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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 27709683)

  • 21. PLA2G6 mutations cause motor dysfunction phenotypes of young-onset dystonia-parkinsonism type 14 and can be relieved by DHA treatment in animal models.
    Yeh TH; Liu HF; Chiu CC; Cheng ML; Huang GJ; Huang YC; Liu YC; Huang YZ; Lu CS; Chen YC; Chen HY; Cheng YC
    Exp Neurol; 2021 Dec; 346():113863. PubMed ID: 34520727
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Reply to: Juvenile PLA2G6-parkinsonism due to Indian 'Asian' p.R741Q mutation, and response to STN DBS.
    Magrinelli F; Rajapaksha I; Kobylecki C; Latorre A; Mulroy E; Estevez-Fraga C; Houlden H; Tinazzi M; Bhatia KP
    Mov Disord; 2022 Mar; 37(3):658-662. PubMed ID: 35152491
    [No Abstract]   [Full Text] [Related]  

  • 23. Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's disease.
    Wirth T; Weibel S; Montaut S; Bigaut K; Rudolf G; Chelly J; Tranchant C; Anheim M
    Parkinsonism Relat Disord; 2017 Aug; 41():127-129. PubMed ID: 28549837
    [No Abstract]   [Full Text] [Related]  

  • 24. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
    Paisán-Ruiz C; Guevara R; Federoff M; Hanagasi H; Sina F; Elahi E; Schneider SA; Schwingenschuh P; Bajaj N; Emre M; Singleton AB; Hardy J; Bhatia KP; Brandner S; Lees AJ; Houlden H
    Mov Disord; 2010 Sep; 25(12):1791-800. PubMed ID: 20669327
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Early-onset autosomal-recessive parkinsonian-pyramidal syndrome.
    Lai HJ; Lin CH; Wu RM
    Acta Neurol Taiwan; 2012 Sep; 21(3):99-107. PubMed ID: 23196729
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Disruption of Golgi morphology and altered protein glycosylation in PLA2G6-associated neurodegeneration.
    Davids M; Kane MS; He M; Wolfe LA; Li X; Raihan MA; Chao KR; Bone WP; Boerkoel CF; Gahl WA; Toro C
    J Med Genet; 2016 Mar; 53(3):180-9. PubMed ID: 26668131
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.
    Galimberti D; Cioffi SM; Fenoglio C; Serpente M; Oblak AL; Rodriguez-Porcel F; Oldoni E; Hagen MC; Arcaro M; Scarpini E; Ghetti B; Espay AJ
    Mov Disord; 2017 Mar; 32(3):476-478. PubMed ID: 27859661
    [No Abstract]   [Full Text] [Related]  

  • 28. Novel mutations in siblings with later-onset PLA2G6-associated neurodegeneration (PLAN).
    Bower MA; Bushara K; Dempsey MA; Das S; Tuite PJ
    Mov Disord; 2011 Aug; 26(9):1768-9. PubMed ID: 21520282
    [No Abstract]   [Full Text] [Related]  

  • 29. PLA2G6-Associated Dystonia Parkinsonism.
    Sachan D; Yadav A; Yadav D
    Indian Pediatr; 2021 Jan; 58(1):77-78. PubMed ID: 33452780
    [No Abstract]   [Full Text] [Related]  

  • 30. Motor and non-motor responses of STN DBS in early onset PLA2G6 related Parkinsonism with compound heterozygous mutation from China.
    Chen S; Zhang H; Zhang J; Jiang B; He Z; Zhang B; Liu Y; Xu S; Zhao C
    Parkinsonism Relat Disord; 2023 Jan; 106():105237. PubMed ID: 36509027
    [No Abstract]   [Full Text] [Related]  

  • 31. Identification of a novel mutation in PLA2G6 gene and phenotypic heterogeneity analysis of PLA2G6-related neurodegeneration.
    Ji Y; Li Y; Shi C; Gao Y; Yang J; Liang D; Yang Z; Xu Y
    Parkinsonism Relat Disord; 2019 Aug; 65():159-164. PubMed ID: 31196701
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort.
    Romani M; Kraoua I; Micalizzi A; Klaa H; Benrhouma H; Drissi C; Turki I; Castellana S; Mazza T; Valente EM; Gouider-Khouja N
    Eur J Neurol; 2015 Jan; 22(1):178-86. PubMed ID: 25164370
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Expanded phenotype and hippocampal involvement in a novel compound heterozygosity of adult PLA2G6 associated neurodegeneration (PARK14).
    Michelis JP; Hattingen E; Gaertner FC; Minnerop M; Träber F; Biskup S; Klockgether T; Paus S
    Parkinsonism Relat Disord; 2017 Apr; 37():111-113. PubMed ID: 28094106
    [No Abstract]   [Full Text] [Related]  

  • 34. [A novel homozygous mutation in PLA2G6 gene causes infantile neuroaxonal dystrophy in a case].
    Wang J; Wu W; Chen X; Zhang L; Wang X; Dong G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):64-7. PubMed ID: 26829737
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegeneration.
    Chen YJ; Chen YC; Dong HL; Li LX; Ni W; Li HF; Wu ZY
    Parkinsonism Relat Disord; 2018 Apr; 49():88-94. PubMed ID: 29454663
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Aripiprazole in a Patient of PLA2G6-Associated Neurodegeneration With Psychosis.
    Huang MH; Chiu YC; Tsai CF
    Clin Neuropharmacol; 2018; 41(4):136-137. PubMed ID: 29916839
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family.
    Lossos A; Reches A; Gal A; Newman JP; Soffer D; Gomori JM; Boher M; Ekstein D; Biran I; Meiner Z; Abramsky O; Rosenmann H
    J Neurol; 2003 Jun; 250(6):733-40. PubMed ID: 12796837
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene.
    Remes AM; Hinttala R; Kärppä M; Soini H; Takalo R; Uusimaa J; Majamaa K
    Parkinsonism Relat Disord; 2008 Dec; 14(8):652-4. PubMed ID: 18321754
    [TBL] [Abstract][Full Text] [Related]  

  • 39. PLA2G6 variant in Parkinson's disease.
    Tomiyama H; Yoshino H; Ogaki K; Li L; Yamashita C; Li Y; Funayama M; Sasaki R; Kokubo Y; Kuzuhara S; Hattori N
    J Hum Genet; 2011 May; 56(5):401-3. PubMed ID: 21368765
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism.
    Kirola L; Behari M; Shishir C; Thelma BK
    Parkinsonism Relat Disord; 2016 Oct; 31():124-128. PubMed ID: 27496670
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.