184 results on '"Manca, L."'
Search Results
2. 18-FDG PET for large vessel vasculitis diagnosis and follow-up
3. A comparison between the β-globin gene clusters of domestic sheep (Ovis aries) and Sardinian mouflon (Ovis gmelini musimon)
4. PROGNOSTIC VALUE OF THE COMBINATION OF NON INVASIVE TEST (TWA-HRV-FE-HOLTER) IN THE HEART FAILURE POST AMI: 19.4
5. OMEGA 3 POLYUNSATURATED FATTY ACID (PUFA) AND MICROVOLTS T WAVE ALTERNANS (MTWA) IN PATIENTS WITH ICD: 19.5
6. A comparison between the β-globin gene clusters of domestic sheep (Ovis aries) and Sardinian mouflon (Ovis gmelini musimon)
7. Long-Term Follow-Up of 106 Multiple Sclerosis Patients Undergoing Interferon-β 1a or 1b Therapy: Predictive Factors of Thyroid Disease Development and Duration
8. The C→G transition in the α2-globin gene of a normal αα-chromosome is responsible for the Hb G-Philadelphia variant in Sardinians
9. Maximal γ-globin expression in the compound heterozygous state for-175 Gγ HPFH and β°39 nonsense thalassaemia: a case study
10. Multilingual Lexicon of Bone Industry, Version 2 (Français-Anglais- Allemand, Danois, Espagnol, Italien, Portugais, Roumain, Bulgare, Polonais, Russe, Hongrois). GDRE PREHISTOS ARCHAEOLOGICAL STUDIES II 2015
11. Visual displays for automated driving: A survey
12. Photovoltaic properties of PSi impregnated with eumelanin
13. PND91 PREDICTORS OF NON-ADHERENCE AMONG PATIENTS WITH MULTIPLE SCLEROSIS NEWLY INITIATING ONCE- OR TWICE-DAILY ORAL DISEASE-MODIFYING DRUGS
14. ND3 USE OF GROUP-BASED TRAJECTORY MODELING TO IDENTIFY ADHERENCE CLUSTERS IN PATIENTS WITH MULTIPLE SCLEROSIS NEWLY-INITIATING ONCE- OR TWICE-DAILY ORAL DISEASE-MODIFYING DRUGS
15. DNA polymorphisms in north Sardinian newborns and their linkage with abnormal γ globin gene arrangements and with βo-thalassemia
16. Predictors of mortality and hospitalization for cardiac causes in patients with heart failure and nonischemic heart disease: a subanalysis of the ALPHA study
17. Predicting all-cause mortality in non-ischemic heart failure patients, interesting outsiders?
18. (464) Identification of Subgroups in Responses to pregabalin in patients with Painful Diabetic Peripheral Neuropathy (pDPN) Enables Utilization of Randomized Controlled Trial (RCT) Data to Reduce Covariate Bias in Observational Study (OS) Data
19. (403) Positive Predictive Value of Responses to Pregabalin in Patients with Severe Painful Diabetic Peripheral Neuropathy (pDPN) using Integrated Time-Series Randomized Controlled Trial (RCT) and Observational Study (OS) data
20. Natural parasitism of Bemisia tabaci and Trialeurodes vaporariorum in an horticultural area of Sardinia, Italy
21. Beta-thalassaemia-87 C > G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients
22. Adult and fetal haemoglobin J-Sardegna [alpha 50(CE8)His -> Asp]: functional and molecular modelling studies
23. FUNCTIONAL ALTERATIONS IN ADULT AND FETAL HEMOGLOBIN SASSARI ASP-ALPHA-126(H9) -] HIS - THE ROLE OF ALPHA(1)ALPHA(2) CONTACT
24. AN ANTIBODY REACTIVITY-BASED ASSAY FOR DIAGNOSIS OF INVASIVE CANDIDIASIS USING PROTEIN ARRAY.
25. PROTEIN MICROARRAYS ON MIDTRIMESTER AMNIOTIC FLUIDS: A NOVEL APPROACH FOR THE DIAGNOSIS OF EARLY INTRAUTERINE INFLAMMATION RELATED TO PRETERM DELIVERY.
26. Proportion of patients needing an implantable cardioverter defibrillator on the basis of current guidelines: impact on healthcare resources in Italy and the USA. Data from the ALPHA study registry.
27. A New, Electrophoretically Silent, Fetal Hemoglobin Variant: Hb F-Calabria [Gγ118(GH1)Phe→Leu].
28. Characterization by DNA Sequencing of Hb F-Columbus-GA [Gγ94(FG1)Asp→Asn] Observed in Sardinian Newborn.
29. Haemoglobin phenotypes of the wild European mouflon sheep living on the island of Sardinia.
30. Maximal γ-globin expression in the compound heterozygous state for -175 Gγ HPFH and β°39 nonsense thalassaemia: a case study.
31. Polymorphism of Foetal Haemoglobin in the Sardinian β+-Thalassaemia.
32. Residual muscle cytochrome c oxidase activity accounts for submaximal exercise lactate threshold in chronic progressive external ophthalmoplegia.
33. The level of Hb F-sardinia (α2A γ2 75IIe→Thr) in the fetal hemoglobin of sardinian β-thalassemic homozygotes determined by isoelectric focusing.
34. Sheep Hb I Variant, or βB13(A10)Gly→Ser, in Breeds From Corsica: Detection by Gene Sequencing.
35. Hb F-Sassari: A Novel Gγ Variant with a Threonine Residue at Position γ75, Characterized by Mass Spectrometry Techniques.
36. Hb G-Miwlo [α64(E13)ASP→ASN] Observed in a Caucasian Family.
37. A Simple Approach To the Determination of the γ Chain Composition of F in Adult Human Blood Samples.
38. Hb Lepore-Baltimore in a North Sardinian Family.
39. Abnormal γ-Globin Gene Arrangements in Sardinians.
40. A Search for Anomalies in the ζ,α,β, and γ Globin Gene Arrangements in Normal Black, Italian, Turkish, and Spanish Newborns.
41. Homozygous βd``-39 Mutation with Thalassemia Intermedia in Northern Sardinia: Clinical, Hematological and Molecular Analysis.
42. Biochemical and Molecular Aspects of β-Thalassemia Types in Northern Sardinia.
43. HB Sassari or α2126(H9)ASP→HISfβ2 Observed in a Family from Northern Sardinia.
44. Hemoglobin Hamilton [β11(A8)VAL →] in Sardinia.
45. The Gamma Globin Chain Heterogeneity of the Sardinian Newborn Baby.
46. A Study of the Switch of Fetal Hemoglobin in Newborn Erythrocytes Fractionated by Density Gradient.
47. Diminished AγT fetal globin levels in Sardinian haplotype II β°-thalassaemia patients are associated with a four base pair deletion in the AγT promoter.
48. Sardinian Haplotype II β0-Thalassemia Is Linked to the Variant AγT-Globin Gene with a 4-Bp Promoter Deletion and Diminished AγT Expressiona,b,.
49. Haemoglobin I: a new β-globin chain variant found in sheep of Italian breeds.
50. Phylogenetic relationships and molecular dating of the main evolutionary events within Caprini tribe inferred by mtDNA and globin genes sequence.
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