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26. [Familial paramyloidotic cardiomyopathy. Hemodynamic and cineangiocardiographic study]. Lima JA; Barbosa J; Lopes AS; Lopes JS; Ginefra P; Benchimol AB Arq Bras Cardiol; 1976 Dec; 29(6):453-8. PubMed ID: 1021072 [No Abstract] [Full Text] [Related]
27. [Metabolic and genetic investigations in childhood cardiomyopathies]. Bonnet D; Rustin P; Rötig A; de Lonlay P; Viot G; Munnich A; Sidi D Arch Mal Coeur Vaiss; 1999 Nov; 92(11):1509-14. PubMed ID: 10598230 [TBL] [Abstract][Full Text] [Related]
28. High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene. Sakata K; Shimizu M; Ino H; Yamaguchi M; Terai H; Fujino N; Hayashi K; Kaneda T; Inoue M; Oda Y; Fujita T; Kaku B; Kanaya H; Mabuchi H Circulation; 2005 Jun; 111(25):3352-8. PubMed ID: 15967842 [TBL] [Abstract][Full Text] [Related]
32. [Familial primary cardiomyopathy]. Gola A; Milewicz A; Turkiewicz R Pol Tyg Lek; 1974 Apr; 29(15):613-4. PubMed ID: 4828041 [No Abstract] [Full Text] [Related]
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37. Prevalence of children with special health care needs in Milwaukee, Wisconsin: data from the Milwaukee metropolitan statistical area. Partington SN; Cisler RA; Blair KA WMJ; 2006 May; 105(3):30-5. PubMed ID: 16749322 [TBL] [Abstract][Full Text] [Related]
38. Noncompaction of the ventricular myocardium. Weiford BC; Subbarao VD; Mulhern KM Circulation; 2004 Jun; 109(24):2965-71. PubMed ID: 15210614 [No Abstract] [Full Text] [Related]
39. Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families. Behr ER; Dalageorgou C; Christiansen M; Syrris P; Hughes S; Tome Esteban MT; Rowland E; Jeffery S; McKenna WJ Eur Heart J; 2008 Jul; 29(13):1670-80. PubMed ID: 18508782 [TBL] [Abstract][Full Text] [Related]
40. [Familial cardiomyopathy in 2 brothers with heart block and auricular flutter]. Dake F; Nakayama H; Hayashi T Naika; 1966 Dec; 18(7):1349-53. PubMed ID: 5980317 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]