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Cytokine levels in children and adults with wheezing and asthma show specific patterns of variability over time

Clinical and experimental immunology, 2021-04, Vol.204 (1), p.152-164

2021

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ePS05.7 Individual caloric intake in cystic fibrosis (CF) – how to calculate?

Journal of cystic fibrosis, 2015-06, Vol.14, p.S51-S51

2015

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81 Specific IgE production against Staphylococcus aureus, Escherichia coli, Hemophilus influenzae and pneumococci in cystic fibrosis patients

Journal of cystic fibrosis, 2017-06, Vol.16, p.S85-S85

2017

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Atypische Mukoviszidose: Erst durch chronische Rhinosinusitis diagnostiziert

HNO, 2009-08, Vol.57 (8), p.804-807

2009

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Acute lymphoblastic leukemia in a 10-year-old boy with cystic fibrosis - improvement of pulmonary function during chemotherapy in spite of intermittent Pseudomonas aeruginosa colonisation

Klinische Padiatrie, 2011-11, Vol.223 (6), p.368-369

2011

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WS21.06 The β-adrenergic sweat secretion test using the AutoBuSTeD software is a novel, high-sensitive CFTR biomarker for patients with inconclusive CFTR genotype and sweat chloride concentration

Journal of cystic fibrosis, 2022-06, Vol.21, p.S41

2022

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P053 Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depend on age and lung disease severity

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

2023

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10-year-old girl with severe edema caused by adder bite

Klinische Padiatrie, 2010-12, Vol.222 (7), p.460

2010

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First colonisation with P. aeruginosa – only detected in the upper airways – eradicated with sinonasal inhalation of Tobramycin

Journal of cystic fibrosis, 2009, Vol.8, p.S69-S69

2009

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Niedrige Seroprävalenz von Hepatitis C bei Flüchtlingen in Deutschland im Jahr 2015

Notfall & Rettungsmedizin, 2017-02, Vol.20 (1), p.1-5

2017

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P010 Newborn screening for cystic fibrosis improves nutritional outcome: monocentric data of the first 4 years in Germany

Journal of cystic fibrosis, 2021, Vol.20, p.S41

2021

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EPS3.08 Evaluation of a fixed-step eradication regime in children with cystic fibrosis and detection of Pseudomonas aeruginosa

Journal of cystic fibrosis, 2021, Vol.20, p.S37

2021

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EPS2.07 Intestinal current and nasal potential difference index cases: diagnostic features of subjects with CFTR-related disorder

Journal of cystic fibrosis, 2018-06, Vol.17, p.S40-S40

2018

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Impact of allergic sensitization on CF-associated chronic rhinosinusitis – Results from a multicentre interdisciplinary study

Journal of cystic fibrosis, 2009, Vol.8, p.S108-S108

2009

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WS09.1 ICM and NPD diagnostics of cases with inconclusive CFTR genetics and sweat test: a single-centre 10-year experience

Journal of cystic fibrosis, 2020-06, Vol.19, p.S15-S15

2020

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Die Mukoviszidose Transitionsambulanz an der Medizinischen Hochschule Hannover

Pneumologie (Stuttgart, Germany), 2014, Vol.68 (S 01)

2014

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WS14.3 Randomised, double-blind, controlled pilot study on safety and efficacy of hypertonic saline as preventive inhalation therapy in infants with CF (PRESIS)

Journal of cystic fibrosis, 2018-06, Vol.17, p.S25-S26

2018

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EPS3.03 Effects of lumacaftor-ivacaftor therapy on CFTR function in Phe508del homozygous patients with cystic fibrosis

Journal of cystic fibrosis, 2018-06, Vol.17, p.S41-S42

2018

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10-Year-Old Girl with Severe Edema Caused by Adder Bite

Klinische Pädiatrie, 2010-12, Vol.222 (7), p.460-461

2010

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Terminale Lungeninsuffizienz bei milder Mukoviszidose?

Pneumologie (Stuttgart, Germany), 2009-04, Vol.63 (4), p.231-234

2009

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Intestinal Current Measurements Detect Activation of Mutant CFTR in Cystic Fibrosis Patients with the G551D Mutation Treated with Ivacaftor

Pneumologie (Stuttgart, Germany), 2015, Vol.69 (7)

2015

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Atypical cystic fibrosis. First diagnosed by chronic rhinosinusitis

HNO, 2009-08, Vol.57 (8), p.804-807

2009

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Terminal pulmonary insufficiency due to mild cystic fibrosis?

Pneumologie (Stuttgart, Germany), 2009-04, Vol.63 (4), p.231

2009

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Atypical cystic fibrosis. First diagnosed by chronic rhinosinusitis

HNO, 2009-08, Vol.57 (8), p.804

2009

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Wertschöpfungskompetenz und Unternehmertum: Rahmenbedingungen Für Entrepreneurship und Innovation in Regionen

2014, 2013

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Cytokine levels in children and adults with wheezing and asthma show specific patterns of variability over time

ePS05.7 Individual caloric intake in cystic fibrosis (CF) – how to calculate?

81 Specific IgE production against Staphylococcus aureus, Escherichia coli, Hemophilus influenzae and pneumococci in cystic fibrosis patients

Atypische Mukoviszidose: Erst durch chronische Rhinosinusitis diagnostiziert

Acute lymphoblastic leukemia in a 10-year-old boy with cystic fibrosis - improvement of pulmonary function during chemotherapy in spite of intermittent Pseudomonas aeruginosa colonisation

WS21.06 The β-adrenergic sweat secretion test using the AutoBuSTeD software is a novel, high-sensitive CFTR biomarker for patients with inconclusive CFTR genotype and sweat chloride concentration

P053 Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depend on age and lung disease severity

10-year-old girl with severe edema caused by adder bite

First colonisation with P. aeruginosa – only detected in the upper airways – eradicated with sinonasal inhalation of Tobramycin

Niedrige Seroprävalenz von Hepatitis C bei Flüchtlingen in Deutschland im Jahr 2015

P010 Newborn screening for cystic fibrosis improves nutritional outcome: monocentric data of the first 4 years in Germany

EPS3.08 Evaluation of a fixed-step eradication regime in children with cystic fibrosis and detection of Pseudomonas aeruginosa

EPS2.07 Intestinal current and nasal potential difference index cases: diagnostic features of subjects with CFTR-related disorder

Impact of allergic sensitization on CF-associated chronic rhinosinusitis – Results from a multicentre interdisciplinary study

WS09.1 ICM and NPD diagnostics of cases with inconclusive CFTR genetics and sweat test: a single-centre 10-year experience

Die Mukoviszidose Transitionsambulanz an der Medizinischen Hochschule Hannover

WS14.3 Randomised, double-blind, controlled pilot study on safety and efficacy of hypertonic saline as preventive inhalation therapy in infants with CF (PRESIS)

EPS3.03 Effects of lumacaftor-ivacaftor therapy on CFTR function in Phe508del homozygous patients with cystic fibrosis

10-Year-Old Girl with Severe Edema Caused by Adder Bite

Terminale Lungeninsuffizienz bei milder Mukoviszidose?

Intestinal Current Measurements Detect Activation of Mutant CFTR in Cystic Fibrosis Patients with the G551D Mutation Treated with Ivacaftor

Atypical cystic fibrosis. First diagnosed by chronic rhinosinusitis

Terminal pulmonary insufficiency due to mild cystic fibrosis?

Atypical cystic fibrosis. First diagnosed by chronic rhinosinusitis

Wertschöpfungskompetenz und Unternehmertum: Rahmenbedingungen Für Entrepreneurship und Innovation in Regionen

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