183 results on '"Schiliro, G"'
Search Results
2. Road Traffic Pollution and Childhood Leukemia: A Nationwide Case-control Study in Italy
3. Air pollution and childhood leukaemia: a nationwide case-control study in Italy
4. Isonymy in Haemoglobinopathies in a Sicilian Sample
5. Road Traffic Pollution and Childhood Leukemia: A Nationwide Case-control Study in Italy
6. Prolyl-hydroxylase and procollagen type III as markers of liver damage in long-term survivors with acute lymphoblastic leukemia (ALL): a biochemical approach of HCV-related liver disease
7. Hb Bronte or alpha93(FG5)Val>Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype
8. General transcription factors TAF13, NC2β, GTF3BAP1 and TAF12 are specifically involved in neuroblastoma pathogenesis
9. Diagnostica delle anemie
10. Phenotype-genotype correlation in Sicilian patients with Hb H
11. LATE PROGRESSION OF A NEUROBLASTOMA AS A MALIGNANT SCHWANNOMA
12. Acute neurotoxicity in children with B-lineage acute lymphoblastic leukemia treated with intermediate risk protocols
13. Malattia epatica e leucemia linfoblastica acuta dell'infanzia: ruolo del virus C e prognosi
14. Characteristics of sicilian women attending cancer screenings
15. Anemia
16. Alloimmunization and autoimmunity in Caucasian patients with sickle cell disease
17. Dysmegakaryopoietic thrombocytopenia in patients with distal chromosome 11q deletion
18. 2. Micromegakarycytes in a patient with partial deletion of the long arm of chromosome 11 del (ll)(q24.2qter)] and chronic thrombocytopenic purpura
19. Thalassaemia strategy in Sicily
20. BETA-S HAPLOTYPES IN VARIOUS WORLD POPULATIONS
21. STUDIES OF DELAYED-HYPERSENSITIVITY RESPONSES IN CHILDREN IN AN INDUSTRIALIZED REGION OF ITALY
22. Comparison of clinical, hematological and molecular findings of Jamaican and Sicilian patients with sickle cell disease
23. Antibodies to hepatitis C virus in sicilian polytransfused thalassemic patient
24. The problem of preventing testicular leukaemia
25. Dysmegakaryopoietic thrombocytopenia in patients with distal chromosome 11q deletion [letter; comment]
26. Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals [letter]
27. Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia
28. γ-mRNA and Hb F levels in β-thalassaemia
29. Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β-thalassaemia due to a homozygosity for the IVS-I-6 (T→C) mutation
30. A mild type of Hb S‐β+‐thalassemia [‐92(C→T)] in a sicilian family
31. Allergy to desferrioxamine
32. Clinical, hematological, and molecular features in sicilians with Hb S‐β‐thalassemia
33. Growth and Development in White Patients with Sickle Cell Diseases
34. Antioxidant enzymatic systems and oxidative stress in erythrocytes with G6PD deficiency: Effect of deferoxamine
35. The Usefulness of Sequence Analysis of Amplified DNA for the Identification of δ Chain Variants
36. Does Endogenous Growth Hormone Influence Immune Function? Immunological Studies in Laron's Dwarfism
37. Hb Agenogi [β90(F6)Glu → Lys] and β°-Thalassa in A Sicilian Family
38. Evidence for the Single Origin of Hb G-San Jose in Sicily.
39. Association of Hb S [β6(A3)Glu→Val] and Hb I-Interlaken [α15(A13)Gly→Asp] in a Sicilian Man; Review of the Occurrence of Hb I-Interlaken in Sicily.
40. A Search for Anomalies in the ζ,α,β, and γ Globin Gene Arrangements in Normal Black, Italian, Turkish, and Spanish Newborns.
41. Incidence of Hemoglobin S Carriers in Sicily.
42. Hb J Baltimore (β 16 (A13) Gly ↣↣ Asp) in Association with β-Thalassemia in a Sicilian Family.
43. Glucose-6-phosphate dehydrogenase deficiency in Sicily. Incidence, biochemical characteristics and clinical implications.
44. Haemoglobin Lepore Boston-Washington in Sicily: clinical, haematological, and biosynthetic studies.
45. Sickle cell disease in Sicily.
46. The Use of Artificial Neural Networks Methodology in the Assessment of "Vulnerability" to Heroin Use among Army Corps Soldiers: A Preliminary Study of 170 Cases inside the Military Hospital of ...
47. Lymphocyte changes in β-thalassaemia major.
48. A new alkali-resistant hemoglobin alpha2J Oxford gammaF2 in a Sicilian baby girl with homozygous beta0 thalassemia
49. Photon scattering as a probe of microviscosity and channel size in gels such as sickle haemoglobin
50. Effects of splenectomy on lymphocyte recirculation. An experimental study
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