A MULTIPLE NEONATAL HAEMANGIOMATOSIS WITH FAVOURABLE OUTCOME FOLLOWING STEROID THERAPYSCHILIRO G; GUARNERI B; RUSSO A et al.1976; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1976; VOL. 65; NO 2; PP. 267-270; BIBL. 14 REF.Article

Reappraisal of high-dose desferrioxamine therapySCHILIRO, G; RUSSO, A.Acta haematologica. 1986, Vol 76, Num 1, pp 63-64, issn 0001-5792Article

HEMOGLOBINOPATHIES IN ITALYMARINUCCI M; SCHILIRO G; RUSSO G et al.1982; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1982; VOL. 6; NO 3; PP. 247-255; BIBL. 11 REF.Article

LEUKOCYTE FUNCTION AND CHARACTERIZATION OF LEUKOCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN SICILIAN MUTANTS.SCHILIRO G; RUSSO A; MAURO L et al.1976; PEDIATR. RES.; U.S.A.; DA. 1976; VOL. 10; NO 8; PP. 739-742; BIBL. 26 REF.Article

K CELL ACTIVITY IN ACUTE LYMPHOBLASTIC LEUKAEMIA OF CHILDHOODSCHILIRO G; MUSUMECI S; SCIOTTO A et al.1980; ACTA HAEMATOL.; ISSN 0001-5792; CHE; DA. 1980; VOL. 64; NO 4; PP. 221-223; BIBL. 9 REF.Article

QUANTITATION OF HUMAN GLOBIN CHAIN SYNTHESIS BY CELLULOSE ACETATE ELECTROPHORESISSALMON JE; NUDEL U; SCHILIRO G et al.1978; ANAL. BIOCHEM.; USA; DA. 1978; VOL. 91; NO 1; PP. 146-157; BIBL. 18 REF.Article

BLOOD GROUP PHENOTYPES AND THE ORIGIN OF SICKLE CELL HEMOGLOBIN IN SILICIANSSANDLER SG; SCHILIRO G; RUSSO A et al.1978; ACTA HAEMATOL.; CHE; DA. 1978; VOL. 60; NO 6; PP. 350-357; BIBL. 36 REF.Article

HEMOLYTIC CRISES OF FAVISM IN SICILIAN FEMALES HETEROZYGOUS FOR G-6-PD DEFICIENCY = CRISES HEMOLYTIQUES DE FAVISME CHEZ DES FILLES SICILIENNES HETEROZYGOTES POUR LE DEFICIT EN G-6-PDRUSSO G; MOLLICA F; PAVONE L et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 49; NO 6; PP. 854-859; BIBL. 22 REF.Serial Issue

DELTA BETA -THALASSAEMIA IN SICILY: REPORT OF A CASE OF DOUBLE HETEROZYGOSITY FOR AGAMMA DELTA BETA -THALASSAEMIA AND AGAMMA GGAMMA DELTA BETA -THALASSAEMIAMUSUMECI S; ROMEO MA; PIZZARELLI G et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 1; PP. 73-75; BIBL. 7 REF.Article

A CASE OF PROBABLE RICKETTSIAL DISEASE IN ACUTE LYMPHOBLASTIC LEUKEMIASCHILIRO G; RUSSO A; MARINO S et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 1; PP. 63-64; BIBL. 11 REF.Article

STUDIES OF THE NEUTROPENIA IN KALA-AZAR: RESULTS IN TWO PATIENTS.MUSUMECI S; D'AGATA A; SCHILIRO G et al.1976; TRANS. R. SOC. TROP. MED. HYG.; G.B.; DA. 1976 PARU 1977; VOL. 70; NO 5-6; PP. 500-503; BIBL. 16 REF.Article

EOSINOPHILIA IN LEUKAEMIARUSSO A; MARINO S; SCIOTTO A et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 47; NO 2; PP. 323-325; BIBL. 8 REF.Article

LENKOKINETIC STUDIES IN MEDITERRANEAN KALA AZAR.MUSUMECI S; D'AGATA A; SCHILIRO G et al.1978; ACTA TROP.; SUISSE; DA. 1978; VOL. 35; NO 2; PP. 183-193; BIBL. 21 REF.Article

