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Journal Abstract Search

484 related items for PubMed ID: 29428506

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  • 4. Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
    Fukuda M, Nagao Y.
    J Med Case Rep; 2019 Oct 21; 13(1):313. PubMed ID: 31630688
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  • 5. Forecasting stroke-like episodes and outcomes in mitochondrial disease.
    Ng YS, Lax NZ, Blain AP, Erskine D, Baker MR, Polvikoski T, Thomas RH, Morris CM, Lai M, Whittaker RG, Gebbels A, Winder A, Hall J, Feeney C, Farrugia ME, Hirst C, Roberts M, Lawthom C, Chrysostomou A, Murphy K, Baird T, Maddison P, Duncan C, Poulton J, Nesbitt V, Hanna MG, Pitceathly RDS, Taylor RW, Blakely EL, Schaefer AM, Turnbull DM, McFarland R, Gorman GS.
    Brain; 2022 Apr 18; 145(2):542-554. PubMed ID: 34927673
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  • 6. Beneficial effect of L-arginine for stroke-like episode in MELAS.
    Kubota M, Sakakihara Y, Mori M, Yamagata T, Momoi-Yoshida M.
    Brain Dev; 2004 Oct 18; 26(7):481-3; discussion 480. PubMed ID: 15351086
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  • 7. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
    El-Hattab AW, Adesina AM, Jones J, Scaglia F.
    Mol Genet Metab; 2015 Oct 18; 116(1-2):4-12. PubMed ID: 26095523
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  • 8. l-Arginine in Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes: A Systematic Review.
    Stefanetti RJ, Ng YS, Errington L, Blain AP, McFarland R, Gorman GS.
    Neurology; 2022 Jun 07; 98(23):e2318-e2328. PubMed ID: 35428733
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  • 10. Impaired nitric oxide production in children with MELAS syndrome and the effect of arginine and citrulline supplementation.
    El-Hattab AW, Emrick LT, Hsu JW, Chanprasert S, Almannai M, Craigen WJ, Jahoor F, Scaglia F.
    Mol Genet Metab; 2016 Apr 07; 117(4):407-12. PubMed ID: 26851065
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  • 11. Assessment of Nitric Oxide Production in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome with the Use of a Stable Isotope Tracer Infusion Technique.
    El-Hattab AW, Jahoor F.
    J Nutr; 2017 Jul 07; 147(7):1251-1257. PubMed ID: 28515163
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  • 12. Heteroplasmic pathogenic m.12315G>A variant in MT-TL2 presenting with MELAS syndrome and depletion of nitric oxide donors.
    Snyder MT, Manor J, Gijavanekar C, Mizerik E, Kralik SF, Elsea SH, Machol K, Emrick L, Scaglia F.
    Am J Med Genet A; 2024 Mar 07; 194(3):e63461. PubMed ID: 37953071
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  • 13. [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 07; 51(2):130-5. PubMed ID: 23527980
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  • 14. Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Chakrabarty S, Govindaraj P, Sankaran BP, Nagappa M, Kabekkodu SP, Jayaram P, Mallya S, Deepha S, Ponmalar JNJ, Arivinda HR, Meena AK, Jha RK, Sinha S, Gayathri N, Taly AB, Thangaraj K, Satyamoorthy K.
    J Neurol; 2021 Jun 07; 268(6):2192-2207. PubMed ID: 33484326
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  • 15. L-Arginine Affects Aerobic Capacity and Muscle Metabolism in MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes) Syndrome.
    Rodan LH, Wells GD, Banks L, Thompson S, Schneiderman JE, Tein I.
    PLoS One; 2015 Jun 07; 10(5):e0127066. PubMed ID: 25993630
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  • 16. MELAS and L-arginine therapy: pathophysiology of stroke-like episodes.
    Koga Y, Povalko N, Nishioka J, Katayama K, Kakimoto N, Matsuishi T.
    Ann N Y Acad Sci; 2010 Jul 07; 1201():104-10. PubMed ID: 20649546
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  • 17. The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
    Mancuso M, Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Donati A, Minetti C, Moggio M, Mongini T, Servidei S, Tonin P, Toscano A, Uziel G, Bruno C, Ienco EC, Filosto M, Lamperti C, Catteruccia M, Moroni I, Musumeci O, Pegoraro E, Ronchi D, Santorelli FM, Sauchelli D, Scarpelli M, Sciacco M, Valentino ML, Vercelli L, Zeviani M, Siciliano G.
    J Neurol; 2014 Mar 07; 261(3):504-10. PubMed ID: 24375076
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  • 18. Pediatric stroke among Hong Kong Chinese subjects.
    Chung B, Wong V.
    Pediatrics; 2004 Aug 07; 114(2):e206-12. PubMed ID: 15286258
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  • 19. Metabolic rescue in pluripotent cells from patients with mtDNA disease.
    Ma H, Folmes CD, Wu J, Morey R, Mora-Castilla S, Ocampo A, Ma L, Poulton J, Wang X, Ahmed R, Kang E, Lee Y, Hayama T, Li Y, Van Dyken C, Gutierrez NM, Tippner-Hedges R, Koski A, Mitalipov N, Amato P, Wolf DP, Huang T, Terzic A, Laurent LC, Izpisua Belmonte JC, Mitalipov S.
    Nature; 2015 Aug 13; 524(7564):234-8. PubMed ID: 26176921
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  • 20. Survival analysis of a cohort of Chinese patients with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) based on clinical features.
    Zhang Z, Zhao D, Zhang X, Xiong H, Bao X, Yuan Y, Wang Z.
    J Neurol Sci; 2018 Feb 15; 385():151-155. PubMed ID: 29406897
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