Your search returned 165 results.

Results
	41.	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)
	42.	Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome. [electronic resource] by Curatolo, P Cilio, M R Del Giudice, E Romano, A Gaggero, R Pessagno, A Producer: 19930806 In: Neuropediatrics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	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)
	44.	High-normal fasting glucose levels are associated with increased prevalence of impaired glucose tolerance in obese children. [electronic resource] by Grandone, A Amato, A Luongo, C Santoro, N Perrone, L del Giudice, E Miraglia Producer: 20090415 In: Journal of endocrinological investigation vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	[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)
	46.	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)
	47.	[Clinical experimental studies of the activity of a cellular extract (TRF). V. Changes of the EEG]. [electronic resource] by Sepe, O De Luca, R Stella, L Del Giudice, E Federico, P Portone, N Producer: 19691202 In: Bollettino della Societa italiana di biologia sperimentale vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	48.	Duchenne and Becker muscular dystrophy presenting as nonalcoholic fatty liver disease. [electronic resource] by Veropalumbo, C Del Giudice, E Capuano, G Gentile, C Di Cosmo, N Vajro, P Producer: 20120202 In: Journal of pediatric gastroenterology and nutrition vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	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)
	50.	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)
	51.	A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia. [electronic resource] by del Giudice, E M Coppola, G Bellini, G Cirillo, G Scuccimarra, G Pascotto, A Producer: 20020123 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis. [electronic resource] by del Giudice, E M Perrotta, S Nobili, B Specchia, C d'Urzo, G Iolascon, A Producer: 19991104 In: Blood vol. 94 Availability: No items available. Save to lists Add to cart (remove)
	53.	Functional gastrointestinal disorders in migrainous children: efficacy of flunarizine. [electronic resource] by Boccia, G Del Giudice, E Crisanti, A F Strisciuglio, C Romano, A Staiano, A Producer: 20061121 In: Cephalalgia : an international journal of headache vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	On the dynamics of self-organization in living organisms. [electronic resource] by Brizhik, L S Del Giudice, E Popp, F-A Maric-Oehler, W Schlebusch, K-P Producer: 20090813 In: Electromagnetic biology and medicine vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	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)
	56.	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)
	57.	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)
	58.	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)
	59.	Mutational screening of the CART gene in obese children: identifying a mutation (Leu34Phe) associated with reduced resting energy expenditure and cosegregating with obesity phenotype in a large family. [electronic resource] by del Giudice, E M Santoro, N Cirillo, G D'Urso, L Di Toro, R Perrone, L Producer: 20010920 In: Diabetes vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	The hospital-based, post-acute geriatric evaluation and management unit: the experience of the acute geriatric unit in Trieste. [electronic resource] by Del Giudice, E Ferretti, E Omiciuolo, C Sceusa, R Zanata, C Manganaro, D Toigo, G Producer: 20100201 In: Archives of gerontology and geriatrics vol. 49 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
1
2
3
4
5
6
7
8
9
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 165 results.