210 results on '"Pietrobattista, Andrea"'
Search Results
2. Metabolic-Associated Steatotic Liver Disease (MASLD): A New Term for a More Appropriate Therapy in Pediatrics?
3. Biliary atresia in preterm infants: a single center experience and review of literature
4. NAFLD in Children: Implication for the Future
5. Consumptive Hypothyroidism due to Hepatic Hemangiomas: A Case Series and Review of the Literature
6. Metabolic-Associated Steatotic Liver Disease (MASLD): A New Term for a More Appropriate Therapy in Pediatrics?
7. Acute Hepatitis of Unknown Origin in Children: Analysis of 17 Cases Admitted to the Bambino Gesù Children's Hospital in Rome.
8. The contribution of plasma oxysterols in the challenging diagnostic work-up of infantile cholestasis
9. Fat soluble vitamins deficiency in pediatric chronic liver disease: The impact of liver transplantation
10. Commentary: Case report: Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) presenting with liver cirrhosis and steroid-responsive interstitial pneumonia
11. Ethylmalonic encephalopathy and liver transplantation: long-term outcome of the first treated patient
12. Histopathological Spectrum and Molecular Characterization of Liver Tumors in the Setting of Fontan-Associated Liver Disease.
13. Article Molecular Profile of Liver Tumors in the Setting of Fontan-Associated Liver Disease
14. The impact of liver transplantation on health‐related quality of life in (acute) intoxication‐type inborn errors of metabolism
15. Gastroenterology: Biliary Atresia, Choledochal Cyst, Cystic Fibrosis
16. Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathies
17. 19: Indications and Success of Intestinal Transplantation in European Children
18. Odevixibat therapy following liver transplantation in patients with FIC1-deficient progressive familial intrahepatic cholestasis: a retrospective case series
19. Clinical features, histology and outcome of pediatric porto-sinusoidal vascular disease
20. Paediatric porto‐sinusoidal vascular disease: Two different clinical phenotypes with subtle histological differences
21. Achievement of operational tolerance in a pediatric liver transplant recipient following successful hematopoietic stem cell transplantation from a different donor
22. Does the Treatment After Kasai Procedure Influence Biliary Atresia Outcome and Native Liver Survival?
23. The Expanding Phenotype of ZTTK Syndrome Due to the Heterozygous Variant of SON Gene Focusing on Liver Involvement: Patient Report and Literature Review
24. Sarcopenia in children with chronic liver disease: Prevalence and impact on liver transplant outcomes
25. THU-313 - Odevixibat therapy following liver transplantation in patients with FIC1-deficient progressive familial intrahepatic cholestasis: a retrospective case series
26. Case report: Unusual and extremely severe lipoprotein X-mediated hypercholesterolemia in extrahepatic pediatric cholestasis
27. Expanding phenotype ofFAM111B‐related disease focusing on liver involvement: Literature review, report of a case with end‐stage liver disease and proposal for a new acronym
28. Gastroenterology: Biliary Atresia, Choledochal Cyst, Cystic Fibrosis
29. “De novo” brain arteriovenous malformation in a child with congenital porto-systemic shunt and multisystemic angiomas
30. Liver transplantation in an infant with cerebrotendinous xanthomatosis, cholestasis, and rapid evolution of liver failure
31. Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations
32. Sarcopenia is associated with poor clinical outcomes in patients with inflammatory bowel disease: a prospective cohort study
33. Impact of Two Antibiotic Therapies on Clinical Outcome and Gut Microbiota Profile in Liver Transplant Paediatric Candidates Colonized by Carbapenem-Resistant Klebsiella pneumoniae CR-KP
34. Macrophage Recruitment by Fibrocystin-Defective Biliary Epithelial Cells Promotes Portal Fibrosis in Congenital Hepatic Fibrosis
35. Expanding phenotype of FAM111B‐related disease focusing on liver involvement: Literature review, report of a case with end‐stage liver disease and proposal for a new acronym.
36. Hyaluronic acid predicts hepatic fibrosis in children with nonalcoholic fatty liver disease
37. AIRE mutation triggering acute liver failure: between genetic testing and treatment options
38. Allograft Fibrosis After Pediatric Liver Transplantation: Incidence, Risk Factors, and Evolution
39. Zinc and Treatment of Wilson’s Disease
40. Seronegative Autoimmune Hepatitis-Associated Severe Aplastic Anemia
41. Transient elastography for assessment of fibrosis in paediatric liver disease
42. THU-285 - Clinical features, histology and outcome of pediatric porto-sinusoidal vascular disease
43. A novel mobile phone application for infant stool color recognition: An easy and effective tool to identify acholic stools in newborns
44. ABO Incompatible Liver Transplantation in Children: A 20 Year Experience from Centres in the TransplantChild European Reference Network
45. Allograft Fibrosis After Pediatric Liver Transplantation: Incidence, Risk Factors, and Evolution.
46. Docosahexaenoic acid supplementation decreases liver fat content in children with non-alcoholic fatty liver disease: double-blind randomised controlled clinical trial
47. Is juvenile liver biopsy unsafe? Putting an end to a common misapprehension
48. WITHDRAWN: Fat soluble vitamins deficiency in pediatric chronic liver disease: The impact of liver transplantation
49. A novel mobile phone application for infant stool color recognition: An easy and effective tool to identify acholic stools in newborns.
50. Establishment of a Seronegative Occult Infection With an Active Hepatitis B Virus Reservoir Enriched of Vaccine Escape Mutations in a Vaccinated Infant After Liver Transplantation
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