LRRK2 variation and dementia with Lewy bodies.
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David T. Jones | C. Jack | R. Petersen | J. Graff‐Radford | B. Boeve | O. Pedraza | T. Ferman | Glenn E. Smith | D. Knopman | V. Lowe | K. Kantarci | M. Murray | D. Dickson | J. Parisi | R. Uitti | M. Heckman | Z. Wszolek | N. Graff-Radford | N. Ertekin-Taner | R. Savica | O. Ross | N. Diehl | R. Walton | O. Lorenzo-Betancor | A. Soto-Ortolaza | C. Labbé | J. V. van Gerpen | R. Rademakers | O. Lorenzo‐Betancor | M. S. Contreras | D. Knopman | Oswaldo Lorenzo-Betancor | Ronald L. Walton | Otto Pedraza
[1] T. Montine,et al. Cognitive profile of LRRK2‐related Parkinson's disease , 2015, Movement disorders : official journal of the Movement Disorder Society.
[2] Chuong B. Do,et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease , 2014, Nature Genetics.
[3] W. M. van der Flier,et al. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies , 2014, Human molecular genetics.
[4] M. Murray,et al. Differential clinicopathologic and genetic features of late-onset amnestic dementias , 2014, Acta Neuropathologica.
[5] M. Nalls,et al. A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. , 2013, JAMA neurology.
[6] Daniel Weintraub,et al. APOE ε4 increases risk for dementia in pure synucleinopathies. , 2013, JAMA neurology.
[7] P. Deyn,et al. DLB and PDD: a role for mutations in dementia and Parkinson disease genes? , 2012, Neurobiology of Aging.
[8] J. Ioannidis,et al. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study , 2011, The Lancet Neurology.
[9] J. Jankovic,et al. Multiple LRRK2 variants modulate risk of Parkinson disease: a chinese multicenter study , 2010, Human mutation.
[10] A. González-Neira,et al. Early-Onset Familial Lewy Body Dementia With Extensive Tauopathy: A Clinical, Genetic, and Neuropathological Study , 2009, Journal of neuropathology and experimental neurology.
[11] M. Toft,et al. CORTICOBASAL SYNDROME AND PRIMARY PROGRESSIVE APHASIA AS MANIFESTATIONS OF LRRK2 GENE MUTATIONS , 2008, Neurology.
[12] J. Molinuevo,et al. Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration , 2008, Journal of the Neurological Sciences.
[13] R. Petersen,et al. Validation of the Neuropathologic Criteria of the Third Consortium for Dementia With Lewy Bodies for Prospectively Diagnosed Cases , 2008, Journal of neuropathology and experimental neurology.
[14] M. Farrer,et al. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease , 2008, Annals of neurology.
[15] J. Trojanowski,et al. Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations , 2008, Neurology.
[16] T. Meitinger,et al. A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease , 2007, Movement disorders : official journal of the Movement Disorder Society.
[17] M. Farrer,et al. Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions , 2007, Acta Neuropathologica.
[18] M. Farrer,et al. Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia. , 2007, Parkinsonism & related disorders.
[19] J. Cappell,et al. Tiagabine-induced nonconvulsive status epilepticus in an adolescent without epilepsy , 2006, Neurology.
[20] Irene Litvan,et al. Lrrk2 and Lewy body disease , 2006, Annals of neurology.
[21] S Minoshima,et al. Diagnosis and management of dementia with Lewy bodies , 2005, Neurology.
[22] Thomas Meitinger,et al. Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology , 2004, Neuron.
[23] D W Dickson,et al. Autosomal dominant parkinsonism associated with variable synuclein and tau pathology , 2004, Neurology.
[24] H. Payami,et al. Genetic Epidemiology of Parkinson's Disease , 1998, Journal of geriatric psychiatry and neurology.
[25] R. Katzman.,et al. Senile Dementia of the Alzheimer Type Without Neocortical Neurofibrillary Tangles , 1987, Journal of neuropathology and experimental neurology.
[26] K Kosaka,et al. Diffuse type of Lewy body disease: progressive dementia with abundant cortical Lewy bodies and senile changes of varying degree--a new disease? , 1984, Clinical neuropathology.
[27] O. Ross,et al. Genetic susceptibility variants in parkinsonism. , 2016, Parkinsonism & Related Disorders.
[28] J. Trojanowski,et al. Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease. , 2015, JAMA neurology.
[29] G. Halliday,et al. α-Synucleinopathy phenotypes. , 2014, Parkinsonism & related disorders.
[30] A. Brice,et al. Role of mendelian genes in "sporadic" Parkinson's disease. , 2012, Parkinsonism & related disorders.
[31] N. Kumar. Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations , 2009 .
[32] H. Braak,et al. Neuropathological stageing of Alzheimer-related changes , 2004, Acta Neuropathologica.