Isabel Conceição Moreira Pereira Alonso
AuthID: R-000-678
21
TITLE: Hereditary spastic paraplegia (HSP) type 15 in five Portuguese patients Full Text
AUTHORS: Sardoeira, A; Alonso, I; Cardoso, M; Ortiz, P; Bastos Lima, AB; Sequeiros, J; Barros, J; Damasio, J;
PUBLISHED: 2018, SOURCE: 4th Congress of the European-Academy-of-Neurology (EAN) in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 25
AUTHORS: Sardoeira, A; Alonso, I; Cardoso, M; Ortiz, P; Bastos Lima, AB; Sequeiros, J; Barros, J; Damasio, J;
PUBLISHED: 2018, SOURCE: 4th Congress of the European-Academy-of-Neurology (EAN) in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 25
INDEXED IN: 
WOS
WOS22
TITLE: When Decrease A beta 1-42 in CSF May Not Mean Alzheimer's Disease Insights From Two Case Reports With Early Onset Dementia
AUTHORS: Filipa Ladeira; Goncalo Cacao; Ana P Correia; Pedro S Pinto; Sara Cavaco; Manuel Melo Pires; Isabel Alonso; Ricardo Taipa;
PUBLISHED: 2018, SOURCE: ALZHEIMER DISEASE & ASSOCIATED DISORDERS, VOLUME: 32, ISSUE: 4
AUTHORS: Filipa Ladeira; Goncalo Cacao; Ana P Correia; Pedro S Pinto; Sara Cavaco; Manuel Melo Pires; Isabel Alonso; Ricardo Taipa;
PUBLISHED: 2018, SOURCE: ALZHEIMER DISEASE & ASSOCIATED DISORDERS, VOLUME: 32, ISSUE: 4
INDEXED IN: 
Scopus WOS
Scopus WOS23
TITLE: Topical timolol for the treatment of pyoderma gangrenosum
AUTHORS: Moreira, C; Lopes, S; Cruz, MJ; Azevedo, F;
PUBLISHED: 2017, SOURCE: BMJ Case Reports, VOLUME: 2017
AUTHORS: Moreira, C; Lopes, S; Cruz, MJ; Azevedo, F;
PUBLISHED: 2017, SOURCE: BMJ Case Reports, VOLUME: 2017
INDEXED IN: Scopus
Scopus24
TITLE: Familial amyloid polyneuropathy in Portugal: New genes modulating age-at-onset
AUTHORS: Diana Santos; Teresa Coelho; Miguel Alves Ferreira; Jorge Sequeiros; Denisa Mendonca ; Isabel Alonso; Carolina Lemos ; Alda Sousa;
PUBLISHED: 2017, SOURCE: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, VOLUME: 4, ISSUE: 2
AUTHORS: Diana Santos; Teresa Coelho; Miguel Alves Ferreira; Jorge Sequeiros; Denisa Mendonca ; Isabel Alonso; Carolina Lemos ; Alda Sousa;
PUBLISHED: 2017, SOURCE: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, VOLUME: 4, ISSUE: 2
25
TITLE: Genetic Contributors to Intergenerational CAG Repeat Instability in Huntington's Disease Knock-In Mice
AUTHORS: Joao L Luis Neto; Jong Min Lee; Ali Afridi; Tammy Gillis; Jolene R Guide; Stephani Dempsey; Brenda Lager; Isabel Alonso; Vanessa C Wheeler; Ricardo Mouro Pinto;
PUBLISHED: 2017, SOURCE: GENETICS, VOLUME: 205, ISSUE: 2
AUTHORS: Joao L Luis Neto; Jong Min Lee; Ali Afridi; Tammy Gillis; Jolene R Guide; Stephani Dempsey; Brenda Lager; Isabel Alonso; Vanessa C Wheeler; Ricardo Mouro Pinto;
PUBLISHED: 2017, SOURCE: GENETICS, VOLUME: 205, ISSUE: 2
INDEXED IN: WOS
WOS26
TITLE: A Portuguese rapid-onset dystonia-parkinsonism case with atypical features Full Text
AUTHORS: Ana Luisa Sousa; Isabel Alonso; Marina Magalhaes;
PUBLISHED: 2017, SOURCE: NEUROLOGICAL SCIENCES, VOLUME: 38, ISSUE: 9
AUTHORS: Ana Luisa Sousa; Isabel Alonso; Marina Magalhaes;
PUBLISHED: 2017, SOURCE: NEUROLOGICAL SCIENCES, VOLUME: 38, ISSUE: 9
INDEXED IN: Scopus WOS
Scopus WOS27
TITLE: Hereditary spastic paraplegia type 11 and 22q11 duplication syndrome in a single family Full Text
AUTHORS: Martins, J; Martins, R; Silva, J; Alonso, I; Pinto Basto, JP; Rendeiro, P; Leal Loureiro, JL; Magalhaes, M;
PUBLISHED: 2017, SOURCE: 3rd Congress of the European-Academy-of-Neurology in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 24
AUTHORS: Martins, J; Martins, R; Silva, J; Alonso, I; Pinto Basto, JP; Rendeiro, P; Leal Loureiro, JL; Magalhaes, M;
PUBLISHED: 2017, SOURCE: 3rd Congress of the European-Academy-of-Neurology in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 24
INDEXED IN: WOS
WOS28
TITLE: IL1B rs16944 and depression symptoms in multiple sclerosis patients Full Text
AUTHORS: Leal, B; Bettencourt, A; Ferreira, AM; Carvalho, C; Moreira, I; Costa, PP ; Martins M Da Silva; Cavaco, S; Martins M Da Silva;
PUBLISHED: 2017, SOURCE: 3rd Congress of the European-Academy-of-Neurology in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 24
AUTHORS: Leal, B; Bettencourt, A; Ferreira, AM; Carvalho, C; Moreira, I; Costa, PP ; Martins M Da Silva; Cavaco, S; Martins M Da Silva;
PUBLISHED: 2017, SOURCE: 3rd Congress of the European-Academy-of-Neurology in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 24
INDEXED IN: WOS
WOS29
TITLE: Charcot-Marie-Tooth 4J with conduction blocks Full Text
AUTHORS: Martins, J; Martins, M; Alonso, I; Ferreira, R; Melo Pires, MM;
PUBLISHED: 2017, SOURCE: 3rd Congress of the European-Academy-of-Neurology in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 24
AUTHORS: Martins, J; Martins, M; Alonso, I; Ferreira, R; Melo Pires, MM;
PUBLISHED: 2017, SOURCE: 3rd Congress of the European-Academy-of-Neurology in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 24
INDEXED IN: WOS
WOS30
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
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
Scopus WOS