223 results on '"Nobili B"'
Search Results
2. The genetic ablation or pharmacological inhibition of TRPV1 signalling is beneficial for the restoration of quiescent osteoclast activity in ovariectomized mice
3. Successful T-cell-depleted, related haploidentical peripheral blood stem cell transplantation in a patient with Fanconi anaemia using a fludarabine-based preparative regimen without radiation
4. Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation
5. Interaction between metabotropic and NMDA glutamate receptors in the periaqueductal grey pain modulatory system
6. Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia
7. ASSESSMENT OF ITALIAN PRACTICE FOR MANAGEMENT OF ACUTE CHILDHOOD IDIOPATHIC THROMBOCYTOPENIC PURPURA.: O2-02
8. Rituximab for the treatment of refractory autoimmune hemolytic anemia in children
9. Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis
10. Diamond-Blackfan anaemia in the Italian population
11. CHROMOSOMAL LOCALIZATION OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE II (CDA-II)
12. Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis
13. CANNABINOID RECEPTOR 2 (CB2) 63 QQ VARIANT IS ASSOCIATED WITH A SEVERE HISTOLOGICAL ACTIVITY INDEX IN PATIENTS WITH CHRONIC HEPATITIS C
14. Management of Chronic Childhood Immune Thrombocytopenic Purpura: AIEOP Consensus Guidelines
15. Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels
16. Fanconi anaemia proteins: major roles in cell protection against oxidative damage
17. Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of S858R variant
18. Clinical and molecular evaluation of non-dominant hereditary spherocytosis
19. CONCORDANZA TRA VISITA OCULISTICA E RM ENCEFALO NELLO SCRRENING DEL GLIOMA DELLE VIE OTTICHE NEI PAZIENTI PEDIATRICI CON NEUROFIBROMATOSI TIPO I
20. Effect of eradication of Helicobacter pylori in children with chronic immune thrombocytopenia: A prospective, controlled, multicenter study
21. Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail:band 3 Vesuvio
22. Toxoplasmosi acquisita atipica con interessamento del nervo ottico: descrizione di un caso
23. Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients withhereditary spherocytosis
24. Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis
25. Anti CD20 monoclonal antibodies in PTI symtomatic refractories
26. Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele
27. A PRACTICAL APPROACH TO DIAGNOSIS AND TREATMENT OF SYMPTOMATIC THROMBOEMBOLIC EVENTS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA: RECOMMENDATIONS OF THE 'COAGULATION DEFECTS' AIEOP WORKING GROUP
28. Assessment of Italian practice for management of acute childhood idiopathic thrombocytopenic purpura
29. The Italian survey on hereditary spherocytosis
30. NEW INSIGHTS INTO THE FUNCTION OF N-TERMINAL 11 AMINO ACIDS OF BAND 3 (AE1) FROM STRUCTURAL AND FUNCTIONAL STUDY OF A NATURALLY OCCURRING BAND 3 VARIANT
31. Iron overload causes osteoporosis in thalassemia major patients through interaction with transient receptor potential vanilloid type 1 (TRPV1) channels
32. Splenectomia in laparoscopia in un bambino affetto da sferocitosi ereditaria
33. Anti-CD20 monoclonal antibody (Rituximab) for life-threatening autoimmune haemolytic anaemia in a patient with systemic lupus erythematosus
34. Impaired intestinal iron absorption in pediatric IBD correlates with disease activity and markers of inflammation
35. Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range
36. 447 CANNABINOID RECEPTOR 2 (CB2) 63 QQ VARIANT IS ASSOCIATED WITH A SEVERE HISTOLOGICAL ACTIVITY INDEX IN PATIENTS WITH CHRONIC HEPATITIS C
37. T-05 Cannabinoid receptor 2 (CB2) 63 QQ variant is associated with a severe histological activity index in patients with chronic hepatitis C
38. Neridronate improves bone mineral density and reduces pain in β-thalassemia patients with osteoporosis: Results from a randomized, open-label study
39. CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura
40. Molecular heterogeneity of hereditary elliptocytosis in Italy
41. The outcome of children with Fanconi anemia given hematopoietic stem cell transplantation and the influence of fludarabine in the conditioning regimen: a report from the Italian pediatric group
42. Inadequate leptin level negatively affects body fat loss during a weight reduction programme for childhood obesity
43. P-065: Serum hepcidin in pediatric inflammatory bowel disease
44. Inadequate leptin level negatively affects body fat loss during a weight reduction programme for childhood obesity
45. Cannabinoid Receptor 2 as Antiobesity Target: Inflammation, Fat Storage, and Browning Modulation
46. The fate of 4-hydroxytryptophan in the rat organism
47. L1 effects on reactive oxygen (ROS) and nitrogen species (RNS) release, hemoglobin oxidation, low molecular weight antioxidants, and antioxidant enzyme activities in red and white blood cells of thalassemic patients
48. THE PROBLEM OF RECESSIVE HEREDITARY SPHEROCYTOSIS (HS)
49. RECOMBINANT ERYTHROPOIETIN IN INFANTS WITH HEREDITARY SPHEROCYTOSIS
50. Evaluation of body iron status in Italian carriers of beta-thalassemia trait
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