Long-term outcomes of transplant kidneys donated after circulatory death von Müller, Amélie K, Breuer, Eva, Hübel, Kerstin, Lehmann, Kuno, Cippà, Pietro, Schachtner, Thomas, Oberkofler, Christian, Müller, Thomas, Weber, Markus, Dutkowski, Philipp, Clavien, Pierre-Alain, de Rougemont, Olivier

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Long-term Outcomes of Transplant Kidneys Donated after Circulatory Death von Müller, Amélie K, Breuer, Eva, Hübel, Kerstin, Lehmann, Kuno, Cippà, Pietro, Schachtner, Thomas, Oberkofler, Christian, Müller, Thomas, Weber, Markus, Dutkowski, Philipp, Clavien, Pierre-Alain, de Rougemont, Olivier

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Targeted Temperature Management for Cardiac Arrest with Nonshockable Rhythm von Lascarrou, Jean-Baptiste, Merdji, Hamid, Le Gouge, Amélie, Colin, Gwenhael, Grillet, Guillaume, Girardie, Patrick, Coupez, Elisabeth, Dequin, Pierre-François, Cariou, Alain, Boulain, Thierry, Brule, Noelle, Frat, Jean-Pierre, Asfar, Pierre, Pichon, Nicolas, Landais, Mickael, Plantefeve, Gaëtan, Quenot, Jean-Pierre, Chakarian, Jean-Charles, Sirodot, Michel, Legriel, Stéphane, Letheulle, Julien, Thevenin, Didier, Desachy, Arnaud, Delahaye, Arnaud, Botoc, Vlad, Vimeux, Sylvie, Martino, Frederic, Giraudeau, Bruno, Reignier, Jean

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Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia von Husain, Ralf A., Grimmel, Mona, Wagner, Matias, Hennings, J. Christopher, Marx, Christian, Feichtinger, René G., Saadi, Abdelkrim, Rostásy, Kevin, Radelfahr, Florentine, Bevot, Andrea, Döbler-Neumann, Marion, Hartmann, Hans, Colleaux, Laurence, Cordts, Isabell, Kobeleva, Xenia, Darvish, Hossein, Bakhtiari, Somayeh, Kruer, Michael C., Besse, Arnaud, Ng, Andy Cheuk-Him, Chiang, Diana, Bolduc, Francois, Tafakhori, Abbas, Mane, Shrikant, Ghasemi Firouzabadi, Saghar, Huebner, Antje K., Buchert, Rebecca, Beck-Woedl, Stefanie, Müller, Amelie J., Laugwitz, Lucia, Nägele, Thomas, Wang, Zhao-Qi, Strom, Tim M., Sturm, Marc, Meitinger, Thomas, Klockgether, Thomas, Riess, Olaf, Klopstock, Thomas, Brandl, Ulrich, Hübner, Christian A., Deschauer, Marcus, Mayr, Johannes A., Bonnen, Penelope E., Krägeloh-Mann, Ingeborg, Wortmann, Saskia B., Haack, Tobias B.

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Effect of Noninvasive Ventilation vs Oxygen Therapy on Mortality Among Immunocompromised Patients With Acute Respiratory Failure: A Randomized Clinical Trial von Lemiale, Virginie, Mokart, Djamel, Resche-Rigon, Matthieu, Pène, Frédéric, Mayaux, Julien, Faucher, Etienne, Nyunga, Martine, Girault, Christophe, Perez, Pierre, Guitton, Christophe, Ekpe, Kenneth, Kouatchet, Achille, Théodose, Igor, Benoit, Dominique, Canet, Emmanuel, Barbier, François, Rabbat, Antoine, Bruneel, Fabrice, Vincent, Francois, Klouche, Kada, Loay, Kontar, Mariotte, Eric, Bouadma, Lila, Moreau, Anne-Sophie, Seguin, Amélie, Meert, Anne-Pascale, Reignier, Jean, Papazian, Laurent, Mehzari, Ilham, Cohen, Yves, Schenck, Maleka, Hamidfar, Rebecca, Darmon, Michael, Demoule, Alexandre, Chevret, Sylvie, Azoulay, Elie

