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Microbial contamination of nebulizers in the home treatment of cystic fibrosis

Child : care, health & development, 2007-07, Vol.33 (4), p.491-495

2007

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Bochdalek diaphragmatic hernia: not only a neonatal disease

Archives of disease in childhood, 2003-06, Vol.88 (6), p.532-535

2003

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Cystic Fibrosis Mutations with Widely Variable Phenotype: The D1152H Example

Pediatric pulmonology, 2006-03, Vol.41 (3), p.250-254

2006

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Computerised paediatric asthma quality of life questionnaires in routine care

Archives of disease in childhood, 2007-08, Vol.92 (8), p.678-682

2007

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The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews

Journal of cystic fibrosis, 2018-09, Vol.17 (5), p.e41-e45

2018

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Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia

The European respiratory journal, 2009-10, Vol.34 (4), p.875-881

2009

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256 Improved outcome in cystic fibrosis – results of the Israeli CF Patient Registry 2005–2013

Journal of cystic fibrosis, 2016-06, Vol.15, p.S117-S117

2016

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ePS05.3 Effect of allergic bronchopulmonary aspergillosis on FEV1 in children and adolescents with cystic fibrosis: an ECFS patient registry analysis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S46-S46

2016

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95 Achromobacter xylosoxidans in cystic fibrosis patients: prevalence and clinical significance

Journal of cystic fibrosis, 2016-06, Vol.15, p.S75-S75

2016

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297 Arab cystic fibrosis patients in Israel

Journal of cystic fibrosis, 2014-06, Vol.13, p.S124-S124

2014

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Nontuberculous mycobacteria in cystic fibrosis patients is associated with disease severity

Paediatric respiratory reviews, 2013-07, Vol.14, p.S51-S51

2013

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P305 Pancreatic function is not a risk factor for cystic fibrosis-related bone disease

Journal of cystic fibrosis, 2024-06, Vol.23, p.S162-S162

2024

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WS02.05 Assessment of respiratory infection following initiation of elexacaftor/tezacaftor/ivacaftor using the European Cystic Fibrosis Society patient registry

Journal of cystic fibrosis, 2024-06, Vol.23, p.S4-S4

2024

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EPS6.03 Factors associated with more frequent and severe pulmonary exacerbations in patients with cystic fibrosis: data from the ECFS Patient Registry

Journal of cystic fibrosis, 2024-06, Vol.23, p.S50-S50

2024

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P102 Methicillin-resistant Staphylococcus aureus and pulmonary outcome in people with cystic fibrosis: a European Cystic Fibrosis Patient Registry data analysis

Journal of cystic fibrosis, 2024-06, Vol.23, p.S116-S116

2024

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115 Rising prevalence of nontuberculous mycobacteria in a CF center

Journal of cystic fibrosis, 2012-06, Vol.11, p.S85-S85

2012

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714 Association between change in Pseudomonas aeruginosa infection and clinical outcomes after elexacaftor/tezacaftor/ivacaftor treatment: data from the European Cystic Fibrosis Society Patient Registry

Journal of cystic fibrosis, 2024-09, Vol.23, p.S404-S404

2024

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WS03.01 Differences in disease severity among different residual function mutations: data from the ECFS Patient Registry

Journal of cystic fibrosis, 2023-06, Vol.22, p.S5-S6

2023

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P222 Airway Achromobacter xylosoxidans and disease severity in cystic fibrosis

Journal of cystic fibrosis, 2024-06, Vol.23, p.S137-S137

2024

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WS01.02 Trends and outcomes of long-term inhaled antimicrobial treatment in people with cystic fibrosis without chronic Pseudomonas aeruginosa infection: an ECFSPR data analysis

Journal of cystic fibrosis, 2022-06, Vol.21, p.S1-S2

2022

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P121 Vaccine coverage in people with cystic fibrosis

Journal of cystic fibrosis, 2023-06, Vol.22, p.S101-S101

2023

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The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants

Archives of disease in childhood, 2005-07, Vol.90 (7), p.675-679

2005

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Clinical and genetic characteristics of patients with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu) – the national Israeli center experience

Paediatric respiratory reviews, 2011, Vol.12, p.S78-S78

2011

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WS20.03 What to hope for when there is no hope

Journal of cystic fibrosis, 2022-06, Vol.21, p.S39-S40

2022

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Incidence of SARS-CoV-2 in people with cystic fibrosis in Europe between February and June 2020

Journal of cystic fibrosis, 2021-07, Vol.20 (4), p.566-577

2021

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Microbial contamination of nebulizers in the home treatment of cystic fibrosis

Bochdalek diaphragmatic hernia: not only a neonatal disease

Cystic Fibrosis Mutations with Widely Variable Phenotype: The D1152H Example

Computerised paediatric asthma quality of life questionnaires in routine care

The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews

Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia

256 Improved outcome in cystic fibrosis – results of the Israeli CF Patient Registry 2005–2013

ePS05.3 Effect of allergic bronchopulmonary aspergillosis on FEV1 in children and adolescents with cystic fibrosis: an ECFS patient registry analysis

95 Achromobacter xylosoxidans in cystic fibrosis patients: prevalence and clinical significance

297 Arab cystic fibrosis patients in Israel

Nontuberculous mycobacteria in cystic fibrosis patients is associated with disease severity

P305 Pancreatic function is not a risk factor for cystic fibrosis-related bone disease

WS02.05 Assessment of respiratory infection following initiation of elexacaftor/tezacaftor/ivacaftor using the European Cystic Fibrosis Society patient registry

EPS6.03 Factors associated with more frequent and severe pulmonary exacerbations in patients with cystic fibrosis: data from the ECFS Patient Registry

P102 Methicillin-resistant Staphylococcus aureus and pulmonary outcome in people with cystic fibrosis: a European Cystic Fibrosis Patient Registry data analysis

115 Rising prevalence of nontuberculous mycobacteria in a CF center

714 Association between change in Pseudomonas aeruginosa infection and clinical outcomes after elexacaftor/tezacaftor/ivacaftor treatment: data from the European Cystic Fibrosis Society Patient Registry

WS03.01 Differences in disease severity among different residual function mutations: data from the ECFS Patient Registry

P222 Airway Achromobacter xylosoxidans and disease severity in cystic fibrosis

WS01.02 Trends and outcomes of long-term inhaled antimicrobial treatment in people with cystic fibrosis without chronic Pseudomonas aeruginosa infection: an ECFSPR data analysis

P121 Vaccine coverage in people with cystic fibrosis

The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants

Clinical and genetic characteristics of patients with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu) – the national Israeli center experience

WS20.03 What to hope for when there is no hope

Incidence of SARS-CoV-2 in people with cystic fibrosis in Europe between February and June 2020

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