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Liver involvement in hereditary hemorrhagic telangiectasia.
Buscarini E, Gandolfi S, Alicante S, Londoni C, Manfredi G. Buscarini E, et al. Among authors: gandolfi s. Abdom Radiol (NY). 2018 Aug;43(8):1920-1930. doi: 10.1007/s00261-018-1671-4. Abdom Radiol (NY). 2018. PMID: 29987403 Review.
Predicting the size of pulmonary arteriovenous malformations on chest computed tomography: a role for transthoracic contrast echocardiography.
Velthuis S, Buscarini E, Mager JJ, Vorselaars VM, van Gent MW, Gazzaniga P, Manfredi G, Danesino C, Diederik AL, Vos JA, Gandolfi S, Snijder RJ, Westermann CJ, Post MC. Velthuis S, et al. Among authors: gandolfi s. Eur Respir J. 2014 Jul;44(1):150-9. doi: 10.1183/09031936.00133713. Epub 2014 Mar 6. Eur Respir J. 2014. PMID: 24603816 Free article.
European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?
Dupuis-Girod S, Shovlin CL, Kjeldsen AD, Mager HJ, Sabba C, Droege F, Fargeton AE, Fialla AD, Gandolfi S, Hermann R, Lenato GM, Manfredi G, Post MC, Rennie C, Suppressa P, Sure U; ePag group; Buscarini E. Dupuis-Girod S, et al. Among authors: gandolfi s. Eur J Med Genet. 2022 Oct;65(10):104575. doi: 10.1016/j.ejmg.2022.104575. Epub 2022 Aug 5. Eur J Med Genet. 2022. PMID: 35940549 Free article.
TMJ disorders and pain: assessment by contrast-enhanced MRI.
Farina D, Bodin C, Gandolfi S, De Gasperi W, Borghesi A, Maroldi R. Farina D, et al. Among authors: gandolfi s. Eur J Radiol. 2009 Apr;70(1):25-30. doi: 10.1016/j.ejrad.2008.01.014. Epub 2008 Mar 7. Eur J Radiol. 2009. PMID: 18329212
245 results