European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)
Eker, Omer F., Boccardi, Edoardo, Sure, Ulrich, Patel, Maneesh C., Alicante, Saverio, Alsafi, Ali, Coote, Nicola, Droege, Freya, Dupuis, Olivier, Fialla, Annette Dam, Jones, Bryony, Kariholu, Ujwal, Kjeldsen, Anette D., Lefroy, David, Lenato, Gennaro M., Mager, Hans Jurgen, Manfredi, Guido, Nielsen, Troels H., Pagella, Fabio, Post, Marco C., Rennie, Catherine, Sabbà, Carlo, Suppressa, Patrizia, Toerring, Pernille M., Ugolini, Sara, Buscarini, Elisabetta, Dupuis-Girod, Sophie, Shovlin, Claire L.
Published in Orphanet journal of rare diseases (29.06.2020)
Published in Orphanet journal of rare diseases (29.06.2020)
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Hereditary Hemorrhagic Telangiectasia: Arteriovenous Malformations in Children
Giordano, Paola, MD, Lenato, Gennaro M., PhD, Suppressa, Patrizia, MD, Lastella, Patrizia, MD, Dicuonzo, Franca, MD, Chiumarulo, Luigi, MD, Sangerardi, Maria, MD, Piccarreta, Paola, MD, Valerio, Raffaella, MD, Scardapane, Arnaldo, MD, Marano, Giuseppe, MD, Resta, Nicoletta, PhD, Quaranta, Nicola, MD, Sabbà, Carlo, MD
Published in The Journal of pediatrics (01.07.2013)
Published in The Journal of pediatrics (01.07.2013)
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A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study
Pierucci, Paola, Lenato, Gennaro M, Suppressa, Patrizia, Lastella, Patrizia, Triggiani, Vincenzo, Valerio, Raffaella, Comelli, Mario, Salvante, Daniela, Stella, Alessandro, Resta, Nicoletta, Logroscino, Giancarlo, Resta, Francesco, Sabbà, Carlo
Published in Orphanet journal of rare diseases (07.06.2012)
Published in Orphanet journal of rare diseases (07.06.2012)
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A large interstitial deletion encompassing the amelogenin gene on the short arm of the Y chromosome
LATTANZI, Wanda, DI GIACOMO, Marilena C, LENATO, Gennaro M, CHIMIENTI, Guglielmina, VOGLINO, Gianfranco, RESTA, Nicoletta, PEPE, Gabriella, GUANTI, Ginevra
Published in Human genetics (01.04.2005)
Published in Human genetics (01.04.2005)
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Role of inflammatory markers in the diagnosis of vascular contributions to cognitive impairment and dementia: a systematic review and meta-analysis
Custodero, Carlo, Ciavarella, Alessandro, Panza, Francesco, Gnocchi, Davide, Lenato, Gennaro M., Lee, Juhan, Mazzocca, Antonio, Sabbà, Carlo, Solfrizzi, Vincenzo
Published in GeroScience (01.06.2022)
Published in GeroScience (01.06.2022)
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Effects of VEGF on phenotypic severity in children with hereditary hemorrhagic telangiectasia
Giordano, Paola, Lenato, Gennaro M, Pierucci, Paola, Suppressa, Patrizia, Altomare, Maria, Del Vecchio, Giancarlo, Di Bitonto, Giovanna, De Mattia, Domenico, Guanti, Ginevra, Sabbà, Carlo
Published in Journal of pediatric hematology/oncology (01.08.2009)
Published in Journal of pediatric hematology/oncology (01.08.2009)
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European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?
