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A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
Neurology. 2005 May 10;64(9):1578-85. doi: 10.1212/01.WNL.0000160116.65034.12.
Neurology. 2005.
PMID: 15883319
Phenotypic variability in familial prion diseases due to the D178N mutation.
Zarranz JJ, Digon A, Atarés B, Rodríguez-Martínez AB, Arce A, Carrera N, Fernández-Manchola I, Fernández-Martínez M, Fernández-Maiztegui C, Forcadas I, Galdos L, Gómez-Esteban JC, Ibáñez A, Lezcano E, López de Munain A, Martí-Massó JF, Mendibe MM, Urtasun M, Uterga JM, Saracibar N, Velasco F, de Pancorbo MM.
Zarranz JJ, et al. Among authors: fernandez maiztegui c.
J Neurol Neurosurg Psychiatry. 2005 Nov;76(11):1491-6. doi: 10.1136/jnnp.2004.056606.
J Neurol Neurosurg Psychiatry. 2005.
PMID: 16227536
Free PMC article.
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Familial prion diseases in the Basque Country (Spain).
Zarranz JJ, Digon A, Atarés B, Arteagoitia JM, Carrera N, Fernández-Manchola I, Fernández-Martínez M, Fernández-Maiztegui C, Forcadas I, Galdos L, Ibáñez A, Lezcano E, Martí-Massó JF, Mendibe MM, Urtasun M, Uterga JM, Saracibar N, Velasco F, González de Galdeano L.
Zarranz JJ, et al. Among authors: fernandez maiztegui c.
Neuroepidemiology. 2005;24(1-2):103-9. doi: 10.1159/000081057. Epub 2004 Sep 24.
Neuroepidemiology. 2005.
PMID: 15459517
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[Treatment pattern of Alzheimer's disease with cholinesterase inhibitors (TRAIN study)].
Gil-Néciga E, Gobartt AL; grupo de investigadores del estudio TRAIN.
Gil-Néciga E, et al.
Rev Neurol. 2008 Apr 16-30;46(8):461-4.
Rev Neurol. 2008.
PMID: 18428102
Free article.
Spanish.
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