Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia
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G. Schellenberg | M. Mesulam | S. Weintraub | T. Siddique | T. Bird | H. Mitsumoto | E. Peskind | S. Przedborski | L. Rowland | N. Johnson | J. Mastrianni | Xiaohong Li
[1] J. Warter,et al. Basis of phenotypic variability in sporadic Creutzfeldt–Jakob disease , 1999, Neurology.
[2] C. Duyckaerts,et al. [Neuropsychological and scintigraphic aspects of frontotemporal dementia preceding amyotrophic lateral sclerosis]. , 2003, Revue neurologique.
[3] A. Hofman,et al. Early cognitive decline is associated with prion protein codon 129 polymorphism , 2003, Annals of neurology.
[4] B. Brooks,et al. El escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis , 1994, Journal of the Neurological Sciences.
[5] C. Henry,et al. Clinical features of variant Creutzfeldt‐Jakob disease , 2002, Reviews in medical virology.
[6] A. LeBlanc,et al. Prion Protein Protects Human Neurons against Bax-mediated Apoptosis* , 2001, The Journal of Biological Chemistry.
[7] C. Lomen‐Hoerth,et al. Characterization of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia , 2004, Dementia and Geriatric Cognitive Disorders.
[8] M. Franceschi,et al. Prion protein gene polymorphism and Alzheimer's disease: one modulatory trait of cognitive decline? , 2001, Journal of neurology, neurosurgery, and psychiatry.
[9] J. Hauw,et al. Polymorphism of the codon 129 of the prion protein (PrP) gene and neuropathology of cerebral ageing , 2003, Acta Neuropathologica.
[10] P. Amouyel,et al. Polymorphism of the prion protein is associated with cognitive impairment in the elderly , 1998, Neurology.
[11] D. Dickson,et al. Familial Primary Progressive Aphasia , 2003, Alzheimer disease and associated disorders.
[12] P Brown,et al. Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects , 1999, Annals of neurology.
[13] T. Asada,et al. Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan , 2003, Annals of neurology.
[14] S H Ferris,et al. Neuropsychological Prediction of Decline to Dementia in Nondemented Elderly , 1999, Journal of geriatric psychiatry and neurology.
[15] M. Mesulam,et al. Primary progressive aphasia--a language-based dementia. , 2003, The New England journal of medicine.
[16] J. Laplanche,et al. Signal transduction through prion protein. , 2000, Science.
[17] A. Aguzzi,et al. Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. , 2004, Brain : a journal of neurology.
[18] John Collinge,et al. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease , 1991, Nature.
[19] J Q Trojanowski,et al. Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease , 1996, Annals of neurology.
[20] D. Dickson,et al. Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS , 2003, Neuropathology and applied neurobiology.
[21] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .
[22] R. Petersen,et al. Fatal Familial Insomnia and Familial Creutzfeldt‐Jakob Disease: Clinical, Pathological and Molecular Features , 1995, Brain pathology.
[23] Y. Agid,et al. Incubation period of Creutzfeldt–Jakob disease in human growth hormone recipients in France , 1999, Neurology.
[24] D. Gajdusek,et al. Genetic studies in relation to kuru: an overview. , 2004, Current molecular medicine.
[25] W. Snow,et al. The NINCDS-ADRDA Work Group criteria for the clinical diagnosis of probable Alzheimerʼs disease: a clinicopathologic study of 57 cases , 1988 .
[26] J. Kimura,et al. A case of primary progressive aphasia with abnormally ubiquitinated neurites in the cerebral cortex , 1996, Acta Neuropathologica.
[27] Raymond Scott Turner,et al. Clinical, neuroimaging, and pathologic features of progressive nonfluent aphasia , 1996, Annals of neurology.
[28] D. Neary,et al. Cognitive change in motor neurone disease/amyotrophic lateral sclerosis (MND/ALS) , 2000, Journal of the Neurological Sciences.
[29] D. Dormont,et al. Genotype at codon 129 and susceptibility to Creutzfeldt-Jakob disease , 1998, The Lancet.
[30] Andrew Kertesz,et al. Primary progressive aphasia and Pick complex , 2003, Journal of the Neurological Sciences.
[31] O. Combarros,et al. Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD , 2000, Neurology.
[32] R. Will,et al. Clinical features of variant Creutzfeldt-Jakob disease. , 2004, Current topics in microbiology and immunology.
[33] S. Haswell,et al. Normal prion protein has an activity like that of superoxide dismutase. , 1999, The Biochemical journal.
[34] D. Westaway,et al. The cellular prion protein binds copper in vivo , 1997, Nature.
[35] S. Folstein,et al. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. , 1975, Journal of psychiatric research.
[36] M. Mesulam,et al. Apolipoprotein E genotypes in primary progressive aphasia , 1997, Neurology.
[37] S. Prusiner,et al. Inherited prion disease caused by the V210I mutation , 2001, Neurology.
[38] H. Budka,et al. Mutations of the prion protein gene phenotypic spectrum. , 2002, Journal of neurology.
[39] J. Metso,et al. Apolipoprotein A-IV polymorphism in the Finnish population: gene frequencies and description of a rare allele. , 1988, Human heredity.
[40] D. Geschwind,et al. Possible association of the tau H1/H1 genotype with primary progressive aphasia , 2003, Neurology.
[41] T. Crow,et al. Codon 129 changes in the prion protein gene in Caucasians. , 1990, American journal of human genetics.
[42] C. Sigurdson,et al. [Prion diseases?]. , 1985, Deutsche medizinische Wochenschrift.
[43] A. Hofman,et al. PRNP Val129 homozygosity increases risk for early‐onset Alzheimer's disease , 2003, Annals of neurology.