João Manuel Monteiro Chaves
AuthID: R-000-PXW
11
TITLE: Two-year follow-up with eslicarbazepine acetate: a consecutive, retrospective, observational study Full Text
AUTHORS: Fernando D Correia; Joel Freitas; Magalhães, R ; Joao Lopes; Joao Ramalheira; Jose Lopes Lima; Joao Chaves;
PUBLISHED: 2014, SOURCE: EPILEPSY RESEARCH, VOLUME: 108, ISSUE: 8
AUTHORS: Fernando D Correia; Joel Freitas; Magalhães, R ; Joao Lopes; Joao Ramalheira; Jose Lopes Lima; Joao Chaves;
PUBLISHED: 2014, SOURCE: EPILEPSY RESEARCH, VOLUME: 108, ISSUE: 8
12
TITLE: Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A Full Text
AUTHORS: Dalia Kasperaviciute; Claudia B Catarino; Mar Matarin; Costin Leu; Jan Novy; Anna Tostevin; Barbara Leal; Ellen V S Hessel; Kerstin Hallmann; Michael S Hildebrand; Hans Henrik M Dahl; Mina Ryten; Daniah Trabzuni; Adaikalavan Ramasamy; Saud Alhusaini; Colin P Doherty; Thomas Dorn; Joerg Hansen; Guenter Kraemer; Bernhard J Steinhoff; ...More
PUBLISHED: 2013, SOURCE: BRAIN, VOLUME: 136, ISSUE: 10
AUTHORS: Dalia Kasperaviciute; Claudia B Catarino; Mar Matarin; Costin Leu; Jan Novy; Anna Tostevin; Barbara Leal; Ellen V S Hessel; Kerstin Hallmann; Michael S Hildebrand; Hans Henrik M Dahl; Mina Ryten; Daniah Trabzuni; Adaikalavan Ramasamy; Saud Alhusaini; Colin P Doherty; Thomas Dorn; Joerg Hansen; Guenter Kraemer; Bernhard J Steinhoff; ...More
PUBLISHED: 2013, SOURCE: BRAIN, VOLUME: 136, ISSUE: 10
13
TITLE: Unverricht -undborg disease: Homozygosity for a new splicing mutation in the cystatin B gene Full Text
AUTHORS: Eugenia Pinto; Joel Freitas; Ana Joana Duarte; Isaura Ribeiro; Diogo Ribeiro; Lopes Lima, JL; Joao Chaves; Olga Amaral;
PUBLISHED: 2012, SOURCE: EPILEPSY RESEARCH, VOLUME: 99, ISSUE: 1-2
AUTHORS: Eugenia Pinto; Joel Freitas; Ana Joana Duarte; Isaura Ribeiro; Diogo Ribeiro; Lopes Lima, JL; Joao Chaves; Olga Amaral;
PUBLISHED: 2012, SOURCE: EPILEPSY RESEARCH, VOLUME: 99, ISSUE: 1-2
14
TITLE: Lack of Cystatin B Protein as a Cause Of Myoclonic Epilepsy Full Text
AUTHORS: Olga Amaral; Ana Duarte; Eugenia Pinto; Isaura Ribeiro; Diogo Ribeiro; Joel Freitas; Joao Chaves;
PUBLISHED: 2012, SOURCE: 8th Anuual Research Meeting of the WORLD Symposium on Lysosomal Disease Networks in MOLECULAR GENETICS AND METABOLISM, VOLUME: 105, ISSUE: 2
AUTHORS: Olga Amaral; Ana Duarte; Eugenia Pinto; Isaura Ribeiro; Diogo Ribeiro; Joel Freitas; Joao Chaves;
PUBLISHED: 2012, SOURCE: 8th Anuual Research Meeting of the WORLD Symposium on Lysosomal Disease Networks in MOLECULAR GENETICS AND METABOLISM, VOLUME: 105, ISSUE: 2
INDEXED IN: 
WOS 
CrossRef
WOS CrossRef15
TITLE: Progressive myoclonus epilepsy with nephropathy C1q due to SCARB2/LIMP-2 deficiency: Clinical report of two siblings Full Text
AUTHORS: Joao Chaves; Idalina Beirao ; Andrea Balreira; Paulo Gaspar; Daniel Caiola; Clara Sa Miranda, MC ; Jose L Lima;
PUBLISHED: 2011, SOURCE: SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, VOLUME: 20, ISSUE: 9
AUTHORS: Joao Chaves; Idalina Beirao ; Andrea Balreira; Paulo Gaspar; Daniel Caiola; Clara Sa Miranda, MC ; Jose L Lima;
PUBLISHED: 2011, SOURCE: SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, VOLUME: 20, ISSUE: 9
16
TITLE: A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome
AUTHORS: Andrea Balreira; Paulo Gaspar; Daniel Caiola; Joao Chaves; Idalina Beirao ; Jose Lopes Lima; Jorge Eduardo Azevedo ; Maria Clara Sa Miranda ;
PUBLISHED: 2008, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 17, ISSUE: 14
AUTHORS: Andrea Balreira; Paulo Gaspar; Daniel Caiola; Joao Chaves; Idalina Beirao ; Jose Lopes Lima; Jorge Eduardo Azevedo ; Maria Clara Sa Miranda ;
PUBLISHED: 2008, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 17, ISSUE: 14
17
TITLE: Eyelid opening apraxia in an AIDS patient Full Text
AUTHORS: Ernestina Santos; Joao Chaves; Jose Lopes Lima;
PUBLISHED: 2008, SOURCE: MOVEMENT DISORDERS, VOLUME: 23, ISSUE: 3
AUTHORS: Ernestina Santos; Joao Chaves; Jose Lopes Lima;
PUBLISHED: 2008, SOURCE: MOVEMENT DISORDERS, VOLUME: 23, ISSUE: 3
