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Mukoviszidose und Diabetes

Diabetologe, 2010, Vol.6 (1), p.16-22

Ballmann, M.

2010

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Long-term effects of a partially supervised conditioning programme in cystic fibrosis

The European respiratory journal, 2010-03, Vol.35 (3), p.578-583

2010

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Steroid dependency despite omalizumab treatment of ABPA in cystic fibrosis

Allergy (Copenhagen), 2010, Vol.65 (1), p.134-135

2010

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Heavy Alkali Metal Manganate Complexes: Synthesis, Structures and Solvent‐Induced Dissociation Effects

Chemistry : a European journal, 2022-10, Vol.28 (55), p.e202201716-n/a

2022

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Calcium catalyzed enantioselective intramolecular alkene hydroamination with chiral C 2 -symmetric bis-amide ligands

Dalton transactions : an international journal of inorganic chemistry, 2021-03, Vol.50 (9), p.3178-3185

2021

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Physical activity is independently related to aerobic capacity in cystic fibrosis

The European respiratory journal, 2006-10, Vol.28 (4), p.734-739

2006

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Application of Bis(amido)alkyl Magnesiates toward the Synthesis of Molecular Rubidium and Cesium Hydrido-magnesiates

Organometallics, 2024-06, Vol.43 (12), p.1393-1401

2024

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Three Oxidative Addition Routes of Alkali Metal Aluminyls to Dihydridoaluminates and Reactivity with CO2

Chemistry : a European journal, 2023-10, Vol.29 (56), p.e202301849-n/a

2023

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A novel sidestream ultrasonic flow sensor for multiple breath washout in children

Pediatric pulmonology, 2008-08, Vol.43 (8), p.731-738

2008

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Synthesis, Characterization, and Structural Analysis of AM[Al(NONDipp)(H)(SiH2Ph)] (AM = Li, Na, K, Rb, Cs) Compounds, Made Via Oxidative Addition of Phenylsilane to Alkali Metal Aluminyls

Inorganic chemistry, 2022-12, Vol.61 (49), p.19838-19846

2022

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Mukoviszidose – wenn die Diagnose unsicher bleibt

Monatsschrift Kinderheilkunde, 2024, Vol.172 (6), p.510-518

2024

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Respiratory viral infections within one year after pediatric lung transplant

Transplant infectious disease, 2009-08, Vol.11 (4), p.304-312

2009

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Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

The Journal of clinical investigation, 2001-12, Vol.108 (11), p.1705-1715

2001

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261 Effect of different treatment regimens of CFRD on clinical status: A register study

Journal of cystic fibrosis, 2013-06, Vol.12, p.S115-S115

2013

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Continuous vs thrice-daily ceftazidime for elective intravenous antipseudomonal therapy in cystic fibrosis

Infection, 2009-10, Vol.37 (5), p.418-423

2009

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WS15.5 An international comparison of insulin use in incident Cystic Fibrosis-Related Diabetes: data from the UK and German Cystic Fibrosis Registries

Journal of cystic fibrosis, 2020-06, Vol.19, p.S26-S26

2020

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Diversity of the basic defect of homozygous CFTR mutation genotypes in humans

Journal of medical genetics, 2008-01, Vol.45 (1), p.47-54

2008

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283 Cystic fibrosis: the thicker, the better? A retrospective longitudinal study over 10 years

Journal of cystic fibrosis, 2011, Vol.10, p.S72-S72

2011

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WS15-1 Long-term follow-up of different treatment regimes of newly diagnosed CFRD: a Registry study from Germany

Journal of cystic fibrosis, 2019-06, Vol.18, p.S28-S28

2019

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WS16.1 Treatment of early diagnosed CFRD with oral drugs versus insulin: An open prospective randomized study

Journal of cystic fibrosis, 2013-06, Vol.12, p.S32-S32

2013

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Development of allergic asthma in an asthmatic recipient of a nonatopic lung under systemic immunosuppression

Allergy (Copenhagen), 2008-05, Vol.63 (5), p.628-629

2008

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Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis

The American journal of gastroenterology, 2000, Vol.95 (8), p.2061-2067

2000

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Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis

The American journal of gastroenterology, 2000-08, Vol.95 (8), p.2061-2067

2000

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Transient correction of the basic defect in sweat glands in an individual with cystic fibrosis carrying the complex CFTR allele F508del-R553Q

Thorax, 2009-02, Vol.64 (2), p.179-180

2009

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202 Exercise testing in children with cystic fibrosis (CF) – risk for adverse events?

Journal of cystic fibrosis, 2011, Vol.10, p.S51-S51

2011

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Mukoviszidose und Diabetes

Long-term effects of a partially supervised conditioning programme in cystic fibrosis

Steroid dependency despite omalizumab treatment of ABPA in cystic fibrosis

Heavy Alkali Metal Manganate Complexes: Synthesis, Structures and Solvent‐Induced Dissociation Effects

Calcium catalyzed enantioselective intramolecular alkene hydroamination with chiral C 2 -symmetric bis-amide ligands

Physical activity is independently related to aerobic capacity in cystic fibrosis

Application of Bis(amido)alkyl Magnesiates toward the Synthesis of Molecular Rubidium and Cesium Hydrido-magnesiates

Three Oxidative Addition Routes of Alkali Metal Aluminyls to Dihydridoaluminates and Reactivity with CO2

A novel sidestream ultrasonic flow sensor for multiple breath washout in children

Synthesis, Characterization, and Structural Analysis of AM[Al(NONDipp)(H)(SiH2Ph)] (AM = Li, Na, K, Rb, Cs) Compounds, Made Via Oxidative Addition of Phenylsilane to Alkali Metal Aluminyls

Mukoviszidose – wenn die Diagnose unsicher bleibt

Respiratory viral infections within one year after pediatric lung transplant

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

261 Effect of different treatment regimens of CFRD on clinical status: A register study

Continuous vs thrice-daily ceftazidime for elective intravenous antipseudomonal therapy in cystic fibrosis

WS15.5 An international comparison of insulin use in incident Cystic Fibrosis-Related Diabetes: data from the UK and German Cystic Fibrosis Registries

Diversity of the basic defect of homozygous CFTR mutation genotypes in humans

283 Cystic fibrosis: the thicker, the better? A retrospective longitudinal study over 10 years

WS15-1 Long-term follow-up of different treatment regimes of newly diagnosed CFRD: a Registry study from Germany

WS16.1 Treatment of early diagnosed CFRD with oral drugs versus insulin: An open prospective randomized study

Development of allergic asthma in an asthmatic recipient of a nonatopic lung under systemic immunosuppression

Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis

Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis

Transient correction of the basic defect in sweat glands in an individual with cystic fibrosis carrying the complex CFTR allele F508del-R553Q

202 Exercise testing in children with cystic fibrosis (CF) – risk for adverse events?

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