Publicaciones
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Ferrer I, Armstrong-Moron J, Capellari S, Parchi P, Arzberger T, Bell J, Budka H, Ströbel T, Giaccone G, Rossi G, Bogdanovic N, Fakai P, Schmitt A, Riederers P, Al-Sarraj S, Ravid R and Kretzschmar H.
Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue:: A BrainNet Europe study
BRAIN PATHOLOGY . 17(3): 297-303. Nº de citas: 119
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Olivé M, Armstrong-Moron J, Miralles F, Pou A, Fardeau M, Gonzalez L, Martínez F, Fischer D, Martínez Matos JA, Shatunov A, Goldfarb L and Ferrer I.
Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene
NEUROMUSCULAR DISORDERS . 17(6): 443-450. Nº de citas: 43
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Armstrong-Moron J, Bonaventura I, Rojo A, González G, Corral J, Nadal N, Volpini V and Ferrer I.
Spinocerebellar ataxia type 2 (SCA2) with white matter involvement
NEUROSCIENCE LETTERS . 381(3): 247-251. Nº de citas: 17
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Corral J, Genís D, Banchs I, San Nicolás H, Armstrong-Moron J and Volpini V.
Giant SCA8 alleles in nine children whose mother has two moderately large ones
ANNALS OF NEUROLOGY . 57(4): 549-553. Nº de citas: 12
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Ballestar E, Ropero S, Alaminos M, Armstrong-Moron J, Setien F, Agrelo R, Fraga MF, Herranz M, Avila S, Pineda M, Monros E and Esteller M.
The impact of MECP2 mutations in the expression patterns of Rett syndrome patients
HUMAN GENETICS . 116(1-2): 91-104. Nº de citas: 73
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Armstrong-Moron J, Aracil A and Pineda M.
Síndrome de Rett, del diagnóstico clínico al diagnóstico molecular
Neurocirugia . (1): 38-43.
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Armstrong-Moron J, Boada M, Rey MJ, Vidal N and Ferrer I.
Familial Alzheimer disease associated with A713T mutation in APP
NEUROSCIENCE LETTERS . 370(2-3): 241-243. Nº de citas: 40
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Armstrong-Moron J, Aibar E, Pineda M, Pérez MM, Gean Molins E, Carrera M, Casas C, Martínez F and Monrós E.
Prenatal diagnosis in Rett syndrome
FETAL DIAGNOSIS AND THERAPY . 17(4): 200-204. Nº de citas: 7
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Monrós E, Armstrong-Moron J, Aibar E, Poo P, Canós I and Pineda M.
Rett syndrome in Spain: mutation analysis and clinical correlations.
BRAIN & DEVELOPMENT . 23 Suppl 1: 251-253. Nº de citas: 78
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Armstrong-Moron J, Pineda M and Monrós E.
Mutation analysis of 16S rRNA in patients with Rett syndrome.
PEDIATRIC NEUROLOGY . 23(1): 85-87. Nº de citas: 6