These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
156 related articles for article (PubMed ID: 37285793)
1. A systematic analysis of genotype-phenotype associations with PLA2G6. Xue J; Ding DX; Xu GY; Wang PZ; Ge YL; Zhang JR; Cheng XY; Wang YM; Jin H; Luo SY; Zheng YH; Chen J; Wang F; Li D; Mao CJ; Li K; Liu CF Parkinsonism Relat Disord; 2023 Jul; 112():105477. PubMed ID: 37285793 [TBL] [Abstract][Full Text] [Related]
2. Catalytic function of PLA2G6 is impaired by mutations associated with infantile neuroaxonal dystrophy but not dystonia-parkinsonism. Engel LA; Jing Z; O'Brien DE; Sun M; Kotzbauer PT PLoS One; 2010 Sep; 5(9):e12897. PubMed ID: 20886109 [TBL] [Abstract][Full Text] [Related]
3. Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients. Dehnavi AZ; Bemanalizadeh M; Kahani SM; Ashrafi MR; Rohani M; Toosi MB; Heidari M; Hosseinpour S; Amini B; Zokaei S; Rezaei Z; Aryan H; Amanat M; Vahidnezhad H; Mohammadi P; Garshasbi M; Tavasoli AR Orphanet J Rare Dis; 2023 Jul; 18(1):177. PubMed ID: 37403138 [TBL] [Abstract][Full Text] [Related]
4. A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy. Iannello G; Graziano C; Cenacchi G; Cordelli DM; Zuntini R; Papa V; Magistà AM; Gagliardi M; Procopio R; Quattrone A; Annesi G J Neurol Sci; 2017 Oct; 381():209-212. PubMed ID: 28991683 [TBL] [Abstract][Full Text] [Related]
5. Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex. Kapoor S; Shah MH; Singh N; Rather MI; Bhat V; Gopinath S; Bindu PS; Taly AB; Sinha S; Nagappa M; Bharath RD; Mahadevan A; Narayanappa G; Chickabasaviah YT; Kumar A PLoS One; 2016; 11(5):e0155605. PubMed ID: 27196560 [TBL] [Abstract][Full Text] [Related]
6. The role of the PLA2G6 gene in neurodegenerative diseases. Deng X; Yuan L; Jankovic J; Deng H Ageing Res Rev; 2023 Aug; 89():101957. PubMed ID: 37236368 [TBL] [Abstract][Full Text] [Related]
7. Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review. Chu YT; Lin HY; Chen PL; Lin CH BMC Neurol; 2020 Mar; 20(1):101. PubMed ID: 32183746 [TBL] [Abstract][Full Text] [Related]
8. Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN). Kurian MA; Morgan NV; MacPherson L; Foster K; Peake D; Gupta R; Philip SG; Hendriksz C; Morton JE; Kingston HM; Rosser EM; Wassmer E; Gissen P; Maher ER Neurology; 2008 Apr; 70(18):1623-9. PubMed ID: 18443314 [TBL] [Abstract][Full Text] [Related]
10. PLA2G6-associated neurodegeneration (PLAN): further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease. Illingworth MA; Meyer E; Chong WK; Manzur AY; Carr LJ; Younis R; Hardy C; McDonald F; Childs AM; Stewart B; Warren D; Kneen R; King MD; Hayflick SJ; Kurian MA Mol Genet Metab; 2014 Jun; 112(2):183-9. PubMed ID: 24745848 [TBL] [Abstract][Full Text] [Related]
11. PLA2G6-associated neurodegeneration in four different populations-case series and literature review. Hanna Al-Shaikh R; Milanowski LM; Holla VV; Kurihara K; Yadav R; Kamble N; Muthusamy B; Bellad A; Koziorowski D; Szlufik S; Hoffman-Zacharska D; Fujioka S; Tsuboi Y; Ross OA; Wierenga K; Uitti RJ; Wszolek Z; Pal PK Parkinsonism Relat Disord; 2022 Aug; 101():66-74. PubMed ID: 35803092 [TBL] [Abstract][Full Text] [Related]
12. Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism. Yoshino H; Tomiyama H; Tachibana N; Ogaki K; Li Y; Funayama M; Hashimoto T; Takashima S; Hattori N Neurology; 2010 Oct; 75(15):1356-61. PubMed ID: 20938027 [TBL] [Abstract][Full Text] [Related]
13. Follow-up study of 25 Chinese children with PLA2G6-associated neurodegeneration. Zhang P; Gao Z; Jiang Y; Wang J; Zhang F; Wang S; Yang Y; Xiong H; Zhang Y; Bao X; Xiao J; Wu X; Wu Y Eur J Neurol; 2013 Feb; 20(2):322-30. PubMed ID: 22934738 [TBL] [Abstract][Full Text] [Related]
14. Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis. Al-Maawali A; Yoon G; Feigenbaum AS; Halliday WC; Clarke JT; Branson HM; Banwell BL; Chitayat D; Blaser SI Neuroradiology; 2016 Oct; 58(10):1035-1042. PubMed ID: 27516098 [TBL] [Abstract][Full Text] [Related]
15. Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis. Iodice A; Spagnoli C; Salerno GG; Frattini D; Bertani G; Bergonzini P; Pisani F; Fusco C Brain Dev; 2017 Feb; 39(2):93-100. PubMed ID: 27884548 [TBL] [Abstract][Full Text] [Related]
16. PLA2G6-associated neurodegeneration: New insights into brain abnormalities and disease progression. Darling A; Aguilera-Albesa S; Tello CA; Serrano M; Tomás M; Camino-León R; Fernández-Ramos J; Jiménez-Escrig A; Poó P; O'Callaghan M; Ortez C; Nascimento A; Fernández Mesaque RC; Madruga M; Arrabal L; Roldan S; Gómez-Martín H; Garrido C; Temudo T; Jou-Muñoz C; Muchart J; Huisman TAGM; Poretti A; Lupo V; Espinós C; Pérez-Dueñas B Parkinsonism Relat Disord; 2019 Apr; 61():179-186. PubMed ID: 30340910 [TBL] [Abstract][Full Text] [Related]
17. Mutation screening of PLA2G6 in Japanese patients with early onset dystonia-parkinsonism. Yamashita C; Funayama M; Li Y; Yoshino H; Yamada H; Seino Y; Tomiyama H; Hattori N J Neural Transm (Vienna); 2017 Apr; 124(4):431-435. PubMed ID: 27942883 [TBL] [Abstract][Full Text] [Related]