T. Lombardo

发表

Presence of an African β‐globin gene cluster haplotype in normal chromosomes in sicily

D. Labie, R. Nagel, A. Ragusa, 1992 .

Asymptomatic and mild β-thalassemia in homozygotes and compound heterozygotes for the IVS 2 + 1 G > A mutation : role of the β-globin gene haplotype

D. Labie, L. Bernini, M. Maier‐Redelsperger, 2003 .

Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype.

D. Labie, L. Bernini, M. Maier‐Redelsperger, 2003, Haematologica.

A leftward deletional α+ thalassemia found in East Sicily in conjunction with heterozygous β-thalassemia

D. Labie, R. Krishnamoorthy, T. Lombardo, 2004, Human Genetics.

Annotated Definition of BCL11A and HMIP-2 Haplotypes Through the Analysis of Sicilian β-Thalassemia Patients with High Levels of Fetal Hemoglobin

D. Labie, M. Buccheri, T. Lombardo, 2013, Hemoglobin.

Possible Evidence for an Increased Factor VIII Antigen Synthesis in Vascular Endothelium of Diabetic Subjects

E. Cacciola, T. Lombardo, N. Catania, 1982, Thrombosis and Haemostasis.

[Considerations on the insulin-binding property of the blood of normal subjects and diabetics never treated with insulin].

T. Lombardo, M. Lunetta, L. Motta, 1968, Acta diabetologica latina.

βS gene in sicily is in linkage disequilibrium with the benin haplotype: Implications for gene flow

D. Labie, R. Nagel, A. Ragusa, 1988, American journal of hematology.

Intriguing Prevalence of Benin‐Type Sickle Cell Gene on Atypical Haplotypes in Sickle Cell/β‐Thalassemia But Not in Sickle Cell Anemia in Sicily a

J. Elion, A. Ragusa, R. Krishnamoorthy, 1990 .

HAPLOTYPE-VI-ASSOCIATED MILD β+-THALASSAEMIA IN SICILY: MEDITERRANEAN TYPE?

D. Labie, R. Cacciola, T. Lombardo, 1983, The Lancet.

HCV and HBV infection among multitransfused thalassemics from Eastern Sicily

R. Russo, B. Cacopardo, S. Cosentino, 1992, Infection.

Prevalence of markers for human immunodeficiency virus types 1 and 2, human T‐lymphotropic virus type I, cytomegalovirus, and hepatitis B and C virus in multiply transfused thalassemia patients. The French Study Group On Thalassaemia

D. Costagliola, R. Girot, S. Cosentino, 1992, Transfusion.

Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily

D. Labie, A. Ragusa, M. Lombardo, 1986, Human Genetics.

Multiple Molecular Bases for Thalassemia Intermedia in East Sicily a

D. Labie, J. Elion, R. Krishnamoorthy, 1985, Annals of the New York Academy of Sciences.

Genetic epidemiology of β‐thalassemia in sicily: Do sequences 5′ to the Gγ gene and 5′ to the β gene interact to enhance HbF expression in β‐thalassemia?

R. Nagel, J. Elion, C. Beldjord, 1992 .

Genetic epidemiology of beta-thalassemia in Sicily: do sequences 5' to the G gamma gene and 5' to the beta gene interact to enhance HbF expression in beta-thalassemia?

R. Nagel, J. Elion, C. Beldjord, 1992, American journal of hematology.

Molecular basis of α-thalassemia in Sicily

M. Fichera, D. Labie, R. Tamouza, 1997, Human Genetics.

Change on Blood Coagulation, Platelet Function and Fibrinolysis in Diabetes Mellitus - Preliminary Report

E. Cacciola, T. Lombardo, R. Giustolisi, 1977, Thrombosis and Haemostasis.

Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haplotypes and are unrelated to fetal hemoglobin expression.

D. Labie, R. Nagel, E. Bouhassira, 1989, American Journal of Human Genetics.

‘μ’ Heavy Chain Type ‘Non‐Excretory’ Myeloma

F. Raimondo, T. Lombardo, P. Guglielmo, 2009 .