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	101.	Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome. [electronic resource] by Iolascon, A Faienza, M F Giordani, L Perrotta, S Ruggiu, G Meloni, G F del Giudice, E M Producer: 19990623 In: European journal of haematology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Cell division cycle alterations and human tumors. [electronic resource] by Della Ragione, F Borriello, A Della Pietra, V Cucciolla, V Oliva, A Barbarisi, A Iolascon, A Zappia, V Producer: 20000427 In: Advances in experimental medicine and biology vol. 472 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	Reduced expression of transforming growth factor-beta receptor type III in high stage neuroblastomas. [electronic resource] by Iolascon, A Giordani, L Borriello, A Carbone, R Izzo, A Tonini, G P Gambini, C Della Ragione, F Producer: 20000405 In: British journal of cancer vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	P16INK4A gene homozygous deletions in human acute leukaemias with alterations of chromosome 9. [electronic resource] by Faienza, M F della Ragione, F Basso, G Coppola, B Miraglia del Giudice, E Schettini, F Iolascon, A Producer: 19960729 In: British journal of haematology vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis). [electronic resource] by Iolascon, A Stewart, G W Ajetunmobi, J F Perrotta, S Delaunay, J Carella, M Zelante, L Gasparini, P Producer: 19990518 In: Blood vol. 93 Availability: No items available. Save to lists Add to cart (remove)
	106.	Rare frequencey of point mutations for codon 12, 13 and 61 of ras gene in italian neuroblastoma. [electronic resource] by Iolascon, A Badiali, M Pession, A Basso, G Losi, L Delgiudice, E Perrotta, S Cutillo, S Tonini, G Producer: 20121002 In: International journal of oncology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis. [electronic resource] by Danise, P Amendola, G Nobili, B Perrotta, S Miraglia Del Giudice, E Matarese, S M Iolascon, A Brugnara, C Producer: 20010920 In: Clinical and laboratory haematology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarray. [electronic resource] by Ingrosso, D D'Angelo, S Perna, A F Iolascon, A Miraglia del Giudice, E Perrotta, S Zappia, V Galletti, P Producer: 19950602 In: European journal of biochemistry vol. 228 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Decreased band 3 anion transport activity and band 3 clusterization in congenital dyserythropoietic anemia type II. [electronic resource] by De Franceschi, L Turrini, F del Giudice, E M Perrotta, S Olivieri, O Corrocher, R Mannu, F Iolascon, A Producer: 19980818 In: Experimental hematology vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	110.	Structural and functional analysis of cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, and CDKN2C) in neuroblastoma. [electronic resource] by Iolascon, A Giordani, L Moretti, A Tonini, G P Lo Cunsolo, C Mastropietro, S Borriello, A Ragione, F D Producer: 19980218 In: Pediatric research vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13. [electronic resource] by Cusano, R Gangarossa, S Forabosco, P Caridi, G Ghiggeri, G M Russo, G Iolascon, A Ravazzolo, R Seri, M Producer: 20001207 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)
	112.	Estrogen-induced proliferation in cultured hepatocytes involves cyclin D1, p21(Cip1) and p27(Kip1). [electronic resource] by Barone, M Ladisa, R Di Leo, A Spano, D Francioso, D Aglio, V Amoruso, A Francavilla, A Iolascon, A Producer: 20060517 In: Digestive diseases and sciences vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin. [electronic resource] by del Giudice, E M Ducluzeau, M T Alloisio, N Wilmotte, R Delaunay, J Perrotta, S Cutillo, S Iolascon, A Producer: 19920825 In: Human genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio. [electronic resource] by Randon, J Miraglia del Giudice, E Bozon, M Perrotta, S De Vivo, M Iolascon, A Delaunay, J Morle, L Producer: 19970417 In: British journal of haematology vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	p27Kip1 accumulation is associated with retinoic-induced neuroblastoma differentiation: evidence of a decreased proteasome-dependent degradation. [electronic resource] by Borriello, A Pietra, V D Criscuolo, M Oliva, A Tonini, G P Iolascon, A Zappia, V Ragione, F D Producer: 20000207 In: Oncogene vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	A genomic deletion causes truncation of α-spectrin and ellipto-poikilocytosis. [electronic resource] by Iolascon, A King, M-J Robertson, S Avvisati, R A Vitiello, F Asci, R Scoppettuolo, M N Delaunay, J Producer: 20110826 In: Blood cells, molecules & diseases vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis. [electronic resource] by del Giudice, E M Hayette, S Bozon, M Perrotta, S Alloisio, N Vallier, A Iolascon, A Delaunay, J Morlé, L Producer: 19960912 In: British journal of haematology vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	Clinical utility of electrophysiological evaluation in Crigler-Najjar syndrome. [electronic resource] by Perretti, A Crispino, G Marcantonio, L Lenta, S Caropreso, M Manganelli, F Scianguetta, S Iorio, R Iolascon, A Vajro, P Producer: 20080314 In: Neuropediatrics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin. [electronic resource] by Lorenzo, F Miraglia del Giudice, E Alloisio, N Morle, L Forissier, A Perrotta, S Sciarratta, G Iolascon, A Delaunay, J Producer: 19930324 In: British journal of haematology vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	120.	Cell division cycle control in embryonal and alveolar rhabdomyosarcomas. [electronic resource] by Moretti, A Borriello, A Monno, F Criscuolo, M Rosolen, A Esposito, G Dello Iacovo, R Della Ragione, F Iolascon, A Producer: 20030121 In: European journal of cancer (Oxford, England : 1990) vol. 38 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 154 results.