Research Topics
| M SternSummaryCountry: Germany Publications
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Detail Information
Publications
Comparative evaluation of serologic tests for celiac disease: a European initiative toward standardizationM Stern
University Children s Hospital, Tubingen, Germany
J Pediatr Gastroenterol Nutr 31:513-9. 2000..However, there is no standardization, and there are no reference protocols and materials...
Benchmarking improves quality in cystic fibrosis care: a pilot project involving 12 centresMartin Stern
University Children s Hospital, University of Tubingen, Hoppe Seyler Str 1, 72076 Tubingen, Germany
Int J Qual Health Care 23:349-56. 2011..Based upon this, continuous quality improvement can be achieved by applying the benchmarking method which is focused on learning from best practice...
From registry to quality management: the German Cystic Fibrosis Quality Assessment project 1995 2006M Stern
University of Tubingen, University Children s Hospital, Hoppe Seyler Str 1, 72076 Tubingen, Germany
Eur Respir J 31:29-35. 2008....
The use of a cystic fibrosis patient registry to assess outcomes and improve cystic fibrosis care in GermanyMartin Stern
Department of General Paediatrics, Haematology, Oncology, University Children s Hospital Tuebingen, Tuebingen, Germany
Curr Opin Pulm Med 17:473-7. 2011..This review describes recent developments in patient registries, outcome research, and pilot projects in quality improvement...
Analysis and clinical effects of gluten in coeliac diseaseM Stern
University Children s Hospital, Tubingen, Germany
Eur J Gastroenterol Hepatol 13:741-7. 2001..The group recommends adherence to a single Codex limit for gluten-free foods. The current limit of 200 ppm gluten is questionable and requires reconsideration based on new information that will be available soon...
Continuous vs thrice-daily ceftazidime for elective intravenous antipseudomonal therapy in cystic fibrosisJ Riethmueller
University Children s Hospital, 72076, Tubingen, Germany
Infection 37:418-23. 2009....
Tobramycin once- vs thrice-daily for elective intravenous antipseudomonal therapy in pediatric cystic fibrosis patientsJ Riethmueller
University Children s Hospital, 72076, Tubingen, Germany
Infection 37:424-31. 2009..Toxicity and practicability may even be improved in the single-dose regimen...
[Routine otorhinolaryngological examination in patients with cystic fibrosis]A Koitschev
Univ HNO Klinik Tübingen
HNO 54:361-4, 366, 368. 2006..A standard annual examination would be useful for definition of risk factors and/or management alternatives for these symptoms...
Sporadic cerebellar ataxia associated with gluten sensitivityK Burk
Department of Neurology, University of Tubingen, Germany
Brain 124:1013-9. 2001....
Bronchodilatory effects of salbutamol, ipratropium bromide, and their combination: double-blind, placebo-controlled crossover study in cystic fibrosisR Ziebach
University Children s Hospital Tubingen, Department 1, Tubingen, Germany
Pediatr Pulmonol 31:431-5. 2001..We conclude that in CF patients bronchodilator therapy with sympathomimetic agents is usually sufficient. Only in cases with proven additional benefit from inhalation by anticholinergics should combination therapy be recommended...
A src-like kinase activates outwardly rectifying chloride channels in CFTR-defective lymphocytesA Lepple-Wienhues
Department for Physiology, University of Tubingen, Tubingen, Germany
FASEB J 15:927-31. 2001..Regulation of I(OR) by p56(lck) thus represents an alternative pathway of stimulating membrane chloride conductance that is left intact in cystic fibrosis...
Coeliac disease in children with Type 1 diabetes mellitus: the effect of the gluten-free dietI Sanchez-Albisua
University Children s Hospital, Tubingen, Germany
Diabet Med 22:1079-82. 2005..Serological screening was performed using anti-gliadin and anti-endomysium antibodies. Data were obtained about clinical symptoms, height and weight-for-height...
Home and hospital antibiotic treatment prove similarly effective in cystic fibrosisJ Riethmueller
University Children s Hospital, Hoppe Seyler Str 1, D 72076 Tuebingen, Germany
Infection 30:387-91. 2002..A prospective clinical study was carried out to compare home and hospital iv antibiotic treatment in CF patients with chronic P. aeruginosa infection...
Evaluation of body mass index percentiles for assessment of malnutrition in children with cystic fibrosisB Wiedemann
Department of Medical Informatics and Biometrics, Technical University Dresden, Dresden, Germany
Eur J Clin Nutr 61:759-68. 2007....
The German cystic fibrosis quality assurance project: clinical features in children and adultsB Wiedemann
Institute for Medical Informatics and Biometrics, Technical University of Dresden, Germany
Eur Respir J 17:1187-94. 2001..The Cystic Fibrosis Quality Assurance project represents an important tool for future progress in the quality of cystic fibrosis care...
[Mucoviscidosis in adults]M Stern
Service de Pneumologie et centre de soins de mucoviscidose, Hopital Foch, 40, rue Worth, 92150 Suresnes
Presse Med 31:263-70. 2002..The discomfort and time the patient has to spend on daily treatments requires regular monitoring, to improve compliance and to improve the quality of life of these patients...
[Bone mineral density in patients with chronic lung diseases]C Brousse
Groupe de transplantation pulmonaire, , BP 36, 40 rue Worth, 92150 Suresnes, France
Rev Mal Respir 18:411-5. 2001..Bone density must be measured in order to prevent and treat osteoporosis...
The metabolic syndrome: time for a critical appraisal. Joint statement from the American Diabetes Association and the European Association for the Study of DiabetesR Kahn
American Diabetes Association, 1701 N Beauregard Street, Alexandria, VA 22311, USA
Diabetologia 48:1684-99. 2005..The term 'metabolic syndrome' refers to a clustering of specific cardiovascular disease (CVD) risk factors whose underlying pathophysiology is thought to be related to insulin resistance...
Nutrition in patients with cystic fibrosis: a European ConsensusM Sinaasappel
Department of Paediatric Gastroenterology, Erasmus Medical Centre, Rotterdam, The Netherlands
J Cyst Fibros 1:51-75. 2002..The purpose of the conference was to develop a consensus document on nutrition in patients with cystic fibrosis based on current evidence...
Clinical outcome following lung transplantation in patients with cystic fibrosis colonised with Burkholderia cepacia complex: results from two French centresV Boussaud
Pôle cardio thoracique, AP HP, HEGP, Paris, France
Thorax 63:732-7. 2008..Infection with Burkholderia cepacia complex (BCC) is a life threatening complication of cystic fibrosis (CF), often seen as a contraindication for lung transplantation...
Poly (D, L-lactide-co-glycolide)/DNA microspheres to facilitate prolonged transgene expression in airway epithelium in vitro, ex vivo and in vivoM Stern
Department of Gene Therapy, Imperial College Faculty of Medicine at the National Heart and Lung Institute, London, UK
Gene Ther 10:1282-8. 2003..These data demonstrate that PLG-mediated gene transfer can produce prolonged gene expression in airway epithelia. However, gene transfer efficiency still requires significant improvement...
An evaluation of the Child Perceptions Questionnaire in the UKZ Marshman
Department of Oral Health and Development, School of Clinical Dentistry, Sheffield, UK
Community Dent Health 22:151-5. 2005..To assess the reliability and validity of the Child Perceptions Questionnaire (CPQ11-14), an oral health related quality of life measure for 11-14 year old children, for use in the UK...
