110 results on '"KRAWCZYK, M."'
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2. Atypische bakterielle Infektionen bei Patienten mit Leberzirrhose
3. Etablierung und Validierung eines Deep-learning basierten Algorithmus zur Diagnose der Eosinophilen Ösophagitis
4. MARC1 p.A165T polymorphism is associated with decreased liver injury and enhanced antioxidant activity in serum in patients with AIH
5. Aktualisierte S2k-Leitlinie nicht-alkoholische Fettlebererkrankung der Deutschen Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten (DGVS) – April 2022 – AWMF-Registernummer: 021–025.
6. Liver fibrosis in conjunction with the prosteatotic PNPLA3 variant affects quality of life in patients with NAFLD: prospective liver stiffness-based study
7. The NLRP3 inflammasome rs10754558 is associated with increased serum ALT activities: analysis of a prospective NAFLD cohort
8. Baseline patient characteristics of the German multicentric prospective real-world NAFLD cohort: The Fatty Liver Assessment in Germany (FLAG) study
9. Carriage of HSD17B13 rs72613567TA is associated with a reduced risk for developing hepatocellular carcinoma in patients with alcohol-related cirrhosis
10. Common variant p.D19 H of the hepatobiliary sterol transporter ABCG5/8 increases the gallstone risk and affects cholesterol homeostasis in children
11. Quantitative trait analysis in Abcb4 deficient mice identifies Pcks9 as a potential modifier gene
12. Prädisponierende Genvarianten bei Divertikulose und Divertikulitis
13. Abcg5/g8-Defizienz im Dünndarm führt zu einer Cholesterinübersättigung der Galle
14. The PNPLA3 p.I148 M polymorphism is associated with increased liver injury in patients with polycystic ovary (PCO) syndrome
15. Leberfibrose und -zirrhose bei Patienten mit Fettleber sind mit einer verminderten Lebensqualität assoziert: Elastografie-basierte prospektive Studie
16. Liver Fibrosis and Metabolic Alterations in Adults with Homozygous Alpha1-antitrypsin Deficiency (PiZZ Genotype)
17. Role of prosteatotic gene variants as modulators of primary sclerosing cholangitis: Analysis of 178 patients with PSC
18. Systems genetics of liver injury in ABCB4 deficiency: identification of genetic modifiers involved in hepatic cholesterol homeostasis
19. Could inherited predisposition drive fatty liver disease in non-obese Germans? Results from eight tertiary referral centers
20. Peculiar cases of ibuprofen-induced acute liver failure with distinct outcomes
21. Effects of gene variants controlling vitamin D metabolism and serum levels on hepatic steatosis
22. Heterozygous carriage of the alpha1-antitrypsin PiZ variant increases the risk to develop liver fibrosis
23. Haemochromatosis (HFE) gene variation and cholangiocarcinoma risk
24. NOD2 gene variants as novel risk factors for secondary sclerosing cholangitis in critically ill patients
25. Common variant p.D19 H of the hepatobiliary sterol transporter ABCG5/8 affects cholesterol homeostasis in children with gallstones
26. Carriers of the adiponutrin (PNPLA3) p.I148 M risk allele might be at-risk of chemotherapy-associated steatohepatitis (CASH)
27. Einnahme von NSAR erhöht selektiv das Risiko für die Entstehung einer Divertikulitis: monozentrische Analyse von Patienten mit Divertikulose
28. Transient elastography correlates with liver injury in PSC patients: Laennec score-based analysis of explanted livers
29. Eine Variante in COL3A1 (rs3134646) ist mit der Entstehung der Divertikulose bei Männern assoziiert
30. Extracorporeal blood purification improves nasobiliary drainage (NBD)-refractory pruritus in a BRIC type 2 patient
31. NOD2 genetic variants confer risk for secondary sclerosing cholangitis in critically ill patients
32. Evaluation der pro-steatotischen Genvariante rs641738 im MBOAT7-Gen bei Patienten mit hepatozellulärem Karzinom (HCC)
33. Presence of the MBOAT7 rs641738 variant might enhance liver fibrosis in patients with fatty liver: analysis of the German NAFLD CSG cohort
34. Biopsy-based analysis of the prosteatotic TM6SF2 p.E167K and PNPLA3 p.I148 M gene variants as potential modifiers of Wilson disease
35. Shear wave elastography of the liver and spleen in patients with autoimmune hepatitis and its variants – A single centre study
36. Frequent polymorphism p.D19 H of the biliary cholesterol transporter ABCG5/8 increases the risk of gallstone disease in children
37. Effects of plasmapheresis on refractory cholestatic pruritus in patients with PBC: prospective analysis of 129 procedures
38. Die lithogene Variante D19 H im Cholesterintransporter Abcg8 verändert das biliäre Cholesterin-/Phosphatidylcholin-Verhältnis in Mäusen
39. Plasma separation and anion adsorption results in rapid improvement of nasobiliary drainage (NBD)-refractory pruritus in BRIC type 2
40. Tumour-associated circulating microparticles: a novel liquid biopsy tool for screening and therapy monitoring of colorectal carcinoma and other epithelial neoplasia
41. The ABCB4 p.T175A allele might be associated with increased liver injury: analysis of two independent cohorts of patients with chronic liver diseases and NAFLD
42. Variant PNPLA3 increases the HCC risk: prospective study in patients treated at the Saarland University Medical Center
43. Common procholestatic variants may confer risk of anabolic steroids induced cholestasis: presentation of two cases
44. Combined effects of the prosteatotic TM6SF2 and PNPLA3 variants on severity of NALFD: multicentre biopsy-based study in German patients
45. Delayed intrahepatic cholestasis induced by anabolic steroids in a patient with haploinsufficiency of the pregnane X receptor (PXR/NR1I2)
46. The power of NGS: Results from a dedicated sequencing panel of 24 genes in 40 patients with cholestatic liver disease
47. FUT2 variant might modulate the course in secondary sclerosing cholangitis in critically ill patients (SC-CIP)
48. Procholestatic gene variants and mutations in secondary sclerosing cholangitis in critically ill patients (SC-CIP)
49. Serum autotaxin is associated with significant impairment of health related quality of life, biochemical and clinical and parameters in patients with PBC
50. Effects of novel prosteatogenic TM6SF2 and NCAN/SUGP1 polymorphisms on hepatic steatosis and non-invasive markers of liver injury in patients with chronic liver diseases
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