Citations 36

Characterization of variants in genes associated with Parkinson’s disease and parkinsonism in the African American population using exome sequencing (P2.079)

Neurology | December 7, 2023 | Volume: 90 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.90.15_supplement.p2.079

TRIO Gene Segregation in a Family with Cerebellar Ataxia (P1.063)

Neurology | December 7, 2023 | Volume: 90 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.90.15_supplement.p1.063

Mayo Clinic Florida Collection Of Human Skin Fibroblast Cultures From Patients With Hereditary Neurodegenerative Disorders (P7.070)

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.p7.070

Three Sib-Pairs of Autopsy-Confirmed Progressive Supranuclear Palsy (P5.248)

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.p5.248

A Family With Corticobasal Degeneration, Parkinson’s Disease, Amyotrophic Lateral Sclerosis, and Dementia (P3.085)

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.p3.085

Analysis of a Large Progressive Supranuclear Palsy Cohort Reporting to a Single Clinical Center (P3.8-024)

Neurology | December 7, 2023 | Volume: 92 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.92.15_supplement.p3.8-024

Patient with Hydrocephalus and SCA15 (ITPR1) Variant (P6.397)

Neurology | December 7, 2023 | Volume: 86 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.86.16_supplement.p6.397

Cancer in Parkinsons Disease in a Collection of the Mayo Clinic (P6.371)

Neurology | December 7, 2023 | Volume: 86 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.86.16_supplement.p6.371

Comparison of Clinical Features Among Parkinson Disease Subtypes (P6.014)

Neurology | December 7, 2023 | Volume: 88 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.88.16_supplement.p6.014

Clinicopathologic phenotypes of four cases with MAPT P301L mutation (P2.164)

Neurology | December 6, 2023 | Volume: 84 | Issue: 14_supplement | Pages: No page available

10.1212/wnl.84.14_supplement.p2.164