
4
IN MY:
ORCID
|
CIÊNCIAVITAE
37
TITLE:
Investigation of Genetic Etiology in Neurodegenerative Dementias: Recommendations from the Centro Hospitalar Sao Joao Neurogenetics Group
Full Text
AUTHORS:
João Massano
; Leao, M;
Garrett, C
;
Carla Pinto Moura
;
Azevedo, E
;
Guimaraes, J
;
Oliveira, JP
;
Castro, P
;
PUBLISHED:
2016
,
SOURCE:
ACTA MEDICA PORTUGUESA,
VOLUME:
29,
ISSUE:
10
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
38
TITLE:
Study of Met34Thr variant in nonsyndromic hearing loss in four Portuguese families
AUTHORS:
D�ria, M
; Fernandes, S;
Carla Pinto Moura
;
PUBLISHED:
2016
,
SOURCE:
Porto Biomedical Journal,
VOLUME:
1,
ISSUE:
1
INDEXED IN:
Scopus
CrossRef
:
1
IN MY:
ORCID
|
CIÊNCIAVITAE
39
TITLE:
Collagen type IV-related nephropathies in Portugal: pathogenic COL4A3 and COL4A4 mutations and clinical characterization of 25 families. Collagen type IV-related nephropathies in Portugal
Full Text
AUTHORS:
Sa, MJN
; Storey, H; Flinter, F; Nagel, M; Sampaio, S; Castro, R; Araujo, JA; Gaspar, MA; Soares, C; Oliveira, A; Henriques, AC; da Costa, AG; Abreu, CP; Ponce, P; Alves, R; Pinho, L; Silva, SE;
Carla Pinto Moura
; Mendonca, L;
Carvalho, F
;
Pestana, M
;
Alves, S;
Carvalho, F
;
Oliveira, JP
;
...More
PUBLISHED:
2015
,
SOURCE:
CLINICAL GENETICS,
VOLUME:
88,
ISSUE:
5
INDEXED IN:
Scopus
WOS
CrossRef
:
16
IN MY:
ORCID
|
CIÊNCIAVITAE
40
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
IN MY:
ORCID
|
CIÊNCIAVITAE
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