MIRAGLIA DEL GIUDICE, Emanuele

MIRAGLIA DEL GIUDICE, Emanuele  

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

Risultati 1 - 20 di 357 (tempo di esecuzione: 0.017 secondi).
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.
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
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
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 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 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 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
A rapid method for the detection of alpha I/65 hereditary elliptocytosis 1-gen-1993 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cutillo, S.
A single-nucleotide polymorphism in the p110beta gene promoter is associated with partial protection from insulin resistance in severely obese adolescents 1-gen-2008 LE STUNFF, C; Dechartres, A; MIRAGLIA DEL GIUDICE, Emanuele; Froguel, P; Bougnères, P.
An abdominal and unexpected cause of persistent fever in a 3-year old boy 1-gen-2016 Marzuillo, Pierluigi; Grandone, Anna; Di Sessa, Anna; Esposito, Tiziana; Della Vecchia, Nicoletta; Capristo, Carlo; MIRAGLIA DEL GIUDICE, Emanuele; Perrone, Laura
Abdominal fat interacts with PNPLA3 I148M, but not with the APOC3 variant in the pathogenesis of liver steatosis in chronic hepatitis C 1-gen-2013 Zampino, R.; Coppola, N.; Cirillo, G.; Boemio, A.; Pisaturo, M.; Marrone, A.; Macera, M.; Sagnelli, E.; Perrone, L.; Adinolfi, L. E.; Miraglia Del Giudice, E.
Abdominal fat interacts with PNPLA3 I148M, but not with the APOC3 variant in the pathogenesis of liver steatosis in chronic hepatitis C 1-gen-2013 Zampino, Rosa; Coppola, Nicola; Cirillo, G; Boemio, A; Pisaturo, M; Marrone, Aldo; Macera, M; Sagnelli, E; Perrone, Laura; Adinolfi, Luigi Elio; MIRAGLIA DEL GIUDICE, Emanuele
Abnormal myocardial deformation properties in obese, non-hypertensive children: An ambulatory blood pressure monitoring, standard echocardiographic, and strain rate imaging study 1-gen-2006 Di Salvo, G.; Pacileo, G.; Del Giudice, E. M.; Natale, F.; Limongelli, G.; Verrengia, M.; Rea, A.; Fratta, F.; Castaldi, B.; D'Andrea, A.; Calabro, P.; Miele, T.; Coppola, F.; Russo, M. G.; Caso, P.; Perrone, L.; Calabro, R.
Acute kidney injury and renal tubular damage in children with type 1 diabetes mellitus onset 1-gen-2021 Marzuillo, Pierluigi; Iafusco, Dario; Zanfardino, Angela; Guarino, Stefano; Piscopo, Alessia; Casaburo, Francesca; Capalbo, Daniela; Ventre, Maria; Arienzo, Maria Rosaria; Cirillo, Grazia; Picione, Carla De Luca; Esposito, Tiziana; Montaldo, Paolo; Di Sessa, Anna; Miraglia Del Giudice, Emanuele
Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors 1-gen-2021 Marzuillo, Pierluigi; Baldascino, Maria; Guarino, Stefano; Perrotta, Silverio; Miraglia Del Giudice, Emanuele; Nunziata, Felice