Search Results - "Cystic Fibrosis/epidemiology"

Data accuracy, consistency and completeness of the national Swiss cystic fibrosis patient registry: Lessons from an ECFSPR data quality project

Authors: Lara Wolf Jakob Usemann Eugénie Collaud et al.

Contributors: Lara Wolf Jakob Usemann Eugénie Collaud et al.

Source: Journal of cystic fibrosis, vol. 23, no. 3, pp. 506-511
Wolf, Lara; Usemann, Jakob; Collaud, Eugénie; Derkenne, Marie-France; Fischer, Reta; Hensen, Maxime; Hitzler, Michael; Hofer, Markus; Inci, Demet; Irani, Sarosh; Jahn, Kathleen; Koutsokera, Angela; Kusche, Rachel; Kurowski, Thomas; Latzin, Philipp; Lin, Dagmar; Mioranza, Laurence; Moeller, Alexander; Mornand, Anne; Mueller-Suter, Dominik; ... (2024). Data accuracy, consistency and completeness of the national Swiss cystic fibrosis patient registry: Lessons from an ECFSPR data quality project. Journal of cystic fibrosis, 23(3), pp. 506-511. Elsevier 10.1016/j.jcf.2023.08.015 <http://dx.doi.org/10.1016/j.jcf.2023.08.015>

Subject Terms: Pulmonary and Respiratory Medicine, Male, Adult, Cystic Fibrosis, Adolescent, Patient registries, 610 Medicine & health, Pediatrics, Cystic Fibrosis/epidemiology, Humans, Registries/statistics & numerical data, Switzerland/epidemiology, Data Accuracy, Child, Female, Reproducibility of Results, Cystic fibrosis, Data quality, Data quality audit, 2735 Pediatrics, Perinatology and Child Health, Registries, Perinatology and Child Health, 3. Good health, 2740 Pulmonary and Respiratory Medicine, 10178 Clinic for Pneumology, Switzerland

File Description: application/pdf; 1_s2.0_S1569199323009049_main.pdf - application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/37996316
https://serval.unil.ch/notice/serval:BIB_C948FE31CEA8
https://serval.unil.ch/resource/serval:BIB_C948FE31CEA8.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_C948FE31CEA87
https://boris.unibe.ch/189340/

Mucoviscidose au Maroc : que valent les mots sans les actes ?

Authors: Amenzoui, Naima Bousfiha, Aziz Bauwens, Nathalie et al.

Subject Terms: paediatric, Cystic Fibrosis, Infant, Newborn, Pilot Projects, Cystic Fibrosis/epidemiology, ethics, Sciences de la santé humaine, Low-middle-income countries, Reference Center, Centre de référence, CFTR, Human health sciences, Génétique, Mucoviscidose, Mutations

Access URL: https://hdl.handle.net/2268/333862

Mucoviscidose au Maroc : que valent les mots sans les actes ? ; Cystic fibrosis in Morroco : what do words mean without action ?.

Authors: Amenzoui, Naima Bousfiha, Aziz Bauwens, Nathalie et al.

Source: Revue Médicale de Liège, 79 (3), 175 - 180 (2024-03)

Subject Terms: Cystic Fibrosis, Low-middle-income countries, ethics, Infant, Newborn, Pilot Projects, Cystic Fibrosis/epidemiology, CFTR, Génétique, Mucoviscidose, Centre de référence, paediatric, Reference Center, Mutations, Human health sciences, Sciences de la santé humaine

Relation: urn:issn:0370-629X; urn:issn:2566-1566; https://orbi.uliege.be/handle/2268/333862; info:hdl:2268/333862; info:pmid:38487912

Availability: https://orbi.uliege.be/handle/2268/333862
https://orbi.uliege.be/bitstream/2268/333862/1/Mucoviscidose%20au%20Maroc%20-%20que%20valent%20les%20mots%20sans%20les%20actes.pdf

The global impact of SARS-CoV-2 in 181 people with cystic fibrosis

Authors: Elliot McClenaghan Rebecca Cosgriff Keith Brownlee et al.

Contributors: Elliot McClenaghan Rebecca Cosgriff Keith Brownlee et al.

