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	41.	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)
	42.	Molecular screening of the ghrelin gene in Italian obese children: the Leu72Met variant is associated with an earlier onset of obesity. [electronic resource] by Miraglia del Giudice, E Santoro, N Cirillo, G Raimondo, P Grandone, A D'Aniello, A Di Nardo, M Perrone, L Producer: 20040429 In: International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	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)
	44.	Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues. [electronic resource] by Iolascon, A Lania, A Badiali, M Pession, A Saglio, G Giangaspero, F Miraglia del Giudice, E Perrotta, S Cutillo, S Producer: 19910726 In: Medical and pediatric oncology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Weight loss in obese children carrying the proopiomelanocortin R236G variant. [electronic resource] by Santoro, N Perrone, L Cirillo, G Raimondo, P Amato, A Coppola, F Santarpia, M D'Aniello, A Miraglia Del Giudice, E Producer: 20060609 In: Journal of endocrinological investigation vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	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)
	47.	Low frequency of melanocortin-4 receptor (MC4R) mutations in a Mediterranean population with early-onset obesity. [electronic resource] by Miraglia Del Giudice, E Cirillo, G Nigro, V Santoro, N D'Urso, L Raimondo, P Cozzolino, D Scafato, D Perrone, L Producer: 20020624 In: International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role. [electronic resource] by Ingrosso, D D'Angelo, S Perrotta, S d'Urzo, G Iolascon, A Perna, A F Galletti, P Zappia, V Miraglia del Giudice, E Producer: 19960531 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)
	49.	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. [electronic resource] by Miraglia del Giudice, E Vallier, A Maillet, P Perrotta, S Cutillo, S Iolascon, A Tanner, M J Delaunay, J Alloisio, N Producer: 19970219 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)
	50.	Hereditary spherocytosis (HS) due to loss of anion exchange transporter. [electronic resource] by Iolascon, A Miraglia del Giudice, E Perrotta, S Pinto, L Fiorelli, G Cappellini, D M Vasseur, C Bursaux, E Cutillo, S Producer: 19930325 In: Haematologica vol. 77 Availability: No items available. Save to lists Add to cart (remove)
	51.	1-Hour plasma glucose in obese youth. [electronic resource] by Manco, M Miraglia Del Giudice, E Spreghini, M R Cappa, M Perrone, L Brufani, C Rustico, C Morino, G Caprio, S Producer: 20130513 In: Acta diabetologica vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy). [electronic resource] by Iolascon, A Pinto, L Nobili, B Lania, A Iafusco, D Miraglia del Giudice, E Matarese, S M Salvati, P Cutillo, S Producer: 19880217 In: Birth defects original article series vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	53.	Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency. [electronic resource] by Miraglia del Giudice, E Lombardi, C Francese, M Nobili, B Conte, M L Amendola, G Cutillo, S Iolascon, A Perrotta, S Producer: 19980618 In: British journal of haematology vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	Increased membrane protein phosphorylation and anion transport activity in chorea-acanthocytosis. [electronic resource] by Olivieri, O De Franceschi, L Bordin, L Manfredi, M Miraglia del Giudice, E Perrotta, S De Vivo, M Guarini, P Corrocher, R Producer: 19980402 In: Haematologica vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	55.	Patients affected by dent disease 2 could be predisposed to hidradenitis suppurativa. [electronic resource] by Marzuillo, P Piccolo, V Mascolo, M Apicella, A Argenziano, G Della Vecchia, N Guarino, S Miraglia Del Giudice, E La Manna, A Producer: 20191113 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum. [electronic resource] by Alloisio, N Texier, P Denoroy, L Berger, C Miraglia del Giudice, E Perrotta, S Iolascon, A Gilsanz, F Berger, G Guichard, J Producer: 19960716 In: Blood vol. 87 Availability: No items available. Save to lists Add to cart (remove)
	57.	TM6SF2 Glu167Lys polymorphism is associated with low levels of LDL-cholesterol and increased liver injury in obese children. [electronic resource] by Grandone, A Cozzolino, D Marzuillo, P Cirillo, G Di Sessa, A Ruggiero, L Di Palma, M R Perrone, L Miraglia Del Giudice, E Producer: 20160829 In: Pediatric obesity vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Evaluation of leptin protein levels in patients with Cooley's anaemia. [electronic resource] by Miraglia Del Giudice, E Perrotta, S Carbone, M T Calabrò, C Esposito, L De Rosa, C Saviano, A Di Toro, R Perrone, L Producer: 19990721 In: British journal of haematology vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia. [electronic resource] by Alfinito, F Calabro, V Cappellini, M D Fiorelli, G Filosa, S Iolascon, A Miraglia del Giudice, E Perrotta, S Migliorati, R Vallone, D Producer: 19941207 In: British journal of haematology vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysis. [electronic resource] by Cirillo, G Marini, R Ito, S Wakamatsu, K Scianguetta, S Bizzarri, C Romano, A Grandone, A Perrone, L Cappa, M Miraglia Del Giudice, E Producer: 20130606 In: The British journal of dermatology vol. 167 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.