S. Cutillo

发表

Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on the population of Naples

G. Battistuzzi, A. Iolascon, S. Colonna-Romano, 2004, Human Genetics.

Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74).

S. Perrotta, A. Iolascon, E. Miraglia Del Giudice, 1994, Blood.

Spectrin Anastasia (αI/78): a new spectrin variant (α45 Arg Thr) with moderate elliptocytogenic potential

S. Perrotta, A. Iolascon, G. Colonna, 1995 .

Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential.

S. Perrotta, A. Iolascon, G. Colonna, 1995, British journal of haematology.

Insulin response to glucagon in obese children.

F. D'onofrio, G. Stoppoloni, S. Cutillo, 1968, Lancet.

Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locus

S. Perrotta, M. Tanner, A. Iolascon, 1997, British journal of haematology.

Frequent de novo monoallelic expression of β‐spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency

S. Perrotta, A. Iolascon, E. Miraglia Del Giudice, 1998, British journal of haematology.

Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia

S. Perrotta, A. Iolascon, M. Vivo, 2001, Leukemia.

Developmental changes in HbA2 and HbF on neocytes and gerocytes in normal infants during the first year of life.

A. Iolascon, B. Nobili, L. Pinto, 1983, Acta Haematologica.

EFFECT OF OROTIC ACID UPON SERUM BILIRUBIN IN NEWBORN INFANTS WITH ERYTHROCYTE G‐6‐PD DEFICIENCY

T. Meloni, S. Cutillo, A. Dore, 1974, Acta paediatrica Scandinavica.

[Hemolytic-uremic syndrome].

S. Cutillo, 1973, La Pediatria.

[On the behavior of creatine-phosphokinase activity in the serum of patients with progressive muscular dystrophy].

A. Coletta, S. Cutillo, F. Rea, 1963, Bollettino della Societa italiana di biologia sperimentale.

Oxytocic agents and neonatal hyperbilirubinaemia in G.-6-P.D.-deficient newborns.

T. Meloni, G. Careddu, S. Cutillo, 1973, Lancet.

High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis.

S. Perrotta, J. Delaunay, B. Nobili, 1998, The Journal of pediatrics.

Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues.

S. Perrotta, A. Iolascon, A. Pession, 1991, Medical and pediatric oncology.

HEREDITARY SPHEROCYTOSIS CHARACTERIZED BY INCREASED SPECTRIN/BAND 3 RATIO

S. Perrotta, A. Iolascon, M. Cappellini, 1992, British journal of haematology.

Phototherapy for neonatal hyperbilirubinemia in mature newborn infants with erythrocyte G-6-PD deficiency.

T. Meloni, S. Cutillo, A. Dore, 1974, The Journal of pediatrics.

Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis

A. Iolascon, B. Nobili, L. Pinto, 2005, European Journal of Pediatrics.

Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in Sardinia

G. Battistuzzi, L. Luzzatto, U. Testa, 1980, Human Genetics.

Hereditary spherocytosis (HS) due to loss of anion exchange transporter.

S. Perrotta, A. Iolascon, C. Vasseur, 1992, Haematologica.

Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases

S. Perrotta, A. Iolascon, C. Camaschella, 1991, British journal of haematology.

Neonatal jaundice and severity of glucose-6-phosphate dehydrogenase deficiency in Sardinian babies.

L. Luzzatto, U. Testa, T. Meloni, 1987, Early human development.

Neonatal hyperbilirubinaemia in heterozygous giucose‐6‐phosphate dehydrogenase deficient females

G. Forteleoni, S. Cutillo, Tullio Meloni, 1983, British journal of haematology.

Phenobarbital for prevention of hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient newborn infants.

T. Meloni, S. Cutillo, G. Cagnazzo, 1973, The Journal of pediatrics.

Favism and hemolytic anemia in glucose-6-phosphate dehydrogenase-deficient subjects in North Sardinia.

G. Forteleoni, T. Meloni, S. Cutillo, 1983, Acta haematologica.

[On the L-leucine aminopeptidase activity of the blood in childhood].

S. Cutillo, V. Ansanelli, R. Di Toro, 1961, La Pediatria.

Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio.

M. L. Cone, S. Perrotta, A. Iolascon, 1999, Blood.

αI/65 Hereditary elliptocytosis in Southern Italy: Evidence for an African origin

S. Perrotta, A. Iolascon, J. Delaunay, 1992, Human Genetics.

Haptoglobin, hemopexin, hemoglobin and hematocrit in newborns with erythrocyte glucose-6-phosphate dehydrogenase deficiency.

T. Meloni, S. Cutillo, S. Costa, 1975, Acta haematologica.

Agar in control of hyperbilirubinemia of full-term newborn infants with erythrocyte G-6-PD deficiency.

T. Meloni, S. Cutillo, R. Corti, 1978, Biology of the neonate.

Serum concentrations of haptoglobin and hemopexin in favism and thalassemia.

T. Meloni, S. Cutillo, 1974, Acta haematologica.