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au.\*:("PICCARDO, Pedro")

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Biochemical characterization of a neuroserpin variant associated with hereditary dementiaYAZAKI, Masahide; LIEPNIEKS, Juris J; MURRELL, Jill R et al.The American journal of pathology. 2001, Vol 158, Num 1, pp 227-233, issn 0002-9440Article

Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian familyDE MICHELE, Giuseppe; POCCHIARI, Maurizio; BERARDELLI, Alfredo et al.Canadian journal of neurological sciences. 2003, Vol 30, Num 3, pp 233-236, issn 0317-1671, 4 p.Article

Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizuresTAKAO, Masaki; GHETTI, Bernardino; FARLOW, Martin R et al.Journal of neuropathology and experimental neurology. 2001, Vol 60, Num 12, pp 1137-1152, issn 0022-3069Article

Fukuoka-1 strain of transmissible spongiform encephalopathy agent infects murine bone marrow-derived cells with features of mesenchymal stem cellsCERVENAKOVA, Larisa; AKIMOV, Sergey; VASILYEVA, Irina et al.Transfusion (Philadelphia, PA). 2011, Vol 51, Num 8, pp 1755-1768, issn 0041-1132, 14 p.Article

Association between conformational mutations in neuroserpin and onset and severity of dementiaDAVIS, Richard L; SHRIMPTON, Antony E; PICCARDO, Pedro et al.Lancet (British edition). 2002, Vol 359, Num 9325, pp 2242-2247, issn 0140-6736Article

Neuroserpin mutation S52R causes Neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsyTAKAO, Masaki; BENSON, Merrill D; FARLOW, Martin R et al.Journal of neuropathology and experimental neurology. 2000, Vol 59, Num 12, pp 1070-1086, issn 0022-3069Article

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