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Allergen extract‐ and component‐based diagnostics in children of the ALLIANCE asthma cohort

Clinical and experimental allergy, 2021-10, Vol.51 (10), p.1331-1345

2021

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Use of elexacaftor/tezacaftor/ivacaftor leads to changes in detection frequencies of Staphylococcus aureus and Pseudomonas aeruginosa dependent on age and lung function in people with cystic fibrosis

International journal of infectious diseases, 2024-02, Vol.139, p.124-131

2024

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Gene correction of human induced pluripotent stem cells repairs the cellular phenotype in pulmonary alveolar proteinosis

American journal of respiratory and critical care medicine, 2014-01, Vol.189 (2), p.167-182

2014

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Impact of Elexacaftor/Tezacaftor/Ivacaftor Therapy on the Cystic Fibrosis Airway Microbial Metagenome

Microbiology spectrum, 2022-10, Vol.10 (5), p.e0145422

2022

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The all age asthma cohort (ALLIANCE) - from early beginnings to chronic disease: a longitudinal cohort study

BMC pulmonary medicine, 2018-08, Vol.18 (1), p.140-140, Article 140

2018

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Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two F508del Alleles

American journal of respiratory and critical care medicine, 2022-03, Vol.205 (5), p.540-549

2022

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Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test

BMJ open respiratory research, 2020-10, Vol.7 (1), p.e000736

2020

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Preventive Inhalation of Hypertonic Saline in Infants with Cystic Fibrosis (PRESIS). A Randomized, Double-Blind, Controlled Study

American journal of respiratory and critical care medicine, 2019-05, Vol.199 (10), p.1238-1248

2019

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Listen Carefully: The Hairy Polyp as an Unusual Cause of Neonatal Stridor

American journal of respiratory and critical care medicine, 2019-10, Vol.200 (7), p.924-925

2019

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Lung transplantation for end-stage cystic fibrosis before and after the availability of elexacaftor-tezacaftor-ivacaftor, Germany, 2012-2021

The European respiratory journal, 2023-01, Vol.61 (1), p.2201402

2023

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IL-17A from innate and adaptive lymphocytes contributes to inflammation and damage in cystic fibrosis lung disease

The European respiratory journal, 2021-06, Vol.57 (6), p.1900716

2021

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Analysis of CF patient survival confirms STAT3 as a CF-modifying gene with changing impact over time

Human molecular genetics, 2023-01, Vol.32 (4), p.543-550

2023

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Analysis of CFTR mRNA and Protein in Peripheral Blood Mononuclear Cells via Quantitative Real-Time PCR and Western Blot

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6367

2024

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COL4A3 is degraded in allergic asthma and degradation predicts response to anti-IgE therapy

The European respiratory journal, 2021-12, Vol.58 (6), p.2003969

2021

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Comparison of Three Eradication Treatment Protocols for Pseudomonas Aeruginosa in Children and Adolescents with Cystic Fibrosis

Klinische Padiatrie, 2023-03, Vol.235 (2), p.75-83

2023

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Flow Volume Loop and Regional Ventilation Assessment Using Phase-Resolved Functional Lung (PREFUL) MRI: Comparison With 129 Xenon Ventilation MRI and Lung Function Testing

Journal of magnetic resonance imaging, 2021-04, Vol.53 (4), p.1092-1105

2021

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Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del- CFTR Homozygous Patient Populations

Genes, 2021-09, Vol.12 (10), p.1554

2021

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Effects of Lumacaftor/Ivacaftor on Cystic Fibrosis Disease Progression in Children 2 through 5 Years of Age Homozygous for F508del-CFTR : A Phase 2 Placebo-controlled Clinical Trial

Annals of the American Thoracic Society, 2023-08, Vol.20 (8), p.1144-1155

2023

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PREFUL MRI for Monitoring Perfusion and Ventilation Changes after Elexacaftor-Tezacaftor-Ivacaftor Therapy for Cystic Fibrosis: A Feasibility Study

Radiology. Cardiothoracic imaging, 2024-04, Vol.6 (2), p.e230104-e230104

2024

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X-linked agammaglobulinaemia and Pneumocystis carinii pneumonia: an unusual coincidence?

