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173 related items for PubMed ID: 34596368

  • 1. Endocrine disorders in a patient with a suspicion of a mitochondrial disease, MELAS syndrome - a case report and literature review.
    Baszyńska-Wilk M, Moszczyńska E, Szarras-Czapnik M, Wysocka-Mincewicz M, Wątrobińska U, Kozłowska A, Szalecki M.
    Pediatr Endocrinol Diabetes Metab; 2021; 27(3):213-218. PubMed ID: 34596368
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  • 2.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, El-Hattab AW, Almannai M, Scaglia F.
    ; 1993. PubMed ID: 20301411
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  • 4. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
    El-Hattab AW, Adesina AM, Jones J, Scaglia F.
    Mol Genet Metab; 2015; 116(1-2):4-12. PubMed ID: 26095523
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  • 6. [Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
    Liu XL, Bao XH, Ma YN, Chang XZ, Qin J, Wu XR.
    Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):130-5. PubMed ID: 23527980
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  • 9. [MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes].
    Mierzewska H, Mroczek K, Pronicki M, Pronicka E, Karczmarewicz E, Bartnik E, Zdzienicka E, Seniów J, Schmidt-Sidor B, Taraszewska A, Palasik W.
    Neurol Neurochir Pol; 2002 Feb; 36(3):457-70. PubMed ID: 12185802
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  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2.
    Endres D, Süß P, Maier SJ, Friedel E, Nickel K, Ziegler C, Fiebich BL, Glocker FX, Stock F, Egger K, Lange T, Dacko M, Venhoff N, Erny D, Doostkam S, Komlosi K, Domschke K, Tebartz van Elst L.
    Front Immunol; 2019 Sep; 10():412. PubMed ID: 30949164
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  • 14. Regression of stroke-like lesions in MELAS-syndrome after seizure control.
    Finsterer J, Barton P.
    Epileptic Disord; 2010 Dec; 12(4):330-4. PubMed ID: 21059492
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  • 15. 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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  • 16. [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 18; 52(5):851-855. PubMed ID: 33047718
    [Abstract] [Full Text] [Related]

  • 17. Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes - a case report.
    Sinnecker T, Andelova M, Mayr M, Rüegg S, Sinnreich M, Hench J, Frank S, Schaller A, Stippich C, Wuerfel J, Bonati LH.
    BMC Neurol; 2019 May 08; 19(1):91. PubMed ID: 31068171
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  • 19. Mitochondrial encephalomyopathy with lactic acidosis and strokelike episodes (MELAS): a mitochondrial disorder presents as fibromyalgia.
    DeSouza RA, Cardenas RJ, Lindler TU, De la Fuente FA, Mayorquin FJ, Trochtenberg DS.
    South Med J; 2004 May 08; 97(5):528-31. PubMed ID: 15180033
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  • 20. When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?
    Lorenzoni PJ, Werneck LC, Kay CS, Silvado CE, Scola RH.
    Arq Neuropsiquiatr; 2015 Nov 08; 73(11):959-67. PubMed ID: 26517220
    [Abstract] [Full Text] [Related]

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