Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Patrizia Matarazzo"'
Autor:
Anna Castiglione, Giovannino Ciccone, Enrico Brignardello, Margherita Dionisi-Vici, Nicoletta Fortunati, Patrizia Matarazzo, Eleonora Biasin, Franca Fagioli, Francesco Felicetti
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(12)
BACKGROUND Potentially gonadotoxic protocols are currently used for the treatment of childhood hematologic malignancies. This study aims to evaluate the prevalence of gonadal dysfunction and the most important associated risk factors in a cohort of h
Autor:
Malgorzata Wasniewska, Maria Chiara Pellegrin, Rita Fischetto, Francesca Macchi, Antonella Lonero, Sara Osimani, A. Crinò, Adriana Franzese, Sarah Bocchini, Gilda Cassano, Luana Nosetti, Annamaria Perri, Giuseppa Patti, Maria Rosaria Licenziati, Michele Sacco, Stefano Stagi, Alessandro Salvatoni, G. Trifirò, Rosanna Lia, Simona Filomena Madeo, Irene Rutigliano, Lorenzo Iughetti, Paola Giordano, Danilo Fintini, Gianluca Tornese, Alessio Convertino, Patrizia Matarazzo, Graziano Grugni, S. Ferraris, Emanuela Scarano, Domenico Corica, Valentina Fattorusso, Viviana Valeria Palmieri, Roberta Pajno, L. Ragusa, Maurizio Delvecchio
Pediatric patients with Prader-Willi syndrome (PWS) can be treated with recombinant human GH (rhGH). These patients are highly sensitive to rhGH and the standard doses suggested by the international guidelines often result in IGF-1 above the normal r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7a8e3ec15413420522c8d0ddc251830
http://hdl.handle.net/11588/770080
http://hdl.handle.net/11588/770080
Autor:
Patrizia Matarazzo, Martina Tetti, Xavier Jeunemaitre, Jacopo Burrello, Silvia Monticone, Barbara Pasini, Franco Veglio, Paolo Mulatero
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 812 (2018)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Liddle syndrome is an inherited form of low-renin hypertension, transmitted with an autosomal dominant pattern. The molecular basis of Liddle syndrome resides in germline mutations of the SCNN1A, SCNN1B and SCNN1G genes, encoding the α, β, and γ-s
Autor:
Caterina Guiot, Giuseppe Migliaretti, Silvia Vannelli, Federica Cavallo, Ilaria Stura, Serena Ditaranto, Nazario Cappello, Patrizia Matarazzo
Recombinant GH has been offered to GH-deficient (GHD) subjects for more than 30 years, in order to improve height and growth velocity in children and to enhance metabolic effects in adults. The aim of our work is to describe the long-term effect of r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0b9f498e78c6c6e7a5b8043dd704e0a
http://hdl.handle.net/2318/1676427
http://hdl.handle.net/2318/1676427
Autor:
Daniele Tessaris, Alison M. Boyce, Roberto Lala, Michael T. Collins, Luisa De Sanctis, Margaret Zacharin, Patrizia Matarazzo
Publikováno v:
Clinical endocrinology. 89(1)
CONTEXT In fibrous dysplasia (BFD), normal bone and bone marrow are replaced by fibro-osseous tissue, leading to fracture, deformity and pain. BFD may be isolated, or in association with cutaneous hyperpigmentation and/or hyperfunctioning endocrinopa
Autor:
