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371 results
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SPG11 compound mutations in spastic paraparesis with thin corpus callosum.
Samaranch L, Riverol M, Masdeu JC, Lorenzo E, Vidal-Taboada JM, Irigoyen J, Pastor MA, de Castro P, Pastor P. Samaranch L, et al. Among authors: pastor p, pastor ma. Neurology. 2008 Jul 29;71(5):332-6. doi: 10.1212/01.wnl.0000319646.23052.d1. Neurology. 2008. PMID: 18663179
A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
Zarranz JJ, Ferrer I, Lezcano E, Forcadas MI, Eizaguirre B, Atarés B, Puig B, Gómez-Esteban JC, Fernández-Maiztegui C, Rouco I, Pérez-Concha T, Fernández M, Rodríguez O, Rodríguez-Martínez AB, de Pancorbo MM, Pastor P, Pérez-Tur J. Zarranz JJ, et al. Among authors: pastor p. Neurology. 2005 May 10;64(9):1578-85. doi: 10.1212/01.WNL.0000160116.65034.12. Neurology. 2005. PMID: 15883319
[Sporadic and familial Parkinson's disease: comparative study].
Muñoz E, Pastor P, José Martí M, Valldeoriola F, Oliva R, Tolosa E. Muñoz E, et al. Among authors: pastor p. Med Clin (Barc). 2001 May 5;116(16):601-4. doi: 10.1016/s0025-7753(01)71919-7. Med Clin (Barc). 2001. PMID: 11412643 Spanish.
371 results