Source: J Cyst Fibros
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
journal of cystic fibrosis, Vol. 19, no.6, p. 868–871 (2021)
Journal of Cystic Fibrosis

Subject Terms: Male, Outcome Assessment, Cystic Fibrosis, Coronavirus, COVID-19, Cystic fibrosis, SARS-CoV-2, Transplant, Respiratory System, Comorbidity, Global Health, Lung/diagnostic imaging, Respiratory Function Tests/methods, Congenital, COVID-19 Testing, 0302 clinical medicine, 7.1 Individual care needs, Risk Factors, COVID-19 Testing/methods, Outcome Assessment, Health Care, Registries, Tomography, Lung, SARS-CoV-2/isolation & purification, Cystic Fibrosis/epidemiology surgery, Registries/statistics & numerical data, Age Factors, X-Ray Computed/methods, X-Ray Computed, Respiratory Function Tests, 3. Good health, [SDV] Life Sciences [q-bio], Hospitalization, Infectious Diseases, Pneumonia & Influenza, Female, Infection, Life Sciences & Biomedicine, Lung Transplantation, Pulmonary and Respiratory Medicine, Adult, Lung Transplantation/statistics & numerical data, Short Communication, 03 medical and health sciences, Rare Diseases, Sex Factors, Clinical Research, Humans, Pediatrics, Perinatology, and Child Health, Mortality, Hospitalization/statistics & numerical data, Aged, Transplantation, Science & Technology, Prevention, 1103 Clinical Sciences, Pneumonia, Global Registry Harmonization Group, Health Care, Emerging Infectious Diseases, Orphan Drug, COVID-19/epidemiology prevention & control therapy, Tomography, X-Ray Computed

File Description: application/pdf; Print-Electronic

Access URL: http://www.cysticfibrosisjournal.com/article/S1569199320308778/pdf
https://pubmed.ncbi.nlm.nih.gov/33183965
https://hdl.handle.net/20.500.12530/81239
https://cris.maastrichtuniversity.nl/en/publications/56721003-7828-4a30-ad63-7ce0c557320f
https://doi.org/10.1016/j.jcf.2020.10.003
https://hdl.handle.net/2078.1/243367
https://hal.science/hal-03827774v1/document
https://hal.science/hal-03827774v1
https://doi.org/10.1016/j.jcf.2020.10.003

A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype

Authors: Hergersberg, M. Balakrishnan, J. Bettecken, T. et al.

Subject Terms: Cystic Fibrosis/epidemiology/*genetics Cystic Fibrosis Transmembrane Conductance Regulator/*genetics DNA Primers Founder Effect Gene Frequency Genetic Screening Humans *Mutation Polymerase Chain Reaction Sequence Analysis, DNA Switzerland/epidemiology

Relation: Human Genetics; https://iris.unil.ch/handle/iris/110868; serval:BIB_4D8E7E366390; A1997XL68600014; 9254853

Availability: https://iris.unil.ch/handle/iris/110868
https://doi.org/10.1007/s004390050494

Newborn screening for cystic fibrosis - The parent perspective.

Authors: Rueegg, C.S. Barben, J. Hafen, G.M. et al.

Contributors: Rueegg, C.S. Barben, J. Hafen, G.M. et al.

Subject Terms: Adult, Consumer Behavior, Consumer Health Information/methods, Consumer Health Information/organization & administration, Consumer Health Information/standards, Cystic Fibrosis/diagnosis, Cystic Fibrosis/epidemiology, Cystic Fibrosis/genetics, Cystic Fibrosis/psychology, Cystic Fibrosis Transmembrane Conductance Regulator/genetics, Female, Genetic Testing/methods, Humans, Infant, Newborn, Male, Needs Assessment, Neonatal Screening/organization & administration, Neonatal Screening/psychology, Neonatal Screening/standards, Parents/psychology, Perinatal Care/methods, Perinatal Care/organization & administration, Pregnancy, Surveys and Questionnaires, Switzerland/epidemiology, Cystic fibrosis, False-positives, Newborn screening, Parents

Relation: Journal of Cystic Fibrosis; https://iris.unil.ch/handle/iris/239570; serval:BIB_DE3AB6811BED; 000382350700009

Availability: https://iris.unil.ch/handle/iris/239570
https://doi.org/10.1016/j.jcf.2015.12.003

Renal involvement in cystic fibrosis: diseases spectrum and clinical relevance

Authors: Yahiaoui, Y. Jablonski, M. Hubert, D. et al.

