Maria Clara Barcelos de Morais Barbot
AuthID: R-000-AQR
11
TITLE: Involving the microRNA Targetome in Esophageal-Cancer Development and Behavior Full Text
AUTHORS: Francisca Dias; Mariana Morais; Ana Luisa Teixeira; Rui Medeiros ;
PUBLISHED: 2018, SOURCE: CANCERS, VOLUME: 10, ISSUE: 10
AUTHORS: Francisca Dias; Mariana Morais; Ana Luisa Teixeira; Rui Medeiros ;
PUBLISHED: 2018, SOURCE: CANCERS, VOLUME: 10, ISSUE: 10
12
TITLE: MicroRNAs and altered metabolism of clear cell renal cell carcinoma: Potential role as aerobic glycolysis biomarkers Full Text
AUTHORS: Mariana Morais; Francisca Dias; Ana L Teixeira; Rui Medeiros ;
PUBLISHED: 2017, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, VOLUME: 1861, ISSUE: 9
AUTHORS: Mariana Morais; Francisca Dias; Ana L Teixeira; Rui Medeiros ;
PUBLISHED: 2017, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, VOLUME: 1861, ISSUE: 9
13
TITLE: Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Type 4
AUTHORS: Jose Bras; Isabel Alonso; Clara Barbot; Maria Manuela Costa; Lee Darwent; Tatiana Orme; Jorge Sequeiros; John Hardy; Paula Coutinho; Rita Guerreiro;
PUBLISHED: 2015, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 96, ISSUE: 3
AUTHORS: Jose Bras; Isabel Alonso; Clara Barbot; Maria Manuela Costa; Lee Darwent; Tatiana Orme; Jorge Sequeiros; John Hardy; Paula Coutinho; Rita Guerreiro;
PUBLISHED: 2015, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 96, ISSUE: 3
14
TITLE: Liver transplantation prevents progressive neurological impairment in argininemia
AUTHORS: Silva, ES; Cardoso, ML; Vilarinho, L; Medina, M; Barbot, C; Martins, E ;
PUBLISHED: 2013, SOURCE: JIMD Reports, VOLUME: 11
AUTHORS: Silva, ES; Cardoso, ML; Vilarinho, L; Medina, M; Barbot, C; Martins, E ;
PUBLISHED: 2013, SOURCE: JIMD Reports, VOLUME: 11
15
TITLE: Síndrome de Sturge-Weber: variabilidad clínica y de neuroimagen
AUTHORS: Rios, M; Barbot, C; P.S Pinto; Salício, L; Santos, M; Carrilho, I; Temudo, T;
PUBLISHED: 2012, SOURCE: Anales de Pediatría, VOLUME: 77, ISSUE: 6
AUTHORS: Rios, M; Barbot, C; P.S Pinto; Salício, L; Santos, M; Carrilho, I; Temudo, T;
PUBLISHED: 2012, SOURCE: Anales de Pediatría, VOLUME: 77, ISSUE: 6
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TITLE: Maxia with oculomotor apraxia type 2 (AOA2): Clinical and molecular delineation, genotype to phenotype correlations and strategy for diagnosis
AUTHORS: Anheim, M; Fleury, M; Charles, P; Barbot, C; Salih, M; P Delaunoy; Arning, L; Schols, L; Sequeiros, J; Goizet, C; Marelli, C; Le Ber, I; Koht, J; Gazulla, J; Drouot, N; Ali Pacha, L; Chbicheb, M; Chabrol, B; MZahem, A; Calvas, P; ...More
PUBLISHED: 2009, SOURCE: 13th International Congress of Parkinsons Disease and Movement Disorders in MOVEMENT DISORDERS, VOLUME: 24
AUTHORS: Anheim, M; Fleury, M; Charles, P; Barbot, C; Salih, M; P Delaunoy; Arning, L; Schols, L; Sequeiros, J; Goizet, C; Marelli, C; Le Ber, I; Koht, J; Gazulla, J; Drouot, N; Ali Pacha, L; Chbicheb, M; Chabrol, B; MZahem, A; Calvas, P; ...More
PUBLISHED: 2009, SOURCE: 13th International Congress of Parkinsons Disease and Movement Disorders in MOVEMENT DISORDERS, VOLUME: 24
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ResearcherID17
TITLE: Utilidad del análisis del líquido cefalorraquídeo para el estudio de las deficiencias del metabolismo de neurotransmisores y pterinas y del transporte de glucosa y folato a través de la barrera hematoencefálica
AUTHORS: Aida Ormazabal; Àngels García Cazorla; Belén Pérez Dueñas; Mercé Pineda; Ángeles Ruiz; Eduardo López Laso; Maite García Silva; Inés Carilho; Clara Barbot; Bru Cormand; Marta Ribases; Lisbeth Moller; Emilio Fernández Álvarez; Jaume Campistol; Rafael Artuch;
PUBLISHED: 2006, SOURCE: Medicina Clínica, VOLUME: 127, ISSUE: 3
AUTHORS: Aida Ormazabal; Àngels García Cazorla; Belén Pérez Dueñas; Mercé Pineda; Ángeles Ruiz; Eduardo López Laso; Maite García Silva; Inés Carilho; Clara Barbot; Bru Cormand; Marta Ribases; Lisbeth Moller; Emilio Fernández Álvarez; Jaume Campistol; Rafael Artuch;
PUBLISHED: 2006, SOURCE: Medicina Clínica, VOLUME: 127, ISSUE: 3
18
TITLE: Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 Full Text
AUTHORS: Moreira, MC; Klur, S; Barbot, C; Tachi, N; Bomont, P; Watanabe, M; Shoji, M; Warter, JM; Aubourg, P; Durr, A; Nemeth, AH; Amouri, R; Hentati, F; Alurkar, A; Divekar, D; Mendoca, P; Sequeiros, J ; Coutinho, P; Koenig, M;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
AUTHORS: Moreira, MC; Klur, S; Barbot, C; Tachi, N; Bomont, P; Watanabe, M; Shoji, M; Warter, JM; Aubourg, P; Durr, A; Nemeth, AH; Amouri, R; Hentati, F; Alurkar, A; Divekar, D; Mendoca, P; Sequeiros, J ; Coutinho, P; Koenig, M;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
INDEXED IN: WOS
WOS19
TITLE: Ocular apraxia in recessive ataxia - Reply
AUTHORS: Coutinho, P; Barbot, C;
PUBLISHED: 2002, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 59, ISSUE: 5
AUTHORS: Coutinho, P; Barbot, C;
PUBLISHED: 2002, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 59, ISSUE: 5
INDEXED IN: WOS
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TITLE: Type 1 neurofibromatosis: The experience of a hospital in Porto, Portugal
AUTHORS: Madalena, C; Pereira, SA; Rosario, C; Santos, M; Barbot, C;
PUBLISHED: 2001, SOURCE: REVISTA DE NEUROLOGIA, VOLUME: 33, ISSUE: 8
AUTHORS: Madalena, C; Pereira, SA; Rosario, C; Santos, M; Barbot, C;
PUBLISHED: 2001, SOURCE: REVISTA DE NEUROLOGIA, VOLUME: 33, ISSUE: 8
INDEXED IN: WOS
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