C. Vullo

发表

Impaired HLA capping capacity of peripheral blood lymphocytes in Duchenne muscular dystrophy.

A. Sensi, A. Venturoli, S. Traniello, 1984, Journal of medical genetics.

Alpha and beta cell evaluation in patients with thalassaemia intermedia and iron overload.

B. Bagni, V. De Sanctis, C. Vullo, 1985, Postgraduate medical journal.

Haemoglobin levels and blood requirement in thalassaemia.

G. Masera, A. Piga, A. D. Di Palma, 1982, Archives of disease in childhood.

Osteopenia in Thalassemic Patients with Primary and Secondary Amenorrhea

B. Bagni, G. Bonaccorsi, C. Vullo, 1995 .

Endocrine Abnormalities in Thalassemia

A. Hoffbrand, B. Bagni, G. Tolis, 1990, Annals of the New York Academy of Sciences.

beta (+)-Thalassaemia in the Po river delta region (northern Italy): genotype and beta globin synthesis.

Y. Kan, L. del Senno, F. Bernardi, 1985, Journal of medical genetics.

Reproductive behaviour of families segregating for Cooley's anaemia before and after the availability of prenatal diagnosis.

I. Barrai, B. Anderson, M. Lucci, 1991, Journal of medical genetics.

Effect of different treatment regimes on linear growth and final height in β‐thalassaemia major

B. Bagni, C. Vullo, V. Sanctis, 1994, Clinical endocrinology.

Induction of spermatogenesis in thalassaemia.

B. Bagni, V. De Sanctis, C. Vullo, 1988, Fertility and sterility.

Haplotypes of thalassaemic families from the Po river delta: Importance for prenatal diagnosis of β‐thalassaemia

A. Venturoli, M. Lucci, C. Vullo, 1988, European journal of haematology.

Ferrara β0 thalassaemia caused by the β39 nonsense mutation

Y. Kan, M. Pirastu, C. Vullo, 1984, Nature.

Biological performance in β‐thal heterozygotes and normals: results of a longitudinal comparison in a former malarial environment

I. Barrai, G. Barbujani, C. Vullo, 1987, Annals of human genetics.

Hepatitis C virus antibodies in a long-term follow-up of beta-thalassaemic children with acute and chronic non-A non-B hepatitis

E. Zammarchi, C. Azzari, A. Vierucci, 1992, European Journal of Pediatrics.

Prevalence of Hepatitis C Vims Antibody in Beta‐Thalassemic Polytransfused Children in a Long‐Term Follow‐Up

C. Azzari, A. Vierucci, M. Resti, 1991, Vox sanguinis.

Beta-thalassemia in the Po Delta: selection, geography, and population structure.

I. Barrai, C. Scapoli, G. Barbujani, 1984, American journal of human genetics.

Appearance of β globin synthesis in erythroid cells of Ferrara β°-thalassaemic patients following blood transfusion

D. Labie, C. Vullo, F. Conconi, 1975, Nature.

Growth and development in thalassaemia major patients with severe bone lesions due to desferrioxamine

C. Vullo, V. Sanctis, M. Gamberini, 1996, European Journal of Pediatrics.

Growth and sexual maturation in thalassemia major.

G. Masera, A. Piga, V. De Sanctis, 1985, The Journal of pediatrics.

Gonadal function in patients with beta thalassaemia major.

B. Bagni, V. De Sanctis, C. Vullo, 1988, Journal of clinical pathology.

Gonadal function after allogenic bone marrow transplantation for thalassaemia.

G. Lucarelli, V. De Sanctis, M. Galimberti, 1991, Archives of disease in childhood.

Growth and endocrine function after bone marrow transplantation for thalassemia major.

G. Lucarelli, V. De Sanctis, M. Galimberti, 1989, Progress in clinical and biological research.

Hypoparathyroidism in Beta-Thalassemia major

B. Bagni, C. Vullo, V. Sanctis, 1992 .

Hypoparathyroidism in beta-thalassemia major. Clinical and laboratory observations in 24 patients.

B. Bagni, V. De Sanctis, C. Vullo, 1992, Acta haematologica.

Transabdominal chorionic villus sampling: Analysis of 350 consecutive cases

N. Rizzo, C. Vullo, Luciano Bovicelli, 1988, Prenatal diagnosis.

Primary hypothyroidism and the low T3 syndrome in thalassaemia major

B. Bagni, V. De Sanctis, C. Vullo, 1983, Archives of disease in childhood.

Decrease of Alpha‐Hasharon Globin in Beta‐Thalassaemia

G. Mariuzzi, C. Vullo, F. Conconi, 1978, British journal of haematology.

alpha-Thalassemia trait in the region of Ferrara.

