101
TITLE: Paula coutinho’s outstanding contribution to the definition of Machado-Joseph disease [A excepcional contribuição de paula coutinho na definição da doença de Machado-Joseph]
AUTHORS: Garcia, BCM; Germiniani, FMB; Marques, P; Sequeiros, J; Teive, HAG;
PUBLISHED: 2017, SOURCE: Arquivos de Neuro-Psiquiatria, VOLUME: 75, ISSUE: 10
INDEXED IN: Scopus
IN MY: ORCID
102
TITLE: Rare neurodegenerative diseases: Clinical and genetic update
AUTHORS: Matilla Dueñas, A; Corral Juan, M; Rodríguez Palmero Seuma, A; Vilas, D; Ispierto, L; Morais, S; Sequeiros, J; Alonso, I; Volpini, V; Serrano Munuera, C; Pintos Morell, G; Álvarez, R; Sánchez, I;
PUBLISHED: 2017, SOURCE: Advances in Experimental Medicine and Biology, VOLUME: 1031
INDEXED IN: Scopus CrossRef: 27
IN MY: ORCID
103
TITLE: Incorporating scoring risk models for care planning of the elderly with chronic kidney disease  Full Text
AUTHORS: Santos, J; Fonseca, I ;
PUBLISHED: 2017, SOURCE: Current Gerontology and Geriatrics Research, VOLUME: 2017
INDEXED IN: Scopus CrossRef: 3
104
TITLE: Hemoglobin Himeji and inconsistent hemoglobin A1c values: A case report  Full Text
AUTHORS: Guedes, V; Bettencourt Silva, R; Queirós, J; Esteves, MDL; Teles, MJ; Carvalho, D ;
PUBLISHED: 2017, SOURCE: Journal of Medical Case Reports, VOLUME: 11, ISSUE: 1
INDEXED IN: Scopus CrossRef: 4
105
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 Handle
IN MY: ORCID
106
TITLE: Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil  Full Text
AUTHORS: Gheno, TC; Furtado, GV; Saute, JAM; Donis, KC; Fontanari, AMV; Emmel, VE; Pedroso, JL; Barsottini, O; Godeiro Junior, C; van der Linden, H; Pereira, ET; Cintra, VP; Marques, W; de Castilhos, RM; Alonso, I; Sequeiros, J; Cornejo Olivas, M; Mazzetti, P; Leotti, VB; Jardim, LB; Saraiva Pereira, ML; ...More
PUBLISHED: 2017, SOURCE: EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 24, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 14
IN MY: ORCID
107
TITLE: Subjects At-Risk for Genetic Diseases in Portugal: Illness Representations  Full Text
AUTHORS: Leite, A ; Dinis, Maria Alzira Pimenta ; Sequeiros, J; Constança Paul ;
PUBLISHED: 2016, SOURCE: JOURNAL OF GENETIC COUNSELING, VOLUME: 25, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 9 Handle
IN MY: ORCID
108
TITLE: Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M)  Full Text
AUTHORS: Diana Santos; Teresa Coelho; Miguel Alves Ferreira; Jorge Sequeiros; Denisa Mendonca ; Isabel Alonso; Carolina Lemos ; Alda Sousa;
PUBLISHED: 2016, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 24, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 37
IN MY: ORCID
109
TITLE: How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence
AUTHORS: Alvaro Mendes ; Milena Paneque ; Liliana Sousa ; Angus Clarke; Jorge Sequeiros;
PUBLISHED: 2016, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 24, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 66
IN MY: ORCID
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