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 *

171 related articles for article (PubMed ID: 23606313)

  • 21. Barth syndrome in a female patient.
    Cosson L; Toutain A; Simard G; Kulik W; Matyas G; Guichet A; Blasco H; Maakaroun-Vermesse Z; Vaillant MC; Le Caignec C; Chantepie A; Labarthe F
    Mol Genet Metab; 2012 May; 106(1):115-20. PubMed ID: 22410210
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Barth Syndrome: Connecting Cardiolipin to Cardiomyopathy.
    Ikon N; Ryan RO
    Lipids; 2017 Feb; 52(2):99-108. PubMed ID: 28070695
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Atypical Clinical Presentations of TAZ Mutations: An Underdiagnosed Cause of Growth Retardation?
    Thiels C; Fleger M; Huemer M; Rodenburg RJ; Vaz FM; Houtkooper RH; Haack TB; Prokisch H; Feichtinger RG; Lücke T; Mayr JA; Wortmann SB
    JIMD Rep; 2016; 29():89-93. PubMed ID: 26724946
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of novel mitochondrial localization signals in human Tafazzin, the cause of the inherited cardiomyopathic disorder Barth syndrome.
    Dinca AA; Chien WM; Chin MT
    J Mol Cell Cardiol; 2018 Jan; 114():83-92. PubMed ID: 29129703
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Phospholipid abnormalities in children with Barth syndrome.
    Schlame M; Kelley RI; Feigenbaum A; Towbin JA; Heerdt PM; Schieble T; Wanders RJ; DiMauro S; Blanck TJ
    J Am Coll Cardiol; 2003 Dec; 42(11):1994-9. PubMed ID: 14662265
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Barth syndrome: cardiolipin, cellular pathophysiology, management, and novel therapeutic targets.
    Zegallai HM; Hatch GM
    Mol Cell Biochem; 2021 Mar; 476(3):1605-1629. PubMed ID: 33415565
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Barth syndrome.
    Clarke SL; Bowron A; Gonzalez IL; Groves SJ; Newbury-Ecob R; Clayton N; Martin RP; Tsai-Goodman B; Garratt V; Ashworth M; Bowen VM; McCurdy KR; Damin MK; Spencer CT; Toth MJ; Kelley RI; Steward CG
    Orphanet J Rare Dis; 2013 Feb; 8():23. PubMed ID: 23398819
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism.
    Vaz FM; Houtkooper RH; Valianpour F; Barth PG; Wanders RJ
    J Biol Chem; 2003 Oct; 278(44):43089-94. PubMed ID: 12930833
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cardiolipin remodeling by TAZ/tafazzin is selectively required for the initiation of mitophagy.
    Hsu P; Liu X; Zhang J; Wang HG; Ye JM; Shi Y
    Autophagy; 2015 Apr; 11(4):643-52. PubMed ID: 25919711
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel mutation of the TAZ gene in Barth syndrome: acute exacerbation after contrast-dye injection.
    Kim GB; Kwon BS; Bae EJ; Noh CI; Seong MW; Park SS
    J Korean Med Sci; 2013 May; 28(5):784-7. PubMed ID: 23678274
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutation characterization and genotype-phenotype correlation in Barth syndrome.
    Johnston J; Kelley RI; Feigenbaum A; Cox GF; Iyer GS; Funanage VL; Proujansky R
    Am J Hum Genet; 1997 Nov; 61(5):1053-8. PubMed ID: 9345098
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype.
    Bowron A; Honeychurch J; Williams M; Tsai-Goodman B; Clayton N; Jones L; Shortland GJ; Qureshi SA; Heales SJ; Steward CG
    J Inherit Metab Dis; 2015 Mar; 38(2):279-86. PubMed ID: 25112388
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Intra-individual plasticity of the TAZ gene leading to different heritable mutations in siblings with Barth syndrome.
    Ferri L; Donati MA; Funghini S; Cavicchi C; Pensato V; Gellera C; Natacci F; Spaccini L; Gasperini S; Vaz FM; Cooper DN; Guerrini R; Morrone A
    Eur J Hum Genet; 2015 Dec; 23(12):1708-12. PubMed ID: 25782672
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Barth syndrome: an X-linked cardiomyopathy with a novel mutation.
    Aljishi E; Ali F
    Indian J Pediatr; 2010 Dec; 77(12):1432-3. PubMed ID: 20981509
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Delayed appearance of 3-methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosis.
    Baban A; Adorisio R; Corica B; Rizzo C; Calì F; Semeraro M; Taurisano R; Magliozzi M; Carrozzo R; Parisi F; Dallapiccola B; Vaz FM; Drago F; Dionisi-Vici C
    Am J Med Genet A; 2020 Jan; 182(1):64-70. PubMed ID: 31729175
    [TBL] [Abstract][Full Text] [Related]  

  • 36. AAV Gene Therapy Prevents and Reverses Heart Failure in a Murine Knockout Model of Barth Syndrome.
    Wang S; Li Y; Xu Y; Ma Q; Lin Z; Schlame M; Bezzerides VJ; Strathdee D; Pu WT
    Circ Res; 2020 Apr; 126(8):1024-1039. PubMed ID: 32146862
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy.
    Borna NN; Kishita Y; Ishikawa K; Nakada K; Hayashi JI; Tokuzawa Y; Kohda M; Nyuzuki H; Yamashita-Sugahara Y; Nasu T; Takeda A; Murayama K; Ohtake A; Okazaki Y
    J Hum Genet; 2017 Apr; 62(5):539-547. PubMed ID: 28123175
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Differing clinical courses and outcomes in two siblings with Barth syndrome and left ventricular noncompaction.
    Momoi N; Chang B; Takeda I; Aoyagi Y; Endo K; Ichida F
    Eur J Pediatr; 2012 Mar; 171(3):515-20. PubMed ID: 21987083
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cardiolipin metabolism and Barth Syndrome.
    Hauff KD; Hatch GM
    Prog Lipid Res; 2006 Mar; 45(2):91-101. PubMed ID: 16442164
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cardiac and clinical phenotype in Barth syndrome.
    Spencer CT; Bryant RM; Day J; Gonzalez IL; Colan SD; Thompson WR; Berthy J; Redfearn SP; Byrne BJ
    Pediatrics; 2006 Aug; 118(2):e337-46. PubMed ID: 16847078
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.