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Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome von Warejko, Jillian K, Tan, Weizhen, Daga, Ankana, Schapiro, David, Lawson, Jennifer A, Shril, Shirlee, Lovric, Svjetlana, Ashraf, Shazia, Rao, Jia, Hermle, Tobias, Jobst-Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J, Schneider, Ronen, Gee, Heon Yung, Schmidt, J Magdalena, Vivante, Asaf, van der Ven, Amelie T, Ityel, Hadas, Chen, Jing, Sadowski, Carolin E, Kohl, Stefan, Pabst, Werner L, Nakayama, Makiko, Somers, Michael J G, Rodig, Nancy M, Daouk, Ghaleb, Baum, Michelle, Stein, Deborah R, Ferguson, Michael A, Traum, Avram Z, Soliman, Neveen A, Kari, Jameela A, El Desoky, Sherif, Fathy, Hanan, Zenker, Martin, Bakkaloglu, Sevcan A, Müller, Dominik, Noyan, Aytul, Ozaltin, Fatih, Cadnapaphornchai, Melissa A, Hashmi, Seema, Hopcian, Jeffrey, Kopp, Jeffrey B, Benador, Nadine, Bockenhauer, Detlef, Bogdanovic, Radovan, Stajić, Nataša, Chernin, Gil, Ettenger, Robert, Fehrenbach, Henry, Kemper, Markus, Munarriz, Reyner Loza, Podracka, Ludmila, Büscher, Rainer, Serdaroglu, Erkin, Tasic, Velibor, Mane, Shrikant, Lifton, Richard P, Braun, Daniela A, Hildebrandt, Friedhelm

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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation von Balak, Chris, Benard, Marianne, Schaefer, Elise, Iqbal, Sumaiya, Ramsey, Keri, Ernoult-Lange, Michèle, Mattioli, Francesca, Llaci, Lorida, Geoffroy, Véronique, Courel, Maité, Naymik, Marcus, Bachman, Kristine K., Pfundt, Rolph, Rump, Patrick, ter Beest, Johanna, Wentzensen, Ingrid M., Monaghan, Kristin G., McWalter, Kirsty, Richholt, Ryan, Le Béchec, Antony, Jepsen, Wayne, De Both, Matt, Belnap, Newell, Boland, Anne, Piras, Ignazio S., Deleuze, Jean-François, Szelinger, Szabolcs, Dollfus, Hélène, Chelly, Jamel, Muller, Jean, Campbell, Arthur, Lal, Dennis, Rangasamy, Sampathkumar, Mandel, Jean-Louis, Narayanan, Vinodh, Huentelman, Matt, Weil, Dominique, Piton, Amélie

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Bias correction of OMI HCHO columns based on FTIR and aircraft measurements and impact on top-down emission estimates von Müller, Jean-François, Stavrakou, Trissevgeni, Oomen, Glenn-Michael, Opacka, Beata, De Smedt, Isabelle, Guenther, Alex, Vigouroux, Corinne, Langerock, Bavo, Aquino, Carlos Augusto Bauer, Grutter, Michel, Hannigan, James, Hase, Frank, Kivi, Rigel, Lutsch, Erik, Mahieu, Emmanuel, Makarova, Maria, Metzger, Jean-Marc, Morino, Isamu, Murata, Isao, Nagahama, Tomoo, Notholt, Justus, Ortega, Ivan, Palm, Mathias, Röhling, Amelie, Stremme, Wolfgang, Strong, Kimberly, Sussmann, Ralf, Té, Yao, Fried, Alan

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Randomized Trial of Fetal Surgery for Severe Left Diaphragmatic Hernia von Deprest, Jan A, Nicolaides, Kypros H, Benachi, Alexandra, Gratacos, Eduard, Ryan, Greg, Persico, Nicola, Sago, Haruhiko, Johnson, Anthony, Wielgoś, Mirosław, Berg, Christoph, Van Calster, Ben, Russo, Francesca M

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Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype von Garber, Alison, Weingarten, Lisa S., Abreu, Nicolas J., Elloumi, Houda Zghal, Haack, Tobias, Hildebrant, Clara, Martínez‐Gil, Núria, Mathews, Jennifer, Müller, Amelie Johanna, Valenzuela Palafoll, Irene, Steigerwald, Connolly, Chung, Wendy K.

