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 *

157 related articles for article (PubMed ID: 31756516)

  • 21. Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.
    Wang YX; Le WD
    Chin Med J (Engl); 2015 Jul; 128(13):1820-5. PubMed ID: 26112726
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes.
    Mukai M; Nagata E; Mizuma A; Yamano M; Sugaya K; Nishino I; Goto YI; Takizawa S
    Intern Med; 2017; 56(1):95-99. PubMed ID: 28050007
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome.
    Li JY; Hsieh RH; Peng NJ; Lai PH; Lee CF; Lo YK; Wei YH
    J Formos Med Assoc; 2007 Jul; 106(7):528-36. PubMed ID: 17660142
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Adult onset MELAS Syndrome Presenting as A Mimic of Herpes Simplex Encephalitis.
    Chen WT; Lin YS; Wang YF; Fuh JL
    Acta Neurol Taiwan; 2019 Jun; 28(2)():46-51. PubMed ID: 31867706
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report.
    Lahiri D; Sawale VM; Banerjee S; Dubey S; Roy BK; Das SK
    J Med Case Rep; 2019 Mar; 13(1):63. PubMed ID: 30837005
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A Case of Myopathy, Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome with Intracardiac Thrombus [corrected].
    Joo JC; Seol MD; Yoon JW; Lee YS; Kim DK; Choi YH; Ahn HS; Cho WH
    Korean Circ J; 2013 Mar; 43(3):204-6. PubMed ID: 23613701
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comparison of magnetic resonance spectroscopy (MRS) with arterial spin labeling (ASL) in the differentiation between mitochondrial encephalomyopathy, lactic Acidosis, plus stroke-like episodes (MELAS) and acute ischemic stroke (AIS).
    Li X; Wang Y; Wang Z; Lu J; Xu Y; Ye J; Kuang Z; Li B; Pan M; Chen W; Lu S; Zhou Z; Cheng L; Wang H
    J Clin Neurosci; 2018 Sep; 55():65-70. PubMed ID: 29921486
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Spinal anesthesia in MELAS syndrome: a case with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Hsiao PN; Cheng YJ; Tseng HC; Chuang YH; Kao PF; Tsai SK
    Acta Anaesthesiol Sin; 2000 Jun; 38(2):107-10. PubMed ID: 11000676
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cerebral blood flow in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.
    Ooiwa Y; Uematsu Y; Terada T; Nakai K; Itakura T; Komai N; Moriwaki H
    Stroke; 1993 Feb; 24(2):304-9. PubMed ID: 8421833
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Chen JC; Tsai TC; Liu CS; Lu CT
    Acta Neurol Taiwan; 2007 Sep; 16(3):168-72. PubMed ID: 17966957
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy.
    Mukai M; Nagata E
    Intern Med; 2017 Oct; 56(19):2695. PubMed ID: 28883258
    [No Abstract]   [Full Text] [Related]  

  • 32. MR OEF imaging in MELAS.
    Xie S
    Methods Enzymol; 2014; 547():433-44. PubMed ID: 25416369
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation.
    Moteki H; Azaiez H; Booth KT; Hattori M; Sato A; Sato Y; Motobayashi M; Sloan CM; Kolbe DL; Shearer AE; Smith RJ; Usami S
    Ann Otol Rhinol Laryngol; 2015 May; 124 Suppl 1(1 0):177S-83S. PubMed ID: 25788561
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Decreased ATP synthesis is phenotypically expressed during increased energy demand in fibroblasts containing mitochondrial tRNA mutations.
    James AM; Sheard PW; Wei YH; Murphy MP
    Eur J Biochem; 1999 Jan; 259(1-2):462-9. PubMed ID: 9914528
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Effect of coenzyme Q10 in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): evaluation by noninvasive tissue oximetry.
    Abe K; Matsuo Y; Kadekawa J; Inoue S; Yanagihara T
    J Neurol Sci; 1999 Jan; 162(1):65-8. PubMed ID: 10064171
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Shoji Y; Sato W; Hayasaka K; Takada G
    J Inherit Metab Dis; 1993; 16(1):27-30. PubMed ID: 8487499
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Elevated glutamate and decreased glutamine levels in the cerebrospinal fluid of patients with MELAS syndrome.
    Guerrero-Molina MP; Morales-Conejo M; Delmiro A; Morán M; Domínguez-González C; Arranz-Canales E; Ramos-González A; Arenas J; Martín MA; González de la Aleja J
    J Neurol; 2022 Jun; 269(6):3238-3248. PubMed ID: 35088140
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes].
    Carmi E; Defossez C; Morin G; Fraitag S; Lok C; Westeel PF; Canaple S; Denoeux JP
    Ann Dermatol Venereol; 2001 Oct; 128(10 Pt 1):1031-5. PubMed ID: 11907964
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W; Hayasaka K; Shoji Y; Takahashi T; Takada G; Saito M; Fukawa O; Wachi E
    Biochem Mol Biol Int; 1994 Aug; 33(6):1055-61. PubMed ID: 7804130
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Detection of preclinically latent hyperperfusion due to stroke-like episodes by arterial spin-labeling perfusion MRI in MELAS patients.
    Ikawa M; Yoneda M; Muramatsu T; Matsunaga A; Tsujikawa T; Yamamoto T; Kosaka N; Kinoshita K; Yamamura O; Hamano T; Nakamoto Y; Kimura H
    Mitochondrion; 2013 Nov; 13(6):676-80. PubMed ID: 24095972
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.