Search Results - "Crocione, Claudia"

Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia by Faughnan, Marie E, Mager, Johannes J, Hetts, Steven W, Palda, Valerie A, Lang-Robertson, Kelly, Buscarini, Elisabetta, Deslandres, Erik, Kasthuri, Raj S, Lausman, Andrea, Poetker, David, Ratjen, Felix, Chesnutt, Mark S, Clancy, Marianne, Whitehead, Kevin J, Al-Samkari, Hanny, Chakinala, Murali, Conrad, Miles, Cortes, Daniel, Crocione, Claudia, Darling, Jama, de Gussem, Els, Derksen, Carol, Dupuis-Girod, Sophie, Foy, Patrick, Geisthoff, Urban, Gossage, James R, Hammill, Adrienne, Heimdal, Ketil, Henderson, Katharine, Iyer, Vivek N, Kjeldsen, Anette D, Komiyama, Masaki, Korenblatt, Kevin, McDonald, Jamie, McMahon, Jack, McWilliams, Justin, Meek, Mary E, Mei-Zahav, Meir, Olitsky, Scott, Palmer, Sara, Pantalone, Rose, Piccirillo, Jay F, Plahn, Beth, Porteous, Mary E M, Post, Marco C, Radovanovic, Ivan, Rochon, Paul J, Rodriguez-Lopez, Josanna, Sabba, Carlo, Serra, Marcelo, Shovlin, Claire, Sprecher, Dennis, White, Andrew J, Winship, Ingrid, Zarrabeitia, Roberto

“…Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease with an estimated prevalence of 1 in 5000 that is characterized by the presence of…”
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Characterization of epidemiological distribution and outcome of COVID-19 in patients with hereditary hemorrhagic telangiectasia: a nationwide retrospective multi-centre study during first wave in Italy by Suppressa, Patrizia, Pagella, Fabio, Lenato, Gennaro Mariano, Gaetani, Eleonora, Serio, Ilaria, Masala, Maristella Salvatora, Spinozzi, Giuseppe, Lizzio, Roberta, Matti, Elina, De Silvestri, Annalisa, Passali, Giulio Cesare, Aguglia, Maria, Crocione, Claudia, Sabbà, Carlo

“…Abstract Background Coronavirus Disease 2019 (COVID-19) continues to have a devastating impact across the world. A number of pre-existing common clinical…”
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Time to diagnosis and determinants of diagnostic delays of people living with a rare disease: results of a Rare Barometer retrospective patient survey by Faye, Fatoumata, Crocione, Claudia, Anido de Peña, Roberta, Bellagambi, Simona, Escati Peñaloza, Luciana, Hunter, Amy, Jensen, Lene, Oosterwijk, Cor, Schoeters, Eva, de Vicente, Daniel, Faivre, Laurence, Wilbur, Michael, Le Cam, Yann, Dubief, Jessie

“…Timely diagnosis is one of the most serious challenges faced by people living with a rare disease (PLWRD), and this study estimates that in Europe, the average…”
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Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia by Buscarini, Elisabetta, Botella, Luisa Maria, Geisthoff, Urban, Kjeldsen, Anette D, Mager, Hans Jurgen, Pagella, Fabio, Suppressa, Patrizia, Zarrabeitia, Roberto, Dupuis-Girod, Sophie, Shovlin, Claire L

“…Hereditary hemorrhagic telangiectasia (HHT) is a multisystemic inherited vascular dysplasia that leads to nosebleeds and visceral arteriovenous malformations…”
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European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)? by 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

“…Hereditary haemorrhagic telangiectasia (HHT) is a rare vascular multisystemic disease that leads to epistaxis, anaemia due to blood loss, and arteriovenous…”
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Impact of SARS-CoV-2 infection in patients with hereditary hemorrhagic telangiectasia: epidemiological and clinical data from the comprehensive Italian retrospective multicenter study by Suppressa, Patrizia, Maiorano, Eugenia, Gaetani, Eleonora, Matti, Elina, Lenato, Gennaro Mariano, Serio, Ilaria, Masala, Maristella Salvatora, Passali, Giulio Cesare, Aguglia, Maria, Crocione, Claudia, Lopalco, Pietro Luigi, Caneschi, Francesca, Musella, Valeria, De Silvestri, Annalisa, Gambini, Giulia, Spinozzi, Giuseppe, Sabbà, Carlo, Pagella, Fabio

“…Rare Disease patients manifested high concern regarding the possible increased risk of severe outcomes and worsening of disease-specific clinical manifestation…”
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