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FAIENZA, Maria Felicia

FAIENZA, Maria Felicia  

DIPARTIMENTO DI MEDICINA DI PRECISIONE E RIGENERATIVA E AREA JONICA DiMePRe-J  

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(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome 1-gen-1999 Iolascon, A; Faienza, Maria Felicia; Centra, M; Storelli, S; Zelante, L; Savoia, A.
17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotypic Variability and Molecular Findings 1-gen-2012 Faienza, Maria Felicia; Cavallo, Luciano
17beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotipic Variability and Molecular Findings. 1-gen-2011 Faienza, Maria Felicia; Cavallo, Luciano
17beta-hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 1-gen-2009 Bertelloni, S; Balsamo, A; Giordani, L; Fischetto, R; Russo, G; Delvecchio, M; Gennari, M; Nicoletti, A; Maggio, Mc; Concolino, D; Cavallo, Luciano; Cicognani, A; Chiumello, G; Hiort, O; Baroncelli, Gi; Faienza, Maria Felicia
17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-up 1-gen-2020 Faienza, Mf; Baldinotti, F; Marrocco, G; Tyutyusheva, N; Peroni, D; Baroncelli, Gi; Bertelloni, S.
46 XY DISORDERS OF SEXUAL DEVELOPMENT (DSD) CAUSED BY A RARE MUTATION OF THE 17 beta HYDROXYSTEROID DEHYDROGENASE TYPE 3 GENE (HSD17B3) 1-gen-2007 Clara, Zeccino; Faienza, Maria Felicia; Lucia, Giordani; Angelo, Acquafredda; Leggio, Samuele; Todarello, Orlando; Mariangela, D'Aniello; MAURIZIO DEL, Vecchio; Suppl, LUCIANO C. A. V. A. L. L. O. . HORMONE R. E. S. E. A. R. C. H. V. O. L.; Issn, P. P.
46,XY disorders of sexual development (DSD) caused by a rare mutation of the 17-β-hydroxysteroid dehydrogenase type 3 gene (HSD17B3) 1-gen-2007 Zecchino, C; Faienza, Maria Felicia; Giordani, L; Acquafredda, A; Leggio, S; Todarello, Orlando; Daniello, M; Delvecchio, M; Cavallo, Luciano
46,XY disorders of sexual development (DSD) caused by a rare mutation of the 17-beta-hydroxysteroid dehydrogenase type 3 gene (HSD17B3) 1-gen-2007 Zecchino, C; Faienza, Maria Felicia; Giordani, L; Acquafredda, A; Leggio, S; Todarello, Orlando; D’Aniello, M; Delvecchio, M; Cavallo, Luciano
46,XY DSD caused by a rare mutation of the 17ß-hydroxysteroid dehydrogenase type 3 gene 1-gen-2007 Faienza, Maria Felicia; L., Giordani; A., Acquafredda; Leggio, Samuele; Todarello, Orlando; S., Trabucco; M., D'Aniello; C., Zecchino; M., Delvecchio; Cavallo, Luciano
A case of pseudohypoparathyroidism (PHP) with multiple hormone resistance and maternal psoriasis 1-gen-2007 Faienza, Maria Felicia; De Sanctis, L; Acquafredda, A; Zecchino, C; Giordani, L; Delvecchio, M; Cavallo, Luciano
A case of type 1a pseudohypoparathyroidism (PHP) with multiple hormones resistance and maternal psoriasis 1-gen-2007 Faienza, Maria Felicia; DE SANCTIS, L; Acquafredda, A; Zecchino, C; Giordani, L; Delvecchio, M; Cavallo, Luciano
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 novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing 1-gen-2011 Vivenza, D; Godi, M; Faienza, Maria Felicia; Mellone, S; Moia, S; Rapa, A; Petri, A; Bellone, S; Riccomagno, S; Cavallo, Luciano; Giordano, M; Bona, G.
A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency. 1-gen-2014 Macchiaroli, A; Kelbermanb, D; Auriemma R., S; Drury, S; Islam, L; Giangiobbe, S; Ironi, G; Lench, N; Sowden J., C; Colao, A; Pivonello, R; Cavallo, Luciano; Gasperi, M; Faienza, Maria Felicia
A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency 1-gen-2016 Lonero, Antonella; Delvecchio, Maurizio; Primignani, Paola; Caputo, Roberto; Bargiacchi, Sara; Penco, Silvana; Mauri, Lucia; Andreucci, Elena; Faienza, Maria Felicia; Cavallo, Luciano
A Novel OTX2 Gene Mutation in a Child with Growth Hormone Deficiency 1-gen-2015 Lonero, A; Delvecchio, Maurizio; Caputo, R; De Palma, F; Faienza, Maria Felicia; Cavallo, Luciano
Acute pancreatitis in a girl with panhypopituitarism due to craniopharyngioma on growth hormone treatment. A combination of risk factors 1-gen-2009 Faienza, Maria Felicia; DELVECCHIO M., INDRIO F; Francavilla, Ruggiero; Acquafredda, A; Cavallo, Luciano
Aggressive therapeutic approach in a newborn with chronic myeloid childhood leukemia | APPROCCIO TERAPEUTICO AGGRESSIVO IN UN LATTANTE AFFETTO DA LEUCEMIA MIELOIDE CRONICA JUVENILE 1-gen-1994 Santoro, N.; Iacobelli, S.; Faienza, M. F.; Alifano, I.; Carrrassi, A.; De Mattia, D.
Alteration of cell division cycle regulation in human cancers: The role of CDKN2A gene 1-gen-1998 Della Ragione, F; Faienza, Maria Felicia; Coppola, B; Mercurio, C; Della Pietra, V; Mastropietro, S; Borriello, A; Moretti, A; Giordani, L; Monno, F; Iolascon, A.