Maria Clara Barcelos de Morais Barbot


AuthID: R-000-AQR

Confirmed Publications: 58



41
TITLE: Liver transplantation in a case of argininaemia  Full Text
AUTHORS: Silva, ES; Martins, E ; Cardoso, ML; Barbot, C ; Vilarinho, L; Medina, M;
PUBLISHED: 2001, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 24, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 12
IN MY: ORCID | ResearcherID
42
TITLE: Periventricular heterotopia in male sex - case reports [Heterotopia periventricular no sexo masculino a propósito de dois casos clínicos]
AUTHORS: Ramalho, H; Santos, M; Barbot, C ;
PUBLISHED: 2001, SOURCE: Nascer e Crescer, VOLUME: 10, ISSUE: 1
INDEXED IN: Scopus
IN MY: ORCID
43
TITLE: Prothrombotic study in full term neonates with arterial stroke.
AUTHORS: Carrilho, I; Costa, E ; Barreirinho, MS; Santos, M; Barbot, C ; Barbot, J;
PUBLISHED: 2001, SOURCE: Haematologica, VOLUME: 86, ISSUE: 8
INDEXED IN: Scopus
IN MY: ORCID
44
TITLE: Recessive ataxia with ocular apraxia - Review of 22 Portuguese patients
AUTHORS: Barbot, C ; Coutinho, P ; Chorao, R; Ferreira, C; Barros, José ; Fineza, I; Dias, K; Monteiro, JP; Guimaraes, A; Mendonca, P; Moreira, MD; Sequeiros, J ;
PUBLISHED: 2001, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 58, ISSUE: 2
INDEXED IN: Scopus WOS
IN MY: ORCID | ResearcherID
45
TITLE: The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin  Full Text
AUTHORS: Moreira, MC; Barbot, C ; Tachi, N; Kozuka, N; Uchida, E; Gibson, T; Mendonca, P; Costa, M; Barros, José ; Yanagisawa, T; Watanabe, M; Ikeda, Y; Aoki, M; Nagata, T; Coutinho, P ; Sequeiros, J ; Koenig, M;
PUBLISHED: 2001, SOURCE: NATURE GENETICS, VOLUME: 29, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 307
IN MY: ORCID | ResearcherID
46
TITLE: Type 1 neurofibromatosis: The experience of a hospital in Porto, Purtugal [Neurofibromatosis tipo 1: Experiencia en un hospital de Oporto, Portugal. Aspectos clínicos]
AUTHORS: Magdalena, C; Pereira, SA; Rosario, C; Santos, M; Barbot, C ;
PUBLISHED: 2001, SOURCE: Revista de Neurologia, VOLUME: 33, ISSUE: 8
INDEXED IN: Scopus
IN MY: ORCID
47
TITLE: Clinical and molecular studies in three Portuguese mtDNA T8993G families  Full Text
AUTHORS: Vilarinho, L; Leao, E; Barbot, C ; Santos, M; Rocha, H; Santorelli, FM;
PUBLISHED: 2000, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 22, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | ResearcherID
48
TITLE: Etiological evaluation of paediatric ischemic stroke [Avaliacao etiologica do acidente vascular cerebral isquemico na crianca]
AUTHORS: Barreirinho, MS; Santos, M; Barbot, C ; Costa, E ; Barbot, J;
PUBLISHED: 2000, SOURCE: Nascer e Crescer, VOLUME: 9, ISSUE: 2
INDEXED IN: Scopus
IN MY: ORCID
49
TITLE: High germinal instability of the (CTG)(n) at the SCA8 locus of both expanded and normal alleles
AUTHORS: Silveira, I ; Alonso, I ; Guimaraes, L ; Mendonca, P; Santos, C; Maciel, P ; de Matos, JMF; Costa, M; Barbot, C ; Tuna, A; Barros, José ; Jardim, L; Coutinho, P ; Sequeiros, J ;
PUBLISHED: 2000, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 66, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 65
IN MY: ORCID | ResearcherID
50
TITLE: Sjörgren - Larsson syndrome [Síndrome de Sjögren-larsson - Caso clínico]
AUTHORS: Oliveira, T; Rosario, C; Selores, M; Martins, E ; Barbot, C ;
PUBLISHED: 2000, SOURCE: Nascer e Crescer, VOLUME: 9, ISSUE: 4
INDEXED IN: Scopus
IN MY: ORCID
Page 5 of 6. Total results: 58.

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