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The Arecibo Legacy Fast ALFA Survey. I. Science Goals, Survey Design, and Strategy von Giovanelli, Riccardo, Haynes, Martha P, Kent, Brian R, Perillat, Philip, Saintonge, Amelie, Brosch, Noah, Catinella, Barbara, Hoffman, G. Lyle, Stierwalt, Sabrina, Spekkens, Kristine, Lerner, Mikael S, Masters, Karen L, Momjian, Emmanuel, Rosenberg, Jessica L, Springob, Christopher M, Boselli, Alessandro, Charmandaris, Vassilis, Darling, Jeremy K, Davies, Jonathan, Lambas, Diego Garcia, Gavazzi, Giuseppe, Giovanardi, Carlo, Hardy, Eduardo, Hunt, Leslie K, Iovino, Angela, Karachentsev, Igor D, Karachentseva, Valentina E, Koopmann, Rebecca A, Marinoni, Christian, Minchin, Robert, Muller, Erik, Putman, Mary, Pantoja, Carmen, Salzer, John J, Scodeggio, Marco, Skillman, Evan, Solanes, Jose M, Valotto, Carlos, van Driel, Wim, van Zee, Liese

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Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities von Cali, Elisa, Suri, Mohnish, Scala, Marcello, Ferla, Matteo P., Alavi, Shahryar, Faqeih, Eissa Ali, Bijlsma, Emilia K., Wigby, Kristen M., Baralle, Diana, Mehrjardi, Mohammad Y.V., Schwab, Jennifer, Platzer, Konrad, Steindl, Katharina, Hashem, Mais, Jones, Marilyn, Niyazov, Dmitriy M., Jacober, Jennifer, Littlejohn, Rebecca Okashah, Weis, Denisa, Zadeh, Neda, Rodan, Lance, Goldenberg, Alice, Lecoquierre, François, Dutra-Clarke, Marina, Horvath, Gabriella, Young, Dana, Orenstein, Naama, Bawazeer, Shahad, Vulto-van Silfhout, Anneke T., Herenger, Yvan, Dehghani, Mohammadreza, Seyedhassani, Seyed Mohammad, Bahreini, Amir, Nasab, Mahya E., Ercan-Sencicek, A. Gulhan, Firoozfar, Zahra, Movahedinia, Mojtaba, Efthymiou, Stephanie, Striano, Pasquale, Karimiani, Ehsan Ghayoor, Salpietro, Vincenzo, Taylor, Jenny C., Redman, Melody, Stegmann, Alexander P.A., Laner, Andreas, Abdel-Salam, Ghada, Li, Megan, Bengala, Mario, Müller, Amelie Johanna, Digilio, Maria C., Rauch, Anita, Gunel, Murat, Titheradge, Hannah, Schweitzer, Daniela N., Kraus, Alison, Valenzuela, Irene, McLean, Scott D., Phornphutkul, Chanika, Salih, Mustafa, Begtrup, Amber, Schnur, Rhonda E., Torti, Erin, Haack, Tobias B., Prada, Carlos E., Alkuraya, Fowzan S., Houlden, Henry, Maroofian, Reza

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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation von Balak, Chris, Bénard, Marianne, Schaefer, Elise, Iqbal, Sumaiya, Ramsey, Keri, Ernoult-Lange, Michèle, Mattioli, Francesca, Llaci, Lorida, Geoffroy, Véronique, Courel, Maité, Naymik, Marcus, Bachman, Kristine K., Pfundt, Rolph, Rump, Patrick, Beest, Johanna Ter, Wentzensen, Ingrid M., Monaghan, Kristin G., Mcwalter, Kirsty, Richholt, Ryan, Béchec, Antony Le, Jepsen, Wayne, Both, Matt De, Belnap, Newell, Boland, Anne, Piras, Ignazio S., Deleuze, Jean-François, Szelinger, Szabolcs, Dollfus, Hélène, Chelly, Jamel, Muller, Jean, Campbell, Arthur, Lal, Dennis, Rangasamy, Sampathkumar, Mandel, Jean-Louis, Narayanan, Vinodh, Huentelman, Matt, Weil, Dominique, Piton, Amélie

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Rotational complexity increases cropping system output under poorer growing conditions von Bybee-Finley, K. Ann, Muller, Katherine, White, Kathryn E., Cavigelli, Michel A., Han, Eunjin, Schomberg, Harry H., Snapp, Sieglinde, Viens, Frederi, Correndo, Adrian A., Deiss, Leonardo, Fonteyne, Simon, Garcia y Garcia, Axel, Gaudin, Amélie C.M., Hooker, David C., Janovicek, Ken, Jin, Virginia, Johnson, Gregg, Karsten, Heather, Liebman, Matt, McDaniel, Marshall D., Sanford, Gregg, Schmer, Marty R., Strock, Jeffrey, Sykes, Virginia R., Verhulst, Nele, Wilke, Brook, Bowles, Timothy M.

