Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

By Laplanche Jean-Louis   Hachimi Khalid Hamid El   Durieux Isabelle   Thuillet Pascaline   Defebvre Luc   Delasnerie-Lauprêtre Nicole   Peoc'h Katell   Foncin Jean-François  

Brain, Vol. 122, Iss. 12, 1999-12 ,pp. : 2375-2386

Oxford University Press

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Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

By Webb T. E. F.  

Brain, Vol. 131, Iss. 10, 2008-10 ,pp. : 2632-2646

Oxford University Press

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Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein

By Wadsworth Jonathan D. F.   Joiner Susan   Linehan Jacqueline M.   Cooper Sharon   Powell Caroline   Mallinson Gary   Buckell Jennifer   Gowland Ian   Asante Emmanuel A.   Budka Herbert   Brandner Sebastian   Collinge John  

Brain, Vol. 129, Iss. 6, 2006-06 ,pp. : 1557-1569

Oxford University Press

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Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene

By Mallucci G. R.   Campbell T. A.   Dickinson A.   Beck J.   Holt M.   Plant G.   de Pauw K. W.   Hakin R. N.   Clarke C. E.   Howell S.   Davies-Jones G. A. B.   Lawden M.   Smith C. M. L.   Ince P.   Ironside J. W.   Bridges L. R.   Dean A.   Weeks I.  

Brain, Vol. 122, Iss. 10, 1999-10 ,pp. : 1823-1837

Oxford University Press

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Primary Myopathy and Accumulation of PrP^Sc-Like Molecules in Peripheral Tissues of Transgenic Mice Expressing a Prion Protein Insertional Mutation

By Chiesa R.   Pestronk A.   Schmidt R.E.   Tourtellotte W.G.   Ghetti B.   Piccardo P.   Harris D.A.  

Neurobiology of Disease, Vol. 8, Iss. 2, 2001-04 ,pp. : 279-288

Academic Press

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