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Manuel Jorge Rocha Melo Pires
AuthID:
R-000-PMA
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (24)
Letter (2)
Article in Press (2)
Abstract (1)
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Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
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Title Dsc
Results:
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Confirmed Publications: 29
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:
Maia, N
;
Soares, AR
;
Fortuna, AM
;
Marques, I
;
Goncalves, A
;
Santos, R
;
Pires, MM
; de Brouwer, APM;
Jorge, P
;
PUBLISHED:
2020
,
SOURCE:
CLINICAL CASE REPORTS,
VOLUME:
8,
ISSUE:
12
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
3
TITLE:
Clinical, histological and molecular characterization of Duchenne/Becker Muscular Dystrophy patients with a pathogenic variant involving exon 44 in DMD gene - a study from a multidisciplinary Unit in a tertiary Hospital
Full Text
AUTHORS:
Ana R Soares
;
Ana Goncalves
;
Ricardo Taipa
;
Cristina Garrido
;
Melo Pires
; Ana M Fortuna;
Teresa Coelho
;
Rosario Santos
;
Manuela Santos
;
PUBLISHED:
2019
,
SOURCE:
22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH)
in
MEDICINE,
VOLUME:
98,
ISSUE:
26
INDEXED IN:
WOS
4
TITLE:
Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database
AUTHORS:
Oliveira, J;
Oliveira, ME
; Kress, W;
Taipa, R
;
Pires, MM
; Hilbert, P; Baxter, P; Santos, M; Buermans, H; den Dunnen, JT; Santos, R;
PUBLISHED:
2013
,
SOURCE:
EUROPEAN JOURNAL OF HUMAN GENETICS,
VOLUME:
21,
ISSUE:
5
INDEXED IN:
Scopus
WOS
CrossRef
Handle
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:
Moniz, S;
Martinho, O
;
Pinto, F
; Sousa, B; Loureiro, C;
Oliveira, MJ
;
Moita, LF
; Honavar, M;
Pinheiro, C
;
Pires, M
;
Lopes, JM
; Jones, C; Costello, JF;
Paredes, J
;
Reis, RM
;
Jordan, P
;
PUBLISHED:
2013
,
SOURCE:
HUMAN MOLECULAR GENETICS,
VOLUME:
22,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
:
43
Handle
IN MY:
ORCID
6
TITLE:
McArdle's disease and multiple sclerosis - Rare association of two diseases McArdle's disease and multiple sclerosis - A rare association [Doença de McArdle e esclerose múltipla - Associação rara de duas doenças McArdle's disease and multiple sclerosis - A rare association]
AUTHORS:
Figueira, C; Palavra, F; Guilherme, A;
Melo Pires, M
; Goncalves, G;
PUBLISHED:
2013
,
SOURCE:
Sinapse,
VOLUME:
13,
ISSUE:
1
INDEXED IN:
Scopus
IN MY:
ORCID
7
TITLE:
Monocarboxylate transporters (MCTs) in gliomas: expression and exploitation as therapeutic targets
AUTHORS:
Vera Miranda Goncalves
; Mrinalini Honavar;
Celine Pinheiro
;
Olga Martinho
;
Manuel M Pires
;
Celia Pinheiro
;
Michelle Cordeiro
;
Gil Bebiano
; Paulo Costa;
Isabel Palmeirim
;
Rui M Reis
;
Fatima Baltazar
;
PUBLISHED:
2013
,
SOURCE:
NEURO-ONCOLOGY,
VOLUME:
15,
ISSUE:
2
INDEXED IN:
Scopus
WOS
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
:
40
IN MY:
ORCID
10
TITLE:
Clinical, Neuropathological, and Genetic Characteristics of the Novel IVS9+1delG GRN Mutation in a Patient with Frontotemporal Dementia
AUTHORS:
Taipa, R
; Tuna, A;
Damasio, J
; Pinto, PS;
Cavaco, S
; Pereira, S; Milterberger Miltenyi, G; Galimberti, D;
Melo Pires, M
;
PUBLISHED:
2012
,
SOURCE:
JOURNAL OF ALZHEIMERS DISEASE,
VOLUME:
30,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
:
6
IN MY:
ORCID
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