471 results on '"Francalanci, Paola"'
Search Results
2. Hemodynamic Assessment of a Large Pulmonary Arteriovenous Malformation in a Neonate: Case Report and Review of Literature
3. Epstein–Barr virus‐associated smooth muscle tumor in a female with ataxia telangiectasia: A case report
4. Changes in Total Homocysteine and Glutathione Levels After Laparoscopic Sleeve Gastrectomy in Children with Metabolic-Associated Fatty Liver Disease
5. Diagnostic approach to neonatal and infantile cholestasis: A position paper by the SIGENP liver disease working group
6. Biliary atresia in preterm infants: a single center experience and review of literature
7. Pediatric Autoimmune Hepatitis
8. Evaluation of Gastroesophageal Reflux Disease 1 Year after Esophageal Atresia Repair: Paradigms Lost from a Single Snapshot?
9. Focal adhesion kinase and its epigenetic interactors as diagnostic and therapeutic hints for pediatric hepatoblastoma.
10. Lymphomonocytic inflammatory infiltrate with numerous eosinophilic granulocytes in the interstitium in a surviving heart transplant recipient: a case report.
11. MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase Phenotype
12. A novel ABCB11 variant in compound heterozygosity: BRIC2 or PFIC2?
13. Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2
14. Molecular Profiling of a Hepatocellular Neoplasm Not Otherwise Specified (HCN-NOS) Demonstrates Distinct Molecular Features in Hepatoblastoma and HCC-Like Components
15. Application of a pattern‐based approach to histological diagnosis in very early onset IBD (VEO‐IBD) in a multicentric cohort of children with emphasis on monogenic disease with IBD‐like morphology
16. Case Report: The impact of severe cryptosporidiosis on the gut microbiota of a pediatric patient with CD40L immunodeficiency
17. A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant
18. Pattern-based Histologic Approach in Very Early Onset IBD: Main Features and Differential Diagnosis
19. Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept
20. Molecular Profiling of a Hepatocellular Neoplasm Not Otherwise Specified (HCN-NOS) Demonstrates Distinct Molecular Features in Hepatoblastoma and HCC-Like Components.
21. Application of a pattern‐based approach to histological diagnosis in very early onset IBD (VEO‐IBD) in a multicentric cohort of children with emphasis on monogenic disease with IBD‐like morphology.
22. Histopathological Spectrum and Molecular Characterization of Liver Tumors in the Setting of Fontan-Associated Liver Disease.
23. Article Molecular Profile of Liver Tumors in the Setting of Fontan-Associated Liver Disease
24. Biallelic truncating variants in children with titinopathy represent a recognizable condition with distinctive muscular and cardiac characteristics: a report on five patients
25. Case report: Coronary allograft vasculopathy: an accurate reflection of the histopathological findings on cardiovascular magnetic resonance imaging
26. Oral viscous budesonide in children with eosinophilic esophagitis after repaired esophagealatresia: a clinical trial.
27. Achievement of operational tolerance in a pediatric liver transplant recipient following successful hematopoietic stem cell transplantation from a different donor
28. ERNICA guidelines for the management of rectosigmoid Hirschsprung’s disease
29. The Expanding Phenotype of ZTTK Syndrome Due to the Heterozygous Variant of SON Gene Focusing on Liver Involvement: Patient Report and Literature Review
30. Remember Friedreich ataxia even in a toddler with apparently isolated dilated (not hypertrophic!) cardiomyopathy. Revisited
31. Oral Viscous Budesonide in Children With Eosinophilic Esophagitis After Repaired Esophageal Atresia: A Clinical Trial.
32. New Onset Cardiac Murmur and Exertional Dyspnea in an Apparently Healthy Child: A Rare Localization of Obstructive Myxoma in the Right Ventricle Outflow Tract without Pulmonary Embolization—A Case Report and Literature Review
33. Decellularized esophageal tubular scaffold microperforated by quantum molecular resonance technology and seeded with mesenchymal stromal cells for tissue engineering esophageal regeneration
34. 3D bioprinting in airway reconstructive surgery: A pilot study
35. Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection
36. Case report: Unusual and extremely severe lipoprotein X-mediated hypercholesterolemia in extrahepatic pediatric cholestasis
37. Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients
38. Pathomorphogenesis of Glycogen-Ground Glass Hepatocytic Inclusions (Polyglucosan Bodies) in Children after Liver Transplantation
39. 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
40. Hemoadsorption for severe MIS-C in critically ill children, should we consider it as a therapeutic opportunity?
41. Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty yearsʼ experience
42. Mineralization of alpha-1-antitrypsin inclusion bodies in Mmalton alpha-1-antitrypsin deficiency
43. Decreased CDKN1C Expression in Congenital Alveolar Rhabdomyosarcoma Associated with Beckwith-Wiedemann Syndrome
44. Jejunal Adenocarcinoma in a 16-Year-Old Patient: An Unusual Case
45. Liver transplantation in an infant with cerebrotendinous xanthomatosis, cholestasis, and rapid evolution of liver failure
46. Non-Invasive Diagnostic Test for Advanced Fibrosis in Adolescents With Non-Alcoholic Fatty Liver Disease
47. How should eosinophilic cystitis be treated in patients with chronic granulomatous disease?
48. MYO5B Gene Mutations
49. Pediatric autoimmune disorders with gastrointestinal expressions: from bench to bedside
50. Not only a small liver - The pathologist’s perspective in the pediatric liver transplant setting
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