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Journal Abstract Search

735 related items for PubMed ID: 24576561

  • 21. Muscle coenzyme Q: a potential test for mitochondrial activity and redox status.
    Miles L, Miles MV, Tang PH, Horn PS, Wong BL, DeGrauw TJ, Morehart PJ, Bove KE.
    Pediatr Neurol; 2005 May; 32(5):318-24. PubMed ID: 15866432
    [Abstract] [Full Text] [Related]

  • 22. Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
    Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, Emma F, Gulhan B, Boyer O, Trautmann A, Xu H, Shen Q, Rao J, Riedhammer KM, Heemann U, Hoefele J, Stenton SL, Tsygin AN, Ng KH, Fomina S, Benetti E, Aurelle M, Prikhodina L, Schreuder MF, Tabatabaeifar M, Jankowski M, Baiko S, Mao J, Feng C, Liu C, Sun S, Deng F, Wang X, Clavé S, Stańczyk M, Bałasz-Chmielewska I, Fila M, Durkan AM, Levart TK, Dursun I, Esfandiar N, Haas D, Bjerre A, Anarat A, Benz MR, Talebi S, Hooman N, Ariceta G, PodoNet Consortium, mitoNET Consortium, CCGKDD Consortium, Schaefer F.
    Kidney Int; 2022 Sep; 102(3):604-612. PubMed ID: 35643375
    [Abstract] [Full Text] [Related]

  • 23. Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum.
    Barca E, Kleiner G, Tang G, Ziosi M, Tadesse S, Masliah E, Louis ED, Faust P, Kang UJ, Torres J, Cortes EP, Vonsattel JP, Kuo SH, Quinzii CM.
    J Neuropathol Exp Neurol; 2016 Jul; 75(7):663-72. PubMed ID: 27235405
    [Abstract] [Full Text] [Related]

  • 24. Mitochondrial Dysfunction due to Novel COQ8A Variation with Poor Response to CoQ10 Treatment: A Comprehensive Study and Review of Literatures.
    Wang J, Lin Y, Xu Z, Yan C, Zhao Y, Ji K.
    Cerebellum; 2024 Oct; 23(5):1824-1838. PubMed ID: 38429489
    [Abstract] [Full Text] [Related]

  • 25. Coenzyme Q10 deficiencies: pathways in yeast and humans.
    Awad AM, Bradley MC, Fernández-Del-Río L, Nag A, Tsui HS, Clarke CF.
    Essays Biochem; 2018 Jul 20; 62(3):361-376. PubMed ID: 29980630
    [Abstract] [Full Text] [Related]

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  • 27. Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q10 Deficiency.
    Romero-Moya D, Santos-Ocaña C, Castaño J, Garrabou G, Rodríguez-Gómez JA, Ruiz-Bonilla V, Bueno C, González-Rodríguez P, Giorgetti A, Perdiguero E, Prieto C, Moren-Nuñez C, Fernández-Ayala DJ, Victoria Cascajo M, Velasco I, Canals JM, Montero R, Yubero D, Jou C, López-Barneo J, Cardellach F, Muñoz-Cánoves P, Artuch R, Navas P, Menendez P.
    Stem Cells; 2017 Jul 20; 35(7):1687-1703. PubMed ID: 28472853
    [Abstract] [Full Text] [Related]

  • 28. Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency.
    Desbats MA, Lunardi G, Doimo M, Trevisson E, Salviati L.
    J Inherit Metab Dis; 2015 Jan 20; 38(1):145-56. PubMed ID: 25091424
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  • 30. Altered redox status of coenzyme Q9 reflects mitochondrial electron transport chain deficiencies in Caenorhabditis elegans.
    Vasta V, Sedensky M, Morgan P, Hahn SH.
    Mitochondrion; 2011 Jan 20; 11(1):136-8. PubMed ID: 20849980
    [Abstract] [Full Text] [Related]

