DE LUCA, Filippo

DE LUCA, Filippo  

Dipartimento di Scienze Pediatriche, Ginecologiche, Microbiologiche e Biomediche (attivo dal 10/07/2012 al 31/12/2015)  

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11-Hydroxylase deficiency as a cause of pre-pubertal gynecomastia 1-gen-2009 Wasniewska, Malgorzata Gabriela; Arrigo, Teresa; Lombardo, Fortunato; Crisafulli, Giuseppe; Salzano, Giuseppina; DE LUCA, Filippo
1ST-PHASE INSULIN-RESPONSE TO INTRAVENOUS GLUCOSE IN CYSTIC- FIBROSIS PATIENTS WITH DIFFERENT DEGREES OF GLUCOSE-TOLERANCE 1-gen-1994 CUCINOTTA D.; DELUCA F; ARRIGO T; DIBENEDETTO A; SFERLAZZAS C; GIGANTE A; RIGOLI L; MAGAZZU' G
48, XXYY syndrome in a newborn with ambiguous genitalia 1-gen-2012 Messina, Maria Francesca; Mami', Carmelo; Valenzise, Mariella; Russo, B; DE LUCA, Filippo
[Celiac disease and short stature] 1-gen-1984 Magazzu', Giuseppe; Sferlazzas, C; Ruggeri, C; DE LUCA, Filippo
[Cholestatic hepatopathy in a child with congenital hypopituitarism]. 1-gen-1986 De Luca F; Pandullo E; Polimeni A; Sindoni A; Gemelli M.
[Thyro-gastric autoimmunity in a pediatric population of type-I diabetics] 1-gen-1985 DE LUCA, Filippo; Vanelli, M; Magazzu', Giuseppe; Pandullo, E; Muritano, M; Sindoni, A; Trimarchi, Francesco; Bernasconi, S.
[Transient biological hypothyroidism in an infant carrier of celiac disease] 1-gen-1983 Magazzu', Giuseppe; DE LUCA, Filippo; Benvenga, S; Trimarchi, F.
A case of adenohypophysitis in a boy affected by sinusitis and acute meningitis: outcome 1-gen-2013 Arasi, Stefania; Wasniewska, Malgorzata Gabriela; Valenzise, Mariella; Pitrolo, E; Corica, D; Santucci, S; Romeo, M; DE LUCA, Filippo
A case of congenital goiter in an endemic area: histological, immunohistochemical and ultrastructural observations]. 1-gen-1981 Barresi, Gaetano; DE LUCA, Filippo; Galatioto, S.; Tuccari, Giovanni; Trimarchi, Francesco
A characteristic cognitive and behavioural pattern as a clue to suspect Klinefelter syndrome in prepubertal age. 1-gen-2012 Messina, Maria Francesca; Sgrò, Dl; Aversa, Tommaso; Pecoraro, M; Valenzise, Mariella; DE LUCA, Filippo
A combined treatment with ketoconazole and cyproterone acetate may slow down the progression of male precocious puberty in McCune-Albright syndrome 1-gen-2007 Messina, Maria Francesca; Wasniewska, Malgorzata Gabriela; Rulli, I; Zirilli, G; Arrigo, Teresa; DE LUCA, Filippo
A congenitally hypothyroid young man (Seated Dwarf, Goya’s Studio, 19th century) 1-gen-2018 Trimarchi, F.; De Luca, F.
A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty 1-gen-1999 Kremer, H; Martens, Jwm; VAN REEN, M; VERHOEF POST, M; Wit, Jm; Otten, Bj; Drop, Sls; DELEMARRE VAN DE WAAL, Ha; POMBO ARIAS, M; DE LUCA, Filippo; Potau, N; Buckler, Jmh; Jansen, M; Parks, Js; Latif, Ha; Moll, Gw; Epping, W; Saggese, G; Mariman, Ecm; Themmen, Apn; Brunner, Hg
A not very essential obesity: the Rohhad syndrome. Description of two cases and review of the literature 1-gen-2013 Ramistella, Vincenzo; Wasniewska, Malgorzata Gabriela; Valenzise, Mariella; Corica, D; Cantucci, S; Pitrolo, E; Romeo, M; DE LUCA, Filippo
A novel frameshift mutation of DAX 1 gene in a boy with apparently isolated X-linked adrenal hypoplasia congenita 1-gen-2001 Wasniewska, Malgorzata Gabriela; Arrigo, Teresa; Messina, Maria Francesca; Lombardo, Fortunato; Vaccaro, T.; DE LUCA, Filippo
A novel frameshift mutation of the DAX-1 gene in a boy with Xlinked adrenal hypoplasia congenita and no early impairement of the hypothalamus-pituitary-gonadal axis 1-gen-2001 Wasniewska, Malgorzata Gabriela; DE LUCA, Filippo; Lombardo, Fortunato; Messina, Maria Francesca; Valenzise, Mariella; Lasco, A; Arrigo, Teresa
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 1-gen-2010 Salzano, Giuseppina; DE LUCA, Filippo; Messina, M. F.; Priolo, M.; Laganà, C; Valenzise, Mariella
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 1-gen-2011 Messina, Maria Francesca; Lombardo, Fortunato; Comito, Valentina; Aversa, Tommaso; Danila, Pecoraro; Valenzise, Mariella; DE LUCA, Filippo
A very rare karyotype in TS syndrome: 45X0, 46X, i(Xq10),X, i(Xq10), i (Xq10) 1-gen-2012 Messina, Maria Francesca; Civa, R; Salzano, Giuseppina; Randazzo, A; DE LUCA, Filippo
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: Comparison with conventional clinical, laboratory, and imaging approaches 1-gen-2001 Corrias, A; Einaudi, S; Chiorboli, E; Weber, G; Crino, A; Andreo, M; Cesaretti, G; DE SANCTIS, L; Messina, Maria Francesca; Segni, M; Cicchetti, M; Vigone, M; Pasquino, Am; Spera, S; DE LUCA, Filippo; Mussa, Gc; Bona, G.