Výsledky vyhledávání - Mauri, Lucia
- Zobrazuji výsledky 1 - 7 z 7
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SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa Autor Chiereghin, Chiara, Robusto, Michela, Mauri, Lucia, Primignani, Paola, Castorina, Pierangela, Ambrosetti, Umberto, Duga, Stefano, Asselta, Rosanna, Soldà, Giulia
Vydáno 2021Text -
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Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma Autor Mauri, Lucia, Uebe, Steffen, Sticht, Heinrich, Vossmerbaeumer, Urs, Weisschuh, Nicole, Manfredini, Emanuela, Maselli, Edoardo, Patrosso, Mariacristina, Weinreb, Robert N., Penco, Silvana, Reis, André, Pasutto, Francesca
Vydáno 2016Text -
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Successful Extracorporeal Membrane Oxygenation After Incidental Azygos Vein Cannulation in a Neonate With Right-Sided Congenital Diaphragmatic Hernia Interruption of the Inferior V... Autor Mayer, Alessandra, Raffaeli, Genny, Schena, Federico, Parente, Valeria, Sorrentino, Gabriele, Macchini, Francesco, Colli, Anna Maria, Mauri, Lucia, Neri, Simona, Borzani, Irene, Leva, Ernesto, Mosca, Fabio, Cavallaro, Giacomo
Vydáno 2019Text -
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Enterovirus fulminant myocarditis as cause of acute heart failure in a newborn Autor Annoni, Giuseppe, De Rienzo, Francesca, Nonini, Sandra, Pugni, Lorenza, Marianeschi, Stefano M., Mauri, Luigi, Gatelli, Italo, Mauri, Lucia, Aresta, Francesca, Bramerio, Manuela, Francescato, Gaia, Carro, Cristina, Picciolli, Irene, Nava, Alice, Fanti, Diana, Galli, Cristina, Mosca, Fabio, Martinelli, Stefano, Ammirati, Enrico
Vydáno 2022Text -
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Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma Autor Siggs, Owen M., Souzeau, Emmanuelle, Pasutto, Francesca, Dubowsky, Andrew, Smith, James E. H., Taranath, Deepa, Pater, John, Rait, Julian L., Narita, Andrew, Mauri, Lucia, Del Longo, Alessandra, Reis, André, Chappell, Angela, Kearns, Lisa S., Staffieri, Sandra E., Elder, James E., Ruddle, Jonathan B., Hewitt, Alex W., Burdon, Kathryn P., Mackey, David A., Craig, Jamie E.
Vydáno 2019Text -
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Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity Autor Souma, Tomokazu, Tompson, Stuart W., Thomson, Benjamin R., Siggs, Owen M., Kizhatil, Krishnakumar, Yamaguchi, Shinji, Feng, Liang, Limviphuvadh, Vachiranee, Whisenhunt, Kristina N., Maurer-Stroh, Sebastian, Yanovitch, Tammy L., Kalaydjieva, Luba, Azmanov, Dimitar N., Finzi, Simone, Mauri, Lucia, Javadiyan, Shahrbanou, Souzeau, Emmanuelle, Zhou, Tiger, Hewitt, Alex W., Kloss, Bethany, Burdon, Kathryn P., Mackey, David A., Allen, Keri F., Ruddle, Jonathan B., Lim, Sing-Hui, Rozen, Steve, Tran-Viet, Khanh-Nhat, Liu, Xiaorong, John, Simon, Wiggs, Janey L., Pasutto, Francesca, Craig, Jamie E., Jin, Jing, Quaggin, Susan E., Young, Terri L.
Vydáno 2016Text