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MIRAGLIA DEL GIUDICE, Emanuele

MIRAGLIA DEL GIUDICE, Emanuele  

Dipartimento della Donna, del Bambino e di Chirurgia Generale e Specialistica  

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Titolo Data di pubblicazione Autore(i) File
1-Hour plasma glucose in obese youth 1-gen-2012 Manco, M; MIRAGLIA DEL GIUDICE, Emanuele; Spreghini, Mr; Cappa, M; Perrone, Laura; Brufani, C; Rustico, C; Morino, G; Caprio, S.
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 1-gen-1999 Perrotta, Silverio; Iolascon, A; Polito, R; D'Urzo, G; Conte, Ml; MIRAGLIA DEL GIUDICE, Emanuele
[Health consequences of obesity in children and adolescents. 1-gen-2014 Valerio, G; Licenziati, Mr; Manco, M; Ambruzzi, Am; Bacchini, Dario; Baraldi, E; Bona, G; Bruzzi, P; Cerutti, F; Corciulo, N; Crinò, A; Franzese, A; Grugni, G; Iughetti, L; Lenta, S; Maffeis, C; Marzuillo, P; MIRAGLIA DEL GIUDICE, Emanuele; Morandi, A; Morino, G; Moro, B; Perrone, Laura; Prodam, F; Ricotti, R; Santamaria, F; Zito, E; Tanas, R.
A 23-month-old girl with chronic seborrhoeic' dermatitis, dehydration and failure to thrive 1-gen-2019 Marzuillo, Pierluigi; Grandone, Anna; Guarino, Stefano; Apicella, Andrea; Panarese, Iacopo; Picciano, Ludovica; Fedele, Maria Cristina; Palladino, Federica; Perrotta, Silverio; Miraglia Del Giudice, Emanuele
A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene 1-gen-2015 Grandone, Anna; Cantelmi, Grazia; Cirillo, Grazia; Marzuillo, Pierluigi; Luongo, Caterina; MIRAGLIA DEL GIUDICE, Emanuele; Perrone, Laura
A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood. 1-gen-2015 Tornese, G; Marzuillo, P; Pellegrin, Mc; Germani, C; Faleschini, E; Zennaro, F; Grandone, Anna; MIRAGLIA DEL GIUDICE, Emanuele; Perrone, Laura; Ventura, A.
A case report of a boy suffering from type 1 diabetes mellitus and familial Mediterranean fever 1-gen-2021 Gicchino, Mf; Iafusco, D; Zanfardino, A; MIRAGLIA DEL GIUDICE, Emanuele; Olivieri, An.
A common CTLA4 polymorphism confers susceptibility to autoimmune thyroid disease in celiac children. 1-gen-2009 Tolone, Carlo; Cirillo, G.; Papparella, Alfonso; Tolone, Salvatore; Santoro, N.; Grandone, Anna; Perrone, Laura; MIRAGLIA DEL GIUDICE, Emanuele
A common functional variant in the p110 B gene promoter acts as a cis-acting eQTL (expression quantitative trait locus) to protect obese adolescents from insulin resistance 1-gen-2008 C., Le Stunff; A., Dechartres; MIRAGLIA DEL GIUDICE, Emanuele; D., Meyre; P., Bougneres
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli 1-gen-1994 Wilmotte, R; MIRAGLIA DEL GIUDICE, Emanuele; Marechal, J; Perrotta, Silverio; DE MATTIA, D; Delaunay, J; Iolascon, A.
A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array 1-gen-2015 Morandi, A; Bonnefond, A; Lobbens, S; Carotenuto, Marco; MIRAGLIA DEL GIUDICE, Emanuele; Froguel, P; Maffeis, C.
A high selective and sensitive liquid chromatography-tandem mass spectrometry method for quantization of BPA urinary levels in children. 1-gen-2013 Nicolucci, C.; Rossi, S. Menale C.; MIRAGLIA DEL GIUDICE, Emanuele; Perrone, Laura; Gallo, P.; Mita, D. G.; Diano, Nadia
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis 1-gen-1989 Pinto, L; Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Nobili, Bruno
A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia 1-gen-2001 MIRAGLIA DEL GIUDICE, Emanuele; Coppola, G; Bellini, Giulia; Cirillo, G; Scuccimarra, G; Pascotto, Antonio
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype 1-gen-2022 Palumbo, S; Cirillo, G; Sanchez, G; Aiello, F; Fachin, A; Baldo, F; Pellegrin, M C; Cassio, A; Salerno, M; Maghnie, M; Faienza, M F; Wasniewska, M; Fintini, D; Giacomozzi, C; Ciccone, S; Miraglia Del Giudice, E; Tornese, G; Grandone, A
A new formula to improve the screening of impaired glucose tolerance in youths with overweight or obesity 1-gen-2022 Di Bonito, Procolo; Licenziati, Maria Rosaria; Corica, Domenico; Wasniewska, Malgorzata Gabriela; Di Sessa, Anna; Miraglia Del Giudice, Emanuele; Morandi, Anita; Maffeis, Claudio; Faienza, Maria Felicia; Mozzillo, Enza; Calcaterra, Valeria; Maltoni, Giulio; Franco, Francesca; Valerio, Giuliana
A new index to simplify the screening of hypertension in overweight or obese youth 1-gen-2017 Di Bonito, P.; Valerio, G.; Pacifico, L.; Chiesa, C.; Invitti, C.; Morandi, A.; Maffeis, C.; Licenziati, M. R.; Manco, M.; Miraglia Del Giudice, E.; Baroni, M. G.; Loche, S.; Tornese, G.; Tomat, M.; De Simone, G.; Gilardini, L.; Sanguigno, E.; Franco, Francesco; Grandone, A.; Luciano, R.; Incani, M.; Pellegrin, M. C.
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists 1-gen-2004 Castaldo, P; Stefanoni, P; Miceli, F; Coppola, G; MIRAGLIA DEL GIUDICE, Emanuele; Bellini, Giulia; Pascotto, Antonio; Trudell, Jr; Harrison, Nl; Annunziato, L; Taglialatela, M.
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes 1-gen-2003 Coppola, G; Castaldo, P; MIRAGLIA DEL GIUDICE, Emanuele; Bellini, Giulia; Galasso, F; Soldovieri, Mv; Anzalone, L; Sferro, C; Annunziato, L; Pascotto, Antonio; Taglialatela, M.
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 1-gen-2003 MIRAGLIA DEL GIUDICE, Emanuele; Coppola, G; Bellini, Giulia; Ledaal, P; Hertz, Jm; Pascotto, Antonio