Left ventricular noncompaction syndrome

    • [DOC File]DNA Sample Submission to Asper Biotech

      https://info.5y1.org/left-ventricular-noncompaction-syndrome_1_ec4a94.html

      24) Howard TS, Valdes SO, Hope KD, Landstrom AP, Schneider AE, Miyake CY, de la Uz CM, Kim JJ. Wolff Parkinson White Syndrome associated with left ventricular non-compaction: Population description, electrophysiological characteristics and ablation. …

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    • [DOCX File]The Natural History of Left Ventricular Non-Compaction ...

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      Bennett et al. (2016) The Current Approach to Diagnosis and Management of Left Ventricular Noncompaction Cardiomyopathy: Review of the Literature. Cardiology Research and Practice. 2016:5172308 (PMID: 26881173) Rooms et al. (2015) Non-compaction cardiomyopathy: a genetically and clinically heterogeneous disorder.

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    • [DOCX File]GeneDx

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      Isolated left ventricular non-compaction: An emerging cause of heart failure in adults. Postgraduate Medical Journal. 85 (1002) (pp 202-207), 2009. Exclude, review

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    • [DOCX File]GeneDx

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      Left Ventricular Noncompaction Cardiomyopathy NGS panel of genes with CNV Long QT Syndrome NGS panel of genes with CNV Del/dup analysis of KCNH2, KCNQ1genes by MLPA Noonan Spectrum Disorders/Rasopathies NGS panel of genes with CNV. Deletion/duplication analysis of selected regions by Chromosomal Microarray Analysis

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    • Addendum to the TCE Document Entitled “Assessing the ...

      Cardiomyopathy is defined as disease of the heart muscle and has many different presentations, including hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), left ventricular noncompaction (LVNC), and arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC).

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    • [DOC File]ANDREW P - Sites@Duke | sites.duke.edu

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      Right to Left Shunt Resulting in Right to Left Confusion: Malignancy Associated Gerstmann Syndrome. Albert Jang1, Tameka Smith2, Stephen Trainor3, Peter Caldwell4 ... A Rare Case Presentation of Left Ventricular Noncompaction Cardiomyopathy. Ankita Tandon1, awa drame2. 1University of South Florida , 2university of south florida.

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    • [DOC File]CURRICULUM VITAE

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      Heterozygous NKX2.5 mutations account for about 4% of all CCDs; atrial septal defects (ASD) are most common, but ventricular septal defects (VSD), left ventricle noncompaction, Teratology of Fallot (TOF), double-outlet right ventricle (DORV), subvalvular aortic stenosis, and Ebstein anomaly of the tricuspid valve have also been observed.

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    • [DOCX File]www.onlinejcf.com

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      Hermida-Prieto M, Monserrat L, Castro-Beiras A, et al. Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations. Am J Cardiol 2004;94:50–54. Chang B, Nishizawa T, Furutani M et al. Identi!cation of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death.

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    • [DOC File]Heart | A leading international cardiology journal from ...

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      Clinical features and long term outcomes of left ventricular noncompaction in childhood: Results from a national population based study of childhood cardiomyopathy. Bharucha T, Lee K, Daubeney PEF, Nugent AW, Turner C, Sholler G, Robertson T, Justo R, Ramsay J, Carlin JB, Colan SD, Davis AM, King I, Weintraub RG.

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