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VX-659–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

The New England journal of medicine, 2018-10, Vol.379 (17), p.1599-1611

2018

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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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Is ritual circumcision a risk factor for neonatal urinary tract infections?

Archives of disease in childhood, 2009-03, Vol.94 (3), p.191-194

2009

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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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Bacterial susceptibility to oral antibiotics in community acquired urinary tract infection

Archives of disease in childhood, 2003-03, Vol.88 (3), p.215-218

2003

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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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Presence of Viremia in Patients with Primary Herpetic Gingivostomatitis

Clinical infectious diseases, 2004-09, Vol.39 (5), p.636-640

2004

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C105 DISORDERS OF RESPIRATORY PHYSIOLOGY AND SLEEP IN CHILDREN: Effect Of Gestational Age Of Children Born Prematurely And Neonatal Intensive Care Unit History On Their Lung Function At School Age

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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P410 Patient satisfaction after transition to adult CF clinic

Journal of cystic fibrosis, 2024-06, Vol.23, p.S193-S194

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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P091 Dual inhaled antibiotics for treatment of pulmonary exacerbations in cystic fibrosis – a real life pilot study

Journal of cystic fibrosis, 2024-06, Vol.23, p.S95-S95

2024

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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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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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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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P074 Treatment effects of CFTR modulators on people with cystic fibrosis carrying the Georgian mutation (Q359K/T360K)

Journal of cystic fibrosis, 2023-06, Vol.22, p.S86-S86

2023

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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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P066 Treatment effects of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis heterozygous for 3849 + 10 kbC->T

Journal of cystic fibrosis, 2024-06, Vol.23, p.S87-S87

2024

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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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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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P121 Vaccine coverage in people with cystic fibrosis

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

2023

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EPS9.01 Utilizing intestinal organoids to assess in-vitro responses to CFTR modulators in rare CFTR variants

Journal of cystic fibrosis, 2024-06, Vol.23, p.S60-S60

2024

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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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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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WS07.3 The lonely patient: “I survived, now what?”

Journal of cystic fibrosis, 2018-06, Vol.17, p.S13-S13

2018

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Lactic dehydrogenase isoenzymes in cerebrospinal fluid of children with Guillain–Barré syndrome

Archives of disease in childhood, 2002-09, Vol.87 (3), p.255-256

2002

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VX-659–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

Microbial contamination of nebulizers in the home treatment of cystic fibrosis

Is ritual circumcision a risk factor for neonatal urinary tract infections?

The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews

Bacterial susceptibility to oral antibiotics in community acquired urinary tract infection

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

Presence of Viremia in Patients with Primary Herpetic Gingivostomatitis

C105 DISORDERS OF RESPIRATORY PHYSIOLOGY AND SLEEP IN CHILDREN: Effect Of Gestational Age Of Children Born Prematurely And Neonatal Intensive Care Unit History On Their Lung Function At School Age

P410 Patient satisfaction after transition to adult CF clinic

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

P091 Dual inhaled antibiotics for treatment of pulmonary exacerbations in cystic fibrosis – a real life pilot study

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

Cystic Fibrosis Mutations with Widely Variable Phenotype: The D1152H Example

Nontuberculous mycobacteria in cystic fibrosis patients is associated with disease severity

P074 Treatment effects of CFTR modulators on people with cystic fibrosis carrying the Georgian mutation (Q359K/T360K)

Computerised paediatric asthma quality of life questionnaires in routine care

P066 Treatment effects of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis heterozygous for 3849 + 10 kbC->T

P222 Airway Achromobacter xylosoxidans and disease severity in cystic fibrosis

115 Rising prevalence of nontuberculous mycobacteria in a CF center

P121 Vaccine coverage in people with cystic fibrosis

EPS9.01 Utilizing intestinal organoids to assess in-vitro responses to CFTR modulators in rare CFTR variants

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

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

WS07.3 The lonely patient: “I survived, now what?”

Lactic dehydrogenase isoenzymes in cerebrospinal fluid of children with Guillain–Barré syndrome

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