11
TITLE: Plasma Extracellular Vesicle-Derived TIMP-1 mRNA as a Prognostic Biomarker in Clear Cell Renal Cell Carcinoma: A Pilot Study  Full Text
AUTHORS: Francisca Dias; Ana Luisa Teixeira; Ines Nogueira; Mariana Morais; Joana Maia; Cristian Bodo; Marta Ferreira; Isabel Vieira; Jose Silva; Joao Lobo; Jose Pedro Sequeira; Joaquina Mauricio; Jorge Oliveira; Carlos Palmeira; Gabriela Martins; Klaas Kok; Bruno Costa Silva; Rui Medeiros ;
PUBLISHED: 2020, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 21, ISSUE: 13
INDEXED IN: Scopus WOS CrossRef: 10
13
TITLE: Spastic-ataxia in a Portuguese cohort of hereditary ataxias  Full Text
AUTHORS: Damasio, J; Alonso, I; Barbot, C; Brandao, AF; Sardoeira, A; Pina, S; Coutinho, P; Barros, J; Sequeiros, J;
PUBLISHED: 2018, SOURCE: 4th Congress of the European-Academy-of-Neurology (EAN) in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 25
INDEXED IN: WOS
14
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
INDEXED IN: Scopus WOS CrossRef: 6
16
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
INDEXED IN: WOS CrossRef: 23
17
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
INDEXED IN: Scopus WOS CrossRef: 40
18
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
INDEXED IN: CrossRef
IN MY: ORCID
19
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; Murphy, R; Watanabe, M; Coutinho, P; Tazir, M; Monga, B; Durr, A; Brice, A; Tranchant, C; Koenig, M; ...More
PUBLISHED: 2009, SOURCE: 13th International Congress of Parkinsons Disease and Movement Disorders in MOVEMENT DISORDERS, VOLUME: 24
INDEXED IN: WOS
20
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
INDEXED IN: CrossRef
IN MY: ORCID
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