  • 31. Coenzyme Q10 and immunity: A case report and new implications for treatment of recurrent infections in metabolic diseases.
    Farough S, Karaa A, Walker MA, Slate N, Dasu T, Verbsky J, Fusunyan R, Canapari C, Kinane TB, Van Cleave J, Sweetser DA, Sims KB, Walter JE.
    Clin Immunol; 2014 Dec 20; 155(2):209-12. PubMed ID: 25264263
    [Abstract] [Full Text] [Related]

  • 32. Human COQ10A and COQ10B are distinct lipid-binding START domain proteins required for coenzyme Q function.
    Tsui HS, Pham NVB, Amer BR, Bradley MC, Gosschalk JE, Gallagher-Jones M, Ibarra H, Clubb RT, Blaby-Haas CE, Clarke CF.
    J Lipid Res; 2019 Jul 20; 60(7):1293-1310. PubMed ID: 31048406
    [Abstract] [Full Text] [Related]

  • 33. Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency.
    Doimo M, Trevisson E, Airik R, Bergdoll M, Santos-Ocaña C, Hildebrandt F, Navas P, Pierrel F, Salviati L.
    Biochim Biophys Acta; 2014 Jan 20; 1842(1):1-6. PubMed ID: 24140869
    [Abstract] [Full Text] [Related]

  • 34. The Paradox of Coenzyme Q10 in Aging.
    Díaz-Casado ME, Quiles JL, Barriocanal-Casado E, González-García P, Battino M, López LC, Varela-López A.
    Nutrients; 2019 Sep 14; 11(9):. PubMed ID: 31540029
    [Abstract] [Full Text] [Related]

  • 35. Coenzyme Q10 modulates sulfide metabolism and links the mitochondrial respiratory chain to pathways associated to one carbon metabolism.
    González-García P, Hidalgo-Gutiérrez A, Mascaraque C, Barriocanal-Casado E, Bakkali M, Ziosi M, Abdihankyzy UB, Sánchez-Hernández S, Escames G, Prokisch H, Martín F, Quinzii CM, López LC.
    Hum Mol Genet; 2020 Nov 25; 29(19):3296-3311. PubMed ID: 32975579
    [Abstract] [Full Text] [Related]

  • 36. Oral coenzyme Q10 supplementation improves clinical symptoms and recovers pathologic alterations in blood mononuclear cells in a fibromyalgia patient.
    Cordero MD, Cotán D, del-Pozo-Martín Y, Carrión AM, de Miguel M, Bullón P, Sánchez-Alcazar JA.
    Nutrition; 2012 Nov 25; 28(11-12):1200-3. PubMed ID: 22898267
    [Abstract] [Full Text] [Related]

  • 37. Disorders of Human Coenzyme Q10 Metabolism: An Overview.
    Hargreaves I, Heaton RA, Mantle D.
    Int J Mol Sci; 2020 Sep 13; 21(18):. PubMed ID: 32933108
    [Abstract] [Full Text] [Related]

  • 38. Primary coenzyme Q10 (CoQ 10) deficiencies and related nephropathies.
    Ozaltin F.
    Pediatr Nephrol; 2014 Jun 13; 29(6):961-9. PubMed ID: 23736673
    [Abstract] [Full Text] [Related]

  • 39. The dilemma of diagnosing coenzyme Q10 deficiency in muscle.
    Louw R, Smuts I, Wilsenach KL, Jonck LM, Schoonen M, van der Westhuizen FH.
    Mol Genet Metab; 2018 Sep 13; 125(1-2):38-43. PubMed ID: 29530532
    [Abstract] [Full Text] [Related]

  • 40. Primary coenzyme Q10 deficiency and the brain.
    Naini A, Lewis VJ, Hirano M, DiMauro S.
    Biofactors; 2003 Sep 13; 18(1-4):145-52. PubMed ID: 14695930
    [Abstract] [Full Text] [Related]

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