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	1.	[Indomethacin in the treatment of some vertiginous syndromes]. [electronic resource] by Amorelli, A Miraglia Del Giudice, E Producer: 19710407 In: Archivii italiani di laringologia vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Histaminolytic property of various micro-organisms (herpes virus, Brucella melitensis and Staphylococcus aureus) in relation to the biological significance of inflammation and shock]. [electronic resource] by MAGGIO, E MIRAGLIA DEL GIUDICE, E Producer: 20030501 In: Bollettino della Societa italiana di biologia sperimentale vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	3.	Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis. [electronic resource] by Iolascon, A Miraglia del Giudice, E Camaschella, C Producer: 19921116 In: Haematologica vol. 77 Availability: No items available. Save to lists Add to cart (remove)
	4.	[The use of neuroleptoanalgesia in ORL surgery]. [electronic resource] by Bellotti, C Miraglia Del Giudice, E Morelli, G Producer: 19700516 In: Archivii italiani di laringologia vol. 76 Availability: No items available. Save to lists Add to cart (remove)
	5.	A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis. [electronic resource] by Pinto, L Iolascon, A Miraglia del Giudice, E Nobili, B Producer: 19891003 In: Acta haematologica vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infant. [electronic resource] by Miraglia del Giudice, E Perrotta, S Lombardi, C Iolascon, A Producer: 19980624 In: Haematologica vol. 83 Availability: No items available. Save to lists Add to cart (remove)
	7.	Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis. [electronic resource] by Cutillo, S Pinto, L Nobili, B Miraglia del Giudice, E Iolascon, A Producer: 19920206 In: European journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis. [electronic resource] by Miraglia del Giudice, E Iolascon, A Pinto, L Nobili, B Perrotta, S Producer: 19950130 In: British journal of haematology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A rapid method for the detection of alpha I/65 hereditary elliptocytosis. [electronic resource] by Iolascon, A Miraglia del Giudice, E Perrotta, S Pinto, L Cutillo, S Producer: 19930521 In: Acta haematologica vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Frequency of Gilbert's syndrome associated with UGTA1 (TA)(7) polymorphism in Southern Italy. [electronic resource] by Iolascon, A Perrotta, S Coppola, B Carbone, R Miraglia Del Giudice, E Producer: 20000816 In: Haematologica vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	11.	UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis. [electronic resource] by Iolascon, A Faienza, M F Moretti, A Perrotta, S Miraglia del Giudice, E Producer: 19980218 In: Blood vol. 91 Availability: No items available. Save to lists Add to cart (remove)
	12.	Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype. [electronic resource] by Miraglia del Giudice, E Perrotta, S Nobili, B Pinto, L Cutillo, L Iolascon, A Producer: 19940422 In: British journal of haematology vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele. [electronic resource] by Miraglia del Giudice, E Francese, M Polito, R Nobili, B Iolascon, A Perrotta, S Producer: 19970919 In: Haematologica vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	14.	New treatment modalities for obesity. [electronic resource] by Grandone, A Di Sessa, A Umano, G R Toraldo, R Miraglia Del Giudice, E Producer: 20181211 In: Best practice & research. Clinical endocrinology & metabolism vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II). [electronic resource] by Iolascon, A Miraglia del Giudice, E Perrotta, S Granatiero, M Zelante, L Gasparini, P Producer: 19971208 In: Blood vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	16.	[Genetics in the infant obesity]. [electronic resource] by Miraglia Del Giudice, E Marzuillo, P Cresta, N Tartaglione, N Pascotto, C Perrone, L Producer: 20100623 In: Minerva pediatrica vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	17.	Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child. [electronic resource] by Gangarossa, S Romano, V Miraglia del Giudice, E Perrotta, S Iolascon, A Schiliro, G Producer: 19950525 In: Acta haematologica vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor. [electronic resource] by Miraglia del Giudice, E Coppola, G Scuccimarra, G Cirillo, G Bellini, G Pascotto, A Producer: 20010222 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Hereditary spherocytosis: from clinical to molecular defects. [electronic resource] by Iolascon, A Miraglia del Giudice, E Perrotta, S Alloisio, N Morlé, L Delaunay, J Producer: 19980610 In: Haematologica vol. 83 Availability: No items available. Save to lists Add to cart (remove)
	20.	Adolescents carrying a missense mutation in the CART gene exhibit increased anxiety and depression. [electronic resource] by Miraglia del Giudice, E Santoro, N Fiumani, P Dominguez, G Kuhar, M J Perrone, L Producer: 20060628 In: Depression and anxiety vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 74 results.