European journal of pediatrics, 2003-06, Vol.162 (6), p.432-433

2003

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NEMO mutations in 2 unrelated boys with severe infections and conical teeth

Pediatrics (Evanston), 2005-05, Vol.115 (5), p.e615-e619

2005

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17q21 Variants Disturb Mucosal Host Defense in Childhood Asthma

American journal of respiratory and critical care medicine, 2024-04, Vol.209 (8), p.947-959

2024

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Validation of the Asthma Severity Scoring System (ASSESS) in the ALLIANCE Cohort

Journal of allergy and clinical immunology, 2023-06, Vol.151 (6), p.1525-1535.e4

2023

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Rapid Whole Blood Flow Cytometric Test to Detect ICOS Deficiency in Patients with Common Variable Immunodeficiency

International Archives of Allergy and Immunology, 2006-01, Vol.140 (4), p.342-344

2006

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Different isoforms of glutathione peroxidase cause opposing effects during the development of allergic asthma in mice

Antioxidants & redox signaling, 2011-01, Vol.14 (1), p.169-170

2011

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Allergen extract‐ and component‐based diagnostics in children of the ALLIANCE asthma cohort

Use of elexacaftor/tezacaftor/ivacaftor leads to changes in detection frequencies of Staphylococcus aureus and Pseudomonas aeruginosa dependent on age and lung function in people with cystic fibrosis

Gene correction of human induced pluripotent stem cells repairs the cellular phenotype in pulmonary alveolar proteinosis

Impact of Elexacaftor/Tezacaftor/Ivacaftor Therapy on the Cystic Fibrosis Airway Microbial Metagenome

The all age asthma cohort (ALLIANCE) - from early beginnings to chronic disease: a longitudinal cohort study

Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two F508del Alleles

Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test

Preventive Inhalation of Hypertonic Saline in Infants with Cystic Fibrosis (PRESIS). A Randomized, Double-Blind, Controlled Study

Listen Carefully: The Hairy Polyp as an Unusual Cause of Neonatal Stridor

Lung transplantation for end-stage cystic fibrosis before and after the availability of elexacaftor-tezacaftor-ivacaftor, Germany, 2012-2021

IL-17A from innate and adaptive lymphocytes contributes to inflammation and damage in cystic fibrosis lung disease

Analysis of CF patient survival confirms STAT3 as a CF-modifying gene with changing impact over time

Analysis of CFTR mRNA and Protein in Peripheral Blood Mononuclear Cells via Quantitative Real-Time PCR and Western Blot

COL4A3 is degraded in allergic asthma and degradation predicts response to anti-IgE therapy

Comparison of Three Eradication Treatment Protocols for Pseudomonas Aeruginosa in Children and Adolescents with Cystic Fibrosis

Flow Volume Loop and Regional Ventilation Assessment Using Phase-Resolved Functional Lung (PREFUL) MRI: Comparison With 129 Xenon Ventilation MRI and Lung Function Testing

Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del- CFTR Homozygous Patient Populations

Effects of Lumacaftor/Ivacaftor on Cystic Fibrosis Disease Progression in Children 2 through 5 Years of Age Homozygous for F508del-CFTR : A Phase 2 Placebo-controlled Clinical Trial

PREFUL MRI for Monitoring Perfusion and Ventilation Changes after Elexacaftor-Tezacaftor-Ivacaftor Therapy for Cystic Fibrosis: A Feasibility Study

X-linked agammaglobulinaemia and Pneumocystis carinii pneumonia: an unusual coincidence?

NEMO mutations in 2 unrelated boys with severe infections and conical teeth

17q21 Variants Disturb Mucosal Host Defense in Childhood Asthma

Validation of the Asthma Severity Scoring System (ASSESS) in the ALLIANCE Cohort

Rapid Whole Blood Flow Cytometric Test to Detect ICOS Deficiency in Patients with Common Variable Immunodeficiency

Different isoforms of glutathione peroxidase cause opposing effects during the development of allergic asthma in mice

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