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Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus

PloS one, 2016-11, Vol.11 (11), p.e0166220-e0166220

2016

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High Nuclease Activity of Long Persisting Staphylococcus aureus Isolates Within the Airways of Cystic Fibrosis Patients Protects Against NET-Mediated Killing

Frontiers in immunology, 2019-11, Vol.10, p.2552-2552

2019

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Association of Diverse Staphylococcus aureus Populations with Pseudomonas aeruginosa Coinfection and Inflammation in Cystic Fibrosis Airway Infection

mSphere, 2021-06, Vol.6 (3), p.e0035821-e0035821

2021

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Kasuistik einer früh im Lebensverlauf an Morbus Addison erkrankten 14 Jahre alten Patientin bei Verdachtsdiagnose einer Anorexia nervosa: Zum Verwechseln ähnlich und doch so verschieden?

Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 2024-01

2024

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Nasal Staphylococcus aureus Carriage Is Not a Risk Factor for Lower-Airway Infection in Young Cystic Fibrosis Patients

Journal of Clinical Microbiology, 2007-09, Vol.45 (9), p.2979-2984

2007

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Emergence of respiratory Streptococcus agalactiae isolates in cystic fibrosis patients

PloS one, 2009-02, Vol.4 (2), p.e4650-e4650

2009

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Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Journal der Deutschen Dermatologischen Gesellschaft, 2020-07, Vol.18 (7), p.734-736

2020

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Impact of Newborn Screening on Adult Height in Patients With Congenital Adrenal Hyperplasia (CAH)

The journal of clinical endocrinology and metabolism, 2023-10, Vol.108 (11), p.e1199-e1204

2023

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Case Report of a 14-Year-Old Girl with Addison's Disease Under Initial Presumptive Diagnosis of Anorexia Nervosa: Confusingly Similar and Yet so Different?

Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 2024-01

2024

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Increased Prevalence and Resistance of Important Pathogens Recovered from Respiratory Specimens of Cystic Fibrosis Patients During a Decade

The Pediatric infectious disease journal, 2015-07, Vol.34 (7), p.700-705

2015

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Staphylococcus aureus in the airways of cystic fibrosis patients - A retrospective long-term study

International journal of medical microbiology, 2018-08, Vol.308 (6), p.631-639

2018

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Disorders of Pubertal Development

Deutsches Ärzteblatt international, 2009-04

2009

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Extended Staphylococcus aureus persistence in cystic fibrosis is associated with bacterial adaptation

International journal of medical microbiology, 2013-12, Vol.303 (8), p.685-692

2013

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The prevalence of Staphylococcus aureus with mucoid phenotype in the airways of patients with cystic fibrosis—A prospective study

International journal of medical microbiology, 2019-07, Vol.309 (5), p.283-287

2019

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Dermale Osteome als erstes Symptom einer hereditären Albright‐Osteodystrophie bei einem zehn Monate alten Mädchen

Journal der Deutschen Dermatologischen Gesellschaft, 2020-07, Vol.18 (7), p.734-736

2020

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Dermal osteomata as first symptom of Albright’s hereditary osteodystrophy in a 10‐month‐old girl

Journal der Deutschen Dermatologischen Gesellschaft, 2020-07, Vol.18 (7), p.734-736

2020

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Antibiotic Treatment and Age Are Associated With Staphylococcus aureus Carriage Profiles During Persistence in the Airways of Cystic Fibrosis Patients

Frontiers in microbiology, 2020-02, Vol.11, p.230-230

2020

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Prevalence and persistence of Escherichia coli in the airways of cystic fibrosis patients—An unrecognized CF pathogen?

International journal of medical microbiology, 2014-05, Vol.304 (3), p.415-421

2014

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Disorders of pubertal development

Deutsches Ärzteblatt international, 2009-04, Vol.106 (17), p.295-303; quiz 304

2009

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Determination of CFTR densities in erythrocyte plasma membranes using recognition imaging

Nanotechnology, 2008-09, Vol.19 (38), p.384017-384017

2008

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Factor V Leiden, protein C, and lipoprotein (a) in catheter-related thrombosis in childhood: A prospective study

The Journal of pediatrics, 1997-10, Vol.131 (4), p.608-612

1997

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Physiological Concept for a Blood Based CFTR Test

Cellular physiology and biochemistry, 2006-01, Vol.17 (1-2), p.29-36

2006

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Dermal osteomata as first symptom of Albright's hereditary osteodystrophy in a 10-month-old girl

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2020, Vol.18 (7), p.734-736

2020

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Pharmacology of all-trans-retinoic acid in children with acute promyelocytic leukemia

Medical and pediatric oncology, 2003-05, Vol.40 (5), p.293-301

2003

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Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus

High Nuclease Activity of Long Persisting Staphylococcus aureus Isolates Within the Airways of Cystic Fibrosis Patients Protects Against NET-Mediated Killing

Association of Diverse Staphylococcus aureus Populations with Pseudomonas aeruginosa Coinfection and Inflammation in Cystic Fibrosis Airway Infection

Kasuistik einer früh im Lebensverlauf an Morbus Addison erkrankten 14 Jahre alten Patientin bei Verdachtsdiagnose einer Anorexia nervosa: Zum Verwechseln ähnlich und doch so verschieden?

Nasal Staphylococcus aureus Carriage Is Not a Risk Factor for Lower-Airway Infection in Young Cystic Fibrosis Patients

Emergence of respiratory Streptococcus agalactiae isolates in cystic fibrosis patients

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Impact of Newborn Screening on Adult Height in Patients With Congenital Adrenal Hyperplasia (CAH)

Case Report of a 14-Year-Old Girl with Addison's Disease Under Initial Presumptive Diagnosis of Anorexia Nervosa: Confusingly Similar and Yet so Different?

Increased Prevalence and Resistance of Important Pathogens Recovered from Respiratory Specimens of Cystic Fibrosis Patients During a Decade

Staphylococcus aureus in the airways of cystic fibrosis patients - A retrospective long-term study

Disorders of Pubertal Development

Extended Staphylococcus aureus persistence in cystic fibrosis is associated with bacterial adaptation

The prevalence of Staphylococcus aureus with mucoid phenotype in the airways of patients with cystic fibrosis—A prospective study

Dermale Osteome als erstes Symptom einer hereditären Albright‐Osteodystrophie bei einem zehn Monate alten Mädchen

Dermal osteomata as first symptom of Albright’s hereditary osteodystrophy in a 10‐month‐old girl

Antibiotic Treatment and Age Are Associated With Staphylococcus aureus Carriage Profiles During Persistence in the Airways of Cystic Fibrosis Patients

Prevalence and persistence of Escherichia coli in the airways of cystic fibrosis patients—An unrecognized CF pathogen?

Disorders of pubertal development

Determination of CFTR densities in erythrocyte plasma membranes using recognition imaging

Factor V Leiden, protein C, and lipoprotein (a) in catheter-related thrombosis in childhood: A prospective study

Physiological Concept for a Blood Based CFTR Test

Dermal osteomata as first symptom of Albright's hereditary osteodystrophy in a 10-month-old girl

Pharmacology of all-trans-retinoic acid in children with acute promyelocytic leukemia

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