69 related articles for article (PubMed ID: 32814227)
1. Neuropathological findings in PINK1-associated Parkinson's disease.
Nybø CJ; Gustavsson EK; Farrer MJ; Aasly JO
Parkinsonism Relat Disord; 2020 Sep; 78():105-108. PubMed ID: 32814227
[TBL] [Abstract][Full Text] [Related]
2. Parkinson's disease with Lewy bodies associated with a heterozygous PARKIN dosage mutation.
Sharp ME; Marder KS; Côté L; Clark LN; Nichols WC; Vonsattel JP; Alcalay RN
Mov Disord; 2014 Apr; 29(4):566-8. PubMed ID: 24375549
[TBL] [Abstract][Full Text] [Related]
3. Gait function and locus coeruleus Lewy body pathology in 51 Parkinson's disease patients.
Mills KA; Mari Z; Bakker C; Johnson V; Pontone GM; Pantelyat A; Troncoso JC; Pletnikova O; Dawson TM; Rosenthal LS
Parkinsonism Relat Disord; 2016 Dec; 33():102-106. PubMed ID: 27693194
[TBL] [Abstract][Full Text] [Related]
4. Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central Europe.
Milanowski ŁM; Lindemann JA; Hoffman-Zacharska D; Soto-Beasley AI; Barcikowska M; Boczarska-Jedynak M; Deutschlander A; Kłodowska G; Dulski J; Fedoryshyn L; Friedman A; Jamrozik Z; Janik P; Karpinsky K; Koziorowski D; Krygowska-Wajs A; Jasińska-Myga B; Opala G; Potulska-Chromik A; Pulyk A; Rektorova I; Sanotsky Y; Siuda J; Sławek J; Śmiłowska K; Szczechowski L; Rudzińska-Bar M; Walton RL; Ross OA; Wszolek ZK
Parkinsonism Relat Disord; 2021 May; 86():48-51. PubMed ID: 33845304
[TBL] [Abstract][Full Text] [Related]
5. Evidence for early and progressive ultrasonic vocalization and oromotor deficits in a PINK1 gene knockout rat model of Parkinson's disease.
Grant LM; Kelm-Nelson CA; Hilby BL; Blue KV; Paul Rajamanickam ES; Pultorak JD; Fleming SM; Ciucci MR
J Neurosci Res; 2015 Nov; 93(11):1713-27. PubMed ID: 26234713
[TBL] [Abstract][Full Text] [Related]
6. α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?
Kiely AP; Asi YT; Kara E; Limousin P; Ling H; Lewis P; Proukakis C; Quinn N; Lees AJ; Hardy J; Revesz T; Houlden H; Holton JL
Acta Neuropathol; 2013 May; 125(5):753-69. PubMed ID: 23404372
[TBL] [Abstract][Full Text] [Related]
7. Human Induced Pluripotent Stem Cell Phenotyping and Preclinical Modeling of Familial Parkinson's Disease.
Kim J; Daadi EW; Oh T; Daadi ES; Daadi MM
Genes (Basel); 2022 Oct; 13(11):. PubMed ID: 36360174
[TBL] [Abstract][Full Text] [Related]
8. Comprehensive assessment of PINK1 variants in Parkinson's disease.
Krohn L; Grenn FP; Makarious MB; Kim JJ; Bandres-Ciga S; Roosen DA; Gan-Or Z; Nalls MA; Singleton AB; Blauwendraat C;
Neurobiol Aging; 2020 Jul; 91():168.e1-168.e5. PubMed ID: 32249012
[TBL] [Abstract][Full Text] [Related]
9. Association of Parkinson disease risk loci with mild parkinsonian signs in older persons.
Shulman JM; Yu L; Buchman AS; Evans DA; Schneider JA; Bennett DA; De Jager PL
JAMA Neurol; 2014 Apr; 71(4):429-35. PubMed ID: 24514572
[TBL] [Abstract][Full Text] [Related]
