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Mukoviszidose – eine Erfolgsgeschichte der Kinderheilkunde

Monatsschrift Kinderheilkunde, 2023-07

Dittrich, Anna-Maria

2023

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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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The Anion Channel TMEM16a/Ano1 Modulates CFTR Activity, but Does Not Function as an Apical Anion Channel in Colonic Epithelium from Cystic Fibrosis Patients and Healthy Individuals

International journal of molecular sciences, 2023-09, Vol.24 (18), p.14214

2023

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IL-27 Is Essential for Suppression of Experimental Allergic Asthma by the TLR7/8 Agonist R848 (Resiquimod)

The Journal of immunology (1950), 2016-12, Vol.197 (11), p.4219-4227

2016

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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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The human respiratory tract microbial community structures in healthy and cystic fibrosis infants

NPJ biofilms and microbiomes, 2020-12, Vol.6 (1), p.61-61, Article 61

2020

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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-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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Differential effects of ELX/TEZ/IVA on organ-specific CFTR function in two patients with the rare CFTR splice mutations c.273+1G>A and c.165-2A>G

Frontiers in pharmacology, 2023, Vol.14, p.1153656-1153656

2023

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Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy

Frontiers in pharmacology, 2023-01, Vol.14, p.1114584-1114584

2023

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

Frontiers in pharmacology, 2023-07, Vol.14, p.1171544-1171544

2023

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A Fast Scoring of Human Primary Respiratory Epithelia Grown at Air-Liquid Interface (ALI) to Assess Epithelial Morphology in Research and Personalized Medicine Settings

Journal of personalized medicine, 2024-01, Vol.14 (1), p.109

2024

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Interleukin‐17A and interleukin‐22 production by conventional and non‐conventional lymphocytes in three different end‐stage lung diseases

Clinical & translational immunology, 2022, Vol.11 (6), p.e1398-n/a

2022

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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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Delineating the role of histamine-1- and -4-receptors in a mouse model of Th2-dependent antigen-specific skin inflammation

PloS one, 2014-02, Vol.9 (2), p.e87296-e87296

2014

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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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TRACK-CF prospective cohort study: Understanding early cystic fibrosis lung disease

Frontiers in medicine, 2023-01, Vol.9, p.1034290-1034290

2023

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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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Severity of Allergic Airway Disease Due to House Dust Mite Allergen Is Not Increased after Clinical Recovery of Lung Infection with Chlamydia pneumoniae in Mice

Infection and Immunity, 2013-09, Vol.81 (9), p.3366-3374

2013

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Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on Lung Clearance Index and Magnetic Resonance Imaging in Patients with Cystic Fibrosis and One or Two F508del Alleles

American journal of respiratory and critical care medicine, 2022-08, Vol.206 (3), p.311-320

2022

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Mukoviszidose – eine Erfolgsgeschichte der Kinderheilkunde

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

The Anion Channel TMEM16a/Ano1 Modulates CFTR Activity, but Does Not Function as an Apical Anion Channel in Colonic Epithelium from Cystic Fibrosis Patients and Healthy Individuals

IL-27 Is Essential for Suppression of Experimental Allergic Asthma by the TLR7/8 Agonist R848 (Resiquimod)

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

The human respiratory tract microbial community structures in healthy and cystic fibrosis infants

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

Differential effects of ELX/TEZ/IVA on organ-specific CFTR function in two patients with the rare CFTR splice mutations c.273+1G>A and c.165-2A>G

Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy

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

A dual center and dual vendor comparison study of automated perfusion‐weighted phase‐resolved functional lung magnetic resonance imaging with dynamic contrast‐enhanced magnetic resonance imaging in patients with cystic fibrosis

A Fast Scoring of Human Primary Respiratory Epithelia Grown at Air-Liquid Interface (ALI) to Assess Epithelial Morphology in Research and Personalized Medicine Settings

Interleukin‐17A and interleukin‐22 production by conventional and non‐conventional lymphocytes in three different end‐stage lung diseases

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

Delineating the role of histamine-1- and -4-receptors in a mouse model of Th2-dependent antigen-specific skin inflammation

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

TRACK-CF prospective cohort study: Understanding early cystic fibrosis lung disease

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

Multicentre feasibility of multiple-breath washout in preschool children with cystic fibrosis and other lung diseases

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

Severity of Allergic Airway Disease Due to House Dust Mite Allergen Is Not Increased after Clinical Recovery of Lung Infection with Chlamydia pneumoniae in Mice

Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on Lung Clearance Index and Magnetic Resonance Imaging in Patients with Cystic Fibrosis and One or Two F508del Alleles

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