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A Higher Tidal Volume May Be Used for Athletes according to Measured FVC

TheScientificWorld, 2013-01, Vol.2013 (1), p.526138-526138

2013

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ePS04.1 Cleaning and infection control of devices in CF patients

Journal of cystic fibrosis, 2016-06, Vol.15, p.S43-S43

2016

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Clinical implication of lung fluid balance in the perinatal period

Journal of perinatology, 2011-04, Vol.31 (4), p.230-235

2011

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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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Evaluation of the health effects of occupational exposure of analytic laboratory workers processing illicit drug investigation files

Clinical toxicology (Philadelphia, Pa.), 2013-05, Vol.51 (4), p.237-242

2013

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299 Cultural differences in illness perception and treatment adherence

Journal of cystic fibrosis, 2015-06, Vol.14, p.S134-S134

2015

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113 Compassionate nitric oxide adjuvant treatment of persistent Mycobacterium infection in cystic fibrosis patients

Journal of cystic fibrosis, 2017-06, Vol.16, p.S94-S94

2017

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176 The effect of treatment with intermittent inhaled tobramycin powder on systemic cytokines response in CF patients colonized with Pseudomonas aeruginosa

Journal of cystic fibrosis, 2017-06, Vol.16, p.S111-S112

2017

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WS01.2 Phase II clinical trial results of alidornase alfa for the treatment of cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S1-S1

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

229 The use of telehealth (WhatsApp and Skype based communication) in patients with cystic fibrosis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S109-S109

2016

Volltextzugriff (PDF)

EPS2.6 Prevalence and characteristics of attention deficit hyperactivity disorder in patients with cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S40-S40

2017

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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

Volltextzugriff (PDF)

Wheeze monitoring in children for assessment of nocturnal asthma and response to therapy

The European respiratory journal, 2003-04, Vol.21 (4), p.621-626

2003

Volltextzugriff (PDF)

Prevalence of rhinosinusitis among atypical cystic fibrosis patients

European archives of oto-rhino-laryngology, 2011-04, Vol.268 (4), p.519-524

2011

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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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301 Our adaptive means to encourage treatment adherence in CF patients

Journal of cystic fibrosis, 2012-06, Vol.11, p.S134-S134

2012

Volltextzugriff (PDF)

Foreign-body aspiration as an aetiology for brain abscess

Archives of disease in childhood, 2009-08, Vol.94 (8), p.601-601

2009

Volltextzugriff (PDF)

300 Prevalence and characteristics of attention deficit hyperactivity disorder (ADHD) in patients with cystic fibrosis (CF)

Journal of cystic fibrosis, 2015-06, Vol.14, p.S134-S134

2015

Volltextzugriff (PDF)

P201 Clinical significance of mucor in airway culture of immunocompetent patients with cystic fibrosis and other chronic lung diseases

Journal of cystic fibrosis, 2024-06, Vol.23, p.S131-S131

2024

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147 Causes of failure to eradicate Pseudomonas aeruginosa in patients with CF

Journal of cystic fibrosis, 2014-06, Vol.13, p.S84-S84

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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P081 Theratyping – extending the success of highly effective CFTR modulators to rare mutations

Journal of cystic fibrosis, 2023-06, Vol.22, p.S88-S88

2023

Volltextzugriff (PDF)

Nasal potential difference measurements in patients with atypical cystic fibrosis

The European respiratory journal, 2001-06, Vol.17 (6), p.1208-1215

2001

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A Higher Tidal Volume May Be Used for Athletes according to Measured FVC

ePS04.1 Cleaning and infection control of devices in CF patients

Clinical implication of lung fluid balance in the perinatal period

The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews

Evaluation of the health effects of occupational exposure of analytic laboratory workers processing illicit drug investigation files

299 Cultural differences in illness perception and treatment adherence

113 Compassionate nitric oxide adjuvant treatment of persistent Mycobacterium infection in cystic fibrosis patients

176 The effect of treatment with intermittent inhaled tobramycin powder on systemic cytokines response in CF patients colonized with Pseudomonas aeruginosa

WS01.2 Phase II clinical trial results of alidornase alfa for the treatment of cystic fibrosis

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

229 The use of telehealth (WhatsApp and Skype based communication) in patients with cystic fibrosis

EPS2.6 Prevalence and characteristics of attention deficit hyperactivity disorder in patients with cystic fibrosis

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

Wheeze monitoring in children for assessment of nocturnal asthma and response to therapy

Prevalence of rhinosinusitis among atypical cystic fibrosis patients

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

301 Our adaptive means to encourage treatment adherence in CF patients

Foreign-body aspiration as an aetiology for brain abscess

300 Prevalence and characteristics of attention deficit hyperactivity disorder (ADHD) in patients with cystic fibrosis (CF)

P201 Clinical significance of mucor in airway culture of immunocompetent patients with cystic fibrosis and other chronic lung diseases

147 Causes of failure to eradicate Pseudomonas aeruginosa in patients with CF

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

P081 Theratyping – extending the success of highly effective CFTR modulators to rare mutations

Nasal potential difference measurements in patients with atypical cystic fibrosis

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