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Journal Abstract Search

262 related items for PubMed ID: 11506313

  • 1. An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure.
    Yanagihara C, Oyama A, Tanaka M, Nakaji K, Nishimura Y.
    Intern Med; 2001 Jul; 40(7):662-5. PubMed ID: 11506313
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  • 2. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA.
    Terauchi A, Tamagawa K, Morimatsu Y, Kobayashi M, Sano T, Yoda S.
    Brain Dev; 1996 Jul; 18(3):224-9. PubMed ID: 8836506
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  • 3. Sigmoid volvulus in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): a rare occurrence.
    Hallac A, Keshava HB, Morris-Stiff G, Ibrahim S.
    BMJ Case Rep; 2016 Mar 02; 2016():. PubMed ID: 26935953
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  • 4. An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with intestinal bleeding in chronic renal failure.
    Mima A, Shiota F, Matsubara T, Iehara N, Akagi T, Abe H, Nagai K, Matsuura M, Murakami T, Kishi S, Araoka T, Kishi F, Kondo N, Shigeta R, Yoshikawa K, Kita T, Doi T, Fukatsu A.
    Ren Fail; 2011 Mar 02; 33(6):622-5. PubMed ID: 21631236
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  • 5. [Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with chronic renal failure: report of mother-child cases].
    Ihara M, Tanaka H, Yashiro M, Nishimura Y.
    Rinsho Shinkeigaku; 1996 Sep 02; 36(9):1069-73. PubMed ID: 8976130
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  • 8. A MELAS Patient Developing Fatal Acute Renal Failure with Lactic Acidosis and Rhabdomyolysis.
    Ito H, Fukutake S, Odake S, Okeda R, Tokunaga O, Kamei T.
    Intern Med; 2020 Nov 01; 59(21):2773-2776. PubMed ID: 32641653
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  • 10. Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report.
    Alenezi AF, Almelahi MA, Fekih-Romdhana F, Jahrami HA.
    J Med Case Rep; 2022 Oct 10; 16(1):361. PubMed ID: 36210452
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  • 11. Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu(UUR) gene.
    Kishnani PS, Van Hove JL, Shoffner JS, Kaufman A, Bossen EH, Kahler SG.
    Eur J Pediatr; 1996 Oct 10; 155(10):898-903. PubMed ID: 8891562
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  • 12. MELAS Syndrome and Kidney Disease Without Fanconi Syndrome or Proteinuria: A Case Report.
    Rudnicki M, Mayr JA, Zschocke J, Antretter H, Regele H, Feichtinger RG, Windpessl M, Mayer G, Pölzl G.
    Am J Kidney Dis; 2016 Dec 10; 68(6):949-953. PubMed ID: 27683045
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  • 14. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.
    Lu J, He B, Wang D.
    Neurosciences (Riyadh); 2011 Apr 10; 16(2):162-3. PubMed ID: 21427669
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  • 15. Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome: A case-report and literature review (CARE-complaint).
    Wang S, Song T, Wang S.
    Medicine (Baltimore); 2020 Jun 12; 99(24):e20310. PubMed ID: 32541454
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  • 16. Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes/Leigh syndrome overlap patient with a novel m.3482A>G mutation in MT-ND1.
    Hayashi Y, Iwasaki Y, Yoshikura N, Yamada M, Kimura A, Inuzuka T, Miyahara H, Goto Y, Nishino I, Yoshida M, Shimohata T.
    Neuropathology; 2021 Feb 12; 41(1):84-90. PubMed ID: 33300189
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  • 17. Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutation.
    Smith ML, Hua XY, Marsden DL, Liu D, Kennaway NG, Ngo KY, Haas RH.
    J Clin Endocrinol Metab; 1997 Sep 12; 82(9):2826-31. PubMed ID: 9284704
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  • 18. Adult-onset mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): a diagnostic challenge.
    Acquaah J, Ferdinand P, Roffe C.
    BMJ Case Rep; 2024 Feb 26; 17(2):. PubMed ID: 38413140
    [Abstract] [Full Text] [Related]

  • 19. A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome.
    Emmanuele V, Sotiriou E, Rios PG, Ganesh J, Ichord R, Foley AR, Akman HO, Dimauro S.
    J Child Neurol; 2013 Feb 26; 28(2):236-42. PubMed ID: 22638077
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  • 20. Increased risk of stroke in patients with the A12308G polymorphism in mitochondria.
    Pulkes T, Sweeney MG, Hanna MG.
    Lancet; 2000 Dec 16; 356(9247):2068-9. PubMed ID: 11145497
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