ABEM consensus for the brazilian medical schools’ communication curriculum von Grosseman, Suely, Hokama, Newton Key, Cruvinel, Agnes de Fátima Pereira, Franzoi, Ana Cristina, Moura, Eliane Perlatto, Muraguchi, Evelin Massae Ogatta, Novaes, Fernanda Patrícia Soares Souto, Raimondi, Gustavo Antonio, Moura, Josemar de Almeida, Torreão, Lara de Araújo, Pereira, Maria Amélia Dias, Philippi, Miriam May, Oliveira, Mônica da Cunha, Alves, Rosana

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Percepção de lésbicas, gays e bissexuais em relação aos serviços de saúde - doi: 10512/ucs.v11i2.1837 von Carvalho, Laudenize Souza, Philippi, Miriam May

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Consenso Abem para o ensino de comunicação nas escolas médicas brasileiras von Grosseman, Suely, Hokama, Newton Key, Cruvinel, Agnes de Fátima Pereira, Franzoi, Ana Cristina, Moura, Eliane Perlatto, Muraguchi, Evelin Massae Ogatta, Novaes, Fernanda Patrícia Soares Souto, Raimondi, Gustavo Antonio, Moura, Josemar de Almeida, Torreão, Lara de Araújo, Pereira, Maria Amélia Dias, Philippi, Miriam May, Oliveira, Mônica da Cunha, Alves, Rosana

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ABEM consensus for the brazilian medical schools’ communication curriculum von Grosseman, Suely, Hokama, Newton Key, Cruvinel, Agnes de Fátima Pereira, Franzoi, Ana Cristina, Moura, Eliane Perlatto, Muraguchi, Evelin Massae Ogatta, Novaes, Fernanda Patrícia Soares Souto, Raimondi, Gustavo Antonio, Moura, Josemar de Almeida, Torreão, Lara de Araújo, Pereira, Maria Amélia Dias, Philippi, Miriam May, Oliveira, Mônica da Cunha, Alves, Rosana

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Methylphosphonate-driven methane formation and its link to primary production in the oligotrophic North Atlantic von von Arx, Jan N., Kidane, Abiel T., Philippi, Miriam, Mohr, Wiebke, Lavik, Gaute, Schorn, Sina, Kuypers, Marcel M. M., Milucka, Jana

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A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly von Abdulkarim, Baroj, Nicolino, Marc, Igoillo-Esteve, Mariana, Daures, Mathilde, Romero, Sophie, Philippi, Anne, Senée, Valérie, Lopes, Miguel, Cunha, Daniel A, Harding, Heather P, Derbois, Céline, Bendelac, Nathalie, Hattersley, Andrew T, Eizirik, Décio L, Ron, David, Cnop, Miriam, Julier, Cécile

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Purple sulfur bacteria fix N2 via molybdenum-nitrogenase in a low molybdenum Proterozoic ocean analogue von Philippi, Miriam, Kitzinger, Katharina, Berg, Jasmine S., Tschitschko, Bernhard, Kidane, Abiel T., Littmann, Sten, Marchant, Hannah K., Storelli, Nicola, Winkel, Lenny H. E., Schubert, Carsten J., Mohr, Wiebke, Kuypers, Marcel M. M.

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Rhizobia–diatom symbiosis fixes missing nitrogen in the ocean von Tschitschko, Bernhard, Esti, Mertcan, Philippi, Miriam, Kidane, Abiel T., Littmann, Sten, Kitzinger, Katharina, Speth, Daan R., Li, Shengjie, Kraberg, Alexandra, Tienken, Daniela, Marchant, Hannah K., Kartal, Boran, Milucka, Jana, Mohr, Wiebke, Kuypers, Marcel M. M.

