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 *

159 related articles for article (PubMed ID: 30972844)

  • 1. 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]  

  • 2. MERRF/MELAS overlap syndrome due to the m.3291T>C mutation.
    Liu K; Zhao H; Ji K; Yan C
    Metab Brain Dis; 2014 Mar; 29(1):139-44. PubMed ID: 24338029
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Histochemical and molecular genetic study of MELAS and MERRF in Korean patients.
    Kim DS; Jung DS; Park KH; Kim IJ; Kim CM; Lee WH; Rho SK
    J Korean Med Sci; 2002 Feb; 17(1):103-12. PubMed ID: 11850598
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case of MELAS associated with histochemical findings of muscles characteristic of MERRF].
    Suzuki H; Ono M; Kojima Y; Kanda M; Shibasaki H; Oki M; Nakano S
    Rinsho Shinkeigaku; 2016; 56(3):196-9. PubMed ID: 26960269
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cerebral lactic acidosis correlates with neurological impairment in MELAS.
    Kaufmann P; Shungu DC; Sano MC; Jhung S; Engelstad K; Mitsis E; Mao X; Shanske S; Hirano M; DiMauro S; De Vivo DC
    Neurology; 2004 Apr; 62(8):1297-302. PubMed ID: 15111665
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
    Vastagh I; Gál A; Reményi V; Semjén J; Lukács T; Valikovics A; Molnár MJ
    Ideggyogy Sz; 2011 Nov; 64(11-12):399-403. PubMed ID: 22611618
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ophthalmologic manifestations in MELAS syndrome.
    Fang W; Huang CC; Lee CC; Cheng SY; Pang CY; Wei YH
    Arch Neurol; 1993 Sep; 50(9):977-80. PubMed ID: 8363452
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
    Naini AB; Lu J; Kaufmann P; Bernstein RA; Mancuso M; Bonilla E; Hirano M; DiMauro S
    Arch Neurol; 2005 Mar; 62(3):473-6. PubMed ID: 15767514
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M; Yabe I; Sudo A; Hosoki K; Yaguchi H; Saitoh S; Sasaki H
    J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytochrome c oxidase activity is deficient in blood vessels of patients with myoclonus epilepsy with ragged-red fibers.
    Hasegawa H; Matsuoka T; Goto Y; Nonaka I
    Acta Neuropathol; 1993; 85(3):280-4. PubMed ID: 8384773
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Ultrastructural and clinical findings of mitochondrial encephalomyopathy:report of 27 cases].
    Zhang Q; Sun YL; Zhang CP; Qu BQ; Zhang ZQ
    Zhonghua Bing Li Xue Za Zhi; 2019 Apr; 48(4):298-302. PubMed ID: 30955266
    [No Abstract]   [Full Text] [Related]  

  • 13. Classical MERRF phenotype associated with mitochondrial tRNA(Leu) (m.3243A>G) mutation.
    Brackmann F; Abicht A; Ahting U; Schröder R; Trollmann R
    Eur J Pediatr; 2012 May; 171(5):859-62. PubMed ID: 22270878
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.
    Zeviani M; Muntoni F; Savarese N; Serra G; Tiranti V; Carrara F; Mariotti C; DiDonato S
    Eur J Hum Genet; 1993; 1(1):80-7. PubMed ID: 8069654
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
    Fabrizi GM; Cardaioli E; Grieco GS; Cavallaro T; Malandrini A; Manneschi L; Dotti MT; Federico A; Guazzi G
    J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W; Li W; Chen G; Cao H; Tang H; Tang X; Jin Q; Sun Z; Zhao H; Zhou W; He S; Lv Y; Zhao J; Zhang X
    Biosens Bioelectron; 2009 Apr; 24(8):2371-6. PubMed ID: 19155171
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Development of a DNA biochip for detection of known mtDNA mutations associated with MELAS and MERRF syndromes.].
    Chen G; Li W; DU WD; Cao HM; Tang HY; Tang XF; Sun ZW; Zhao H; Jin QH; Zhao JL; Zhang XJ
    Yi Chuan; 2008 Oct; 30(10):1279-86. PubMed ID: 18930887
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SPECT findings in mitochondrial encephalomyopathy.
    Watanabe Y; Hashikawa K; Moriwaki H; Oku N; Seike Y; Kodaka R; Ono J; Uehara T; Kusuoka H; Nishimura T
    J Nucl Med; 1998 Jun; 39(6):961-4. PubMed ID: 9627326
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
    Campos Y; Martin MA; Lorenzo G; Aparicio M; Cabello A; Arenas J
    Muscle Nerve; 1996 Feb; 19(2):187-90. PubMed ID: 8559168
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High cytochrome c oxidase expression links to severe skeletal energy failure by (31)P-MRS spectroscopy in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.
    Liu AH; Niu FN; Chang LL; Zhang B; Liu Z; Chen JY; Zhou Q; Wu HY; Xu Y
    CNS Neurosci Ther; 2014 Jun; 20(6):509-14. PubMed ID: 24674659
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.