Dupuis-Girod, Sophie, Shovlin, Claire L., Kjeldsen, Anette D., Mager, Hans-Jurgen, Sabba, Carlo, Droege, Freya, Fargeton, Anne-Emmanuelle, Fialla, Annette D., Gandolfi, Silvia, Hermann, Ruben, Lenato, Gennaro M., Manfredi, Guido, Post, Marco C., Rennie, Catherine, Suppressa, Patrizia, Sure, Ulrich, Crocione, Claudia, Blom, Ria, Botella, Luisa Maria, Brocca, Fernando, Coxall, Caroline, Druckman, Karen T., Erasme, Didier, Federici, Paolo, Grabowski, Christina, Lundgren, Mildred, Søderman, Tone, Woods, Dara, Buscarini, Elisabetta
Published in European journal of medical genetics (01.10.2022)
Published in European journal of medical genetics (01.10.2022)
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Liver involvement in a large cohort of patients with hereditary hemorrhagic telangiectasia: Echo-color-Doppler vs multislice computed tomography study
Buonamico, Paolo, Suppressa, Patrizia, Lenato, Gennaro M, Pasculli, Giovanna, D’Ovidio, Francesco, Memeo, Maurizio, Scardapane, Arnaldo, Sabbà, Carlo
Published in Journal of hepatology (01.05.2008)
Published in Journal of hepatology (01.05.2008)
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Pulmonary Arteriovenous Malformations and Cerebral Abscess Recurrence in a Child With Hereditary Hemorrhagic Telangiectasia
Giordano, Paola, Sangerardi, Maria, Suppressa, Patrizia, Lastella, Patrizia, Attolini, Ettore, Valente, Federica, Fiorella, Maria L, Lenato, Gennaro M, Sabbà, Carlo
Published in Journal of pediatric hematology/oncology (01.04.2015)
Published in Journal of pediatric hematology/oncology (01.04.2015)
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Hepatic angiodynamic profile in paediatric patients with hereditary haemorrhagic telangiectasia type 1 and type 2
Giordano, Paola, Francavilla, Mariantonietta, Buonamico, Paolo, Suppressa, Patrizia, Lastella, Patrizia, Sangerardi, Maria, Miniello, Vito L, Scardapane, Arnaldo, Lenato, Gennaro M, Sabbà, Carlo
Published in VASA (01.05.2017)
Published in VASA (01.05.2017)
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Liver involvement in hereditary hemorrhagic telangiectasia: can breath test unmask impaired hepatic first-pass effect?
Candelli, Marcello, Pompili, Maurizio, Suppressa, Patrizia, Lenato, Gennaro M., Bosco, Giulia, Rapaccini, Gian Ludovico, Gasbarrini, Antonio, Scardapane, Arnaldo, Sabbà, Carlo
Published in Internal and emergency medicine (01.08.2012)
Published in Internal and emergency medicine (01.08.2012)
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Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1
Fernandez-L, Africa, Sanz-Rodriguez, Francisco, Zarrabeitia, Roberto, Perez-Molino, Alfonso, Morales, Carmelo, Restrepo, Carlos M., Ramirez, Jose R., Coto, Eliecer, Lenato, Gennaro M., Bernabeu, Carmelo, Botella, Luisa M.
Published in Human mutation (01.03.2006)
Published in Human mutation (01.03.2006)
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Journal Article
DHPLC-based mutation analysis of ENG and ALK-1 genes in HHT Italian population
Lenato, Gennaro M., Lastella, Patrizia, Di Giacomo, Marilena C., Resta, Nicoletta, Suppressa, Patrizia, Pasculli, Giovanna, Sabbà, Carlo, Guanti, Ginevra
Published in Human mutation (01.02.2006)
Published in Human mutation (01.02.2006)
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Journal Article
Rare diseases in the elderly: a new perspective for the specialist in geriatrics
Carlo Sabbà, Gennaro M. Lenato, Carlo Custodero, Patrizia Suppressa
Published in Geriatric care (Pavia) (01.12.2019)
Published in Geriatric care (Pavia) (01.12.2019)
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Journal Article
European Reference Network for Rare Vascular Diseases
Eker, Omer F, Boccardi, Edoardo, Sure, Ulrich, Patel, Maneesh C, Alicante, Saverio, Alsafi, Ali, Coote, Nicola, Droege, Freya, Dupuis, Olivier, Fialla, Annette Dam, Jones, Bryony, Kariholu, Ujwal, Kjeldsen, Anette D, Lefroy, David, Lenato, Gennaro M, Mager, Hans Jurgen, Manfredi, Guido, Nielsen, Troels H, Pagella, Fabio, Post, Marco C, Rennie, Catherine, Sabbà, Carlo, Suppressa, Patrizia, Toerring, Pernille M, Ugolini, Sara, Buscarini, Elisabetta, Dupuis-Girod, Sophie, Shovlin, Claire L
Published in Orphanet journal of rare diseases (29.06.2020)
Published in Orphanet journal of rare diseases (29.06.2020)
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Journal Article
Safety of reduced or absent antithrombotic therapy after left atrial appendage closure in patients affected by hereditary haemorrhagic telangiectasia and atrial fibrillation
Pepe, Martino, Suppressa, Patrizia, Giuliano, Antonio F, Nestola, Palma L, Bortone, Alessandro S, DE Cillis, Emanuela, Acquaviva, Tommaso, Forleo, Cinzia, Moscarelli, Marco, Lenato, Gennaro M, SabbÀ, Carlo
Published in Minerva cardiology and angiology (11.03.2021)
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Published in Minerva cardiology and angiology (11.03.2021)
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