Subject Terms: Adult, Amyloidosis/epidemiology/pathology, Biopsy, Cystic Fibrosis/*epidemiology, Diabetic Nephropathies/epidemiology/pathology, Female, Follow-Up Studies, Glomerulonephritis/epidemiology/pathology, Glomerulonephritis, IGA/epidemiology/pathology, Humans, Incidence, Kidney/*pathology, Kidney Diseases/*epidemiology/*pathology, Kidney Failure, Chronic/epidemiology/pathology, Male, Middle Aged, Nephrosis, Lipoid/epidemiology/pathology, Paris/epidemiology, Retrospective Studies, Young Adult

Relation: Clinical Journal of the American Society of Nephrology; https://iris.unil.ch/handle/iris/145208; serval:BIB_7A2C2F95814D

Availability: https://iris.unil.ch/handle/iris/145208
https://doi.org/10.2215/CJN.00750209

Cystic fibrosis in Iceland and the high prevalence of the N1303K variant

Authors: Elidottir, Helga Bjarnadottir, Selma R. Baldursson, Olafur et al.

Source: Pediatric Pulmonology; 59(7), pp 1944-1951 (2024) ; ISSN: 8755-6863

Subject Terms: Health Care Service and Management, Health Policy and Services and Health Economy, CFTR gene variants, cystic fibrosis epidemiology, cystic fibrosis incidence, cystic fibrosis prevalence, N1303K gene variant

Relation: http://dx.doi.org/10.1002/ppul.27019; scopus:85190969595; pmid:38629430

Availability: https://lup.lub.lu.se/record/c1fede5f-408e-4bde-a6b8-190ebc339d27
https://doi.org/10.1002/ppul.27019

Absence of a gender gap in survival. An analysis of the Italian registry for cystic fibrosis in the paediatric age

Authors: Viviani L Bossi A ASSAEL, BAROUKHMAURICE et al.

Source: Journal of Cystic Fibrosis. 10:313-317

Subject Terms: Pulmonary and Respiratory Medicine, Male, Adolescent, Cystic Fibrosis, Incidence, Infant, Kaplan-Meier Estimate, 3. Good health, 03 medical and health sciences, Age Distribution, 0302 clinical medicine, Italy, 5. Gender equality, Risk Factors, Child, Preschool, Pediatrics, Perinatology and Child Health, Cystic fibrosis, Child, Cystic Fibrosis/epidemiology, Registries/statistics & numerical data, Humans, Female, Pediatrics, Perinatology, and Child Health, Longitudinal Studies, Registries, Sex Distribution

Access URL: http://www.cysticfibrosisjournal.com/article/S1569199311000476/pdf
https://pubmed.ncbi.nlm.nih.gov/21514901
https://www.sciencedirect.com/science/article/pii/S1569199311000476
https://core.ac.uk/display/82443036
https://www.cysticfibrosisjournal.com/article/S1569-1993(11)00047-6/fulltext
https://europepmc.org/article/MED/21514901
http://www.ncbi.nlm.nih.gov/pubmed/21514901
https://www.cysticfibrosisjournal.com/article/S1569-1993(11)00047-6/pdf
https://hdl.handle.net/11562/431939
https://doi.org/10.1016/j.jcf.2011.03.007
https://www.openaccessrepository.it/record/177602

Impact of polymorphism of Multidrug Resistance-associated Protein 1 (ABCC1) gene on the severity of cystic fibrosis

Authors: MAFFICINI, Andrea Ortombina M Sermet Gaudelius I et al.

Source: Journal of Cystic Fibrosis. 10:228-233

Subject Terms: Pulmonary and Respiratory Medicine, Adult, Male, 0301 basic medicine, Adolescent, Cystic Fibrosis, Databases, Factual, Genotype, ABCC1, Kaplan-Meier Estimate, Polymorphism, Single Nucleotide, Severity of Illness Index, Cystic fibrosis, Cell Line, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Multidrug Resistance-associated Protein 1, Humans, Pseudomonas Infections, Cystic Fibrosis/epidemiology, Cystic Fibrosis/genetics, Cystic Fibrosis/microbiology, Polymorphism, Single Nucleotide/genetics, Pseudomonas Infections/epidemiology, Pediatrics, Perinatology, and Child Health, NT_010393.16:g.15983174C>G polymorphism, Promoter Regions, Genetic, Modifier gene, Infection by Pseudomonas aeruginosa, Epithelial Cells, Pseudomonas aeruginosa, Female, Multidrug Resistance-Associated Proteins, Severity of cystic fibrosis disease

Access URL: http://www.cysticfibrosisjournal.com/article/S1569199311000403/pdf
https://pubmed.ncbi.nlm.nih.gov/21435954
https://www.ncbi.nlm.nih.gov/pubmed/21435954
https://www.sciencedirect.com/science/article/pii/S1569199311000403
http://dial.uclouvain.be/pr/boreal/object/boreal:123476
https://pubmed.ncbi.nlm.nih.gov/21435954/
https://dial.uclouvain.be/pr/boreal/object/boreal:123476
https://iris.univr.it/handle/11562/345850

Comparative demographics of the European cystic fibrosis population: a cross-sectional database analysis

Authors: McCormick, Jonathan D. Mehta, Gita R. Olesen, Hanne Vebert Ebert et al.

