DISSEMINATED INTRAVASCULAR COAGULATION ASSOCIATED WITH HEREDITARY FRUCTOSE INTOLERANCEMAGGIORE G; BORGNA PIGNATTI C.1982; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1982; VOL. 136; NO 2; PP. 169-170; BIBL. 8 REF.Article

Marrow transplantation for ThalassemiaBORGNA-PIGNATTI, C.Annual review of medicine. 1985, Vol 36, pp 329-336, issn 0066-4219Article

FANCONI'S ANEMIA IN INFANCY. REPORT OF A CASE DIAGNOSED IN THE PRE-ANEMIC STAGE.BORGNA PIGNATTI C; BIANCHI E; POLITO E et al.1977; HELV. PAEDIATR. ACTA; SUISSE; DA. 1977; VOL. 32; NO 4-5; PP. 413-418; ABS. ALLEM. FR; BIBL. 15 REF.Article

Evaluation of a new method of administration of the iron chelating agent deferoxamineBORGNA-PIGNATTI, C; COHEN, A.The Journal of pediatrics. 1997, Vol 130, Num 1, pp 86-88, issn 0022-3476Article

A COMBINED BONE MARROW AND SPINAL FLUID ASPIRATION TECHNIQUE USING DISPOSABLE SPINAL NEEDLESURBAN C; BORGNA PIGNATTI C; KAULFERSCH W et al.1983; CLINICAL PEDIATRICS; ISSN 0009-9228; USA; DA. 1983; VOL. 22; NO 4; PP. 304-305; BIBL. 2 REF.Article

CHOLOSTASE RECURRENTE BENIGNEBORGNA PIGNATTI C; MAGGIORE G; DE STEFANO P et al.1980; HELV. PAEDIATR. ACTA; CHE; DA. 1980; VOL. 35; NO 1; PP. 69-74; ABS. GER/ENG; BIBL. 13 REF.Article

Clinical manifestations and therapy of transfusional haemosiderosisGABUTTI; BORGNA-PIGNATTI, C.Baillière's clinical haematology. 1994, Vol 7, Num 4, pp 919-940, issn 0950-3536Article

INTERNAL DISTRIBUTION OF EXCESS IRON AND SOURCES OF SERUM FERRITIN IN PATIENTS WITH THALASSAEMIACAZZOLA M; BORGNA PIGNATTI C; DE STEFANO P et al.1983; SCANDINAVIAN JOURNAL OF HAEMATOLOGY; ISSN 0036-553X; DNK; DA. 1983; VOL. 30; NO 4; PP. 289-296; BIBL. 21 REF.Article

Fatal ceftriaxone-induced hemolysis a child with acquired immunodeficiency syndromeBORGNA-PIGNATTI, C; BEZZI, T. M; REVERBERI, R et al.The Pediatric infectious disease journal. 1995, Vol 14, Num 12, pp 1116-1117, issn 0891-3668Article

CHOLELITHIASIS IN CHILDREN WITH THALASSEMIA MAJOR: AN ULTRASONOGRAPHIC STUDYBORGNA PIGNATTI C; DE STEFANO P; PAJNO D et al.1981; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1981; VOL. 99; NO 2; PP. 243-244; BIBL. 10 REF.Article

PULMONARY ARTERIOVENOUS FISTULAS: AN UNUSUAL COMPLICATION OF CONGENITAL HEPATIC FIBROSISMAGGIORE G; BORGNA PIGNATTI C; MARNI E et al.1983; JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION; ISSN 0277-2116; USA; DA. 1983; VOL. 2; NO 1; PP. 183-186; BIBL. 12 REF.Article

Penicillin compliance in splenectomized thalassemicsBORGNA-PIGNATTI, C; DE STEFANO, P; BARONE, F et al.European journal of pediatrics. 1984, Vol 142, Num 2, pp 83-85, issn 0340-6199Article

Radiological case of the monthDE STEFANO, P; BORGNA PIGNATTI, C; BAILO, C et al.American journal of diseases of children (1960). 1985, Vol 139, Num 8, pp 793-794, issn 0002-922XArticle

Successful pregnancy after bone marrow transplantation for thalassaemiaBORGNA-PIGNATTI, C; MARRADI, P; RUGOLOTTO, S et al.Bone marrow transplantation (Basingstoke). 1996, Vol 18, Num 1, pp 235-236, issn 0268-3369Article

MARROW TRANSPLANTATION FOR THALASSAEMIATHOMAS ED; BUCKNER CD; SANDERS JE et al.1982; LANCET (BR. ED.); ISSN 0140-6736; GBR; DA. 1982; VOL. 2; NO 8292; PP. 227-229; BIBL. 27 REF.Article

Hepatocellular carcinoma in thalassemia majorBORGNA-PIGNATTI, C; DE STEFANO, P; SESSA, F et al.Medical and pediatric oncology. 1986, Vol 14, Num 6, pp 327-328, issn 0098-1532Article

The sicca syndrome in thalassaemia majorBORGNA-PIGNATTI, C; CAMMARERI, V; DE STEFANO, P et al.British medical journal (1857). 1984, Vol 288, Num 6418, pp 668-669, issn 0007-1447Article

Thiamine-responsive anemia in DIDMOAD syndromeBORGNA-PIGNATTI, C; MARRADI, P; PINELLI, L et al.The Journal of pediatrics. 1989, Vol 114, Num 3, pp 405-410, issn 0022-3476Article

Delayed separation of an appendix-containing umbilical stumpBORGNA-PIGNATTI, C; BERGAMO ANDREIS, I. A; BETTILI, G et al.Journal of pediatric surgery. 1995, Vol 30, Num 12, pp 1717-1718, issn 0022-3468Article

Transient neurologic disturbances in a child treated with moderate-dose methotrexateBORGNA-PIGNATTI, C; BATTISTI, L; MARRADI, P et al.British journal of haematology. 1992, Vol 81, Num 3, issn 0007-1048, p. 448Article

Electroretinographic and visual-evoked potential abnormalities in patients with beta-thalassemia majorGELMI, C; BORGNA-PIGNATTI, C; FRANCHIN, S et al.Ophthalmologica (Basel). 1988, Vol 196, Num 1, pp 29-34, issn 0030-3755Article

Spleen iron content is low in thalassemiaBORGNA-PIGNATTI, C; DE STEFANO, P; BONGO, I. G et al.The American journal of pediatric hematology/oncology. 1984, Vol 6, Num 3, pp 340-343, issn 0192-8562Article

Safety and efficacy of subcutaneous bolus injection of deferoxamine in adult patients with iron overloadFRANCHINI, M; GANDINI, G; DE GIRONCOLI, M et al.Blood. 2000, Vol 95, Num 9, pp 2776-2779, issn 0006-4971Article

Subcutaneous bolus injection of deferoxamine in adult patients affected by onco-hematologic diseases and iron overloadBORGNA-PIGNATTI, C; FRANCHINI, M; GANDINI, G et al.Haematologica - Journal of hematology. 1998, Vol 83, Num 9, pp 788-790Article

A moderate transfusion regimen may reduce iron loading in β-thalassemia major without producing excessive expansion of erythropoiesisCAZZOLA, M; BORGNA-PIGNATTI, C; LOCATELLI, F et al.Transfusion (Philadelphia, PA). 1997, Vol 37, Num 2, pp 135-140, issn 0041-1132Article