Marco Braghero, Annamaria Staiano, Eleonora Biasin, Patrizia Matarazzo, Silvia Einaudi, Rosaria Manicone, Francesco Felicetti, Enrico Brignardello, Franca Fagioli, Elisabetta Bignamini, Elena Nave, F. Callea, C. Concato, E. Fiscarelli, S. Garrone, M.Rossi de Gasperis, Patrizia Calzi, Grazia Marinelli, Roberto Besana, Carlo Caffarelli, Antonio Di Peri, Irene Lapetina, Patrizia Cincinnati, Rosalia Maria Da Riol, Mario De Curtis, Lucia Dito, Chiara Protano, Susanna Esposito, Dante Ferrara, Rossella Galiano, Pasquale Novellino, Eric Heath Kossoff, Andrzej Krzysztofiak, Elena Bozzola, Laura Lancella, Alessandra Marchesi, Alberto Villani, Paola Lago, Elisabetta Garetti, Anna Pirelli, Paola Marchisio, Maria Santagati, Stefania Stefani, Nicola Principi, Valeria d’Apolito, Luigi Memo, Angelo Selicorni, Vito Leonardo Miniello, Lucia Diaferio, Antonella Palmieri, Luciana Parola, Ettore Piro, Claudio Romano, Maria Ausilia Catena, Sabrina Cardile, Oliviero Sacco, Donata Girosi, Roberta Olcese, Mariangela Tosca, Giovanni Arturo Rossi, Sergio Salerno, Maria Chiara Terranova, Francesca Santamaria, Giorgia Mancano, Silvia Maitz, Virginia A. Stallings, Chiara Berlolaso, Carolyn McAnlis, Joan I. Schall, Pasquale Striano, Rita Tanas, Giulia De Iaco, Maria Marsella, Guido Caggese, Paolo Toma, Piero Valentini, Danilo Buonsenso, David Pata, Manuela Ceccarelli, Elvira Verduci, Marta Brambilla, Benedetta Mariani, Carlotta Lassandro, Alice Re Dionigi, Sara Vizzuso, Giuseppe Banderali, Gianvito Panzarino, Claudia Di Paolantonio, Alberto Verrotti, Laura Cursi, Annalisa Grandin, Raffaele Virdis, Patrizia Carletti, Giovanna Weber, Silvana Caiulo, Maria Cristina Vigone
Publikováno v:
Italian Journal of Pediatrics. 43
Autor:
Malgorzata Wasniewska, Tommaso Aversa, Maria Francesca Messina, Domenico Corica, Andrea Corrias, Mariacarolina Salerno, Mariella Valenzise, Patrizia Matarazzo, Filippo De Luca, Laura Mazzanti
Aim: To prospectively investigate, during a 5-year follow-up, whether the prognosis of thyroid function with Hashimoto thyroiditis (HT) is different in euthyroid girls with Turner syndrome (TS) than in euthyroid girls without TS. Design: In 66 TS gir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf94301bd5b0d912405bfc229d331e5
http://hdl.handle.net/11588/700282
http://hdl.handle.net/11588/700282
McCune-Albright syndrome (MAS) is characterized by the triad of polyostotic bone fibrous dysplasia (PFD), endocrine disorders, and café-au-lait skin pigmentation. Ninety percent of MAS patients have fibrous dysplasia (FD) craniofacial lesions. Osteo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9465729ada82c97e244819440187310f
http://hdl.handle.net/2318/1556588
http://hdl.handle.net/2318/1556588
Autor:
Daniele Tessaris, Patrizia Matarazzo, L. de Sanctis, Malgorzata Wasniewska, Andrea Corrias, Roberto Lala, M. F. Messina, Maria Cristina Vigone
Publikováno v:
Hormone Research in Paediatrics. 78:151-157
Background: To date, there is no agreement about the frequency or the features of thyroid abnormalities in McCune-Albright syndrome (MAS). The aim of our study was to detect thyroid abnormalities in a cohort of MAS children and adolescents and to giv
Autor:
Patrizia Matarazzo, Alessandro Mussa, Gerdi Tuli, Marialia Repici, Francesco Porta, Ludovica Fiore
Publikováno v:
Ultrasound in Medicine & Biology. 36:726-732
The aim of the present study is to investigate bone status by phalangeal quantitative ultrasound (QUS) in a cohort of hypopituitaric pediatric subjects, and to relate measurement outcome to their clinical, laboratory, and therapeutical features. Fort