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	21.	Inadequate leptin level negatively affects body fat loss during a weight reduction programme for childhood obesity. [electronic resource] by Miraglia, del Giudice E Santoro, N Marotta, A Nobili, B Di, Toro R Perrone, L Producer: 20021010 In: Acta paediatrica (Oslo, Norway : 1992) vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia. [electronic resource] by Miraglia Del Giudice, E Coppola, G Bellini, G Ledaal, P Hertz, J M Pascotto, A Producer: 20030805 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Molecular heterogeneity of hereditary elliptocytosis in Italy. [electronic resource] by Miraglia del Giudice, E Perrotta, S Sannino, E De Angelis, F Nobili, B Iolascon, A Producer: 19950309 In: Haematologica vol. 79 Availability: No items available. Save to lists Add to cart (remove)
	24.	4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis. [electronic resource] by Perrotta, S Iolascon, A Polito, R d'Urzo, G Conte, M L Miraglia del Giudice, E Producer: 19990824 In: Haematologica vol. 84 Availability: No items available. Save to lists Add to cart (remove)
	25.	Clinical and molecular evaluation of non-dominant hereditary spherocytosis. [electronic resource] by Miraglia del Giudice, E Nobili, B Francese, M D'Urso, L Iolascon, A Eber, S Perrotta, S Producer: 20010315 In: British journal of haematology vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Variations of retinol binding protein 4 levels are not associated with changes in insulin resistance during puberty. [electronic resource] by Santoro, N Perrone, L Cirillo, G Brienza, C Grandone, A Cresta, N Miraglia del Giudice, E Producer: 20091214 In: Journal of endocrinological investigation vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases. [electronic resource] by Iolascon, A Miraglia del Giudice, E Camaschella, C Pinto, L Nobili, B Perrotta, S Cutillo, S Producer: 19911107 In: British journal of haematology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis. [electronic resource] by Miraglia del Giudice, E Francese, M Nobili, B Morlé, L Cutillo, S Delaunay, J Perrotta, S Producer: 19980224 In: The Journal of pediatrics vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Screening for impaired glucose tolerance in obese children and adolescents: a validation and implementation study. [electronic resource] by Morandi, A Maschio, M Marigliano, M Miraglia Del Giudice, E Moro, B Peverelli, P Maffeis, C Producer: 20141027 In: Pediatric obesity vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Hereditary spherocytosis characterized by increased spectrin/band 3 ratio. [electronic resource] by Miraglia del Giudice, E Perrotta, S Pinto, L Cappellini, M D Fiorelli, G Cutillo, S Iolascon, A Producer: 19920330 In: British journal of haematology vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli. [electronic resource] by Wilmotte, R Miraglia del Giudice, E Marechal, J Perrotta, S de Mattia, D Delaunay, J Iolascon, A Producer: 19950202 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)
	32.	Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects. [electronic resource] by De Franceschi, L Olivieri, O Miraglia del Giudice, E Perrotta, S Sabato, V Corrocher, R Iolascon, A Producer: 19970904 In: American journal of hematology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions. [electronic resource] by Concolino, D Iembo, M A Rossi, E Giglio, S Coppola, G Miraglia Del Giudice, E Strisciuglio, P Producer: 20020729 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential. [electronic resource] by Perrotta, S Iolascon, A De Angelis, F Pagano, L Colonna, G Cutillo, S Miraglia del Giudice, E Producer: 19950713 In: British journal of haematology vol. 89 Availability: No items available. Save to lists Add to cart (remove)
	35.	Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74). [electronic resource] by Perrotta, S Miraglia del Giudice, E Alloisio, N Sciarratta, G Pinto, L Delaunay, J Cutillo, S Iolascon, A Producer: 19940627 In: Blood vol. 83 Availability: No items available. Save to lists Add to cart (remove)
	36.	Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations. [electronic resource] by Miraglia del Giudice, E Cirillo, G Santoro, N D'Urso, L Carbone, M T Di Toro, R Perrone, L Producer: 20011205 In: International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	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)
	38.	Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search. [electronic resource] by Gasparini, P Miraglia del Giudice, E Delaunay, J Totaro, A Granatiero, M Melchionda, S Zelante, L Iolascon, A Producer: 19971212 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Hyperekplexia caused by dominant-negative suppression of glyra1 function. [electronic resource] by Bellini, G Miceli, F Mangano, S Miraglia del Giudice, E Coppola, G Barbagallo, A Taglialatela, M Pascotto, A Producer: 20070712 In: Neurology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	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)

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