L. del Senno, F. Bernardi, G. Marchetti, 1981, Haematologica.

Psychosocial Integration of Adolescents and Young Adults with Thalassemia Major

B. Zani, C. Vullo, A. Palma, 1998, Annals of the New York Academy of Sciences.

Psychosocial aspects of chronic illness in adolescents with thalassaemia major

B. Zani, C. Vullo, A. Palma, 1995 .

Organization of α‐Globin Genes and mRNA Translation in Subjects Carrying Haemoglobin Hasharon (α47 Asp → His) from the Ferrara Region (Northern Italy)

F. Bernardi, G. Marchetti, C. Vullo, 2005 .

Duchenne muscular dystrophy . peripheral blood lymphocytes in Impaired HLA capping capacity of

C. Vullo, P. Mattiuz, R. Baricordi, 2022 .

Low red blood cell glutathione reductase and pyridoxine phosphate oxidase activities not related to dietary riboflavin: selection by malaria?

B. Anderson, C. Vullo, G. Perry, 1993, The American journal of clinical nutrition.

A Multi‐Center Safety Trial of the Oral Iron Chelator Deferiprone

A. Piga, F. Tricta, C. Vullo, 1998, Annals of the New York Academy of Sciences.

Raised IgE levels in beta-thalassaemia: correlation with splenectomy and hepatitis B virus infection.

M. de Martino, W. London, A. Vierucci, 1984, Clinical and experimental immunology.

Elusive blood clots and fluctuating ventricular dilatation after neonatal intraventricular haemorrhage

G. Masera, A. Piga, C. Vullo, 2006 .

Pubertal development in thalassaemic patients after allogenic bone marrow transplantation

B. Bagni, G. Lucarelli, D. Baronciani, 1993, European Journal of Pediatrics.

Survival studies of thalassemic erythrocytes transfused into donors, into subjects with thalassemia minor and into normal and splenectomized subjects.

C. Vullo, A. M. Tunioli, 1958, Blood.

Glutathione reductase activity and its relationship to pyridoxine phosphate activity in G6PD deficiency

B. Anderson, C. Vullo, G. Perry, 1987, European journal of haematology.

Pattern of iron excretion in relation to haemoglobin level and iron load in 8 haematological patients following the administration of subcutaneous deferrioxamine

F. Fagioli, C. Vullo, G. Atti, 1994, European journal of haematology.

Altered T Cell Subsets and Function in Polytransfused β‐Thalassemia Patients: Correlation with Sex and Age at First Transfusion

A. Vierucci, C. Vullo, M. Rossi, 1985, Vox sanguinis.

Red‐cell GSH regeneration and glutathione reductase activity in G6PD variants in the Ferrara area

B. Anderson, M. Lucci, C. Vullo, 1987, British journal of haematology.

Sexual performance and fertility potential in patients with beta thalassemia major.

A. Hoffbrand, B. Bagni, V. De Sanctis, 1989, Progress in clinical and biological research.

Endocrine assessment of hypogonadism in patients affected by thalassaemia major

B. Bagni, C. Vullo, V. Sanctis, 1980, La Ricerca in clinica e in laboratorio.

Genetic and other influences on red‐cell flavin enzymes, pyridoxine phosphate oxidase and glutathione reductase in families with β‐thalassaemia

B. Anderson, C. Vullo, R. Fashola, 1989, European journal of haematology.

Hereditary Pyruvate Kinase Deficiency: Role of the Abnormal Enzyme in Red Cell Pathophysiology

A. Zanella, P. Rebulla, G. Sirchia, 1978, British journal of haematology.

New developments in stem cell transplantation with special reference to the first in utero transplants in humans.

D. Frappaz, M. Roncarolo, F. Freycon, 1991, Bone marrow transplantation.

The Selective Destruction of “Compatible” Red Cells Transfused in a Patient Suffering from Thalassaemia Major

C. Vullo, A. M. Tunioli, 1961, Vox sanguinis.

The Use of Biomagnetic Liver Susceptometry in the Ferrara-Hamburg-Turin Study on Thalassemia

A. Piga, F. Tricta, R. Fischer, 2000 .

Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution

A. Piazza, P. Pignatti, A. Villani, 1997, Annals of human genetics.

marrow transplantation for thalassaemia . Gonadal function after allogenic bone

G. Lucarelli, M. Galimberti, P. Polchi, 2007 .

Deficiency of two red-cell flavin enzymes in a population in Sardinia: was glutathione reductase deficiency specifically selected for by malaria?

