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 *

162 related articles for article (PubMed ID: 32364361)

  • 1. [Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene].
    Illés A; Balicza P; Gál A; Pentelényi K; Csabán D; Gézsi A; Molnár V; Molnár MJ
    Orv Hetil; 2020 May; 161(20):821-828. PubMed ID: 32364361
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
    Luoma P; Melberg A; Rinne JO; Kaukonen JA; Nupponen NN; Chalmers RM; Oldfors A; Rautakorpi I; Peltonen L; Majamaa K; Somer H; Suomalainen A
    Lancet; 2004 Sep 4-10; 364(9437):875-82. PubMed ID: 15351195
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel
    Ma L; Mao W; Xu E; Cai Y; Wang C; Chhetri JK; Chan P
    Int J Neurosci; 2020 Apr; 130(4):319-321. PubMed ID: 31613174
    [No Abstract]   [Full Text] [Related]  

  • 4. POLG R964C and GBA L444P mutations in familial Parkinson's disease: Case report and literature review.
    Hsieh PC; Wang CC; Tsai CL; Yeh YM; Lee YS; Wu YR
    Brain Behav; 2019 May; 9(5):e01281. PubMed ID: 30941926
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations.
    Tzoulis C; Tran GT; Schwarzlmüller T; Specht K; Haugarvoll K; Balafkan N; Lilleng PK; Miletic H; Biermann M; Bindoff LA
    Brain; 2013 Aug; 136(Pt 8):2393-404. PubMed ID: 23625061
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders.
    Palin EJ; Paetau A; Suomalainen A
    Brain; 2013 Aug; 136(Pt 8):2379-92. PubMed ID: 23811324
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Parkinsonism, cognitive deficit and behavioural disturbance caused by a novel mutation in the polymerase gamma gene.
    Delgado-Alvarado M; de la Riva P; Jiménez-Urbieta H; Gago B; Gabilondo A; Bornstein B; Rodríguez-Oroz MC
    J Neurol Sci; 2015 Mar; 350(1-2):93-7. PubMed ID: 25724872
    [TBL] [Abstract][Full Text] [Related]  

  • 8. POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.
    Van Goethem G; Luoma P; Rantamäki M; Al Memar A; Kaakkola S; Hackman P; Krahe R; Löfgren A; Martin JJ; De Jonghe P; Suomalainen A; Udd B; Van Broeckhoven C
    Neurology; 2004 Oct; 63(7):1251-7. PubMed ID: 15477547
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Monogenic Parkinson's disease and parkinsonism: clinical phenotypes and frequencies of known mutations.
    Puschmann A
    Parkinsonism Relat Disord; 2013 Apr; 19(4):407-15. PubMed ID: 23462481
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MRI findings in SANDO variety of the ataxia-neuropathy spectrum with a novel mutation in POLG (c.3287G>T): A case report.
    Parada-Garza JD; López-Valencia G; Miranda-García LA; Pérez-García G; Ruiz-Sandoval JL
    Neuromuscul Disord; 2020 Jul; 30(7):590-592. PubMed ID: 32600829
    [TBL] [Abstract][Full Text] [Related]  

  • 11. POLG-related disorders and their neurological manifestations.
    Rahman S; Copeland WC
    Nat Rev Neurol; 2019 Jan; 15(1):40-52. PubMed ID: 30451971
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and Molecular Features of POLG-Related Sensory Ataxic Neuropathy with Dysarthria and Ophthalmoparesis.
    Li LX; Jiang LT; Pan YG; Zhang XL; Pan LZ; Nie ZY; Chen YH; Jin LJ
    J Mol Neurosci; 2021 Dec; 71(12):2462-2467. PubMed ID: 33791913
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India.
    Deepha S; Govindaraj P; Sankaran BP; Chiplunkar S; Kashinkunti C; Nunia V; Nagappa M; Sinha S; Khanna T; Thangaraj K; Taly AB; Gayathri N
    J Mol Neurosci; 2021 Nov; 71(11):2219-2228. PubMed ID: 33469851
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early-onset parkinsonism due to compound heterozygous POLG mutations.
    Rempe T; Kuhlenbäumer G; Krüger S; Biskup S; Matschke J; Hagel C; Deuschl G; van Eimeren T
    Parkinsonism Relat Disord; 2016 Aug; 29():135-7. PubMed ID: 27185166
    [No Abstract]   [Full Text] [Related]  

  • 15. Dopamine-agonist responsive Parkinsonism in a patient with the SANDO syndrome caused by POLG mutation.
    Bandettini di Poggio M; Nesti C; Bruno C; Meschini MC; Schenone A; Santorelli FM
    BMC Med Genet; 2013 Oct; 14():105. PubMed ID: 24099403
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases.
    Hikmat O; Naess K; Engvall M; Klingenberg C; Rasmussen M; Tallaksen CM; Brodtkorb E; Ostergaard E; de Coo IFM; Pias-Peleteiro L; Isohanni P; Uusimaa J; Darin N; Rahman S; Bindoff LA
    J Inherit Metab Dis; 2020 Jul; 43(4):726-736. PubMed ID: 32391929
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease.
    Kim YJ; Jeon J; Shin J; Kim NY; Hong JH; Oh JM; Hong S; Kim YJ; Kim YE; Kang SY; Ma HI; Lee U; Yoon J
    Mov Disord; 2017 Aug; 32(8):1211-1220. PubMed ID: 28548297
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of drug-induced parkinsonism and tardive akathisia with e1143g polymerase γ mutation-innocent bystander or a culprit?
    Idiculla PS; Hussain ST; Siddiqui JH
    J Clin Transl Res; 2021 Jun; 7(3):297-301. PubMed ID: 34179544
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Adult-onset sensory neuropathy and ataxia as a clinical manifestation of POLG gene mutations].
    García-Cabo C; Carvajal-García P; Fernández-Vega I; Peña-Suárez J; Mateos-Marcos V; Suárez-Santos P; Álvarez-Martínez V; Morís-de la Tassa G
    Rev Neurol; 2023 Feb; 76(3):75-81. PubMed ID: 36703500
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and molecular features of POLG-related mitochondrial disease.
    Stumpf JD; Saneto RP; Copeland WC
    Cold Spring Harb Perspect Biol; 2013 Apr; 5(4):a011395. PubMed ID: 23545419
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.