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 *

110 related articles for article (PubMed ID: 32650990)

  • 1. Sensory motor ataxic neuropathy associated dysarthria and ophthalmoplegia "SMANDO" in a consanguineous Moroccan patient with new POLG gene homozygote mutation.
    Rafai MA; Khattab H; Jardel C; Slassi I; Dehbi H; Bouche P
    Rev Neurol (Paris); 2021; 177(1-2):144-146. PubMed ID: 32650990
    [No Abstract]   [Full Text] [Related]  

  • 2. Sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO) in a sibling pair with a homozygous p.A467T POLG mutation.
    McHugh JC; Lonergan R; Howley R; O'Rourke K; Taylor RW; Farrell M; Hutchinson M; Connolly S
    Muscle Nerve; 2010 Feb; 41(2):265-9. PubMed ID: 19813183
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Mitochondrial DNA depletion and POLG mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia].
    Posada IJ; Gallardo ME; Domínguez C; Rivera H; Cabello A; Arenas J; Martín MA; Garesse R; Bornstein B
    Med Clin (Barc); 2010 Oct; 135(10):452-5. PubMed ID: 20576279
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sensory ataxic neuropathy with dysarthria/dysphagia and ophthalmoplegia (SANDO). Two case reports.
    Gáti I; Danielsson O; Jonasson J; Landtblom AM
    Acta Myol; 2011 Dec; 30(3):188-90. PubMed ID: 22616202
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel mutation in spacer region of POLG associated with ataxia neuropathy spectrum and gastroparesis.
    Bostan A; Glibert G; Dachy B; Dan B
    Auton Neurosci; 2012 Sep; 170(1-2):70-2. PubMed ID: 22805437
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Early-onset ataxia with progressive external ophthalmoplegia associated with POLG mutation: autosomal recessive mitochondrial ataxic syndrome or SANDO?
    Habek M; Barun B; Adamec I; Mitrović Z; Ozretić D; Brinar VV
    Neurologist; 2012 Sep; 18(5):287-9. PubMed ID: 22931735
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sensory ataxic neuropathy with ophthalmoparesis caused by POLG mutations.
    Milone M; Brunetti-Pierri N; Tang LY; Kumar N; Mezei MM; Josephs K; Powell S; Simpson E; Wong LJ
    Neuromuscul Disord; 2008 Aug; 18(8):626-32. PubMed ID: 18585914
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sensory ataxic neuropathy with dysarthria and ophthalmoparesis (SANDO) in late life due to compound heterozygous POLG mutations.
    Weiss MD; Saneto RP
    Muscle Nerve; 2010 Jun; 41(6):882-5. PubMed ID: 20513108
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sensory ataxic neuropathy as the presenting feature of a novel mitochondrial disease.
    Fadic R; Russell JA; Vedanarayanan VV; Lehar M; Kuncl RW; Johns DR
    Neurology; 1997 Jul; 49(1):239-45. PubMed ID: 9222196
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia.
    Van Goethem G; Martin JJ; Dermaut B; Löfgren A; Wibail A; Ververken D; Tack P; Dehaene I; Van Zandijcke M; Moonen M; Ceuterick C; De Jonghe P; Van Broeckhoven C
    Neuromuscul Disord; 2003 Feb; 13(2):133-42. PubMed ID: 12565911
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [SANDO (sensory ataxic neuropathy, dysarthria, and ophthalmoplegia)].
    Goto Y
    Ryoikibetsu Shokogun Shirizu; 2001; (36):172. PubMed ID: 11596360
    [No Abstract]   [Full Text] [Related]  

  • 15. [A case of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis with multiple mitochondrial DNA deletions].
    Tanaka K; Tateishi T; Kawamura N; Ohyagi Y; Urata M; Kira J
    Rinsho Shinkeigaku; 2013; 53(3):205-11. PubMed ID: 23524600
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation.
    Kierdaszuk B; Kaliszewska M; Rusecka J; Kosińska J; Bartnik E; Tońska K; Kamińska AM; Kostera-Pruszczyk A
    Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33396418
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MELAS/SANDO overlap syndrome associated with POLG1 mutations.
    Hansen N; Zwarg T; Wanke I; Zierz S; Kastrup O; Deschauer M
    Neurol Sci; 2012 Feb; 33(1):209-12. PubMed ID: 21647632
    [No Abstract]   [Full Text] [Related]  

  • 18. Patient homozygous for a recessive POLG mutation presents with features of MERRF.
    Van Goethem G; Mercelis R; Löfgren A; Seneca S; Ceuterick C; Martin JJ; Van Broeckhoven C
    Neurology; 2003 Dec; 61(12):1811-3. PubMed ID: 14694057
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Homozygous R627W mutations in POLG cause mitochondrial DNA depletion leading to encephalopathy, seizures and stroke-like episodes.
    Paramasivam A; Venkatapathi C; Sandeep G; Meena AK; Uppin MS; Mohapatra S; Pitceathly RDS; Thangaraj K
    Mitochondrion; 2019 Sep; 48():78-83. PubMed ID: 31425757
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oculomasticatory rhythmic movements, insomnia and stroke-like episodes in a patient with POLG mutation.
    Ramesh R; Amanmahanya C; Krishnamoorthy V; Krishnan V; Palani S; Narasimhan Ranganathan L
    BMJ Case Rep; 2024 Apr; 17(4):. PubMed ID: 38684350
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.