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â–  Abbreviation / Long Form : FDC / familial dilated cardiomyopathy

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Total Number of Papers: 26
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Abbreviation:   FDC  (>> Co-occurring Abbreviation)
Long Form:   familial dilated cardiomyopathy
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No. Year Title Co-occurring Abbreviation
2018 A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy. DCM
2018 Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing. DCM, EYA1, LMNA
2013 Family history of dilated cardiomyopathy among patients with heart failure from the HF-ACTION genetic ancillary study. DCM, FH
2013 Health status of cardiac genetic disease patients and their at-risk relatives. ARVC, CPVT, HCM, LQTS, PCS and MCS, SF-36
2013 Return of genetic results in the familial dilated cardiomyopathy research project. IDC
2011 Review and metaanalysis of the frequency of familial dilated cardiomyopathy. ---
2011 Update 2011: clinical and genetic issues in familial dilated cardiomyopathy. IDC
2010 Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals. DCM, IDC, IDC
2010 Familial dilated cardiomyopathy--a case report from western Nepal. DCM
10  2009 [Familial predisposition and microbial etiology in dilated cardiomyopathy]. DCM
11  2008 Anesthetic considerations for cesarean section in the parturient with familial cardiomyopathy. DCM, LVEDD
12  2008 Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy. CMR, IDC, LV, MBF
13  2008 Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. DCM, IDC
14  2007 Lamin A/C mutations associated with familial and sporadic cases of dilated cardiomyopathy in Koreans. DCM, LMNA
15  2006 Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy. FH, IDC
16  2005 Clinical and genetic issues in familial dilated cardiomyopathy. IDC
17  2002 A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation. ---
18  2002 Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy. IDC
19  2002 Periodic rescreening is indicated for family members at risk of developing familial dilated cardiomyopathy. HF, IDC, SCD
20  2001 Genetic Counseling and Screening Issues in Familial Dilated Cardiomyopathy. ECG, IDC
21  2001 Low proportion of familial dilated cardiomyopathy in an arab population with a high prevalence of consanguineous marriages. IDC
22  1999 Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: preliminary recommendations for clinical practice. IDC, LVE
23  1999 Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected. BMIs, BSA, FS, LVE, LVEDD, NHLBI
24  1999 Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. DCM
25  1998 Advances in molecular genetics of dilated cardiomyopathy. The Heart Muscle Disease Study Group. ---
26  1997 Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. FDC-CDM