Generic versions of enoxaparin available for clinical use in Brazil are similar to the original drug von GLAUSER, B. F., VAIRO, B. C., OLIVEIRA, C. P. M., CINELLI, L. P., PEREIRA, M. S., MOURÃO, P. A. S.

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Heparins from porcine and bovine intestinal mucosa: Are they similar drugs? von Aquino, Rafael S., Pereira, Mariana S., Vairo, Bruno C., Cinelli, Leonardo P., Santos, Gustavo R. C., Fonseca, Roberto J. C., Mourão, Paulo A. S.

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Heparin from bovine intestinal mucosa: Glycans with multiple sulfation patterns and anticoagulant effects von Tovar, A. M. F., Capillé, N. V. M., Santos, G. R. C., Vairo, B. C., Oliveira, S.-N. M. C. G., Fonseca, R. J. C., Mourão, P. A. S.

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Heparin from bovine intestinal mucosa: Glycans with multiple sulfation patterns and anticoagulant effects von Tovar, Ana M. F., Capillé, Nina V. M., Santos, Gustavo R. C., Vairo, Bruno C., Oliveira, Stephan-Nicollas M. C. G., Fonseca, Roberto J. C., Mourão, Paulo A. S.

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Structure and haemostatic effects of generic versions of enoxaparin available for clinical use in Brazil: Similarity to the original drug von Glauser, Bianca F., Vairo, Bruno C., Oliveira, Stephan-Nicollas M. C. G., Cinelli, Leonardo P., Pereira, Mariana S., Mourão, Paulo A.S.

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Molecular characterization of SARS-CoV-2 from the first case of COVID-19 in Italy von Capobianchi, M.R., Rueca, M., Messina, F., Giombini, E., Carletti, F., Colavita, F., Castilletti, C., Lalle, E., Bordi, L., Vairo, F., Nicastri, E., Ippolito, G., Gruber, C.E.M., Bartolini, B.

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Diagnostic yield of exome and genome sequencing after non-diagnostic multi-gene panels in patients with single-system diseases von Wilke, Matheus V M B, Klee, Eric W, Dhamija, Radhika, Fervenza, Fernando C, Thomas, Brittany, Leung, Nelson, Hogan, Marie C, Hager, Megan M, Kolbert, Kayla J, Kemppainen, Jennifer L, Loftus, Elle C, Leitzen, Katie M, Vitek, Carolyn R, McAllister, Tammy, Lazaridis, Konstantinos N, Pinto E Vairo, Filippo

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Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency von Boisson, Bertrand, Laplantine, Emmanuel, Prando, Carolina, Giliani, Silvia, Israelsson, Elisabeth, Xu, Zhaohui, Abhyankar, Avinash, Israël, Laura, Trevejo-Nunez, Giraldina, Bogunovic, Dusan, Cepika, Alma-Martina, MacDuff, Donna, Chrabieh, Maya, Hubeau, Marjorie, Bajolle, Fanny, Debré, Marianne, Mazzolari, Evelina, Vairo, Donatella, Agou, Fabrice, Virgin, Herbert W, Bossuyt, Xavier, Rambaud, Caroline, Facchetti, Fabio, Bonnet, Damien, Quartier, Pierre, Fournet, Jean-Christophe, Pascual, Virginia, Chaussabel, Damien, Notarangelo, Luigi D, Puel, Anne, Israël, Alain, Casanova, Jean-Laurent, Picard, Capucine

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Identification of Genetic Causes of Focal Segmental Glomerulosclerosis Increases With Proper Patient Selection von Miao, Jing, Pinto e Vairo, Filippo, Hogan, Marie C., Erickson, Stephen B., El Ters, Mireille, Bentall, Andrew J., Kukla, Aleksandra, Greene, Eddie L., Hernandez, Loren Herrera, Sethi, Sanjeev, Lazaridis, Konstantinos N., Pichurin, Pavel N., Lisi, Emily, Prochnow, Carri A., Zand, Ladan, Fervenza, Fernando C.

