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 *

186 related articles for article (PubMed ID: 16551460)

  • 1. Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case.
    Orcesi S; Gorni K; Termine C; Uggetti C; Veggiotti P; Carrara F; Zeviani M; Berardinelli A; Lanzi G
    J Child Neurol; 2006 Jan; 21(1):79-82. PubMed ID: 16551460
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers.
    Monden Y; Mori M; Kuwajima M; Goto T; Yamagata T; Momoi MY
    Brain Dev; 2013 Jun; 35(6):582-5. PubMed ID: 22981260
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fibrous dysplasia in a child with mitochondrial A8344G mutation.
    Chen ST; Fan PC; Hwu WL; Wu MH
    J Child Neurol; 2008 Dec; 23(12):1447-50. PubMed ID: 18772492
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review.
    Tsao CY; Herman G; Boué DR; Prior TW; Lo WD; Atkin JF; Rusin J
    J Child Neurol; 2003 Jan; 18(1):62-4. PubMed ID: 12661941
    [TBL] [Abstract][Full Text] [Related]  

  • 5. When should MERRF (myoclonus epilepsy associated with ragged-red fibers) be the diagnosis?
    Lorenzoni PJ; Scola RH; Kay CS; Silvado CE; Werneck LC
    Arq Neuropsiquiatr; 2014 Oct; 72(10):803-11. PubMed ID: 25337734
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation].
    Hou Y; Zhao XT; Xie ZY; Yuan Y; Wang ZX
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 52(5):851-855. PubMed ID: 33047718
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical heterogeneity associated with mitochondrial DNA A8344G point mutation].
    Zhao J; Zhao DH; Zhang W; Lü H; Yuan Y; Qi Y; Wang ZX
    Zhonghua Yi Xue Za Zhi; 2012 Oct; 92(40):2835-8. PubMed ID: 23290212
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unusual presentations of patients with the mitochondrial MERRF mutation A8344G.
    Wiedemann FR; Bartels C; Kirches E; Mawrin C; Wallesch CW
    Clin Neurol Neurosurg; 2008 Sep; 110(8):859-63. PubMed ID: 18657354
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case report.
    Sitburana O; Witoonpanich R; Phudhichareonrat S; Lertrit P; Supavilai R
    J Med Assoc Thai; 2001 Jul; 84(7):1051-5. PubMed ID: 11759966
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas.
    Larsson NG; Tulinius MH; Holme E; Oldfors A
    Muscle Nerve Suppl; 1995; 3():S102-6. PubMed ID: 7603509
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys.
    Horvath R; Kley RA; Lochmüller H; Vorgerd M
    Neurology; 2007 Jan; 68(1):56-8. PubMed ID: 17200493
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MERRF-like phenotype associated with a rare mitochondrial trnaile mutation (m.4284 G>A).
    Hahn A; Schänzer A; Neubauer BA; Gizewski E; Ahting U; Rolinski B
    Neuropediatrics; 2011 Aug; 42(4):148-51. PubMed ID: 21766266
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosis.
    Naumann M; Kiefer R; Toyka KV; Sommer C; Seibel P; Reichmann H
    Muscle Nerve; 1997 Jul; 20(7):833-9. PubMed ID: 9179155
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome.
    Shtilbans A; Shanske S; Goodman S; Sue CM; Bruno C; Johnson TL; Lava NS; Waheed N; DiMauro S
    J Child Neurol; 2000 Nov; 15(11):759-61. PubMed ID: 11108511
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Decreased heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation.
    Chen CY; Chen HF; Gi SJ; Chi TH; Cheng CK; Hsu CF; Ma YS; Wei YH; Liu CS; Hsieh M
    Mitochondrion; 2011 Sep; 11(5):739-49. PubMed ID: 21679777
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Generation of an induced pluripotent stem cell (iPSC) line from a 40-year-old patient with the A8344G mutation of mitochondrial DNA and MERRF (myoclonic epilepsy with ragged red fibers) syndrome.
    Wu YT; Hsu YH; Huang CY; Ho MC; Cheng YC; Wen CH; Ko HW; Lu HE; Chen YC; Tsai CL; Hsu YC; Wei YH; Hsieh PCH
    Stem Cell Res; 2018 Mar; 27():10-14. PubMed ID: 29288969
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autopsied case with MERRF/MELAS overlap syndrome accompanied by stroke-like episodes localized to the precentral gyrus.
    Miyahara H; Matsumoto S; Mokuno K; Dei R; Akagi A; Mimuro M; Iwasaki Y; Yoshida M
    Neuropathology; 2019 Jun; 39(3):212-217. PubMed ID: 30972844
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Fukuhara disease].
    Fukuhara N
    Brain Nerve; 2008 Jan; 60(1):53-8. PubMed ID: 18232333
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epileptic phenotypes associated with mitochondrial disorders.
    Canafoglia L; Franceschetti S; Antozzi C; Carrara F; Farina L; Granata T; Lamantea E; Savoiardo M; Uziel G; Villani F; Zeviani M; Avanzini G
    Neurology; 2001 May; 56(10):1340-6. PubMed ID: 11376185
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.