338 results on '"vom Dahl, Stephan"'
Search Results
2. Transition seltener Leberkrankheiten im Kindesalter – was kommt auf die Hepatologie zu?
3. Diagnosis and management of secondary causes of steatohepatitis
4. Everyday Life, Dietary Practices, and Health Conditions of Adult PKU Patients : A Multicenter, Cross-Sectional Study
5. Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders
6. Favourable Outcome in Two Pregnancies in a Patient with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
7. Management and monitoring recommendations for the use of eliglustat in adults with type 1 Gaucher disease in Europe
8. Hepatocellular carcinoma in Gaucher disease: an international case series
9. Rare and genetic diseases of the liver – an introduction
10. Kapitel 65 - Morbus Gaucher
11. Reply to Letter to the Editor: “The added benefit of contrast-enhanced CT in the evaluation of incidental FDG-avid colon lesions”
12. Management, vaccination status and COVID-19 morbidity of patients with Gaucher disease in Germany during the COVID-19 pandemic
13. Incidence of hepatic adenomas in adult glycogen storage disease type Ia/b
14. Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision
15. Radiofrequency Pulmonary Vein Isolation without Esophageal Temperature Monitoring: Contact-Force Characteristics and Incidence of Esophageal Thermal Damage
16. Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision
17. Percutaneous transhepatic or endoscopic ultrasound-guided biliary drainage in malignant distal bile duct obstruction using a self-expanding metal stent: Study protocol for a prospective European multicenter trial (PUMa trial)
18. Impact of pregnancy planning and preconceptual dietary training on metabolic control and offspring's outcome in phenylketonuria
19. Cerebrotendinous xanthomatosis: long-term course in 5 patients and first description of a successful pregnancy management during therapy with chenodesoxycholic acid (CDCA)
20. Whole body MRI in type I Gaucher patients: Evaluation of skeletal involvement
21. The management of pregnancy in Gaucher disease
22. Activation of Integrins by Urea in Perfused Rat Liver
23. Lysosomal storage diseases as differential diagnosis of hepatosplenomegaly
24. A validated disease severity scoring system for adults with type 1 Gaucher disease
25. Force Majeure: Therapeutic measures in response to restricted supply of imiglucerase (Cerezyme) for patients with Gaucher disease
26. Digital single-operator cholangioscopy with EHL as salvage therapy of an internalized and stone-impacted biliary stent 13 years after implantation
27. Niemann-Pick type B as ultra-rare differential diagnosis in hepatomegaly, steatohepatitis, low HDL and increased plasma chitotriosidase activity: three case reports
28. Adult cholesteryl ester storage disease (CESD): Three case reports
29. Understanding the natural history of Gaucher disease
30. Dose-response relationships for enzyme replacement therapy with imiglucerase/alglucerase in patients with Gaucher disease type 1
31. The female Gaucher patient: The impact of enzyme replacement therapy around key reproductive events (menstruation, pregnancy and menopause)
32. Long-term clinical outcomes in type 1 Gaucher disease following 10 years of imiglucerase treatment
33. An obligatory requirement for the heterotrimeric G protein [G.sub.i3] in the antiautophagic action of insulin in the liver
34. Diagnose und Therapie des Morbus Gaucher Aktuelle Empfehlungen der deutschen Therapiezentren im Jahr 2000: Aktuelle Empfehlungen der deutschen Therapiezentren im Jahr 2000
35. Characteristics of type I Gaucher disease associated with persistent thrombocytopenia after treatment with imiglucerase for 4–5 years
36. Hepatorenal Tyrosinaemia: Impact of a Simplified Diet on Metabolic Control and Clinical Outcome
37. Cardiometabolic risk factor clustering in patients with deficient branched‐chain amino acid catabolism: A case‐control study
38. Hepatic Gaucheroma mimicking focal nodular hyperplasia#
39. Prevalence of Type 1 Gaucher Disease in the United States
40. Effects of urea on K+ fluxes and cell volume in perfused rat liver
41. Involvement of Integrins and Src in Insulin Signaling toward Autophagic Proteolysis in Rat Liver
42. Ca2+-dependent Protein Kinase C Isoforms Induce Cholestasis in Rat Liver
43. Nutritional state and the swelling-induced inhibition of proteolysis in perfused rat liver
44. Gaucher disease type 1: Revised recommendations on evaluations and monitoring for adult patients
45. Detection of colorectal polyps by multislice CT colonography with ultra-low-dose technique: comparison with high-resolution videocolonoscopy
46. Clinical monitoring after cessation of enzyme replacement therapy in m. gaucher
47. FRI283 - Cerebrotendinous xanthomatosis: long-term course in 5 patients and first description of a successful pregnancy management during therapy with chenodesoxycholic acid (CDCA)
48. Involvement of integrins and Src in tauroursodeoxycholate-induced and swelling-induced choleresis
49. Hepatic encephalopathy in chronic liver disease: a clinical manifestation of astrocyte swelling and low-grade cerebral edema?
50. Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase −1 exon 8 splice junction mutation
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.