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DNAJC3 deficiency induces β-cell mitochondrial apoptosis and causes syndromic young-onset diabetes von Lytrivi, Maria, Senée, Valérie, Salpea, Paraskevi, Fantuzzi, Federica, Philippi, Anne, Abdulkarim, Baroj, Sawatani, Toshiaki, Marín-Cañas, Sandra, Pachera, Nathalie, Degavre, Anne, Singh, Pratibha, Derbois, Céline, Lechner, Doris, Ladrière, Laurence, Igoillo-Esteve, Mariana, Cosentino, Cristina, Marselli, Lorella, Deleuze, Jean-François, Marchetti, Piero, Eizirik, Décio L, Nicolino, Marc, Chaussenot, Annabelle, Julier, Cécile, Cnop, Miriam

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Dark aerobic sulfide oxidation by anoxygenic phototrophs in anoxic waters von Berg, Jasmine S., Pjevac, Petra, Sommer, Tobias, Buckner, Caroline R.T., Philippi, Miriam, Hach, Philipp F., Liebeke, Manuel, Holtappels, Moritz, Danza, Francesco, Tonolla, Mauro, Sengupta, Anupam, Schubert, Carsten J., Milucka, Jana, Kuypers, Marcel M.M.

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Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders von Travaglini, Lorena, Brancati, Francesco, Silhavy, Jennifer, Iannicelli, Miriam, Nickerson, Elizabeth, Elkhartoufi, Nadia, Scott, Eric, Spencer, Emily, Gabriel, Stacey, Thomas, Sophie, Ben-Zeev, Bruria, Bertini, Enrico, Boltshauser, Eugen, Chaouch, Malika, Cilio, Maria Roberta, de Jong, Mirjam M, Kayserili, Hulya, Ogur, Gonul, Poretti, Andrea, Signorini, Sabrina, Uziel, Graziella, Zaki, Maha S, Johnson, Colin, Attié-Bitach, Tania, Gleeson, Joseph G, Valente, Enza Maria

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Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies von Iannicelli, Miriam, Brancati, Francesco, Mougou-Zerelli, Soumaya, Mazzotta, Annalisa, Thomas, Sophie, Elkhartoufi, Nadia, Travaglini, Lorena, Gomes, Céline, Luigi Ardissino, Gian, Bertini, Enrico, Boltshauser, Eugen, Castorina, Pierangela, D'Arrigo, Stefano, Fischetto, Rita, Leroy, Brigitte, Loget, Philippe, Bonnière, Maryse, Starck, Lena, Tantau, Julia, Gentilin, Barbara, Majore, Silvia, Swistun, Dominika, Flori, Elizabeth, Lalatta, Faustina, Pantaleoni, Chiara, Penzien, Johannes, Grammatico, Paola, Dallapiccola, Bruno, Gleeson, Joseph G, Attie-Bitach, Tania, Valente, Enza Maria

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MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement von Brancati, Francesco, Iannicelli, Miriam, Travaglini, Lorena, Mazzotta, Annalisa, Bertini, Enrico, Boltshauser, Eugen, D'Arrigo, Stefano, Emma, Francesco, Fazzi, Elisa, Gallizzi, Romina, Gentile, Mattia, Loncarevic, Damir, Mejaski-Bosnjak, Vlatka, Pantaleoni, Chiara, Rigoli, Luciana, Salpietro, Carmelo D, Signorini, Sabrina, Stringini, Gilda Rita, Verloes, Alain, Zabloka, Dominika, Dallapiccola, Bruno, Gleeson, Joseph G, Valente, Enza Maria

