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 *

214 related articles for article (PubMed ID: 27943471)

  • 1. A novel RAB39B gene mutation in X-linked juvenile parkinsonism with basal ganglia calcification.
    Shi CH; Zhang SY; Yang ZH; Yang J; Shang DD; Mao CY; Liu H; Hou HM; Shi MM; Wu J; Xu YM
    Mov Disord; 2016 Dec; 31(12):1905-1909. PubMed ID: 27943471
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.
    Ciammola A; Carrera P; Di Fonzo A; Sassone J; Villa R; Poletti B; Ferrari M; Girotti F; Monfrini E; Buongarzone G; Silani V; Cinnante CM; Mignogna ML; D'Adamo P; Bonati MT
    Parkinsonism Relat Disord; 2017 Nov; 44():142-146. PubMed ID: 28851564
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Generation of induced pluripotent stem cell line (ZZUi005-A) from a 21-year-old patient with a novel RAB39B gene mutation in X-linked juvenile parkinsonism.
    Wang Y; Sun H; Wang Z; Yang Z; Shi M; Yang J; Liu Y; Liu H; Zhang S; Shi C; Xu Y
    Stem Cell Res; 2017 Dec; 25():132-135. PubMed ID: 29128816
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RAB39B gene mutations are not linked to familial Parkinson's disease in China.
    Kang JF; Luo Y; Tang BS; Wan CM; Yang Y; Li K; Liu ZH; Sun QY; Xu Q; Yan XX; Guo JF
    Sci Rep; 2016 Oct; 6():34502. PubMed ID: 27694831
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies.
    Hodges K; Brewer SS; Labbé C; Soto-Ortolaza AI; Walton RL; Strongosky AJ; Uitti RJ; van Gerpen JA; Ertekin-Taner N; Kantarci K; Lowe VJ; Parisi JE; Savica R; Graff-Radford J; Jones DT; Knopman DS; Petersen RC; Murray ME; Graff-Radford NR; Ferman TJ; Dickson DW; Wszolek ZK; Boeve BF; Ross OA; Lorenzo-Betancor O
    Neurobiol Aging; 2016 Sep; 45():107-108. PubMed ID: 27459931
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease.
    Mata IF; Jang Y; Kim CH; Hanna DS; Dorschner MO; Samii A; Agarwal P; Roberts JW; Klepitskaya O; Shprecher DR; Chung KA; Factor SA; Espay AJ; Revilla FJ; Higgins DS; Litvan I; Leverenz JB; Yearout D; Inca-Martinez M; Martinez E; Thompson TR; Cholerton BA; Hu SC; Edwards KL; Kim KS; Zabetian CP
    Mol Neurodegener; 2015 Sep; 10():50. PubMed ID: 26399558
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease.
    Yuan L; Deng X; Song Z; Yang Z; Ni B; Chen Y; Deng H
    Neurobiol Aging; 2015 Oct; 36(10):2907.e11-2. PubMed ID: 26163985
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.
    Wilson GR; Sim JC; McLean C; Giannandrea M; Galea CA; Riseley JR; Stephenson SE; Fitzpatrick E; Haas SA; Pope K; Hogan KJ; Gregg RG; Bromhead CJ; Wargowski DS; Lawrence CH; James PA; Churchyard A; Gao Y; Phelan DG; Gillies G; Salce N; Stanford L; Marsh AP; Mignogna ML; Hayflick SJ; Leventer RJ; Delatycki MB; Mellick GD; Kalscheuer VM; D'Adamo P; Bahlo M; Amor DJ; Lockhart PJ
    Am J Hum Genet; 2014 Dec; 95(6):729-35. PubMed ID: 25434005
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.
    Lin HH; Wu RM; Lin HI; Chen ML; Tai CH; Lin CH
    Neurobiol Aging; 2017 Feb; 50():169.e3-169.e4. PubMed ID: 27838047
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinical features of familial idiopathic basal ganglia calcification caused by a novel mutation in the SLC20A2 gene].
    Zhu M; Fang C; Li X; Zhou M; Wan H; Hong D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb; 32(1):64-8. PubMed ID: 25636102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel RAB39B loss-of-function mutation in patient with typical early-onset Parkinson's disease.
    Jacobson JR; Piat C; Aksamit AJ; Patane' G; Ross OA; Savica R
    Parkinsonism Relat Disord; 2024 Jun; 123():106038. PubMed ID: 38503262
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification.
    Nicolas G; Pottier C; Charbonnier C; Guyant-Maréchal L; Le Ber I; Pariente J; Labauge P; Ayrignac X; Defebvre L; Maltête D; Martinaud O; Lefaucheur R; Guillin O; Wallon D; Chaumette B; Rondepierre P; Derache N; Fromager G; Schaeffer S; Krystkowiak P; Verny C; Jurici S; Sauvée M; Vérin M; Lebouvier T; Rouaud O; Thauvin-Robinet C; Rousseau S; Rovelet-Lecrux A; Frebourg T; Campion D; Hannequin D;
    Brain; 2013 Nov; 136(Pt 11):3395-407. PubMed ID: 24065723
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Broad clinical phenotype in Parkinsonism associated with a base pair deletion in RAB39B and additional POLG variant.
    Güldner M; Schulte C; Hauser AK; Gasser T; Brockmann K
    Parkinsonism Relat Disord; 2016 Oct; 31():148-150. PubMed ID: 27448726
    [No Abstract]   [Full Text] [Related]  

  • 14. Clinical and Neuropathological Features Associated With Loss of RAB39B.
    Gao Y; Martínez-Cerdeño V; Hogan KJ; McLean CA; Lockhart PJ
    Mov Disord; 2020 Apr; 35(4):687-693. PubMed ID: 31951675
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with an SLC20A2 mutation.
    Kimura T; Miura T; Aoki K; Saito S; Hondo H; Konno T; Uchiyama A; Ikeuchi T; Takahashi H; Kakita A
    Neuropathology; 2016 Aug; 36(4):365-71. PubMed ID: 26635128
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Primary familial brain calcification caused by MYORG mutations in an Italian family.
    Taglia I; Kuipers DJS; Breedveld GJ; Mignarri A; Dotti MT; Federico A; Bonifati V
    Parkinsonism Relat Disord; 2019 Oct; 67():24-26. PubMed ID: 31621601
    [No Abstract]   [Full Text] [Related]  

  • 17. Novel RAB39B variant associated intellectual disability and levodopa-responsive young-onset parkinsonism.
    Abusrair A; Mititelu A; Pfeffer G; Rosenegger L; Aquino CC
    Parkinsonism Relat Disord; 2023 Nov; 116():105855. PubMed ID: 37844350
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RAB39B mutations are a rare finding in Parkinson disease patients.
    Löchte T; Brüggemann N; Vollstedt EJ; Krause P; Domingo A; Rosales R; Lee LV; Hopfner F; Westenberger A; Kühn A; Klein C; Lohmann K
    Parkinsonism Relat Disord; 2016 Feb; 23():116-7. PubMed ID: 26739247
    [No Abstract]   [Full Text] [Related]  

  • 19. New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.
    Puschmann A
    Curr Neurol Neurosci Rep; 2017 Sep; 17(9):66. PubMed ID: 28733970
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease.
    Suleiman J; Hamwi N; El-Hattab AW
    Brain Dev; 2018 Oct; 40(9):824-826. PubMed ID: 29903538
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.