10. Upregulated ECM genes and increased synaptic activity in Parkinson's human DA neurons with PINK1/ PRKN mutations.
Tripathi U; Rosh I; Ben Ezer R; Nayak R; Hussein Y; Choudhary A; Djamus J; Manole A; Houlden H; Gage FH; Stern S
NPJ Parkinsons Dis; 2024 May; 10(1):103. PubMed ID: 38762512
[TBL] [Abstract][Full Text] [Related]
11. A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.
Ben El Haj R; Regragui W; Tazi-Ahnini R; Skalli A; Bouslam N; Benomar A; Yahyaoui M; Bouhouche A
Biomed Res Int; 2016; 2016():3460234. PubMed ID: 27413743
[TBL] [Abstract][Full Text] [Related]
12. Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature.
Schneider SA; Alcalay RN
Mov Disord; 2017 Nov; 32(11):1504-1523. PubMed ID: 29124790
[TBL] [Abstract][Full Text] [Related]
13. Neuroleptic-induced Parkinsonism: Clinicopathological study.
Shuaib UA; Rajput AH; Robinson CA; Rajput A
Mov Disord; 2016 Mar; 31(3):360-5. PubMed ID: 26660063
[TBL] [Abstract][Full Text] [Related]
14. Long-read sequencing unravels the complexity of structural variants in
Cogan G; Daida K; Billingsley KJ; Tesson C; Forlani S; Jornea L; Arnaud L; Tissier L; LeGuern E; Singleton AB; Ferrien M; Gervais Bernard H; Lesage S; Blauwendraat C; Brice A
medRxiv; 2024 May; ():. PubMed ID: 38746197
[TBL] [Abstract][Full Text] [Related]
15. Genetic landscape of Parkinson's disease and related diseases in Luxembourg.
Landoulsi Z; Pachchek S; Bobbili DR; Pavelka L; May P; Krüger R;
Front Aging Neurosci; 2023; 15():1282174. PubMed ID: 38173558
[TBL] [Abstract][Full Text] [Related]
16. Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Daida K; Funayama M; Billingsley KJ; Malik L; Miano-Burkhardt A; Leonard HL; Makarious MB; Iwaki H; Ding J; Gibbs JR; Ishiguro M; Yoshino H; Ogaki K; Oyama G; Nishioka K; Nonaka R; Akamatsu W; Blauwendraat C; Hattori N
Mov Disord; 2023 Dec; 38(12):2249-2257. PubMed ID: 37926948
[TBL] [Abstract][Full Text] [Related]
17. Genetic Identification in Early Onset Parkinsonism among Norwegian Patients.
Gustavsson EK; Trinh J; McKenzie M; Bortnick S; Petersen MS; Farrer MJ; Aasly JO
Mov Disord Clin Pract; 2017; 4(4):499-508. PubMed ID: 30363439
[TBL] [Abstract][Full Text] [Related]
18. Transcriptomic signatures of brain regional vulnerability to Parkinson's disease.
Keo A; Mahfouz A; Ingrassia AMT; Meneboo JP; Villenet C; Mutez E; Comptdaer T; Lelieveldt BPF; Figeac M; Chartier-Harlin MC; van de Berg WDJ; van Hilten JJ; Reinders MJT
Commun Biol; 2020 Mar; 3(1):101. PubMed ID: 32139796
[TBL] [Abstract][Full Text] [Related]
19. PINK1-PD: A compound heterozygote of Filipino ancestry and 7 Tesla MRI findings.
Dulski J; Middlebrooks EH; Wszolek ZK
Parkinsonism Relat Disord; 2024 Jan; 118():105948. PubMed ID: 38043182
[TBL] [Abstract][Full Text] [Related]
20. Long-read sequencing resolves a complex structural variant in
Daida K; Funayama M; Billingsley KJ; Malik L; Miano-Burkhardt A; Leonard HL; Makarious MB; Iwaki H; Ding J; Gibbs JR; Ishiguro M; Yoshino H; Ogaki K; Oyama G; Nishioka K; Nonaka R; Akamatsu W; Blauwendraat C; Hattori N
medRxiv; 2023 Aug; ():. PubMed ID: 37790330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]