A large Calabrian kindred segregating frontotemporal dementia
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A. Paterson | T. Kawarai | A. Bruni | R. Maletta | J. Foncin | S. Palermo | P. Hyslop | M. D. Di Natale | G. Puccio | S. Curcio | M. Perri
[1] W. Kamphorst,et al. Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22. , 2001, Brain : a journal of neurology.
[2] G. Schellenberg,et al. Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia. , 2001, Archives of neurology.
[3] J. Grafman,et al. Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation , 2000, Annals of neurology.
[4] J. Haines,et al. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. , 2000, JAMA.
[5] K. Boone,et al. First Symptoms – Frontotemporal Dementia versus Alzheimer’s Disease , 2000, Dementia and Geriatric Cognitive Disorders.
[6] Sasha Bozeat,et al. Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer's disease? , 2000, Journal of neurology, neurosurgery, and psychiatry.
[7] G. Leuba,et al. Search for a Mutation in the tau Gene in a Swiss Family with Frontotemporal Dementia , 2000, Experimental Neurology.
[8] W. Kamphorst,et al. Phenotypic variation in hereditary frontotemporal dementia with tau mutations , 1999, Annals of neurology.
[9] R. Petersen,et al. Frequency of tau mutations in three series of non‐Alzheimer's degenerative dementia , 1999, Annals of neurology.
[10] D. Geschwind,et al. Inheritance of frontotemporal dementia. , 1999, Archives of neurology.
[11] T. Robbins,et al. Comparative Cognitive Neuropsychological Studies of Frontal Lobe Function: Implications for Therapeutic Strategies in Frontal Variant Frontotemporal Dementia , 1999, Dementia and Geriatric Cognitive Disorders.
[12] D. Geschwind,et al. Tau Mutations in Frontotemporal Dementia , 1999, Dementia and Geriatric Cognitive Disorders.
[13] K. Blennow,et al. Prevalence and Incidence of Clinically Diagnosed Memory Impairments in a Geographically Defined General Population in Sweden , 1999, Neuroepidemiology.
[14] D. Neary,et al. Evaluation of the NINCDS-ADRDA criteria in the differentiation of Alzheimer’s disease and frontotemporal dementia , 1999, Journal of neurology, neurosurgery, and psychiatry.
[15] C. Duijn,et al. High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. , 1999, American journal of human genetics.
[16] D. Geschwind,et al. Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[17] A. Bruni. Cloning of a gene bearing missense mutations in early onset familial Alzheimer's disease: a Calabrian study. , 1998, Functional neurology.
[18] A Klug,et al. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[19] Ronald C. Petersen,et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.
[20] P. Scheltens,et al. Familial aggregation in frontotemporal dementia , 1998, Neurology.
[21] G. Schellenberg,et al. Tau is a candidate gene for chromosome 17 frontotemporal dementia , 1998, Annals of neurology.
[22] L. Thal,et al. Genetic evidence for the involvement of τ in progressive supranuclear palsy , 1997, Annals of neurology.
[23] A A Schäffer,et al. Faster linkage analysis computations for pedigrees with loops or unused alleles. , 1996, Human heredity.
[24] L Kruglyak,et al. Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.
[25] J. Hardy,et al. Familial non-specific dementia maps to chromosome 3. , 1995, Human molecular genetics.
[26] D. Pollen,et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease , 1995, Nature.
[27] M. Ploch,et al. A new Italian pedigree with early-onset Alzheimer's disease. , 1994 .
[28] A. Bruni,et al. Alzheimer's Disease: A Model From the Quantitative Study of a Large Kindred , 1992, Journal of geriatric psychiatry and neurology.
[29] B. L. Miller,et al. Frontal lobe degeneration , 1991, Neurology.
[30] M. Folstein,et al. Clinical diagnosis of Alzheimer's disease , 1984, Neurology.
[31] 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.
[32] J Marshall,et al. Cerebral blood flow in dementia. , 1975, Archives of neurology.
[33] B. Milner,et al. Interhemispheric differences in the localization of psychological processes in man. , 1971, British medical bulletin.
[34] Arthur L. Benton,et al. Word fluency and brain damage , 1967 .
[35] E. Renzi,et al. The token test: A sensitive test to detect receptive disturbances in aphasics. , 1962, Brain : a journal of neurology.
[36] F. Pasquier,et al. Frontotemporal dementia: its rediscovery. , 1997, European neurology.
[37] D. Salmon,et al. Extended Kindreds as a Model for Research on Alzheimer’s Disease , 1988 .
[38] G. Caruso,et al. Démence présénile d'Alzheimer transmise dans une famille étendue. , 1985 .