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Nutritional Status in Childhood as a Prognostic Factor in Patients with Cystic Fibrosis

Lung, 2019-06, Vol.197 (3), p.371-376

2019

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Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis [Erratum]

Journal of asthma and allergy, 2018-01, Vol.11, p.245-246

2018

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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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167 Growing flow to volume dysanapsis in cystic fibrosis – a predictor for lung transplantation?

Journal of cystic fibrosis, 2012-06, Vol.11, p.S99-S99

2012

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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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P073 Clinical efficacy of CFTR modulator therapy in patients carrying the I1234V mutation

Journal of cystic fibrosis, 2023-06, Vol.22, p.S85-S85

2023

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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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Erratum: Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis [Erratum]

Journal of asthma and allergy, 2018, Vol.11, p.245-245

2018

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Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis [Erratum]

Journal of asthma and allergy, 2018-01, Vol.11, p.245

2018

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WS11.1 Response to CFTR modulators in organoids from patients with cystic fibrosis as a tool to select candidates to treatment

Journal of cystic fibrosis, 2020-06, Vol.19, p.S18-S18

2020

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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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A76 WHAT'S IN THE TOOL BOX TO ASSESS LUNG FUNCTION: Difference Between Maximal And Submaximal Effort On Fev1 - Possible Connection To Tracheomegalia In Cystic Fibrosis

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

2017

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Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis

Journal of asthma and allergy, 2018-01, Vol.11, p.101-107

2018

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WS03.3 Childhood nutritional status is a major factor determining lung function in adults with cystic fibrosis

Journal of cystic fibrosis, 2018-06, Vol.17, p.S6-S6

2018

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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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Endocrine abnormalities in ataxia telangiectasia: findings from a national cohort

Pediatric research, 2016-06, Vol.79 (6), p.889-894

2016

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Functional parameter measurements in children with ataxia telangiectasia

Developmental medicine and child neurology, 2020-02, Vol.62 (2), p.207-213

2020

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Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis

The European respiratory journal, 2021-01, Vol.57 (1), p.1902426

2021

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Elevated IgM levels as a marker for a unique phenotype in patients with Ataxia telangiectasia

BMC pediatrics, 2018-06, Vol.18 (1), p.185-185, Article 185

2018

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The Viewpoints of Social Studies Teachers on the Role of Social Studies Education in Promoting the Culture of Self-Sacrifice and Martyrdom among Students

Masāʼil-i kārburdī-i taʻlīm va tarbīyat-i Islāmī, 2017-08, Vol.2 (4), p.123-142

2017

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Cough characteristics and FVC maneuver in cystic fibrosis

Respiratory care, 2014-12, Vol.59 (12), p.1912-1917

2014

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Progressive Flow-to-Volume Dysanapsis in Cystic Fibrosis: A Predictor for Lung Transplantation?

American journal of respiratory and critical care medicine, 2012-07, Vol.186 (1), p.82-87

2012

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Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis

World journal of gastroenterology : WJG, 2015-01, Vol.21 (1), p.318-325

2015

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Phenotypic and molecular characteristics of CF patients carrying the I1234V mutation

Respiratory medicine, 2020-08, Vol.170, p.106027-106027, Article 106027

2020

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Failure to conceive in women with CF is associated with pancreatic insufficiency and advancing age

Journal of cystic fibrosis, 2019-07, Vol.18 (4), p.525-529

2019

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Nutritional Status in Childhood as a Prognostic Factor in Patients with Cystic Fibrosis

Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis [Erratum]

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

167 Growing flow to volume dysanapsis in cystic fibrosis – a predictor for lung transplantation?

297 Arab cystic fibrosis patients in Israel

P073 Clinical efficacy of CFTR modulator therapy in patients carrying the I1234V mutation

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

Erratum: Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis [Erratum]

Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis [Erratum]

WS11.1 Response to CFTR modulators in organoids from patients with cystic fibrosis as a tool to select candidates to treatment

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

A76 WHAT'S IN THE TOOL BOX TO ASSESS LUNG FUNCTION: Difference Between Maximal And Submaximal Effort On Fev1 - Possible Connection To Tracheomegalia In Cystic Fibrosis

Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis

WS03.3 Childhood nutritional status is a major factor determining lung function in adults with cystic fibrosis

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

Endocrine abnormalities in ataxia telangiectasia: findings from a national cohort

Functional parameter measurements in children with ataxia telangiectasia

Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis

Elevated IgM levels as a marker for a unique phenotype in patients with Ataxia telangiectasia

The Viewpoints of Social Studies Teachers on the Role of Social Studies Education in Promoting the Culture of Self-Sacrifice and Martyrdom among Students

Cough characteristics and FVC maneuver in cystic fibrosis

Progressive Flow-to-Volume Dysanapsis in Cystic Fibrosis: A Predictor for Lung Transplantation?

Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis

Phenotypic and molecular characteristics of CF patients carrying the I1234V mutation

Failure to conceive in women with CF is associated with pancreatic insufficiency and advancing age

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