188 related articles for article (PubMed ID: 9382096)
1. The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.
D'Adamo P; Fassone L; Gedeon A; Janssen EA; Bione S; Bolhuis PA; Barth PG; Wilson M; Haan E; Orstavik KH; Patton MA; Green AJ; Zammarchi E; Donati MA; Toniolo D
Am J Hum Genet; 1997 Oct; 61(4):862-7. PubMed ID: 9382096
[TBL] [Abstract][Full Text] [Related]
2. Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome.
Bleyl SB; Mumford BR; Thompson V; Carey JC; Pysher TJ; Chin TK; Ward K
Am J Hum Genet; 1997 Oct; 61(4):868-72. PubMed ID: 9382097
[TBL] [Abstract][Full Text] [Related]
3. X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.
Gedeon AK; Wilson MJ; Colley AC; Sillence DO; Mulley JC
J Med Genet; 1995 May; 32(5):383-8. PubMed ID: 7616547
[TBL] [Abstract][Full Text] [Related]
4. Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle.
Bissler JJ; Tsoras M; Göring HH; Hug P; Chuck G; Tombragel E; McGraw C; Schlotman J; Ralston MA; Hug G
Lab Invest; 2002 Mar; 82(3):335-44. PubMed ID: 11896212
[TBL] [Abstract][Full Text] [Related]
5. Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome.
Ichida F; Tsubata S; Bowles KR; Haneda N; Uese K; Miyawaki T; Dreyer WJ; Messina J; Li H; Bowles NE; Towbin JA
Circulation; 2001 Mar; 103(9):1256-63. PubMed ID: 11238270
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation in the G4.5 (TAZ) gene in a Greek patient with Barth syndrome.
Bachou T; Giannakopoulos A; Trapali C; Vazeou A; Kattamis A
Blood Cells Mol Dis; 2009; 42(3):262-4. PubMed ID: 19261493
[TBL] [Abstract][Full Text] [Related]
7. Barth syndrome.
Jefferies JL
Am J Med Genet C Semin Med Genet; 2013 Aug; 163C(3):198-205. PubMed ID: 23843353
[TBL] [Abstract][Full Text] [Related]
8. A novel X-linked gene, G4.5. is responsible for Barth syndrome.
Bione S; D'Adamo P; Maestrini E; Gedeon AK; Bolhuis PA; Toniolo D
Nat Genet; 1996 Apr; 12(4):385-9. PubMed ID: 8630491
[TBL] [Abstract][Full Text] [Related]
9. Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle.
Ronvelia D; Greenwood J; Platt J; Hakim S; Zaragoza MV
Mol Genet Metab; 2012 Nov; 107(3):428-32. PubMed ID: 23031367
[TBL] [Abstract][Full Text] [Related]
10. X chromosome inactivation in carriers of Barth syndrome.
Orstavik KH; Orstavik RE; Naumova AK; D'Adamo P; Gedeon A; Bolhuis PA; Barth PG; Toniolo D
Am J Hum Genet; 1998 Nov; 63(5):1457-63. PubMed ID: 9792874
[TBL] [Abstract][Full Text] [Related]
11. Novel missense mutation (R94S) in the TAZ ( G4.5) gene in a Japanese patient with Barth syndrome.
Sakamoto O; Kitoh T; Ohura T; Ohya N; Iinuma K
J Hum Genet; 2002; 47(5):229-31. PubMed ID: 12032589
[TBL] [Abstract][Full Text] [Related]
12. Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth.
Steward CG; Newbury-Ecob RA; Hastings R; Smithson SF; Tsai-Goodman B; Quarrell OW; Kulik W; Wanders R; Pennock M; Williams M; Cresswell JL; Gonzalez IL; Brennan P
Prenat Diagn; 2010 Oct; 30(10):970-6. PubMed ID: 20812380
[TBL] [Abstract][Full Text] [Related]
13. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update.
Barth PG; Valianpour F; Bowen VM; Lam J; Duran M; Vaz FM; Wanders RJ
Am J Med Genet A; 2004 May; 126A(4):349-54. PubMed ID: 15098233
[TBL] [Abstract][Full Text] [Related]
14. [Genetics of dilated cardiomyopathy].
Osterziel KJ; Scheffold T; Perrot A; Dietz R;
Z Kardiol; 2001 Jul; 90(7):461-9. PubMed ID: 11515275
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. X-linked fetal cardiomyopathy caused by a novel mutation in the TAZ gene.
Brady AN; Shehata BM; Fernhoff PM
Prenat Diagn; 2006 May; 26(5):462-5. PubMed ID: 16548007
[TBL] [Abstract][Full Text] [Related]
17. Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.
Adès LC; Gedeon AK; Wilson MJ; Latham M; Partington MW; Mulley JC; Nelson J; Lui K; Sillence DO
Am J Med Genet; 1993 Feb; 45(3):327-34. PubMed ID: 8434619
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation in the G4.5 (TAZ) gene in a kindred with Barth syndrome.
Vesel S; Stopar-Obreza M; Trebusak-Podkrajsek K; Jazbec J; Podnar T; Battelino T
Eur J Hum Genet; 2003 Jan; 11(1):97-101. PubMed ID: 12529714
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.
Cantlay AM; Shokrollahi K; Allen JT; Lunt PW; Newbury-Ecob RA; Steward CG
J Pediatr; 1999 Sep; 135(3):311-5. PubMed ID: 10484795
[TBL] [Abstract][Full Text] [Related]
20. Seven functional classes of Barth syndrome mutation.
Whited K; Baile MG; Currier P; Claypool SM
Hum Mol Genet; 2013 Feb; 22(3):483-92. PubMed ID: 23100323
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
