José Felix Martí Massó-rekin lankidetzan egindako argitalpenak (6)

2017

  1. The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics

    PLoS ONE, Vol. 12, Núm. 6

2014

  1. Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2

    Parkinsonism and Related Disorders, Vol. 20, Núm. 10, pp. 1097-1100

2013

  1. Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers

    Neurobiology of Aging, Vol. 34, Núm. 5, pp. 1462-1468

2012

  1. Response to treatment with corticoids in a case of inflammatory amyloid angiopathy without performing a biopsy

    Revista de Neurologia

2011

  1. Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>a progranulin mutation

    Alzheimer Disease and Associated Disorders, Vol. 25, Núm. 1, pp. 93-95

2009

  1. Frontotemporoparietal dementia: Clinical phenotype associated with the c.709-1G>A PGRN mutation

    Neurology, Vol. 73, Núm. 17, pp. 1367-1374