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Targeting of acute myeloid leukemia in vitro and in vivo with an anti-CD123 mAb engineered for optimal ADCC von Busfield, S J, Biondo, M, Wong, M, Ramshaw, H S, Lee, E M, Ghosh, S, Braley, H, Panousis, C, Roberts, A W, He, S Z, Thomas, D, Fabri, L, Vairo, G, Lock, R B, Lopez, A F, Nash, A D

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TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study von Bowles, Bradley, Ferrer, Alejandro, Nishimura, Carla J., Pinto e Vairo, Filippo, Rey, Tristan, Leheup, Bruno, Sullivan, Jennifer, Schoch, Kelly, Stong, Nicholas, Agolini, Emanuele, Cocciadiferro, Dario, Williams, Abigail, Cummings, Alex, Loddo, Sara, Genovese, Silvia, Roadhouse, Chelsea, McWalter, Kirsty, Wentzensen, Ingrid M., Li, Chumei, Babovic‐Vuksanovic, Dusica, Lanpher, Brendan C., Dentici, Maria Lisa, Ankala, Arun, Hamm, J. Austin, Dallapiccola, Bruno, Radio, Francesca Clementina, Shashi, Vandana, Gérard, Benedicte, Bloch‐Zupan, Agnes, Smith, Richard J., Klee, Eric W.

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Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy von Morales-Rosado, Joel A., Schwab, Tanya L., Macklin-Mantia, Sarah K., Foley, A. Reghan, Pinto e Vairo, Filippo, Pehlivan, Davut, Donkervoort, Sandra, Rosenfeld, Jill A., Boyum, Grace E., Hu, Ying, Cong, Anh T.Q., Lotze, Timothy E., Mohila, Carrie A., Saade, Dimah, Bharucha-Goebel, Diana, Chao, Katherine R., Grunseich, Christopher, Bruels, Christine C., Littel, Hannah R., Estrella, Elicia A., Pais, Lynn, Kang, Peter B., Zimmermann, Michael T., Lupski, James R., Lee, Brendan, Schellenberg, Matthew J., Clark, Karl J., Wierenga, Klaas J., Bönnemann, Carsten G., Klee, Eric W.

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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias von Helbig, Katherine L., Lauerer, Robert J., Bahr, Jacqueline C., Souza, Ivana A., Uysal, Betül, Gandini, Maria A., Huang, Sun, Keren, Boris, Mignot, Cyril, Billette de Villemeur, Thierry, Nava, Caroline, Valence, Stéphanie, Buratti, Julien, Fagerberg, Christina R., Soerensen, Kristina P., Kamsteeg, Erik-Jan, Koolen, David A., Gunning, Boudewijn, Schelhaas, H. Jurgen, Fox, Jordana, Bakhtiari, Somayeh, Jarrar, Randa, Lindstrom, Kristin, Jin, Sheng Chih, Zeng, Xue, Bilguvar, Kaya, Papavasileiou, Antigone, Xing, Qinghe, Zhu, Changlian, Boysen, Katja, Vairo, Filippo, Klee, Eric W., Tillema, Jan-Mendelt, Payne, Eric T., Cousin, Margot A., Kruisselbrink, Teresa M., Wick, Myra J., Baker, Joshua, Smith, Nicholas, Angrist, Misha, Ashley, Patricia, Bidegain, Margarita, Chambers, Eileen, Cope, Heidi, Cotten, C. Michael, Curington, Theresa, Davis, Erica E., Fisher, Kimberley, French, Amanda, Gallentine, William, Hill, Kevin, Kansagra, Sujay, Katsanis, Sara, Kurtzberg, Joanne, Marcus, Jeffrey, McDonald, Marie, Mikati, Mohammed, Miller, Stephen, Murtha, Amy, Perilla, Yezmin, Pizoli, Carolyn, Ross, Sherry, Sadeghpour, Azita, Smith, Edward, Wiener, John, Corbett, Mark A., Goldmann, Eva, Kichula, Elizabeth, Segal, Eric, Jackson, Kelly E., Asamoah, Alexander, McCarrier, Julie, Botto, Lorenzo D., Tvrdik, Tatiana, Cascino, Gregory D., Klingerman, Sherry, Neumann, Catherine, Nolan, Melinda A., Snell, Russell G., Lehnert, Klaus, Sadleir, Lynette G., Kvarnung, Malin, Guerrini, Renzo, Friez, Michael J., Lyons, Michael J., Leonhard, Jennifer, Kringlen, Gabriel, El Achkar, Christelle M., Smith, Lacey A., Carss, Keren J., Rankin, Julia, Zeman, Adam, Blyth, Moira, Kerr, Bronwyn, Ruiz, Karla, Urquhart, Jill, Banka, Siddharth, Scheffer, Ingrid E., Zamponi, Gerald W., Mefford, Heather C.

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In vitro and in vivo antimicrobial activity of sodium colistimethate and amikacin-loaded nanostructured lipid carriers (NLC) von Vairo, C., Basas, J., Pastor, M., Palau, M., Gomis, X., Almirante, B., Gainza, E., Hernandez, R.M., Igartua, M., Gavaldà, J., Gainza, G.

