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Anatomical and physiological basis of continuous spike-wave of sleep syndrome after early thalamic lesions. [electronic resource] by
- Leal, Alberto
- Calado, Eulália
- Vieira, José P
- Mendonça, Carla
- Ferreira, José C
- Ferreira, Hugo
- Carvalho, Daniel
- Furtado, Fátima
- Gomes, Roseli
- Monteiro, José P
Producer: 20190201
In:
Epilepsy & behavior : E&B vol. 78
Availability: No items available.
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13.
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Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients. [electronic resource] by
- Santos, Mónica
- Temudo, Teresa
- Kay, Teresa
- Carrilho, Inês
- Medeira, Ana
- Cabral, Helena
- Gomes, Roseli
- Lourenço, Maria Teresa
- Venâncio, Margarida
- Calado, Eulália
- Moreira, Ana
- Oliveira, Guiomar
- Maciel, Patrícia
Producer: 20090930
In:
Journal of child neurology vol. 24
Availability: No items available.
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14.
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Atypical phenotype in two patients with LAMA2 mutations. [electronic resource] by
- Marques, Joana
- Duarte, Sofia T
- Costa, Sónia
- Jacinto, Sandra
- Oliveira, Jorge
- Oliveira, Márcia E
- Santos, Rosário
- Bronze-da-Rocha, Elsa
- Silvestre, Ana Rita
- Calado, Eulália
- Evangelista, Teresinha
Producer: 20141210
In:
Neuromuscular disorders : NMD vol. 24
Availability: No items available.
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Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities. [electronic resource] by
- Marini, Carla
- Mei, Davide
- Temudo, Teresa
- Ferrari, Anna Rita
- Buti, Daniela
- Dravet, Charlotte
- Dias, Ana I
- Moreira, Ana
- Calado, Eulalia
- Seri, Stefano
- Neville, Brian
- Narbona, Juan
- Reid, Evan
- Michelucci, Roberto
- Sicca, Federico
- Cross, Helen J
- Guerrini, Renzo
Producer: 20071010
In:
Epilepsia vol. 48
Availability: No items available.
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16.
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Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type. [electronic resource] by
- Temudo, Teresa
- Ramos, Elisabete
- Dias, Karin
- Barbot, Clara
- Vieira, Jose P
- Moreira, Ana
- Calado, Eulalia
- Carrilho, Ines
- Oliveira, Guiomar
- Levy, Antonio
- Fonseca, Maria
- Cabral, Alexandra
- Cabral, Pedro
- Monteiro, Joao P
- Borges, Luis
- Gomes, Roseli
- Santos, Manuela
- Sequeiros, Jorge
- Maciel, Patricia
Producer: 20081118
In:
Movement disorders : official journal of the Movement Disorder Society vol. 23
Availability: No items available.
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17.
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Identification of novel genetic causes of Rett syndrome-like phenotypes. [electronic resource] by
- Lopes, Fátima
- Barbosa, Mafalda
- Ameur, Adam
- Soares, Gabriela
- de Sá, Joaquim
- Dias, Ana Isabel
- Oliveira, Guiomar
- Cabral, Pedro
- Temudo, Teresa
- Calado, Eulália
- Cruz, Isabel Fineza
- Vieira, José Pedro
- Oliveira, Renata
- Esteves, Sofia
- Sauer, Sascha
- Jonasson, Inger
- Syvänen, Ann-Christine
- Gyllensten, Ulf
- Pinto, Dalila
- Maciel, Patrícia
Producer: 20160712
In:
Journal of medical genetics vol. 53
Availability: No items available.
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18.
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Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes. [electronic resource] by
- Temudo, Teresa
- Santos, Mónica
- Ramos, Elisabete
- Dias, Karin
- Vieira, José Pedro
- Moreira, Ana
- Calado, Eulália
- Carrilho, Inês
- Oliveira, Guiomar
- Levy, António
- Barbot, Clara
- Fonseca, Maria
- Cabral, Alexandra
- Cabral, Pedro
- Monteiro, José
- Borges, Luís
- Gomes, Roseli
- Mira, Graça
- Pereira, Susana Aires
- Santos, Manuela
- Fernandes, Anabela
- Epplen, Jorg T
- Sequeiros, Jorge
- Maciel, Patrícia
Producer: 20110411
In:
Brain & development vol. 33
Availability: No items available.
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