VISCERAL LEISHMANIASIS FOLLOWING A SKIN LESION IN A SIX-YEAR-OLD SICILIAN GIRLSCHILIRO G; RUSSO A; MUSUMECI S et al.1978; TRANS. R. SOC. TROP. MED. HYG.; GBR; DA. 1978; VOL. 72; NO 6; PP. 656-657; BIBL. 17 REF.Article

INSULIN AND GROWTH HORMONE SECRETION IN A LEUKAEMIC GIRL WITH HYPOTHALAMIC SYNDROME.SCHILIRO G; RUSSO A; SCIOTTO A et al.1977; ACTA POEDIATR. SCAND.; SUEDE; DA. 1977; VOL. 66; NO 2; PP. 261-263; BIBL. 21 REF.Article

Comparative approach to the evaluation of hemoglobin A₂ by two different methods : high-performance liquid chromatography and DE-52 microchromatographySAMPERI, P; TESTA, R; MANCUSO, M et al.Acta haematologica. 1990, Vol 83, Num 4, pp 179-182, issn 0001-5792, 4 p.Article

HEMOGLOBIN KOELLIKER (A₂ MINUS 141 ARG BETA ₂) IN FAVISMSCHILIRO G; RUSSO A; AZZIA N et al.1982; ACTA HAEMATOL.; ISSN 0001-5792; CHE; DA. 1982; VOL. 67; NO 3; PP. 229; BIBL. 2 REF.Article

HEMOGLOBIN G COPENHAGEN BETA 47(CD6) ASP->ASN IN A SICILIAN FAMILYSCHILIRO G; MUSUMECI S; RUSSO A et al.1981; HEMOGLOBIN; USA; DA. 1981; VOL. 5; NO 2; PP. 195-198; BIBL. 9 REF.Article

SICKLE CELL DISEASE IN SICILYROTH EF JR; SCHILIRO G; RUSSO A et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 1; PP. 34-38; BIBL. 16 REF.Article

UNUSUAL COMBINATION OF GENETIC DEFECTS IN A SILICIAN BOY: GGAMMA AGAMMA DELTA BETA THALASSEMIA, GGAMMA AGAMMA HETEROCELLULAR HPFH, BETA ^O THALASSEMIA, AND ALBINISMSCHILIRO G; PAVONE L; ROMEO MA et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 2; PP. 225-231; BIBL. 20 REF.Article

HAEMOGLOBIN LEPORE BOSTON-WASHINGTON IN SICILY: CLINICAL, HAEMATOLOGICAL, AND BIOSYNTHETIC STUDIESSCHILIRO G; MUSUMECI S; PIZZARELLI G et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 3; PP. 179-182; BIBL. 25 REF.Article

HOST FACTORS AGAINST SALMONELLA TYPHI IN CHILDREN WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCYSCHILIRO G; RUSSO A; SCIACCA A et al.1980; ACTA PAEDIATR. SCAND.; ISSN 0001-656X; SWE; DA. 1980; VOL. 69; NO 5; PP. 689-690; BIBL. 11 REF.Article

ALPHA THALASSAEMIA IN SICILY: HAEMATOLOGICAL AND BIOSYNTHETIC STUDIESMUSUMECI S; SCHILIRO G; PIZZARELLI G et al.1979; BRIT. J. HAEMATOL.; GBR; DA. 1979; VOL. 43; NO 3; PP. 413-422; BIBL. 36 REF.Article

Sickle hemoglobinopathies in SicilySCHILIRO, G; SPENA, M; GIAMBELLUCA, E et al.American journal of hematology. 1990, Vol 33, Num 2, pp 81-85, issn 0361-8609Article

HAEMOGLOBIN SYNTHESIS IN BONE MARROW OF PATIENTS WITH BETA 0 AND BETA +-THALASSAEMIAMUSUMECI S; SCHILIRO G; ROMEO MA et al.1981; ACTA HAEMATOL.; ISSN 0001-5792; CHE; DA. 1981; VOL. 65; NO 3; PP. 170-176; BIBL. 17 REF.Article