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Mechanisms of Ageing and Development|April 26, 2003
HLA haplotypes and TNF polymorphism do not associate with longevity in the IrishOwen A Ross, Martin D Curran, I Maeve Rea, et al.
Neurology|May 3, 2013
Similarities between familial and sporadic autopsy-proven progressive supranuclear palsyShinsuke Fujioka, Avi A Algom, Melissa E Murray, et al.
Human Mutation|May 6, 2015
Structural and Functional Impact of Parkinson Disease-Associated Mutations in the E3 Ubiquitin Ligase ParkinFabienne C Fiesel, Thomas R Caulfield, Elisabeth L Moussaud-Lamodière, et al.
Brain : a Journal of Neurology|September 6, 2023
Pleiotropy with sex-specific traits reveals genetic aspects of sex differences in Parkinson's diseaseKaja Nordengen, Chiara Cappelletti, Shahram Bahrami, et al.
Stroke|August 21, 2023
Management of Inherited CNS Small Vessel Diseases: The CADASIL Example: A Scientific Statement From the American Heart AssociationJames F Meschia, Bradford B Worrall, Fanny M Elahi, et al.
Acta Neuropathologica Communications|July 6, 2023
Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologiesShunsuke Koga, Aya Murakami, Alexandra I Soto-Beasley, et al.
Neurology|July 1, 2026
Familial Aggregation of Parkinson Disease and Essential Tremor in Early and Late Onset Parkinson Disease CohortsLorenzo Malfer, Tina Liu, Aidan Mullan, et al.
Plos One|August 23, 2012
Evaluation of the role of SNCA variants in survival without neurological diseaseMichael G Heckman, Alexandra I Soto-Ortolaza, Nancy N Diehl, et al.
Clinical Genetics|June 15, 2023
A homozygous founder variant in PDE2A causes paroxysmal dyskinesia with intellectual disabilityHammad Yousaf, Shagufta Rehmat, Muhammad Jameel, et al.
Neurobiology of Aging|November 17, 2012
Supportive evidence for 11 loci from genome-wide association studies in Parkinson's diseaseLasse Pihlstrøm, Gunnar Axelsson, Kari Anne Bjørnarå, et al.
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