Precision Health Database

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Records 1-26 (of 26 Records)

Query Trace: Cardiomyopathy[original query]>>Evidence Synthesis [Product Type]
Cascade health service use in family members following genetic testing in children: a scoping literature review. Cernat Alexandra et al. European journal of human genetics : EJHG 2021 Similar articles in PubMed
Estimating the health benefits of timely diagnosis and treatment of transthyretin amyloid cardiomyopathy. Rozenbaum Mark H et al. Journal of comparative effectiveness research 2021 Similar articles in PubMed
An Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. Jordan Elizabeth et al. Circulation 2021 Similar articles in PubMed
An Integrated Review of Hypertrophic Cardiomyopathy in Black Populations: Underrecognized and Understudied. Arabadjian Milla et al. The Journal of cardiovascular nursing 36(2) 104-115 Similar articles in PubMed
Angiotensinogen M235T polymorphism and susceptibility to hypertrophic cardiomyopathy in Asian population: A meta analysis. Zhen Zhen et al. Journal of the renin-angiotensin-aldosterone system : JRAAS 21(4) 1470320320978100 Similar articles in PubMed
Evaluation of earlier versus later dietary management in long-chain 3-hydroxyacyl-CoA dehydrogenase or mitochondrial trifunctional protein deficiency: a systematic review. Fraser Hannah et al. Orphanet journal of rare diseases 2019 Nov 14(1) 258 Similar articles in PubMed
CLINGEN Actionability Report for Dilated cardiomyopathy - DMD, LMNA, TNNT2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Fabry Disease - GLA ClinGen Actionability Working Group
CLINGEN Actionability Report for Glycogen Storage Disease 2 - GAA ClinGen Actionability Working Group
CLINGEN Actionability Report for Familial Hypertrophic Cardiomyopathy - ACTC1, CSRP3, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNI3, TNNT2, TPM1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Hemochromatosis, Type 1-HFE ClinGen Actionability Working Group
CLINGEN Actionability Report for Catecholaminergic Polymorphic Ventricular Tachycardia - RYR2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Very Long Chain Actyl-CoA Dehydrogenase Deficiency (ACADVLD) - ACADVL ClinGen Actionability Working Group
CLINGEN Actionability Report for Emery-Dreifuss Muscular Dystrophy (AD, XL) - LMNA, EMD, FHL1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary transthyretin-related amyloidosis - TTR ClinGen Actionability Working Group
CLINGEN Actionability Report for Myofibrillar Myopathy -DES, BAG3, FLNC ClinGen Actionability Working Group
CLINGEN Actionability Report for Glycogen Storage Disease V - PYGM ClinGen Actionability Working Group
CLINGEN Actionability Report for Arrhythmogenic Right Ventricular Dysplasia - PKP2, DSP, DSC2, TMEM43, DSG2 ClinGen Actionability Working Group
A cost-effectiveness model of genetic testing and periodical clinical screening for the evaluation of families with dilated cardiomyopathy. Catchpool Max et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jun Similar articles in PubMed
Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes. Ingles Jodie et al. Circulation. Genomic and precision medicine 2019 Jan Similar articles in PubMed
Cost Efficacy of ?-Galactosidase A Enzyme Screening for Fabry Disease. Newman Darrell B et al. Mayo Clinic proceedings 2019 Jan 94(1) 84-88 Similar articles in PubMed
Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review. Naik Rakhi P, et al. Annals of internal medicine 2018 11 0. (9) 619-627 Similar articles in PubMed
Using Decision Analysis to Support Newborn Screening Policy Decisions: A Case Study for Pompe Disease. Prosser Lisa A et al. MDM policy & practice 3(1) Similar articles in PubMed
Next Generation DNA Sequencing: A Review of the Cost Effectiveness and Guidelines Similar articles in PubMed
Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC). Similar articles in PubMed
Clinical utility gene card for: dilated cardiomyopathy (CMD). Similar articles in PubMed