B. Anderson, C. Vullo, L. Corda, 1995, American journal of human genetics.

Did malaria select for primary adult lactase deficiency?

B. Anderson, C. Vullo, 1994, Gut.

Is the flavin-deficient red blood cell common in Maremma, Italy, an important defense against malaria in this area?

B. Anderson, G. Buonocore, P. Galván, 1994, American journal of human genetics.

Gonadal function in long term survivors with B thalassemia major following bone marrow transplantation.

B. Bagni, G. Lucarelli, V. De Sanctis, 1993, Bone marrow transplantation.

Endocrine complications in thalassaemia major.

B. Bagni, V. De Sanctis, A. D. Di Palma, 1989, Progress in clinical and biological research.

Clinical experience using the Androderm testosterone transdermal system in hypogonadal adolescents and young men with beta-thalassemia major.

N. Mazer, V. De Sanctis, C. Vullo, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Hemolysis in vitro and the anemia of leukemia.

W. Crosby, C. Vullo, S. Garriga, 1961, Blood.

major low T 3 syndrome in thalassaemia Primary hypothyroidism and the and

B. Bagni, C. Vullo, V. Sanctis, 2006 .

Effectiveness of partial splenic embolization as treatment for hypersplenism in thalassaemia major: A 7‐year follow up

A. Pinca, B. Bagni, P. Mannella, 1992, European journal of haematology.

Hypothalamic-Pituitary-Gonadal Axis in Thalassemic Patients With Secondary Amenorrhea

B. Bagni, V. De Sanctis, C. Vullo, 1988, Obstetrics and gynecology.

Vitamin E in beta-thalassemia.

R. Miniero, D. Ghigo, C. Vullo, 1982, Acta vitaminologica et enzymologica.

Changes in superoxide anion production in neutrophils from multitransfused beta-thalassemia patients: correlation with ferritin levels and liver damage.

M. de Martino, A. Vierucci, M. Resti, 1984, Acta Haematologica.

Antibodies to HTLV‐III and the Lymphadenopathy Syndrome in Multitransfused β‐Thalassemia Patients

A. Vierucci, C. Vullo, A. Saimot, 1985, Vox sanguinis.

Comparison of structures from frequencies of genes and surnames in the population of Ferrara.

I. Barrai, C. Scapoli, M. Beretta, 1993, Human biology.

Heterozygosity and geographic distances in a limited area

I. Barrai, M. Beretta, G. Barbujani, 1983 .

A study of nine polymorphic systems in the population of the Po Delta.

R. Palmarino, E. Bottini, P. Lucarelli, 1976, American journal of physical anthropology.

Genetic structure of the human population in the Po delta.

M. Beretta, E. Mamolini, R. Barale, 1989, American journal of human genetics.

Pharmacokinetics of sex steroids in patients with beta thalassaemia major.

B. Bagni, V. De Sanctis, C. Vullo, 1993, Journal of clinical pathology.

THE FŒTAL THYMUS

C. Vullo, G. Biasini, A. Montaguti, 1966 .

Early tubular functional changes in autosomal dominant polycystic kidney disease.

L. del Senno, C. Vullo, A. Farinelli, 1989, Nephron.

Endocrine function after bone marrow transplantation for thalassemia.

B. Bagni, G. Lucarelli, V. De Sanctis, 1991, Bone marrow transplantation.

ANTIMALARIAL EFFECTS OF RIBOFLAVIN DEFICIENCY

B. Anderson, H. Powers, C. Bates, 1986, The Lancet.

Semen parameters in patients with homozygous β-thalassemia

C. Vullo, D. Mazzotta, B. Wonke, 1989 .

Safety profile of the oral iron chelator deferiprone: a multicentre study

Vullo, R. Galanello, A. Piga, 2000, British journal of haematology.

Comparison of prolactin response to suckling and breast pump aspiration in lactating mothers

B. Bagni, C. Vullo, V. Sanctis, 1981, La Ricerca in clinica e in laboratorio.

[Effects of heparin in experimental nephrosis].

C. Vullo, P. Careddu, 1956, Bollettino della Societa italiana di biologia sperimentale.