123 results on '"KRAWCZYK, M."'
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2. Etablierung und Validierung eines Deep-learning basierten Algorithmus zur Diagnose der Eosinophilen Ösophagitis
3. MARC1 p.A165T polymorphism is associated with decreased liver injury and enhanced antioxidant activity in serum in patients with AIH
4. MBOAT7 rs641738 POLYMORPHISM IS LINKED TO ALTERED PORTAL BLOOD FLOW ASSESSED USING 13C METHACETIN TEST
5. LIVER STIFFNESS MEASUREMENTS IN EMERGENCY TRIAGE PREDICT INPATIENT HEALTH CARE UTILIZATION
6. HSD17B13 and MBOAT7 as modulators of PNPLA3-associated cirrhosis
7. PNPLA3 and HSD17B13 gene variants exert opposite effects on fatty liver phenotypes: results from the FLAG cohort
8. Common genetic variant c.711A>T in the hepatobiliary phospholipid translocator ABCB4 as risk factor for liver fibrosis
9. Phenotyping non-alcoholic fatty liver disease by the gut microbiota – ready for prime time?
10. Genes involved in hepatic cholesterol homeostasis identified as modifiers of cholestasis in Abcb4 deficient mice
11. Acute pancreatitis in a female patient with HEV (GT 3) infection and a compound CLDN2 – PRSS1 genotype
12. HSD17B13 hepatoprotective variant limits liver disease severity in homozygous carriers of the PNPLA3 p. 148MM risk genotype
13. Quantitative trait analysis in Abcb4 deficient mice identifies Pcsk9 as a potential modifier gene
14. Phänotypisierung der nichtalkoholischen Fettlebererkrankung (NAFLD) durch das intestinale Mikrobiom – Sind wir schon so weit?
15. Kein signifikanter Einfluss des Fruktosekonsums auf die Zusammensetzung der Darmmikrobiota bei Patienten mit bioptisch gesicherter nichtalkoholischer Fettlebererkrankung
16. Effects of the common PNPLA3 p.I148 M polymorphism on the fatty liver phenotypes in German patients: results from the FLAG “real life” cohort
17. Body composition in patients with non-alcoholic fatty liver and fibrosis correlates with impaired health related quality of life
18. Liver fibrosis in conjunction with the prosteatotic PNPLA3 variant affects quality of life in patients with NAFLD: prospective liver stiffness-based study
19. The NLRP3 inflammasome rs10754558 is associated with increased serum ALT activities: analysis of a prospective NAFLD cohort
20. Baseline patient characteristics of the German multicentric prospective real-world NAFLD cohort: The Fatty Liver Assessment in Germany (FLAG) study
21. Carriage of HSD17B13 rs72613567TA is associated with a reduced risk for developing hepatocellular carcinoma in patients with alcohol-related cirrhosis
22. Common variant p.D19 H of the hepatobiliary sterol transporter ABCG5/8 increases the gallstone risk and affects cholesterol homeostasis in children
23. Quantitative trait analysis in Abcb4 deficient mice identifies Pcks9 as a potential modifier gene
24. Prädisponierende Genvarianten bei Divertikulose und Divertikulitis
25. Abcg5/g8-Defizienz im Dünndarm führt zu einer Cholesterinübersättigung der Galle
26. The PNPLA3 p.I148 M polymorphism is associated with increased liver injury in patients with polycystic ovary (PCO) syndrome
27. Leberfibrose und -zirrhose bei Patienten mit Fettleber sind mit einer verminderten Lebensqualität assoziert: Elastografie-basierte prospektive Studie
28. Liver Fibrosis and Metabolic Alterations in Adults with Homozygous Alpha1-antitrypsin Deficiency (PiZZ Genotype)
29. Role of prosteatotic gene variants as modulators of primary sclerosing cholangitis: Analysis of 178 patients with PSC
30. Systems genetics of liver injury in ABCB4 deficiency: identification of genetic modifiers involved in hepatic cholesterol homeostasis
31. Could inherited predisposition drive fatty liver disease in non-obese Germans? Results from eight tertiary referral centers
32. Peculiar cases of ibuprofen-induced acute liver failure with distinct outcomes
33. Effects of gene variants controlling vitamin D metabolism and serum levels on hepatic steatosis
34. Heterozygous carriage of the alpha1-antitrypsin PiZ variant increases the risk to develop liver fibrosis
35. Haemochromatosis (HFE) gene variation and cholangiocarcinoma risk
36. Nicht-alkoholische Fettleberkrankung bei Patienten mit chronisch entzündlichen Darmerkrankungen: Prospektive Untersuchung der Inzidenz und genetischer Risikofaktoren
37. NOD2 gene variants as novel risk factors for secondary sclerosing cholangitis in critically ill patients
38. Common variant p.D19 H of the hepatobiliary sterol transporter ABCG5/8 affects cholesterol homeostasis in children with gallstones
39. Carriers of the adiponutrin (PNPLA3) p.I148 M risk allele might be at-risk of chemotherapy-associated steatohepatitis (CASH)
40. Einnahme von NSAR erhöht selektiv das Risiko für die Entstehung einer Divertikulitis: monozentrische Analyse von Patienten mit Divertikulose
41. Transient elastography correlates with liver injury in PSC patients: Laennec score-based analysis of explanted livers
42. Eine Variante in COL3A1 (rs3134646) ist mit der Entstehung der Divertikulose bei Männern assoziiert
43. Genetik der nicht-alkoholischen Fettlebererkrankung
44. Extracorporeal blood purification improves nasobiliary drainage (NBD)-refractory pruritus in a BRIC type 2 patient
45. NOD2 genetic variants confer risk for secondary sclerosing cholangitis in critically ill patients
46. Evaluation der pro-steatotischen Genvariante rs641738 im MBOAT7-Gen bei Patienten mit hepatozellulärem Karzinom (HCC)
47. Presence of the MBOAT7 rs641738 variant might enhance liver fibrosis in patients with fatty liver: analysis of the German NAFLD CSG cohort
48. Biopsy-based analysis of the prosteatotic TM6SF2 p.E167K and PNPLA3 p.I148 M gene variants as potential modifiers of Wilson disease
49. Shear wave elastography of the liver and spleen in patients with autoimmune hepatitis and its variants – A single centre study
50. Frequent polymorphism p.D19 H of the biliary cholesterol transporter ABCG5/8 increases the risk of gallstone disease in children
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