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Literature DB >> 16969862

Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes.

Jonathan D Rohrer, Simon Mead, Rohani Omar, Mark Poulter, Jason D Warren, John Collinge, Martin N Rossor.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2006 PMID： 16969862 DOI： 10.1002/ana.20931

Source DB: PubMed Journal: Ann Neurol ISSN： 0364-5134 Impact factor: 10.422

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7 in total

1. Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.

Authors: Jolanta Bratosiewicz-Wąsik; Joanna Smoleń-Dzirba; Annemieke J Rozemuller; Casper Jansen; Wim Spliet; Gerard H Jansen; Tomasz J Wąsik; Paweł P Liberski
Journal: Prion Date: 2012-08-16 Impact factor: 3.931

Review 2. Are there susceptibility factors for primary progressive aphasia?

Authors: Emily Rogalski; Sandra Weintraub; M-Marsel Mesulam
Journal: Brain Lang Date: 2013-03-13 Impact factor: 2.381

3. Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene.

Authors: Marka van Blitterswijk; Bianca Mullen; Aleksandra Wojtas; Michael G Heckman; Nancy N Diehl; Matthew C Baker; Mariely DeJesus-Hernandez; Patricia H Brown; Melissa E Murray; Ging-Yuek R Hsiung; Heather Stewart; Anna M Karydas; Elizabeth Finger; Andrew Kertesz; Eileen H Bigio; Sandra Weintraub; Marsel Mesulam; Kimmo J Hatanpaa; Charles L White; Manuela Neumann; Michael J Strong; Thomas G Beach; Zbigniew K Wszolek; Carol Lippa; Richard Caselli; Leonard Petrucelli; Keith A Josephs; Joseph E Parisi; David S Knopman; Ronald C Petersen; Ian R Mackenzie; William W Seeley; Lea T Grinberg; Bruce L Miller; Kevin B Boylan; Neill R Graff-Radford; Bradley F Boeve; Dennis W Dickson; Rosa Rademakers
Journal: Mol Neurodegener Date: 2014-09-20 Impact factor: 14.195

Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes.

1. Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.

Review 2. Are there susceptibility factors for primary progressive aphasia?

3. Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene.

4. Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.

Review 5. Word-finding difficulty: a clinical analysis of the progressive aphasias.

Review 6. Molecular pathology of human prion diseases.

7. Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia.