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Aspergillus fumigatus chronic colonization and lung function decline in cystic fibrosis may have a two-way relationship

European journal of clinical microbiology & infectious diseases, 2015-11, Vol.34 (11), p.2235-2241

2015

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13 Cases of false negative cystic fibrosis newborn screening in Greece

Journal of cystic fibrosis, 2016-06, Vol.15, p.S54-S54

2016

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Rabies outbreak in Greece during 2012–2014: use of Geographical Information System for analysis, risk assessment and control

Epidemiology and infection, 2016-10, Vol.144 (14), p.3068-3079

2016

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230 History of meconium ileus is associated with low fat tissue mass in children and adolescents with cystic fibrosis

Journal of cystic fibrosis, 2015-06, Vol.14, p.S117-S117

2015

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Bovine rabies in Greece in 2013

Veterinary record, 2015-12, Vol.177 (23), p.598-598

2015

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182 Chronic Pseudomonas aeruginosa infection and respiratory muscle impairment in cystic fibrosis

Journal of cystic fibrosis, 2013-06, Vol.12, p.S95-S95

2013

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Re-emergence of animal rabies in northern Greece and subsequent human exposure, October 2012 – March 2013

Euro surveillance : bulletin européen sur les maladies transmissibles, 2013-05, Vol.18 (18), p.1

2013

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24 Basophil Activation Test may facilitate ABPA diagnosis in CF patients

Journal of cystic fibrosis, 2015-06, Vol.14, p.S63-S63

2015

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ePS04.6 Aspergillus fumigatus chronic colonization and lung function decline in CF may have a two-way relationship

Journal of cystic fibrosis, 2015-06, Vol.14, p.S49-S49

2015

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154 Scedosporium apiospermum isolation in cystic fibrosis patients

Journal of cystic fibrosis, 2014-06, Vol.13, p.S86-S86

2014

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173 Basophil activation test: A novel approach to the diagnosis of allergic bronchopulmonary aspergillosis in cystic fibrosis patients

Journal of cystic fibrosis, 2013-06, Vol.12, p.S92-S92

2013

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169 Exercise and respiratory muscle function in patients with cystic fibrosis

Journal of cystic fibrosis, 2012-06, Vol.11, p.S100-S100

2012

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152 Inhaled antibiotics and Candida albicans chronic colonization in cystic fibrosis

Journal of cystic fibrosis, 2014-06, Vol.13, p.S85-S85

2014

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CFTR gene mutations - including three novel nucleotide substitutions - and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease

Human genetics, 2001-03, Vol.108 (3), p.216-221

2001

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96 Aspergillus spp. and Candida spp. detection in CF children: implications on lung function and hospitalizations

Journal of cystic fibrosis, 2012-06, Vol.11, p.S81-S81

2012

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Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis

Clinical genetics, 2007-05, Vol.71 (5), p.451-457

2007

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231 Respiratory muscle function in patients with cystic fibrosis

Journal of cystic fibrosis, 2011, Vol.10, p.S58-S58

2011

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Identification of novel mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene in the Greek population

Journal of cystic fibrosis, 2010, Vol.9, p.S12-S12

2010

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Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individuals

Clinical genetics, 2003-05, Vol.63 (5), p.400-409

2003

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Renal hyperechogenicity: a newly recognized complication of severe dehydration in infants with cystic fibrosis

Journal of cystic fibrosis, 2010, Vol.9, p.S121-S121

2010

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Voriconazole therapy in children with cystic fibrosis and steroid-dependant allergic bronchopulmonary aspergillosis: Efficacy and adverse effects

Journal of cystic fibrosis, 2009, Vol.8, p.S57-S57

2009

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Dehydration: a common clinical feature suggesting the diagnosis of CF in Greece

Journal of cystic fibrosis, 2008-06, Vol.7, p.S11-S11

2008

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Atopic background as a risk factor for allergic bronchopulmonary aspergillosis in cystic fibrosis (CF) patients

Journal of cystic fibrosis, 2008-06, Vol.7, p.S53-S53

2008

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Scedosporium apiospermum colonization in cystic fibrosis patients: incidence and clinical outcome

Journal of cystic fibrosis, 2010, Vol.9, p.S36-S36

2010

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Thyroid dysfunction in newly diagnosed cystic fibrosis patients with pancreatic insufficiency and restitution with enzyme therapy

Journal of cystic fibrosis, 2009, Vol.8, p.S83-S83

2009

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Aspergillus fumigatus chronic colonization and lung function decline in cystic fibrosis may have a two-way relationship

13 Cases of false negative cystic fibrosis newborn screening in Greece

Rabies outbreak in Greece during 2012–2014: use of Geographical Information System for analysis, risk assessment and control

230 History of meconium ileus is associated with low fat tissue mass in children and adolescents with cystic fibrosis

Bovine rabies in Greece in 2013

182 Chronic Pseudomonas aeruginosa infection and respiratory muscle impairment in cystic fibrosis

Re-emergence of animal rabies in northern Greece and subsequent human exposure, October 2012 – March 2013

24 Basophil Activation Test may facilitate ABPA diagnosis in CF patients

ePS04.6 Aspergillus fumigatus chronic colonization and lung function decline in CF may have a two-way relationship

154 Scedosporium apiospermum isolation in cystic fibrosis patients

173 Basophil activation test: A novel approach to the diagnosis of allergic bronchopulmonary aspergillosis in cystic fibrosis patients

169 Exercise and respiratory muscle function in patients with cystic fibrosis

152 Inhaled antibiotics and Candida albicans chronic colonization in cystic fibrosis

CFTR gene mutations - including three novel nucleotide substitutions - and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease

96 Aspergillus spp. and Candida spp. detection in CF children: implications on lung function and hospitalizations

Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis

231 Respiratory muscle function in patients with cystic fibrosis

Identification of novel mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene in the Greek population

Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individuals

Renal hyperechogenicity: a newly recognized complication of severe dehydration in infants with cystic fibrosis

Voriconazole therapy in children with cystic fibrosis and steroid-dependant allergic bronchopulmonary aspergillosis: Efficacy and adverse effects

Dehydration: a common clinical feature suggesting the diagnosis of CF in Greece

Atopic background as a risk factor for allergic bronchopulmonary aspergillosis in cystic fibrosis (CF) patients

Scedosporium apiospermum colonization in cystic fibrosis patients: incidence and clinical outcome

Thyroid dysfunction in newly diagnosed cystic fibrosis patients with pancreatic insufficiency and restitution with enzyme therapy

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