Genomics and Precision Health Database

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Query Trace: all[original query]>>Reviews/Commentaries[Product Type]

Publication
Annual Academy of Sickle Cell and Thalassaemia (ASCAT) conference: a summary of the proceedings. Strunk Crawford et al. BMC proceedings 2020 Dec 14(Suppl 20) 21 Similar articles in PubMed
Integrated Guidance for Enhancing the Care of Familial Hypercholesterolaemia in Australia. Watts Gerald F et al. Heart, lung & circulation 2020 Dec Similar articles in PubMed
Current Clinical Applications of in vivo Gene Therapy with AAVs. Mendell Jerry R et al. Molecular therapy : the journal of the American Society of Gene Therapy 2020 Dec Similar articles in PubMed
Genetic Contribution to Common Heart Failure—Not So Rare? EM McNally et al, JAMA Cardiology, December 15, 2020
A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients. Soltani Saber et al. Tropical medicine and health 2020 Dec 48(1) 96 Similar articles in PubMed
Organoids for personalized treatment of Cystic Fibrosis: Professional perspectives on the ethics and governance of organoid biobanking. Lensink Michael A et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2020 Dec Similar articles in PubMed
Life by the Numbers: Living with Familial Hypercholesterolemia. Walsh Casey Mulligan et al. Circulation. Genomic and precision medicine 2020 Dec Similar articles in PubMed
Novel therapies for familial hypercholesterolemia. Mohamed Farzahna et al. Current opinion in endocrinology, diabetes, and obesity 2020 Dec Similar articles in PubMed
Gene therapy for sickle cell disease. Olowoyeye Abiola et al. The Cochrane database of systematic reviews 2020 Nov 11CD007652 Similar articles in PubMed
CRISPR gene therapy shows promise against blood diseases H Ledford, Nature News, December 10, 2020
Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome. Lorca Rebeca et al. Journal of clinical medicine 2020 Nov 9(12) Similar articles in PubMed
Atrial fibrillation—a complex polygenetic disease JH Andersen et al, EJHG, December 5, 2020
Reimbursing the value of gene therapy care in an era of uncertainty. Noone Declan et al. Haemophilia : the official journal of the World Federation of Hemophilia 2020 Nov Similar articles in PubMed
Addressing patient education priorities in the era of gene therapy for haemophilia: Towards evidence-informed shared decision-making. Woollard Laurence et al. Haemophilia : the official journal of the World Federation of Hemophilia 2020 Nov Similar articles in PubMed
Familial Hypercholesterolemia: A Reportable Disorder. Kullo Iftikhar J et al. Circulation 2020 Nov 142(21) 1999-2001 Similar articles in PubMed
Evolving Role of Pharmacogenetic Biomarkers to Predict Drug-Induced Hematological Disorders. Pattanaik Smita et al. Therapeutic drug monitoring 2020 Nov Similar articles in PubMed
The Changing Face of Cystic Fibrosis and Its Implications for Screening. Naehrlich Lutz et al. International journal of neonatal screening 2020 Jul 6(3) Similar articles in PubMed
Big Data and Artificial Intelligence: Opportunities and Threats in Electrophysiology. van de Leur Rutger R et al. Arrhythmia & electrophysiology review 2020 Nov 9(3) 146-154 Similar articles in PubMed
Artificial Intelligence and Acute Stroke Imaging. Soun J E et al. AJNR. American journal of neuroradiology 2020 Nov Similar articles in PubMed
Emerging Alternatives to Conventional Clinic Visits in the Era of COVID-19: Adoption of Telehealth at VCU Adult Cystic Fibrosis Center. Womack Caitlin et al. International journal of general medicine 2020 131175-1186 Similar articles in PubMed
Why Do We Screen Newborn Infants for Cystic Fibrosis? Barben Jürg et al. International journal of neonatal screening 2020 Jul 6(3) Similar articles in PubMed
Newborn Screening for Cystic Fibrosis: Over the Hump, Still Need to Fine-Tune It. Castellani Carlo et al. International journal of neonatal screening 2020 Jul 6(3) Similar articles in PubMed
Genomics of hypertension: the road to precision medicine. Padmanabhan Sandosh et al. Nature reviews. Cardiology 2020 Nov Similar articles in PubMed
[Clinical pathway for cardiomyopathies: a genetic testing strategy proposed by ANMCO in Tuscany]. Girolami Francesca et al. Giornale italiano di cardiologia (2006) 2020 Dec 21(12) 926-934 Similar articles in PubMed
Patients with Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for Repeat Diagnostic Testing with Next Generation Sequencing. O'Hare Bailey J et al. Circulation. Genomic and precision medicine 2020 Nov Similar articles in PubMed
Familial Hypercholesterolemia: A Reportable Disorder I Kullo, Circulation, November 23, 2020
Pseudomonas aeruginosa adaptation and evolution in patients with cystic fibrosis. Rossi Elio et al. Nature reviews. Microbiology 2020 Nov Similar articles in PubMed
[Artificial intelligence technology in cardiac auscultation screening for congenital heart disease: present and future]. Xu Weize et al. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2020 Oct 49(5) 548-555 Similar articles in PubMed
Role of Non-Coding Variants in Brugada Syndrome. Pérez-Agustín Adrian et al. International journal of molecular sciences 2020 Nov 21(22) Similar articles in PubMed
ACE2 in the Era of SARS-CoV-2: Controversies and Novel Perspectives. Saponaro Federica et al. Frontiers in molecular biosciences 2020 7588618 Similar articles in PubMed