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EUREC.sup.4A von Ament, Felix, Fairall, Christopher, Acquistapace, Claudia, Bodenschatz, Eberhard, Caesar, Kathy-Ann, Delanoë, Julien, Denby, Leif, Ewald, Florian, Fildier, Benjamin, Forde, Marvin, George, Geet, Hagen, Martin, Hausold, Andrea, Heywood, Karen J, Jacob, Marek, Jansen, Friedhelm, Kölling, Tobias, Lothon, Marie, Mohr, Wiebke, Pincus, Robert, Pöhlker, Mira, Reverdin, Gilles, Schulz, Hauke, Siebesma, A. Pier, Stephan, Claudia Christine, Vial, Jessica, Asmath, Hamish, Barrau, Sébastien, Batier, Frédéric, Behrendt, Andreas, Beucher, Florent, Branellec, Pierre, Brilouet, Pierre-Etienne, Brügmann, Björn, Canonici, Jean-Christophe, Chilinski, Michal T, Choularton, Thomas, Chuang, Patrick, Cuypers, Yannis, Damerell, Gillian M, Deneke, Hartwig, Donner, Sebastian, Etienne, Jean-Claude, Faure, Ghislain, Feingold, Graham, Ferrero, Luca, Forster, Linda, Geyskens, Nicolas, Giez, Andreas, Gourbeyre, Christophe, de Graaf, Dörte, Harris, George, Helfer, Kevin C, Ibanez-Landeta, Antonio, Iyer, Suneil, Julien, Fabrice, Kalesse, Heike, Kellman, Alexander, Körner, Mareike, Kretzschmar, Jan, Krüger, Ovid, Kumala, Wojciech, Labaste, Matthieu, Lange, Diego, Leandro, Mason, Li, Qiang, Los, Sebastian, Manta, Gaston, Maury, Nicolas, Mayer, Bernhard, Mayers-Als, Margarette, Mech, Mario, Meroni, Agostino Niyonkuru, Minikin, Andreas, Muller, Caroline, Noisel, Christophe, Parker, Douglas J, Person, Renaud, Plueddemann, Albert, Pörtge, Veronika, Pologne, Lawrence, Reus, Klaus, Rochetin, Nicolas, Rollo, Callum, Sadoulet, Pauline, Saffin, Leo, Sandiford, Sanola, Schäfer, Michael, Schröder, Marcel, Senff, Christoph J, Serikov, Ilya, Shohan, Samkeyat, Szkólka, Wojciech, Totems, Julien, Ubele, Alma Anna, Wagner, Thomas, Wirth, Martin, Wolf, Kevin, Wright, Ethan, Wulfmeyer, Volker

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Expanding CEP290 mutational spectrum in ciliopathies von Travaglini, Lorena, Brancati, Francesco, Attie-Bitach, Tania, Audollent, Sophie, Bertini, Enrico, Kaplan, Josseline, Perrault, Isabelle, Iannicelli, Miriam, Mancuso, Brunella, Rigoli, Luciana, Rozet, Jean-Michel, Swistun, Dominika, Tolentino, Jerlyn, Dallapiccola, Bruno, Gleeson, Joseph G., Valente, Enza Maria

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DNAJC3 deficiency induces mitochondrial β-cell apoptosis and causes young-onset diabetes and neurodegeneration von Lytrivi, Maria, Senée, Valérie, Salpea, Paraskevi, Philippi, Anne, Baroj Abdulkarim, Degavre, Anne, Singh, Pratibha, Derbois, Céline, Lechner, Doris, Igoillo-Esteve, Mariana, Cosentino, Cristina, Marselli, Lorella, Jean-François Deleuze, Marchetti, Piero, Eizirik, Decio L., Nicolino, Marc, Chaussenot, Annabelle, Julier, Cécile, Cnop, Miriam

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A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly von Abdulkarim, Baroj, Nicolino, Marc, Igoillo-Esteve, Mariana, Daures, Mathilde, Romero, Sophie, Philippi, Anne, Senée, Valérie, Lopes, Miguel, Cunha, Daniel A, Harding, Heather, Derbois, Céline, Bendelac, Nathalie, Hattersley, Andrew T, Eizirik, Décio L, Ron, David, Cnop, Miriam, Julier, Cécile

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A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly von Abdulkarim, Baroj, Nicolino, Marc, Igoillo-Esteve, Mariana, Daures, Mathilde, Romero, Sophie, Philippi, Anne, Senée, Valérie, Lopes, Miguel, Cunha, Daniel A, Harding, Heather P, Derbois, Céline, Bendelac, Nathalie, Hattersley, Andrew T, Eizirik, Décio L, Ron, David, Cnop, Miriam, Julier, Cécile

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