1
TITLE: Hypophosphatemia as a possible biomarker for epileptic seizures at the emergency department
AUTHORS: Coutinho, Maria P.; Faustino, Patricia; Ladeira, Filipa; Leita, Lia;
PUBLISHED: 2023, SOURCE: SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, VOLUME: 111
INDEXED IN: Scopus WOS
2
TITLE: Beef Consumers Behaviour and Preferences-The Case of Portugal  Full Text
AUTHORS: Paiva, Teresa; Jacinto, Telma A.; Sarraguca, Mafalda Cruz; Coutinho, Paula;
PUBLISHED: 2022, SOURCE: SUSTAINABILITY, VOLUME: 14, ISSUE: 4
INDEXED IN: Scopus WOS
4
TITLE: Mutational mechanism for DAB1 (ATTTC)(n) insertion in SCA37: ATTTT repeat lengthening and nucleotide substitution  Full Text
AUTHORS: Loureiro, JR; Oliveira, CL; Mota, C; Castro, AF; Costa, C; Loureiro, JL; Coutinho, P; Martins, S ; Sequeiros, J; Silveira, I;
PUBLISHED: 2019, SOURCE: HUMAN MUTATION, VOLUME: 40, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 17
5
TITLE: Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias
AUTHORS: Sara Morais; Laure Raymond; Mathilde Mairey; Paula Coutinho; Eva Brandao; Paula Ribeiro; Jose Leal Loureiro; Jorge Sequeiros; Alexis Brice; Isabel Alonso; Giovanni Stevanin;
PUBLISHED: 2017, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 25, ISSUE: 11
INDEXED IN: Scopus WOS
6
TITLE: A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia
AUTHORS: Seixas, AI; Loureiro, JR; Costa, C; Ordonez Ugalde, A; Marcelino, H; Oliveira, CL; Loureiro, JL; Dhingra, A; Brandao, E; Cruz, VT ; Timoteo, A; Quintans, B; Rouleau, GA; Rizzu, P; Carracedo, A; Bessa, J; Heutink, P; Sequeiros, J; Sobrido, MJ; Coutinho, P; Silveira, I; ...More
PUBLISHED: 2017, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 101, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 110
7
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
8
TITLE: Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia  Full Text
AUTHORS: Marie Coutelier; Cyril Goizet; Alexandra Durr; Florence Habarou; Sara Morais; Alexandre Dionne Laporte; Feifei F Tao; Juliette Konop; Marion Stoll; Perrine Charles; Maxime Jacoupy; Raphael Matusiak; Isabel Alonso; Chantal Tallaksen; Mathilde Mairey; Marina Kennerson; Marion Gaussen; Rebecca Schule; Maxime Janin; Fanny Morice Picard; Christelle M Durand; Christel Depienne; Patrick Calvas; Paula Coutinho; Jean Marie Saudubray; Guy Rouleau; Alexis Brice; Garth Nicholson; Frederic Darios; Jose L Loureiro; Stephan Zuchner; Chris Ottolenghi; Fanny Mochel; Giovanni Stevanin; ...More
PUBLISHED: 2015, SOURCE: BRAIN, VOLUME: 138, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef
9
TITLE: Expertise development in volleyball: The role of early sport activities and players’ age and height
AUTHORS: Coutinho, P; Mesquita, I; Fonseca, AM; Côte, J;
PUBLISHED: 2015, SOURCE: Kinesiology, VOLUME: 47, ISSUE: 2
INDEXED IN: Scopus
10
TITLE: Novel APTX Mutation in a Hispanic Subject Affected by Ataxia with Oculomotor Apraxia Type 1
AUTHORS: Martin Paucar; Isabel Alonso; Mats Eriksson; Stanislav Beniaminov; Paula Coutinho; Per Svenningsson;
PUBLISHED: 2015, SOURCE: MOVEMENT DISORDERS CLINICAL PRACTICE, VOLUME: 2, ISSUE: 1
INDEXED IN: Scopus WOS
Página 1 de 5. Total de resultados: 42.