284 related articles for article (PubMed ID: 7788908)
1. Genetic approaches to cardiovascular disease. Supravalvular aortic stenosis, Williams syndrome, and long-QT syndrome.
Keating MT
Circulation; 1995 Jul; 92(1):142-7. PubMed ID: 7788908
[TBL] [Abstract][Full Text] [Related]
2. Genetics, molecular mechanisms and management of long QT syndrome.
Wang Q; Chen Q; Towbin JA
Ann Med; 1998 Feb; 30(1):58-65. PubMed ID: 9556090
[TBL] [Abstract][Full Text] [Related]
3. [Long QT syndrome].
Nakajima T; Kaneko Y; Taniguchi Y; Nagai R
Nihon Rinsho; 1996 Mar; 54(3):776-81. PubMed ID: 8904236
[TBL] [Abstract][Full Text] [Related]
4. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.
Wang Q; Shen J; Splawski I; Atkinson D; Li Z; Robinson JL; Moss AJ; Towbin JA; Keating MT
Cell; 1995 Mar; 80(5):805-11. PubMed ID: 7889574
[TBL] [Abstract][Full Text] [Related]
5. The LQT syndromes--current status of molecular mechanisms.
Schulze-Bahr E; Wedekind H; Haverkamp W; Borggrefe M; Assmann G; Breithardt G; Funke H
Z Kardiol; 1999 Apr; 88(4):245-54. PubMed ID: 10408028
[TBL] [Abstract][Full Text] [Related]
6. Genetic aspects of supravalvular aortic stenosis.
Morris CA
Curr Opin Cardiol; 1998 May; 13(3):214-9. PubMed ID: 9649945
[TBL] [Abstract][Full Text] [Related]
7. [Molecular genetics in the hereditary form of long QT syndrome].
Georgijević Milić L
Med Pregl; 2000; 53(1-2):51-4. PubMed ID: 10953551
[TBL] [Abstract][Full Text] [Related]
8. Elastin mutation screening in a group of patients affected by vascular abnormalities.
Rodriguez-Revenga L; Badenas C; Carrió A; Milà M
Pediatr Cardiol; 2005; 26(6):827-31. PubMed ID: 15990952
[TBL] [Abstract][Full Text] [Related]
9. Supravalvular aortic stenosis cosegregates with a familial 6; 7 translocation which disrupts the elastin gene.
Morris CA; Loker J; Ensing G; Stock AD
Am J Med Genet; 1993 Jul; 46(6):737-44. PubMed ID: 8362925
[TBL] [Abstract][Full Text] [Related]
10. [Molecular genetics of the long QT syndrome: clinical aspects].
Sepp R; Csanády M
Orv Hetil; 1999 Nov; 140(47):2633-8. PubMed ID: 10613047
[TBL] [Abstract][Full Text] [Related]
11. New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
Li H; Chen Q; Moss AJ; Robinson J; Goytia V; Perry JC; Vincent GM; Priori SG; Lehmann MH; Denfield SW; Duff D; Kaine S; Shimizu W; Schwartz PJ; Wang Q; Towbin JA
Circulation; 1998 Apr; 97(13):1264-9. PubMed ID: 9570196
[TBL] [Abstract][Full Text] [Related]
12. The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biology.
Priori SG; Cantù F; Schwartz PJ
Schweiz Med Wochenschr; 1996 Oct; 126(41):1727-31. PubMed ID: 8893413
[TBL] [Abstract][Full Text] [Related]
13. A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.
Ewart AK; Morris CA; Ensing GJ; Loker J; Moore C; Leppert M; Keating M
Proc Natl Acad Sci U S A; 1993 Apr; 90(8):3226-30. PubMed ID: 8475063
[TBL] [Abstract][Full Text] [Related]
14. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.
Moss AJ; Zareba W; Benhorin J; Locati EH; Hall WJ; Robinson JL; Schwartz PJ; Towbin JA; Vincent GM; Lehmann MH
Circulation; 1995 Nov; 92(10):2929-34. PubMed ID: 7586261
[TBL] [Abstract][Full Text] [Related]
15. The molecular basis of long QT syndrome and prospects for therapy.
Wang Q; Bowles NE; Towbin JA
Mol Med Today; 1998 Sep; 4(9):382-8. PubMed ID: 9791861
[TBL] [Abstract][Full Text] [Related]
16. Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosis.
Fryssira H; Palmer R; Hallidie-Smith KA; Taylor J; Donnai D; Reardon W
J Med Genet; 1997 Apr; 34(4):306-8. PubMed ID: 9138154
[TBL] [Abstract][Full Text] [Related]
17. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.
Ewart AK; Morris CA; Atkinson D; Jin W; Sternes K; Spallone P; Stock AD; Leppert M; Keating MT
Nat Genet; 1993 Sep; 5(1):11-6. PubMed ID: 7693128
[TBL] [Abstract][Full Text] [Related]
18. Molecular genetics of long QT syndrome from genes to patients.
Wang Q; Chen Q; Li H; Towbin JA
Curr Opin Cardiol; 1997 May; 12(3):310-20. PubMed ID: 9243089
[TBL] [Abstract][Full Text] [Related]
19. Sodium channel abnormalities are infrequent in patients with long QT syndrome: identification of two novel SCN5A mutations.
Wattanasirichaigoon D; Vesely MR; Duggal P; Levine JC; Blume ED; Wolff GS; Edwards SB; Beggs AH
Am J Med Genet; 1999 Oct; 86(5):470-6. PubMed ID: 10508990
[TBL] [Abstract][Full Text] [Related]
20. The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis.
Curran ME; Atkinson DL; Ewart AK; Morris CA; Leppert MF; Keating MT
Cell; 1993 Apr; 73(1):159-68. PubMed ID: 8096434
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
