Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Vittoria Baraldini"'
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 31, Iss , Pp 71-76 (2018)
Introduction: Gastrointestinal infantile hemangiomas (IHs) are extremely rare and represent a diagnostic challenge, especially in newborns for the limited applicability of diagnostic approaches.We report two cases of neonates with gastrointestinal bl
Externí odkaz:
https://doaj.org/article/b1f2a985dbeb44aea6ae407f21da219b
Autor:
Daniela Graziani, Giana Izzo, Vittoria Baraldini, Cecilia Parazzini, Chiara Doneda, Valentina Toto, Martina Di Stasi, Elisa Cattaneo, Andrea Righini
Publikováno v:
Neurogenetics. 22(1)
The term PROS (PIK3CA-Related Overgrowth Spectrum) indicates a wide spectrum of overgrowth disorders related to somatic mutations in PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) pathway. We present three cases with
Autor:
Gaetano Bulfamante, Laura Moneghini, Anna Caretti, Luigina Spaccini, Vittoria Baraldini, Delfina Tosi, Daniela Graziani, Giacomo Colletti, Elisa Cattaneo, Alfredo Zocca
Vascular malformations (vMs) encompass a wide range of diseases often associated with somatic or, more rarely, germinal genetic mutations. A mutation in the PIK3Ca/mTOR pathway is more often involved in various vMs. CD10 and CD34 are cellular markers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5daf8e4cb7bece6eaa22feaae211131
https://hdl.handle.net/11380/1251974
https://hdl.handle.net/11380/1251974
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 31, Iss, Pp 71-76 (2018)
Introduction: Gastrointestinal infantile hemangiomas (IHs) are extremely rare and represent a diagnostic challenge, especially in newborns for the limited applicability of diagnostic approaches.We report two cases of neonates with gastrointestinal bl
Publikováno v:
Journal of Pediatric Surgery. 42:381-385
Background/Purpose Surgical excision of critical infantile haemangiomas (HMs) is usually delayed until intralesional blood flow spontaneously decreases, but fibrofatty tissue and exuberant skin invariably remain even after total involution. The aim o
Autor:
Massimo Vaghi, Vittoria Baraldini
Publikováno v:
Hemangiomas and Vascular Malformations ISBN: 9788847056725
The syndromes represent an important chapter of vascular malformations because they are recognized in the classification of rare diseases. The syndromes are usually named with eponyms, and this brought some confusion in the classification of vascular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6d4c59224557d4c6ed103c6182f8eb2
https://doi.org/10.1007/978-88-470-5673-2_37
https://doi.org/10.1007/978-88-470-5673-2_37
Publikováno v:
Journal of Pediatric Surgery. 38:58-61
Background/Purpose: This report reviews the clinical presentation, surgical treatment, and outcome of 8 children treated for the thoracic outlet syndrome (TOS) during the last 3 years. Methods: From 1998 through 2001 31 patients were admitted to our
Publikováno v:
Journal of Pediatric Surgery. 37:232-235
Purpose: The aim of this study was to evaluate the authors' preliminary experience in early surgical treatment of distal venous hypertension (DVH) in children affected by Klippel-Trenaunay syndrome (KTS). Methods: Clinical assessment, surgical manage
Autor:
G. Vercellio, Vittoria Baraldini
Publikováno v:
Hemangiomas and Vascular Malformations ISBN: 9788847005686
Hemangiomas and Vascular Malformations ISBN: 9788847056725
Hemangiomas and Vascular Malformations ISBN: 9788847056725
The surgical management of infantile hemangiomas (IH) usually consists of late correction of contour deformities after completed spontaneous involution with excision of remaining fibrofatty tissue and exuberant skin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15c443428059f924c2dcf06709030914
https://doi.org/10.1007/978-88-470-0569-3_10
https://doi.org/10.1007/978-88-470-0569-3_10