Contributors: McCormick, Jonathan D. Mehta, Gita R. Olesen, Hanne Vebert Ebert et al.

Source: McCormick, J, Mehta, G, Olesen, H V, Viviani, L, Macek, M, Mehta, A & European Registry Working Group 2010, 'Comparative demographics of the European cystic fibrosis population: a cross-sectional database analysis', Lancet, vol. 375, no. 9719, pp. 1007-13. https://doi.org/10.1016/S0140-6736(09)62161-9

Subject Terms: Adult, Adolescent, Cystic Fibrosis, Medical and Health Sciences, Cystic fibrosis, Young Adult, 03 medical and health sciences, AGE, 0302 clinical medicine, Humans, Pulmonary exacerbation, UK, European Union, Registries, Child, Lung, Cystic Fibrosis/epidemiology* Europe/epidemiology, OUTCOMES, MORTALITY, Infant, Middle Aged, Registires, Cross-Sectional Studies, European Union/statistics & numerical data, 3. Good health, Europe, Child, Preschool, Clinical Medicine

File Description: pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/20304245
https://www.bib.irb.hr/740705
https://doi.org/10.1016/s0140-6736(09)62161-9
http://www.sciencedirect.com/science/article/pii/S0140673609621619
https://doi.org/10.1016/S0140-6736(09)62161-9
https://www.ncbi.nlm.nih.gov/pubmed/20304245
http://www.sciencedirect.com/science/article/pii/S0140673609621619
https://air.unimi.it/handle/2434/148220
https://www.sciencedirect.com/science/article/pii/S0140673609621619
https://pubmed.ncbi.nlm.nih.gov/20304245/
https://www.bib.irb.hr/740705
https://hdl.handle.net/2434/148220
https://doi.org/10.1016/S0140-6736(09)62161-9
https://hdl.handle.net/20.500.14279/3666
https://pure.au.dk/portal/en/publications/13e05425-2cc5-4902-9301-d632bf461a1e
https://doi.org/10.1016/S0140-6736(09)62161-9

Liver disease in pediatric patients with cystic fibrosis is associated with glutathione S-transferase P1 polymorphism

Authors: Henrion-Caude, Alexandra Flamant, Cyril Roussey, Michel et al.

Source: Hepatology, Vol. 36, No 4 Pt 1 (2002) pp. 913-7

Subject Terms: Male, 0301 basic medicine, Cystic Fibrosis/*epidemiology/*genetics, Adolescent, Cystic Fibrosis, Genotype, Polymorphism, Single Nucleotide, 03 medical and health sciences, Isoenzymes/*genetics, Risk Factors, Genetic Predisposition to Disease/epidemiology, Humans, Genetic Predisposition to Disease, Child, Glutathione Transferase, 2. Zero hunger, 0303 health sciences, Glutathione Transferase/*genetics, Liver Diseases, Liver Diseases/*epidemiology/*genetics, 3. Good health, Isoenzymes, Glutathione S-Transferase pi, Female

File Description: application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/12297838
https://www.ncbi.nlm.nih.gov/pubmed/12297838
https://aasldpubs.onlinelibrary.wiley.com/doi/pdf/10.1053/jhep.2002.35534
https://archive-ouverte.unige.ch/unige:47138
https://core.ac.uk/display/60933248
https://www.sciencedirect.com/science/article/pii/S0270913902000976
https://aasldpubs.onlinelibrary.wiley.com/doi/abs/10.1053/jhep.2002.35534
https://archive-ouverte.unige.ch/unige:47138
https://archive-ouverte.unige.ch/unige:47138
https://doi.org/10.1053/jhep.2002.35534

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

Authors: By:dork, T Macek, M Mekus, F et al.

Contributors: By:dork, T Macek, M Mekus, F et al.

