Isidro Ferrer Abizanda-rekin lankidetzan egindako argitalpenak (9)

2018

  1. Sporadic Creutzfeldt–Jakob disease with glial PrPRes nuclear and perinuclear immunoreactivity

    Neuropathology, Vol. 38, Núm. 5, pp. 561-567

2017

  1. Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations

    Current Neurology and Neuroscience Reports, Vol. 17, Núm. 4

  2. Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus

    Brain Pathology, Vol. 27, Núm. 1, pp. 95-106

2016

  1. Identification of new molecular alterations in fatal familial insomnia

    Human molecular genetics, Vol. 25, Núm. 12, pp. 2417-2436

  2. Sporadic adult-onset leucodystrophy with axonal spheroids and pigmented glia with no mutations in the known targeted genes

    Histopathology, Vol. 68, Núm. 2, pp. 308-312

2013

  1. A novel form of human disease

    Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210

2012

  1. Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: A case report

    Journal of Medical Case Reports, Vol. 6

2010

  1. A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.

    BMC neurology, Vol. 10, pp. 99

2005

  1. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease

    Neurology, Vol. 64, Núm. 9, pp. 1578-1585