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QCD and strongly coupled gauge theories: challenges and perspectives von Brambilla, N., Eidelman, S., Foka, P., Gardner, S., Kronfeld, A. S., Alford, M. G., Alkofer, R., Butenschoen, M., Cohen, T. D., Erdmenger, J., Fabbietti, L., Faber, M., Goity, J. L., Ketzer, B., Lin, H. W., Llanes-Estrada, F. J., Meyer, H. B., Pakhlov, P., Pallante, E., Polikarpov, M. I., Sazdjian, H., Schmitt, A., Snow, W. M., Vairo, A., Vogt, R., Vuorinen, A., Wittig, H., Arnold, P., Christakoglou, P., Di Nezza, P., Fodor, Z., Garcia i Tormo, X., Höllwieser, R., Janik, M. A., Kalweit, A., Keane, D., Kiritsis, E., Mischke, A., Mizuk, R., Odyniec, G., Papadodimas, K., Pich, A., Pittau, R., Qiu, J.-W., Ricciardi, G., Salgado, C. A., Schwenzer, K., Stefanis, N. G., von Hippel, G. M., Zakharov, V. I.

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Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients von Santiago, K.M., Castro, L.P., Neto, J.P.D., Nóbrega, A.F., Pinto, C.A.L., Ashton‐Prolla, P., Pinto e Vairo, F., Medeiros, P.F.V., Ribeiro, E.M., Ribeiro, B.F.R., Valle, F.F., Doriqui, M.J.R., Leite, C.H.B., Rocha, R.M., Moura, L.M.S., Munford, V., Galante, P.A.F., Menck, C.F.M., Rogatto, S.R., Achatz, M.I.

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Genomics Integration Into Nephrology Practice von Pinto e Vairo, Filippo, Prochnow, Carri, Kemppainen, Jennifer L., Lisi, Emily C., Steyermark, Joan M., Kruisselbrink, Teresa M., Pichurin, Pavel N., Dhamija, Rhadika, Hager, Megan M., Albadri, Sam, Cornell, Lynn D., Lazaridis, Konstantinos N., Klee, Eric W., Senum, Sarah R., El Ters, Mireille, Amer, Hatem, Baudhuin, Linnea M., Moyer, Ann M., Keddis, Mira T., Zand, Ladan, Sas, David J., Erickson, Stephen B., Fervenza, Fernando C., Lieske, John C., Harris, Peter C., Hogan, Marie C.

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Heavy quarkonium: progress, puzzles, and opportunities von Brambilla, N., Eidelman, S., Heltsley, B. K., Vogt, R., Bodwin, G. T., Eichten, E., Frawley, A. D., Meyer, A. B., Mitchell, R. E., Papadimitriou, V., Petreczky, P., Petrov, A. A., Robbe, P., Vairo, A., Andronic, A., Arnaldi, R., Artoisenet, P., Bali, G., Bertolin, A., Bettoni, D., Brodzicka, J., Bruno, G. E., Caldwell, A., Catmore, J., Chang, C.-H., Chao, K.-T., Chudakov, E., Cortese, P., Crochet, P., Drutskoy, A., Ellwanger, U., Faccioli, P., Gabareen Mokhtar, A., Garcia i Tormo, X., Hanhart, C., Harris, F. A., Kaplan, D. M., Klein, S. R., Kowalski, H., Lansberg, J.-P., Levichev, E., Lombardo, V., Lourenço, C., Maltoni, F., Mocsy, A., Mussa, R., Navarra, F. S., Negrini, M., Nielsen, M., Olsen, S. L., Pakhlov, P., Pakhlova, G., Peters, K., Polosa, A. D., Qian, W., Qiu, J.-W., Rong, G., Sanchis-Lozano, M. A., Scomparin, E., Senger, P., Simon, F., Stracka, S., Sumino, Y., Voloshin, M., Weiss, C., Wöhri, H. K., Yuan, C.-Z.

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TGF-α and IL-6 plasma levels selectively identify CML patients who fail to achieve an early molecular response or progress in the first year of therapy von Nievergall, E, Reynolds, J, Kok, C H, Watkins, D B, Biondo, M, Busfield, S J, Vairo, G, Fuller, K, Erber, W N, Sadras, T, Grose, R, Yeung, D T, Lopez, A F, Hiwase, D K, Hughes, T P, White, D L

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Neuromuscular and biomechanical landing performance subsequent to ipsilateral semitendinosus and gracilis autograft anterior cruciate ligament reconstruction von Vairo, Giampietro L., Myers, Joseph B., Sell, Timothy C., Fu, Freddie H., Harner, Christopher D., Lephart, Scott M.

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