Source: Human Genetics

Subject Terms: Male, 0301 basic medicine, Dna mutational analysis, Cystic Fibrosis, DNA Mutational Analysis, Cystic Fibrosis Transmembrane Conductance Regulator, Settore MED/03 - GENETICA MEDICA, DNA Mutational Analysi, CFTR gene, 03 medical and health sciences, Gene Frequency, CFTRdele2, Humans, Preschool, Alleles, Child, Child, Preschool, Europe, Female, Infant, Infant, Newborn, Phenotype, Reverse Transcriptase Polymerase Chain Reaction, Sequence Deletion, Cystic Fibrosi, Allele, 21-kb deletion, 3(21 kb), cystic fibrosis mutation, 0303 health sciences, Europe - epidemiology, Newborn, 3. Good health, Cystic fibrosis - epidemiology - genetics, Human

Access URL: https://pubmed.ncbi.nlm.nih.gov/10798353
https://www.bib.irb.hr/233049
https://doi.org/10.1007/s004390000246
https://link.springer.com/article/10.1007/s004390000246
https://doi.org/10.1007/s004390000246
https://iris.univr.it/handle/11562/225499
https://rd.springer.com/article/10.1007/s004390000246
http://nlm.it/www.nlm.it/documents/2000_cftr_dele_2
3_dork.pdf
https://www.ncbi.nlm.nih.gov/pubmed/10798353
https://core.ac.uk/display/53869629
https://nlm.it/www.nlm.it/documents/2000_cftr_dele_2
3_dork.pdf
https://imagine.imgge.bg.ac.rs/handle/123456789/138
https://hdl.handle.net/11562/225499
https://doi.org/10.1007/s004390000246
https://hdl.handle.net/2108/166508
http://hdl.handle.net/10722/44361

Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations (W1098C, 846delT, P750L, 4160insGGGG and 297-1G→A)

Authors: Tsui, LC Carnevale, A Orozco, L et al.

Source: Human Genetics. 106:360-365

Subject Terms: Male, 0301 basic medicine, 0303 health sciences, Cystic Fibrosis, single-stranded conformational, Cystic Fibrosis Transmembrane Conductance Regulator, Genetic Variation, 3. Good health, Cystic fibrosis transmembrane conductance regulator - genetics, 03 medical and health sciences, Gene Frequency, Cystic fibrosis - epidemiology - genetics, Mutation, Polymorphism, single-stranded conformational, Humans, Female, Polymorphism, Mexico, Variation (genetics), Polymorphism, Single-Stranded Conformational

Access URL: https://pubmed.ncbi.nlm.nih.gov/10798368
http://hub.hku.hk/handle/10722/44359
https://europepmc.org/abstract/MED/10798368
https://rd.springer.com/article/10.1007/s004390000244
https://www.ncbi.nlm.nih.gov/pubmed/10798368
https://pubmed.ncbi.nlm.nih.gov/10798368/
https://link.springer.com/article/10.1007%2Fs004390000244
http://hdl.handle.net/10722/44359

Global trends of young people with chronic and disabling conditions.

Authors: Surís, J.C.

Subject Terms: Adolescent, Adult, Asthma/epidemiology, Bias (Epidemiology), Cerebral Palsy/epidemiology, Child, Preschool, Chronic Disease/epidemiology, Cystic Fibrosis/epidemiology, Diabetes Mellitus/epidemiology, Disabled Persons/statistics & numerical data, Down Syndrome/epidemiology, Female, Humans, Infant, Male, Neoplasms/epidemiology, Prevalence, Survival Rate, World Health

Relation: Journal of Adolescent Health; https://iris.unil.ch/handle/iris/254621; serval:BIB_E1DB8E976FCB; A1995RM10200005; 7578157

Availability: https://iris.unil.ch/handle/iris/254621
https://doi.org/10.1016/1054-139X(95)00075-4

Respiratory infections by Achromobacter xylosoxidans in a cohort of Cystic Fibrosis patients: identification, antimicrobial susceptibility and molecular epidemiology

Authors: Antonietta Lambiase Maria Rosaria Catania Mariassunta Del Pezzo et al.

Source: Microbiologia Medica, Vol 25, Iss 1 (2010)

Subject Terms: Achromobacter xylosoxidans, cystic fibrosis, epidemiology, antimicrobial susceptibility, Microbiology, QR1-502

File Description: electronic resource

Relation: http://www.pagepressjournals.org/index.php/mm/article/view/2486; https://doaj.org/toc/2280-6423

Access URL: https://doaj.org/article/c4175995b8524e93a411514491ee464b

Genomic analysis of an emerging multiresistant Staphylococcus aureus strain rapidly spreading in cystic fibrosis patients revealed the presence of an antibiotic inducible bacteriophage

Authors: Rolain, Jean-Marc Francois, Patrice Hernandez, David et al.

