1
TITLE: Identification of novel genetic causes of Rett syndrome-like phenotypes
AUTHORS: Fatima Lopes; Mafalda Barbosa; Adam Ameur; Gabriela Soares; Joaquim de Sa; Ana Isabel Dias; Guiomar Oliveira; Pedro Cabral; Teresa Temudo; Eulalia Calado; Isabel Fineza Cruz; Jose Pedro Vieira; Renata Oliveira; Sofia Esteves; Sascha Sauer; Inger Jonasson; Ann Christine Syvanen; Ulf Gyllensten; Dalila Pinto; Patricia Maciel;
PUBLISHED: 2016, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 53, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
2
TITLE: Who needs surgery for pediatric myelomeningocele? A retrospective study and literature review
AUTHORS: Humberto Marreiros; Clara Loff; Eulalia Calado;
PUBLISHED: 2015, SOURCE: JOURNAL OF SPINAL CORD MEDICINE, VOLUME: 38, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
3
TITLE: Identification of novel genetic causes of Rett syndrome-like phenotypes by whole exome sequencing  Full Text
AUTHORS: Fatima Lopes; Mafalda Barbosa; Teresa Temudo; Joaquim de Sa; Ana Isabel Dias; Guiomar Oliveira; Pedro Cabra; Eulalia Calado; Isabel Fineza Cruz; Gabriela Soares; Jose Pedro Vieira; Maria Margarida Venancio; Renata Oliveira; Inger Jonasson; Adam Ameur; Dalila Pinto; Ulf Gyllensten; Patricia Maciel;
PUBLISHED: 2015, SOURCE: Joint Meeting of the 20th Biennial Meeting of the International-Society-for-Developmental-Neuroscience / 5th Annual NeuroDevNet Brain Development Conference in INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, VOLUME: 47
INDEXED IN: WOS CrossRef
4
TITLE: Atypical phenotype in two patients with LAMA2 mutations  Full Text
AUTHORS: Joana Marques; Sofia T Duarte; Sonia Costa; Sandra Jacinto; Jorge Oliveira; Marcia E Oliveira; Rosario Santos; Bronze-da-Rocha E; Bronze E; Bronze-Rocha E ; Ana Rita Silvestre; Eulalia Calado; Teresinha Evangelista;
PUBLISHED: 2014, SOURCE: NEUROMUSCULAR DISORDERS, VOLUME: 24, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 24
5
TITLE: Epilepsy and cerebral palsy: Characteristics and trends in children born in 1976-1998  Full Text
AUTHORS: Elodie Sellier; Peter Uldall; Eulalia Calado; Solveig Sigurdardottir; Maria Giulia Torrioli; Mary Jane Platt; Christine Cans;
PUBLISHED: 2012, SOURCE: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, VOLUME: 16, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
6
TITLE: Osteoporosis in paediatric patients with spina bifida
AUTHORS: Humberto Marreiros; Clara Loff; Eulalia Calado;
PUBLISHED: 2012, SOURCE: The Journal of Spinal Cord Medicine, VOLUME: 35, ISSUE: 2
INDEXED IN: CrossRef
7
TITLE: Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes  Full Text
AUTHORS: Teresa Temudo; Monica Santos; Elisabete Ramos ; Karin Dias; Jose Pedro Vieira; Ana Moreira; Eulalia Calado; Ines Carrilho; Guiomar Oliveira ; Antonio Levy; Clara Barbot ; Maria Fonseca; Alexandra Cabral; Pedro Cabral; Jose Monteiro; Luis Borges; Roseli Gomes; Graca Mira; Susana Aires Pereira; Manuela Santos; Anabela Fernandes ; Jorg T Epplen; Jorge Sequeiros ; Patricia Maciel ; ...More
PUBLISHED: 2011, SOURCE: BRAIN & DEVELOPMENT, VOLUME: 33, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 17
8
TITLE: N170 asymmetry as an index of inferior occipital dysfunction in patients with symptomatic occipital lobe epilepsy  Full Text
AUTHORS: Ricardo Lopes; Pedro Cabral; Nuno Canas; Paula Breia; John P Foreid; Eullia Calado; Rita Silva; Alberto Leal ;
PUBLISHED: 2011, SOURCE: CLINICAL NEUROPHYSIOLOGY, VOLUME: 122, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
9
TITLE: Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients
AUTHORS: Minica Santos; Teresa Temudo; Teresa Kay; Ines Carrilho; Ana Medeira; Helena Cabral; Roseli Gomes; Maria Teresa Lourenco; Margarida Venancio; Eulalia Calado; Ana Moreira; Guiomar Oliveira ; Patricia Maciel ;
PUBLISHED: 2009, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 24, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
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