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28 results on '"Gabriella Nebbia"'

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1. Gilbert or Crigler–Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity

2. Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

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3. Ceftriaxone-induced cholestatic hepatitis in a child: A case report and a review of the literature

5. Case Report: Early Treatment With Chenodeoxycholic Acid in Cerebrotendinous Xanthomatosis Presenting as Neonatal Cholestasis

6. KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature

7. Comparative analysis of rs12979860 SNP of the IFNL3 gene in children with hepatitis C and ethnic matched controls using 1000 Genomes Project data.

8. Diagnostic approach to neonatal and infantile cholestasis: A position paper by the SIGENP liver disease working group

9. Transplant-free Survival in Chronic Liver Disease Presenting as Acute Liver Failure in Childhood

10. Pediatric autoimmune liver disease and extra-hepatic immune-mediated comorbidities

11. Transient Hypothyroidism and Autoimmune Thyroiditis in Children With Chronic Hepatitis C Treated With Pegylated-interferon-α-2b and Ribavirin

12. Early ultrasound guided percutaneous liver biopsy in former preterm infants

13. The phenotype of compound heterozygous BSEP deficiency patients is determined by the combined residual function of the two ABCB11 mutations: results from the NAPPED consortium

14. Clinical features and natural history of 1154 Alagille syndrome patients: results from the international multicenter GALA study group

15. Kinetic of Virologic Response to Pegylated Interferon and Ribavirin in Children With Chronic Hepatitis C Predicts the Effect of Treatment

16. Epilepsy surgery in a liver-transplanted girl with temporal lobe epilepsy and hippocampal sclerosis following PRES with status epilepticus

18. P028 Establishing a SIGENP Italian network for the study of biliary atresia

20. Transient hypothyroidism and autoimmune thyroiditis in children with chronic hepatitis C treated with pegylated-interferon-α-2b and ribavirin

21. Recombinant interferon-alfa therapy in children with chronic hepatitis C

24. Posttransfusion and Community-Acquired Hepatitis C in Childhood

25. Nutritional status in Alagille syndrome

26. Neurological involvement in Crigler-Najjar type I syndrome: Role of liver transplantation

27. P0164 PP HCV GENOTYPES AND HEPATITIS C IN CHILDREN