Carolin Kröner

LMU Klinikum — Germany

Medicine · Health Sciences

13h-index657citations41works3.02yr avg
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Research Topics

Neonatal Respiratory Health Research(9), Cystic Fibrosis Research Advances(7), Immunodeficiency and Autoimmune Disorders(7), Psychopathy, Forensic Psychiatry, Sexual Offending(3), Tracheal and airway disorders(3)

Publications41 total

Single-centre prospective evaluation of the first 5 years of cystic fibrosis newborn screening in Germany
ERJ Open Research·2024· 3 citedOpen Access
Vision to cure lung disease in STAT3-Hyper IgE syndrome
Klinische Pädiatrie·2022
Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential
Orphanet Journal of Rare Diseases·2020· 16 citedOpen Access
Retained primary teeth in STAT3 hyper-IgE syndrome: Early intervention in childhood is essential
2019· 3 citedOpen Access
Impaired memory B‐cell development and antibody maturation with a skewing toward IgE in patients with STAT3 hyper‐IgE syndrome
Allergy·2019· 40 citedOpen Access
Lung disease in <scp>STAT</scp>3 hyper‐IgE syndrome requires intense therapy
Allergy·2019· 25 cited
Lung disease caused by<i>ABCA3</i>mutations
Thorax·2016· 146 citedOpen Access
Eradication of methicillin resistant<i>Staphylococcus aureus</i>detected for the first time in cystic fibrosis: A single center observational study
Pediatric Pulmonology·2016· 32 cited
Tools to explore ABCA3 mutations causing interstitial lung disease
Pediatric Pulmonology·2016· 24 cited
Categorizing diffuse parenchymal lung disease in children
Orphanet Journal of Rare Diseases·2015· 52 citedOpen Access
GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders
BMC Pulmonary Medicine·2015· 73 citedOpen Access
Genotype alone does not predict the clinical course of<i>SFTPC</i>deficiency in paediatric patients
European Respiratory Journal·2015· 90 citedOpen Access
Endobronchial Lesions Caused by Nontuberculous Mycobacteria in Apparently Healthy Pediatric Patients
The Pediatric Infectious Disease Journal·2014· 10 cited
Mutation alone does not predict the clinical course of surfactant protein C deficiency in children
2014
The chemokine CCL18 characterises<i>Pseudomonas</i>infections in cystic fibrosis lung disease
European Respiratory Journal·2014· 17 citedOpen Access
The basidiomycetous yeast Trichosporon may cause severe lung exacerbation in cystic fibrosis patients – clinical analysis of Trichosporonpositive patients in a Munich cohort
BMC Pulmonary Medicine·2013· 28 citedOpen Access
Surfactant dysfunction and alveolar proteinosis
European Respiratory Society eBooks·2013
Molecular Epidemiology of Nontuberculous Mycobacteria in a German CF Center and Clinical Course of NTM Positive Patients
Open Journal of Medical Microbiology·2013· 2 citedOpen Access
Erkrankungen des Verdauungstrakts
Springer-Lehrbuch·2010
Erkrankungen des Nervensystems
Springer-Lehrbuch·2010· 1 cited
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Frequent Co-authors

Berthold Koletzko(20), Matthias Griese(14), Matthias Kappler(9), Ralf Zarbock(6), Simone Reu(5), Frank Brasch(5), Beate Hagl(5), Ellen D. Renner(5), Peter Lohse(4), Ann-Christin Grimmelt(4), Benedikt D. Spielberger(4), Thomas Wittmann(3), Veronika Teusch(3), Meike Hengst(3), Andrea Schams(3), Maria Feilcke(3), Ingo Pawlita(3), Jens Neumann(3), Iris Meixner(3), Gregor Dückers(3)