43 results on '"Wilschanski, Michael"'
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2. Evolution of nutritional management in children with cystic fibrosis – a narrative review.
3. The effect of probiotic administration on metabolomics and glucose metabolism in CF patients.
4. Training in Paediatric Clinical Nutrition Across Europe: A Survey of the National Societies Network (2016-2019) of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition.
5. Tumor necrosis factor‐α inhibitor‐induced follicular psoriasiform eruption.
6. Drugs in Focus: Proton Pump Inhibitors.
7. Management of Gastrointestinal and Nutritional Problems in Children With Neurological Impairment: A Survey of Practice.
8. The Use of Fecal Calprotectin Testing in Paediatric Disorders: A Position Paper of the European Society for Paediatric Gastroenterology and Nutrition Gastroenterology Committee.
9. Clinical and Practice Variations in Pediatric Acute Recurrent or Chronic Pancreatitis: Report From the INSPPIRE Study.
10. Diabetes Mellitus in Children with Acute Recurrent and Chronic Pancreatitis: Data From the INternational Study Group of Pediatric Pancreatitis: In Search for a CuRE Cohort.
11. The Use of Jejunal Tube Feeding in Children: A Position Paper by the Gastroenterology and Nutrition Committees of the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition 2019.
12. Chronic Pancreatitis: Pediatric and Adult Cohorts Show Similarities in Disease Progress Despite Different Risk Factors.
13. Increasing Vitamin D Serum Levels Is Associated With Reduced Pulmonary Exacerbations in Patients With Cystic Fibrosis.
14. Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE.
15. Nutritional Considerations in Pediatric Pancreatitis: A Position Paper from the NASPGHAN Pancreas Committee and ESPGHAN Cystic Fibrosis/Pancreas Working Group.
16. Cystic Fibrosis-related Liver Disease: Research Challenges and Future Perspectives.
17. ESPGHAN- Guidelines for the Evaluation and Treatment of Gastrointestinal and Nutritional Complications in Children with Neurological Impairment.
18. Causal Evaluation of Acute Recurrent and Chronic Pancreatitis in Children: Consensus From the INSPPIRE Group.
19. Highlights of the ESPEN-ESPGHAN-ECFS Guidelines on Nutrition Care for Infants and Children With Cystic Fibrosis.
20. Comparison of Nasal Potential Difference and Intestinal Current Measurements as Surrogate Markers for CFTR Function.
21. An international consensus report on a new algorithm for the management of infant diarrhoea.
22. Functional gastro-intestinal disorder algorithms focus on early recognition, parental reassurance and nutritional strategies.
23. ESPGHAN and NASPGHAN Report on the Assessment of Exocrine Pancreatic Function and Pancreatitis in Children.
24. Genetic and Electrophysiological Characteristics of Recurrent Acute Pancreatitis.
25. Role of Polyethylene Glycol in the Treatment of Functional Constipation in Children.
26. Oral Health Status and Salivary Properties in Relation to Gluten-free Diet in Children With Celiac Disease.
27. Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis.
28. Endoscopic retrograde cholangiopancreatography in neonatal cholestasis.
29. Exocrine pancreatic function testing in patients with cystic fibrosis and pancreatic sufficiency: a correlation study.
30. Nasal potential difference in non-classic cystic fibrosis-long term follow up.
31. Vitamins A and E and Pulmonary Exacerbations in Patients With Cystic Fibrosis.
32. Combination of Helicobacter pylori Strain and Tumor Necrosis Factor-α Polymorphism of the Host Increases the Risk of Peptic Ulcer Disease in Children.
33. Treatment regimens for Helicobacter pylori infection in children: is in vitro susceptibility testing helpful?
34. Relative expression and localization of the insulin-like growth factor system components in the fetal, child and adult intestine.
35. Helicobacter pylori genotypes in Israeli children: the significance of geography.
36. Findings on routine abdominal ultrasonography in cystic fibrosis patients.
37. Cystic fibrosis, pregnancy, and recurrent, acute pancreatitis.
38. Neonatal Sclerosing Cholangitis Associated with Autoimmune Phenomena.
39. CFTR Protein Function Modulation Therapy Is Finally Targeting Cystic Fibrosis-related Gastrointestinal Disease.
40. Shwachman-Diamond syndrome presenting as hepatosplenomegaly.
41. Haemophilus Influenzae Neonatal Sepsis-What is Appropriate Initial Therapy?
42. EXPRESSION OF INSULIN-LIKE GROWTH FACTORS AND THEIR RECEPTORS IN THE NORMAL SMALL INTESTINE OF THE CHILD.
43. An international consensus report on a new algorithm for the management of infant diarrhoea
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