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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: Apr 25, 2024
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Cystic Fibrosis[original query]>>Evidence Synthesis [Product Type]
The Psychological Impact on Parents of Children who Receive an Inconclusive Diagnosis for Cystic Fibrosis following Newborn Screening: A Systematic Mini-Review.
Ioanna Loukou et al. Children (Basel) 2024 11(1)
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Effectiveness of preconceptional and prenatal cystic fibrosis carrier screening: a systematic review.
Rita Banzi et al. Epidemiol Prev 2023 47(4-5) 243-256
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Carrier Screening Programs for Cystic Fibrosis, Fragile X Syndrome, Hemoglobinopathies and Thalassemia, and Spinal Muscular Atrophy: A Health Technology Assessment.
et al. Ont Health Technol Assess Ser 2023 23(4) 1-398
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Cost-effectiveness analysis of genetic tools to predict treatment response in patients with cystic fibrosis.
Yeva Sahakyan et al. J Cyst Fibros 2023
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Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemia.
Louise J Geneen et al. The Cochrane database of systematic reviews 2023 3(3) CD012349
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Economic evaluation of population-based expanded reproductive carrier screening for genetic diseases in Australia.
Deborah Schofield et al. Genetics in medicine : official journal of the American College of Medical Genetics 2023 100813
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Needs of people with rare diseases that can be supported by electronic resources: a scoping review.
Long Janet C et al. BMJ open 2022 12(9) e060394
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Interventions for the eradication of meticillin-resistant Staphylococcus aureus (MRSA) in people with cystic fibrosis.
Lo David Kh et al. The Cochrane database of systematic reviews 2022 12CD009650
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Laser therapy for retinopathy in sickle cell disease.
Myint Kay Thi et al. The Cochrane database of systematic reviews 2022 12(12) CD010790
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Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review.
Dawood Sarah N et al. Cureus 2022 14(9) e29359
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Inhaled nitric oxide for treating pain crises in people with sickle cell disease.
Aboursheid Tarek et al. The Cochrane database of systematic reviews 2022 7CD011808
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Implementation of prognostic machine learning algorithms in paediatric chronic respiratory conditions: a scoping review.
Filipow Nicole et al. BMJ open respiratory research 2022 9(1)
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Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research.
Johnson Faye et al. European journal of human genetics : EJHG 2022
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Maternal and foetal outcomes following natural vaginal versus caesarean section (c-section) delivery in women with bleeding disorders and carriers.
Karanth Laxminarayan et al. The Cochrane database of systematic reviews 2021 12CD011059
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The prevalence of CFTR mutations in patients with chronic rhinosinusitis: A systematic review and meta-analysis.
Yong Michael et al. Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery 2021
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Current updates and future perspectives in the evaluation of azoospermia: A systematic review.
Punjani Nahid et al. Arab journal of urology 2021 19(3) 206-214
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Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.
Brunelli Marcela Junqueira et al. The Cochrane database of systematic reviews 2021 9CD009806
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Rituximab for eradicating inhibitors in people with acquired haemophilia A.
Remmington Tracey et al. The Cochrane database of systematic reviews 2021 8CD011907
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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
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The Cost-effectiveness of Genotyping versus Sequencing for Prenatal Cystic Fibrosis Carrier Screening.
Avram Carmen M et al. Prenatal diagnosis 2021
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Systematic Identification of Familial Hypercholesterolaemia in Primary Care-A Systematic Review.
Silva Luisa et al. Journal of personalized medicine 2021 11(4)
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Cost-Effectiveness of Ivacaftor Therapy for Treatment of Cystic Fibrosis Patients With the G551D Gating Mutation.
Wherry Kael et al. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2020 Oct 23(10) 1332-1339
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A systematic review of the clinical and genetic characteristics of Chinese patients with cystic fibrosis.
Shi Ruihe et al. Pediatric pulmonology 2020 Jul
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Cost-effectiveness of the CFTR gene-sequencing test for asymptomatic carriers in the Colombian population
Andrade Ernesto et al. Biomedica : revista del Instituto Nacional de Salud 2020 40(2) 283-295
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Spectrum of mutations of cystic fibrosis in the 22 Arab countries: A systematic review.
Al-Sadeq Duaa et al. Respirology (Carlton, Vic.) 2019 24(2) 127-136
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Prenatal genetic testing for cystic fibrosis: a systematic review of clinical effectiveness and an ethics review.
Kessels Sharon J M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Aug
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Interventions for treating neuropathic pain in people with sickle cell disease.
Asnani Monika R et al. The Cochrane database of systematic reviews 2019 Jul 7CD012943
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A model-based economic evaluation of four newborn screening strategies for cystic fibrosis in Flanders, Belgium.
Schmidt Masja et al. Acta clinica Belgica 2019 Apr 1-9
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Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis.
Zhang Lei et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Feb
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Health economic modelling in Cystic Fibrosis: A systematic review.
Mohindru Bishal et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2019 Feb
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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