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WS18.5 Nasal potential difference and sweat chloride responses to ivacaftor correlate in three patients with non-p.Gly551Asp gating mutations

Journal of cystic fibrosis, 2016-06, Vol.15, p.S30-S31

2016

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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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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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WS15.5 Electrophysiological tests in CF diagnosis: nasal potential difference is more predictive than sweat test – single center study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S28-S28

2017

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Salivary profile and oxidative stress in children and adolescents with cystic fibrosis

Journal of oral pathology & medicine, 2010-01, Vol.39 (1), p.16-21

2010

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223 Infertility among women with cystic fibrosis: prevalence and risk factors

Journal of cystic fibrosis, 2016-06, Vol.15, p.S108-S108

2016

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P082 Optimizing CFTR modulator therapy management for cystic fibrosis through the ReX platform

Journal of cystic fibrosis, 2024-06, Vol.23, p.S92-S92

2024

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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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120 Duplication in CHIT1 gene and the risk for Aspergillus lung disease in CF patients

Journal of cystic fibrosis, 2013-06, Vol.12, p.S79-S79

2013

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P293 An intensive protocol for bowel preparation in people with cystic fibrosis undergoing screening colonoscopy, a single centre experience

Journal of cystic fibrosis, 2023-06, Vol.22, p.S154-S154

2023

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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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P044 Treatment benefits of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying non-F508del mutations

Journal of cystic fibrosis, 2022-06, Vol.21, p.S73

2022

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160 Nasal potential difference in young children is feasible: report from a national referral center

Journal of cystic fibrosis, 2024-09, Vol.23, p.S90-S90

2024

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P052 Efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with normal/near normal FEV1 (≥70%)

Journal of cystic fibrosis, 2023-06, Vol.22, p.S79-S79

2023

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P214 Real-life evaluation of the multi-organ effects of lumacaftor/ivacaftor (Orkambi) on F508del homozygous cystic fibrosis patients

Journal of cystic fibrosis, 2020-06, Vol.19, p.S117-S117

2020

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133 Clinical response to elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with the N1303K and non-modulator responsive mutation

Journal of cystic fibrosis, 2022-10, Vol.21, p.S78-S79

2022

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P266 The effect of lumacaftor/ivacaftor on the severity of cystic fibrosis pulmonary exacerbations in patients with F508del homozygous cystic fibrosis

Journal of cystic fibrosis, 2019-06, Vol.18, p.S132-S132

2019

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P077 Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutation

Journal of cystic fibrosis, 2023-06, Vol.22, p.S87-S87

2023

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Pulmonary outcome of Alport syndrome with familial diffuse esophageal leiomyomatosis

Paediatric respiratory reviews, 2011, Vol.12, p.S85-S85

2011

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Pure versus complicated vulvar vestibulitis: a randomized trial of fluconazole treatment

Gynecologic and obstetric investigation, 2000-01, Vol.50 (3), p.194-197

2000

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P203 Media impact on phenotype and function of an established airway epithelial cell line

Journal of cystic fibrosis, 2020-06, Vol.19, p.S113-S114

2020

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P217 Cystic fibrosis with pancreatic insufficiency is associated with a high incidence of subfertility in women

Journal of cystic fibrosis, 2018-06, Vol.17, p.S121-S121

2018

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P174 Faecal calprotectin in cystic fibrosis patients during respiratory exacerbation

Journal of cystic fibrosis, 2018-06, Vol.17, p.S108-S108

2018

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Salivary gland involvement and oxidative stress in juvenile idiopathic arthritis: novel observation in oligoarticular-type patients

Journal of rheumatology, 2006-12, Vol.33 (12), p.2532

2006

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J11/93 – Vibration response imaging of the lungs in foreign body aspiration

Paediatric respiratory reviews, 2006, Vol.7, p.S313-S313

2006

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WS18.5 Nasal potential difference and sweat chloride responses to ivacaftor correlate in three patients with non-p.Gly551Asp gating mutations

The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews

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

WS15.5 Electrophysiological tests in CF diagnosis: nasal potential difference is more predictive than sweat test – single center study

Salivary profile and oxidative stress in children and adolescents with cystic fibrosis

223 Infertility among women with cystic fibrosis: prevalence and risk factors

P082 Optimizing CFTR modulator therapy management for cystic fibrosis through the ReX platform

297 Arab cystic fibrosis patients in Israel

120 Duplication in CHIT1 gene and the risk for Aspergillus lung disease in CF patients

P293 An intensive protocol for bowel preparation in people with cystic fibrosis undergoing screening colonoscopy, a single centre experience

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

P044 Treatment benefits of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying non-F508del mutations

160 Nasal potential difference in young children is feasible: report from a national referral center

P052 Efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with normal/near normal FEV1 (≥70%)

P214 Real-life evaluation of the multi-organ effects of lumacaftor/ivacaftor (Orkambi) on F508del homozygous cystic fibrosis patients

133 Clinical response to elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with the N1303K and non-modulator responsive mutation

P266 The effect of lumacaftor/ivacaftor on the severity of cystic fibrosis pulmonary exacerbations in patients with F508del homozygous cystic fibrosis

P077 Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutation

Pulmonary outcome of Alport syndrome with familial diffuse esophageal leiomyomatosis

Pure versus complicated vulvar vestibulitis: a randomized trial of fluconazole treatment

P203 Media impact on phenotype and function of an established airway epithelial cell line

P217 Cystic fibrosis with pancreatic insufficiency is associated with a high incidence of subfertility in women

P174 Faecal calprotectin in cystic fibrosis patients during respiratory exacerbation

Salivary gland involvement and oxidative stress in juvenile idiopathic arthritis: novel observation in oligoarticular-type patients

J11/93 – Vibration response imaging of the lungs in foreign body aspiration

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