Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Silvia Vannelli"'
Autor:
Gianpaolo Di Rosa, Francesca Verna, Raffaele Buganza, Luisa de Sanctis, Silvia Vannelli, Daniele Tessaris, Alberto Borraccino, Maria Baffico, Giulia Vinci
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-6 (2020)
Italian Journal of Pediatrics
Italian Journal of Pediatrics
Background The phenotypic features of SHOX deficiency (SHOX-D) are highly variable and can be very mild, especially in young children. The aim of this retrospective study was to evaluate auxological and radiological indicators that could be predictiv
Autor:
Mohamad Maghnie, Federica Messa, Martina Scilipoti, Emanuele Miraglia del Giudice, Stefania Picariello, Lucia Quaglietta, Daniela Cioffi, Anna Grandone, Silvia Vannelli, Natascia Di Iorgi, Maria Parpagnoli, Mario Cirillo, Luisa De Sanctis, Pierluigi Marzuillo, Annalisa Gallizia, Giuseppe Cinalli, Silverio Perrotta, Claudia Santoro
Context Up to 20% of children with neurofibromatosis type 1 (NF1) develop low-grade optic pathway gliomas (OPGs) that can result in endocrine dysfunction. Data on prevalence and type of endocrine disorders in NF1-related OPGs are scarce. Objectives T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e346d485222cd704502939bfe671674
http://hdl.handle.net/11591/428589
http://hdl.handle.net/11591/428589
Autor:
Luisa de Sanctis, Federica Runfola, Antonio Andreacchio, Silvia Vannelli, Ilaria Mussinatto, Raffaele Buganza
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-6 (2020)
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-6 (2020)
BackgroundJaffe-Campanacci syndrome is characterized by multiple non-ossifying fibromas, café-au-lait macules and giant cell granulomas of the jaw. Even if the association between all these peculiar features and neurofibromatosis type 1 have been de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9edd8f4533e2e5abd8e5fb059ae045a7
http://hdl.handle.net/2318/1798041
http://hdl.handle.net/2318/1798041
Publikováno v:
Nutrients, Vol 12, Iss 1941, p 1941 (2020)
Nutrients
Volume 12
Issue 7
Nutrients
Volume 12
Issue 7
Preterm infant growth is a major health indicator and needs to be monitored with an appropriate growth curve to achieve the best developmental and growth potential while avoiding excessive caloric intake that is linked to metabolic syndrome and hyper
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:
Lorenzo Lenzi, Carla Bizzarri, Ivana Rabbone, Riccardo Bonfanti, Mohamad Maghnie, Maria Cristina Maggio, Giuseppe d'Annunzio, Dario Iafusco, Lorenzo Iughetti, Stefano Tumini, Giuseppina Salzano, Gabriella Pozzobon, Marco Marigliano, Stefano Zucchini, Silvia Vannelli, Valentino Cherubini, Andrea Scaramuzza
Background/Aim: Combined growth hormone (GH) and insulin therapy is rarely prescribed by pediatric endocrinologists. We investigated the attitude of Italian physicians to prescribing that therapy in the case of short stature and type-1 diabetes (T1DM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9e0b2db2825280b71d79e0714c5546b
http://hdl.handle.net/11567/773805
http://hdl.handle.net/11567/773805
Autor:
Silvio Boero, Orazio Gabrielli, R. Vivarelli, Eugenio Bonioli, Giuliana Lama, Silvia Vannelli, Guido Morcaldi, Maurizio Clementi, Raffaele Virdis
Neurofibromatosis Type 1 (NF1) is a common autosomal dominant disorder characterized by high penetrance, widely variable expressivity and occurrence of specific skeletal changes such as tibial osteopathy (TO). We collected data on patients referred t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc28c4777e9848a484a95403293429de
http://hdl.handle.net/11577/2573758
http://hdl.handle.net/11577/2573758
Autor:
Maria E. Street, Maria Cristina Maggio, Piero Pirazzoli, Roberto Gastaldi, Silvia Vannelli, Giorgio Radetti, Lorenzo Iughetti, Barbara Stasiowska, Lucia Capone, Laura Mazzanti, Barbara Predieri, Silvano Bertelloni
Background/Aims: Mutations of the short stature homeobox-containing (SHOX) gene on the pseudoautosomal region of the sex chromosomes cause short stature. GH treatment has been recently proposed to improve height in short patients with SHOX deficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09a2fda8659c370a5346b70ac92a2f12
http://hdl.handle.net/11585/411575
http://hdl.handle.net/11585/411575
Autor:
E Cacciari, Giorgio Radetti, F. Deluca, Silvano Milani, Brunetto Boscherini, P. Balestrazzi, A. M. Pasquino, Fabio Buzi, G Mazzilli, Carlo Pintor, Orazio Gabrielli, Cecilia Volta, P Matarazzo, Francesco Carlo Morabito, Giuseppe Chiumello, F. Rigon, F DeMatteis, GTonini (Trieste), S DiMaio, C. Desanctis, Franco Dammacco, Anna Spada, G Giovannelli, L. Benso, Luciano Tatò, Luciano Cavallo, Laura Mazzanti, GP Stoppoloni, V. DeSanctis, Silvia Vannelli, Giuseppe Saggese, U Klain, R Berardi, S. Bernasconi, G. Aicardi, G Nizzoli, A Licursi, P. Borrelli, Francesca Severi, S Lamanna, Daniela Larizza
Publikováno v:
Acta Paediatrica. 83:292-298
In 1990, the Italian Study Group for Turner's Syndrome (ISGTS) undertook a nationwide survey, involving the retrospective collection of cross-sectional data and longitudinal growth profiles of 772 girls with Turner's syndrome born between 1950 and 19
Publikováno v:
Hormone Research. 42:81-85
Twenty-two girls affected by sexual precocity with impaired final height prognosis were followed until they achieved final height. Twelve of them were treated with an intranasal (D-Ser6)-gonadotrophin-releasing hormone (GnRH) analogue (buserelin) adm