Source: ISSN: 1745-6150 ; Biology direct, vol. 4 (2009) 1.

Subject Terms: info:eu-repo/classification/ddc/616.07, info:eu-repo/classification/ddc/616, Anti-Bacterial Agents/*pharmacology, Bacteriophages/*drug effects, Base Sequence, Cell Proliferation/drug effects, Cell Wall/ultrastructure, Cystic Fibrosis/epidemiology/*microbiology, DNA, Bacterial/genetics/metabolism, Drug Resistance, Multiple, Bacterial/*genetics, France/epidemiology, Gene Expression Profiling, Genes, Bacterial, Genome, Humans, Methicillin Resistance/drug effects/genetics, Minisatellite Repeats/genetics, Molecular Sequence Data, Phenotype, Phylogeny, Staphylococcus aureus/*cytology/*genetics/ultrastructure, Transcription, Genetic/drug effects

Relation: info:eu-repo/semantics/altIdentifier/pmid/19144117; unige:19576

Availability: https://archive-ouverte.unige.ch/unige:19576

Cystic fibrosis in the Western health region / Cystisk fibrose i Helseregion Vest

Authors: Fluge, G

Source: Tidsskrift for Den Norske Laegeforening. 120(5):568

First report of CFTR mutations in black cystic fibrosis patients of southern African origin

Authors: Carles S. Desgeorges M. Goldman A. et al.

Contributors: Carles S. Desgeorges M. Goldman A. et al.

Source: Journal of Medical Genetics. 33:802-804

Subject Terms: south africa, Adult, Male, 0301 basic medicine, Heterozygote, Cystic Fibrosis, transmembrane conductance regulator, DNA Mutational Analysis, Molecular Sequence Data, Cystic Fibrosis Transmembrane Conductance Regulator, Cystic Fibrosis/epidemiology, Haploidy, negro, cystic fibrosis, South Africa, 03 medical and health sciences, father, case report, molecular biology, Humans, controlled study, exon, gene mutation, human, cameroon, 0303 health sciences, South Africa/epidemiology, Base Sequence, gene deletion, Homozygote, article, heterozygote, 3. Good health, homozygote, priority journal, nucleic acid base substitution, Cystic Fibrosis Transmembrane Conductance Regulator/genetics, Female

Access URL: https://jmg.bmj.com/content/33/9/802.full.pdf
https://pubmed.ncbi.nlm.nih.gov/8880589
https://scholar.sun.ac.za:443/handle/10019.1/12688
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1050743/
https://jmg.bmj.com/content/33/9/802
https://pubmed.ncbi.nlm.nih.gov/8880589/
http://core.ac.uk/display/3612991
https://jmg.bmj.com/content/33/9/802.full.pdf
https://biblio.vub.ac.be/vubir/first-report-of-cftr-mutations-in-black-cystic-fibrosis-patients-of-southern-african-origin(2561b793-f95c-4be6-b259-bc5c81f93baf).html
https://doi.org/10.1136/jmg.33.9.802
https://hdl.handle.net/20.500.14017/2561b793-f95c-4be6-b259-bc5c81f93baf

Creating longitudinal datasets and cleaning existing data identifiers in a cystic fibrosis registry using a novel Bayesian probabilistic approach from astronomy

Authors: Peter Donald Hurley Seb Oliver Anil Mehta

Source: PLoS One
PLoS ONE, Vol 13, Iss 7, p e0199815 (2018)

Subject Terms: Cystic Fibrosis, Science, Datasets as Topic, Bayes Theorem, Cystic Fibrosis/epidemiology, 01 natural sciences, Data Accuracy, 3. Good health, Datasets as Topic/standards, name=General Biochemistry,Genetics and Molecular Biology, 0103 physical sciences, name=General Agricultural and Biological Sciences, Medicine, Humans, Registries, 0101 mathematics, Research Article

File Description: application/pdf

Access URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0199815&type=printable
https://pubmed.ncbi.nlm.nih.gov/29985939
https://doaj.org/article/c394af5ded3a41e1bf4ca1dd19a3263b
https://pubmed.ncbi.nlm.nih.gov/29985939/
https://discovery.dundee.ac.uk/ws/files/27743350/journal.pone.0199815.pdf
http://sro.sussex.ac.uk/id/eprint/95746/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037350
https://ui.adsabs.harvard.edu/abs/2018PLoSO..1399815H/abstract
https://europepmc.org/article/MED/29985939