O42 – 1909 FOXG1 gene: phenotype–genotype relation in Spanish patients
Pineda Marfa, M, O'Callaghan Gordo, M, Gerotina Mora, E, Quandt Herrera, E, Rabaza Gairí, M, Brandi Tarrau, N, Cortès Saladelafont, E, Roche Martínez, A, Armstrong Morón, J
Published in European journal of paediatric neurology (01.09.2013)
Published in European journal of paediatric neurology (01.09.2013)
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Journal Article
Neurologic presentation in haemolytic-uraemic syndrome
Roche-Martínez, A, Póo, P, Maristany-Cucurella, M, Jiménez-Llort, A, Camacho, J A, Campistol, J
Published in Revista de neurologiá (16.08.2008)
Published in Revista de neurologiá (16.08.2008)
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Journal Article
P20.1 Long term outcome in haemolytic-uraemic syndrome: neurologic symptoms, neuroimaging, motor and neurocognitive performance
Martínez, A. Roche, Argüelles, P. Póo, Cucurella, M. Maristany, Plana, J. Campistol
Published in European journal of paediatric neurology (01.05.2011)
Published in European journal of paediatric neurology (01.05.2011)
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Journal Article
FOXG1, a new gene responsible for the congenital form of Rett syndrome
Roche-Martinez, A, Gerotina, E, Armstrong-Moron, J, Sans-Capdevila, O, Pineda, M
Published in Revista de neurologiá (16.05.2011)
Published in Revista de neurologiá (16.05.2011)
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Journal Article