Αποτελέσματα αναζήτησης - Mauri, Lucia

Connexin 26 variant carriers have a better gastrointestinal health: is this the heterozygote advantage? από Vuckovic, Dragana, Dallapiccola, Bruno, Franzè, Annamaria, Mauri, Lucia, Perrone, Maria Dolores, Gasparini, Paolo

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SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa από Chiereghin, Chiara, Robusto, Michela, Mauri, Lucia, Primignani, Paola, Castorina, Pierangela, Ambrosetti, Umberto, Duga, Stefano, Asselta, Rosanna, Soldà, Giulia

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Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma από 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

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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... από 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

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Enterovirus fulminant myocarditis as cause of acute heart failure in a newborn από 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

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Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma από 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.

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Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity από 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.

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