Результаты поиска - Mauri, Lucia

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

Полный текст Полный текст

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

Полный текст Полный текст Полный текст

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

Полный текст Полный текст Полный текст

Successful Extracorporeal Membrane Oxygenation After Incidental Azygos Vein Cannulation in a Neonate With Right-Sided Congenital Diaphragmatic Hernia Interruption of the Inferior V... по 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

Полный текст Полный текст Полный текст

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

Полный текст Полный текст Полный текст

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

Полный текст Полный текст Полный текст

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

Полный текст Полный текст Полный текст