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 *

234 related articles for article (PubMed ID: 33704555)

  • 21. COQ7 defect causes prenatal onset of mitochondrial CoQ
    Pettenuzzo I; Carli S; Sánchez-Cuesta A; Isidori F; Montanari F; Grippa M; Lanzoni G; Ambrosetti I; Di Pisa V; Cordelli DM; Mondardini MC; Pippucci T; Ragni L; Cenacchi G; Costa R; Lima M; Capristo MA; Tropeano CV; Caporali L; Carelli V; Brunelli E; Maffei M; Ahmed Sheikhmaye H; Fetta A; Brea-Calvo G; Garone C
    Eur J Hum Genet; 2024 Aug; 32(8):938-946. PubMed ID: 38702428
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Primary Coenzyme Q10 Deficiency-7 and Pathogenic
    Xie J; Jiang J; Guo Q
    Front Genet; 2021; 12():776807. PubMed ID: 35154243
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel COQ8A missense variant associated with a mild form of primary coenzyme Q10 deficiency type 4.
    Liu G; Ma D; Li J; Luo C; Sun Y; Zhang J; Hu P; Tang W; Xu Z
    Clin Biochem; 2020 Oct; 84():93-98. PubMed ID: 32553579
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Secondary CoQ
    Navas P; Cascajo MV; Alcázar-Fabra M; Hernández-Camacho JD; Sánchez-Cuesta A; Rodríguez ABC; Ballesteros-Simarro M; Arroyo-Luque A; Rodríguez-Aguilera JC; Fernández-Ayala DJM; Brea-Calvo G; López-Lluch G; Santos-Ocaña C
    Biofactors; 2021 Jul; 47(4):551-569. PubMed ID: 33878238
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review.
    Sonuç Kartal G; Koç Yekedüz M; Köse E; Eminoğlu FT
    J Pediatr Endocrinol Metab; 2024 Mar; 37(3):260-270. PubMed ID: 38353291
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ
    Sondheimer N; Hewson S; Cameron JM; Somers GR; Broadbent JD; Ziosi M; Quinzii CM; Naini AB
    Mol Genet Metab Rep; 2017 Sep; 12():23-27. PubMed ID: 28540186
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure.
    Desbats MA; Vetro A; Limongelli I; Lunardi G; Casarin A; Doimo M; Spinazzi M; Angelini C; Cenacchi G; Burlina A; Rodriguez Hernandez MA; Chiandetti L; Clementi M; Trevisson E; Navas P; Zuffardi O; Salviati L
    Eur J Hum Genet; 2015 Sep; 23(9):1254-8. PubMed ID: 25564041
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review.
    Galosi S; Barca E; Carrozzo R; Schirinzi T; Quinzii CM; Lieto M; Vasco G; Zanni G; Di Nottia M; Galatolo D; Filla A; Bertini E; Santorelli FM; Leuzzi V; Haas R; Hirano M; Friedman J
    Parkinsonism Relat Disord; 2019 Nov; 68():8-16. PubMed ID: 31621627
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Disruption of the human COQ5-containing protein complex is associated with diminished coenzyme Q10 levels under two different conditions of mitochondrial energy deficiency.
    Yen HC; Liu YC; Kan CC; Wei HJ; Lee SH; Wei YH; Feng YH; Chen CW; Huang CC
    Biochim Biophys Acta; 2016 Sep; 1860(9):1864-76. PubMed ID: 27155576
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2).
    Scalais E; Chafai R; Van Coster R; Bindl L; Nuttin C; Panagiotaraki C; Seneca S; Lissens W; Ribes A; Geers C; Smet J; De Meirleir L
    Eur J Paediatr Neurol; 2013 Nov; 17(6):625-30. PubMed ID: 23816342
    [TBL] [Abstract][Full Text] [Related]  

  • 31. COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by CoQ10 Administration.
    Caglayan AO; Gumus H; Sandford E; Kubisiak TL; Ma Q; Ozel AB; Per H; Li JZ; Shakkottai VG; Burmeister M
    Cerebellum; 2019 Jun; 18(3):665-669. PubMed ID: 30847826
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency.
    Salviati L; Trevisson E; Rodriguez Hernandez MA; Casarin A; Pertegato V; Doimo M; Cassina M; Agosto C; Desbats MA; Sartori G; Sacconi S; Memo L; Zuffardi O; Artuch R; Quinzii C; Dimauro S; Hirano M; Santos-Ocaña C; Navas P
    J Med Genet; 2012 Mar; 49(3):187-91. PubMed ID: 22368301
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 38(1):145-56. PubMed ID: 25091424
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The efficacy of coenzyme Q
    Wang Y; Hekimi S
    J Cell Mol Med; 2022 Sep; 26(17):4635-4644. PubMed ID: 35985679
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Intracellular cholesterol accumulation and coenzyme Q
    Suárez-Rivero JM; de la Mata M; Pavón AD; Villanueva-Paz M; Povea-Cabello S; Cotán D; Álvarez-Córdoba M; Villalón-García I; Ybot-González P; Salas JJ; Muñiz O; Cordero MD; Sánchez-Alcázar JA
    Biochim Biophys Acta Mol Basis Dis; 2018 Dec; 1864(12):3697-3713. PubMed ID: 30292637
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Vitamin K2 cannot substitute Coenzyme Q
    Cerqua C; Casarin A; Pierrel F; Vazquez Fonseca L; Viola G; Salviati L; Trevisson E
    Sci Rep; 2019 Apr; 9(1):6553. PubMed ID: 31024065
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Spectrum of clinical manifestations in newborns with the COQ4 mutation: case series and literature review.
    Pan P; Zhou N; Sun Y; Chen Z; Han J; Zhou W
    Front Pediatr; 2024; 12():1410133. PubMed ID: 39398416
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation.
    Eroglu FK; Ozaltin F; Gönç N; Nalçacıoğlu H; Özçakar ZB; Yalnızoğlu D; Güçer Ş; Orhan D; Eminoğlu FT; Göçmen R; Alikaşifoğlu A; Topaloğlu R; Düzova A
    Pediatr Neurol; 2018 Nov; 88():71-74. PubMed ID: 30337132
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis.
    Casarin A; Jimenez-Ortega JC; Trevisson E; Pertegato V; Doimo M; Ferrero-Gomez ML; Abbadi S; Artuch R; Quinzii C; Hirano M; Basso G; Ocaña CS; Navas P; Salviati L
    Biochem Biophys Res Commun; 2008 Jul; 372(1):35-9. PubMed ID: 18474229
    [TBL] [Abstract][Full Text] [Related]  

  • 40. ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency.
    Balreira A; Boczonadi V; Barca E; Pyle A; Bansagi B; Appleton M; Graham C; Hargreaves IP; Rasic VM; Lochmüller H; Griffin H; Taylor RW; Naini A; Chinnery PF; Hirano M; Quinzii CM; Horvath R
    J Neurol; 2014 Nov; 261(11):2192-8. PubMed ID: 25182700
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.