Zobrazeno 1 - 10 of 11 pro vyhledávání: '"Donald, Love"'
1
Akademický článek
Long QT molecular autopsy in sudden unexplained death in the young (1-40 years old): Lessons learnt from an eight year experience in New Zealand.
Autor: Luciana Marcondes, Jackie Crawford, Nikki Earle, Warren Smith, Ian Hayes, Paul Morrow, Tom Donoghue, Amanda Graham, Donald Love, Jonathan R Skinner, Cardiac Inherited Disease Group New Zealand
Publikováno v: PLoS ONE, Vol 13, Iss 4, p e0196078 (2018)
To review long QT syndrome molecular autopsy results in sudden unexplained death in young (SUDY) between 2006 and 2013 in New Zealand.Audit of the LQTS molecular autopsy results, cardiac investigations and family screening data from gene-positive fam
Externí odkaz: https://doaj.org/article/84585226c26443e28f6195b4699136ca
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2
Adult attention deficit hyperactivity disorder clinic: An interprofessional collaboration
Autor: Donald Love, Corinne Johnson, Tyler Casey
Publikováno v: Journal of the American Pharmacists Association. 60:S113-S117
Objective To review the experience of a pharmacist-led interprofessional attention deficit hyperactivity disorder (ADHD) clinic in a large integrated health care system. Practice description Kaiser Permanente Northwest (KPNW) is a nonprofit managed h
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4daa087cc2111054651536dd130c2c46
https://doi.org/10.1016/j.japh.2020.03.020
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3
Impact and predictors of quality of life in adults diagnosed with a genetic muscle disorder: a nationwide population-based study
Autor: Alice, Theadom, Miriam, Rodrigues, Annemarei, Ranta, Gemma, Poke, Donald, Love, Kelly, Jones, Braden Te, Ao, Graeme, Hammond-Tooke, Priya, Parmar, Gina, O'Grady, Richard, Roxburgh
Publikováno v: Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation. 31(6)
To determine the impact of genetic muscle disorders and identify the sociodemographic, illness, and symptom factors influencing quality of life.Adults (aged 16-90 years) with a confirmed clinical or molecular diagnosis of a genetic muscle disorder id
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::62f9d1d8abbb2f7b65bfff29d5017318
https://pubmed.ncbi.nlm.nih.gov/34837601
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4
Detection of sudden death syndromes in New Zealand
Autor: Nikki, Earle, Jackie, Crawford, Kate, Gibson, Donald, Love, Ian, Hayes, Katherine, Neas, Martin, Stiles, Mandy, Graham, Tom, Donoghue, Andrew, Aitken, Jon, Skinner
Publikováno v: The New Zealand medical journal. 129(1445)
To investigate regional variations in the detection of sudden death syndromes across New Zealand by assessing registrations in the national Cardiac Inherited Diseases Registry New Zealand (CIDRNZ).The CIDRNZ has been a national entity since 2009, wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::52dc5057f4ebdda2999d3a6e683f0228
https://pubmed.ncbi.nlm.nih.gov/27857240
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6
Predicting the Pathogenic Potential of BRCA1 and BRCA2 Gene Variants Identified in Clinical Genetic Testing
Autor: Brookes, C., Lai, S., Doherty, E., Donald Love
Publikováno v: Sultan Qaboos University Medical Journal, Vol 15, Iss 2, Pp 218-225 (2015)
Sultan Qaboos University Medical Journal, Vol 15, Iss 2, Pp e218-e225 (2015)
Scopus-Elsevier
Objectives: Missense variants are very commonly detected when screening for mutations in the BRCA1 and BRCA2 genes. Pathogenic mutations in the BRCA1 and BRCA2 genes lead to an increased risk of developing breast, ovarian, prostate and/or pancreatic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ed9320d55867d9666799bf91a02dff05
https://pubmed.ncbi.nlm.nih.gov/26052455
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7
Evaluation of outpatient initiation of antiarrhythmic drug therapy in patients reverting to sinus rhythm after an episode of atrial fibrillation
Autor: Donald Love, David J. Cohen, Vicki E Schreckengost, Peter Zimetbaum, Robert Lemery, Laurence M. Epstein, Roger J. Laham, Mark E. Josephson
Publikováno v: The American Journal of Cardiology. 83:450-452
The safety of a method of outpatient antiarrhythmic drug loading utilizing a continuous loop event recorder was evaluated. The findings suggest that the standard 2-day hospital admission for drug loading is not necessary in all patients and a method
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2edb1c0bc7ad3fd622bb1057af840a0
https://doi.org/10.1016/s0002-9149(98)00885-6
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8
Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype
Autor: Belinda, Chong, Madhuri, Hegde, Matthew, Fawkner, Scott, Simonet, Hamilton, Cassinelli, Mahmut, Coker, John, Kanis, Joerg, Seidel, Cristina, Tau, Beyhan, Tüysüz, Bilgin, Yüksel, Donald, Love
Publikováno v: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18(12)
Homozygous mutations in TNFRSF11B, the gene encoding osteoprotegerin, were found in affected members from six of nine families with idiopathic hyperphosphatasia. The severity of the phenotype was related to the predicted effects of the mutations on o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1a6eb2b9471c9971ef3c573f02ae70d3
https://pubmed.ncbi.nlm.nih.gov/14672344
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