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DLG4-related synaptopathy: a new rare brain disorder von Rodríguez-Palmero, Agustí, Boerrigter, Melissa Maria, Gómez-Andrés, David, Aldinger, Kimberly A., Marcos-Alcalde, Íñigo, Popp, Bernt, Everman, David B., Lovgren, Alysia Kern, Arpin, Stephanie, Bahrambeigi, Vahid, Beunders, Gea, Bisgaard, Anne-Marie, Bjerregaard, V. A., Bruel, Ange-Line, Challman, Thomas D., Cogné, Benjamin, Coubes, Christine, de Man, Stella A., Denommé-Pichon, Anne-Sophie, Dye, Thomas J., Elmslie, Frances, Feuk, Lars, García-Miñaúr, Sixto, Gertler, Tracy, Giorgio, Elisa, Gruchy, Nicolas, Haack, Tobias B., Haldeman-Englert, Chad R., Haukanes, Bjørn Ivar, Hoyer, Juliane, Hurst, Anna C. E., Isidor, Bertrand, Soller, Maria Johansson, Kushary, Sulagna, Kvarnung, Malin, Landau, Yuval E., Leppig, Kathleen A., Lindstrand, Anna, Kleinendorst, Lotte, MacKenzie, Alex, Mandrile, Giorgia, Mendelsohn, Bryce A., Moghadasi, Setareh, Morton, Jenny E., Moutton, Sebastien, Müller, Amelie J., O’Leary, Melanie, Pacio-Míguez, Marta, Palomares-Bralo, Maria, Parikh, Sumit, Pfundt, Rolph, Pode-Shakked, Ben, Rauch, Anita, Repnikova, Elena, Revah-Politi, Anya, Ross, Meredith J., Ruivenkamp, Claudia A. L., Sarrazin, Elisabeth, Savatt, Juliann M., Schlüter, Agatha, Schönewolf-Greulich, Bitten, Shad, Zohra, Shaw-Smith, Charles, Shieh, Joseph T., Shohat, Motti, Spranger, Stephanie, Thiese, Heidi, Mau-Them, Frederic Tran, van Bon, Bregje, van de Burgt, Ineke, van de Laar, Ingrid M. B. H., van Drie, Esmée, van Haelst, Mieke M., van Ravenswaaij-Arts, Conny M., Verdura, Edgard, Vitobello, Antonio, Waldmüller, Stephan, Whiting, Sharon, Zweier, Christiane, Prada, Carlos E., de Vries, Bert B. A., Dobyns, William B., Reiter, Simone F., Gómez-Puertas, Paulino, Pujol, Aurora, Tümer, Zeynep

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A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement von Prasad, Megana K, Geoffroy, Véronique, Vicaire, Serge, Jost, Bernard, Dumas, Michael, Le Gras, Stéphanie, Switala, Marzena, Gasse, Barbara, Laugel-Haushalter, Virginie, Paschaki, Marie, Leheup, Bruno, Droz, Dominique, Dalstein, Amelie, Loing, Adeline, Grollemund, Bruno, Muller-Bolla, Michèle, Lopez-Cazaux, Séréna, Minoux, Maryline, Jung, Sophie, Obry, Frédéric, Vogt, Vincent, Davideau, Jean-Luc, Davit-Beal, Tiphaine, Kaiser, Anne-Sophie, Moog, Ute, Richard, Béatrice, Morrier, Jean-Jacques, Duprez, Jean-Pierre, Odent, Sylvie, Bailleul-Forestier, Isabelle, Rousset, Monique Marie, Merametdijan, Laure, Toutain, Annick, Joseph, Clara, Giuliano, Fabienne, Dahlet, Jean-Christophe, Courval, Aymeric, El Alloussi, Mustapha, Laouina, Samir, Soskin, Sylvie, Guffon, Nathalie, Dieux, Anne, Doray, Bérénice, Feierabend, Stephanie, Ginglinger, Emmanuelle, Fournier, Benjamin, de la Dure Molla, Muriel, Alembik, Yves, Tardieu, Corinne, Clauss, François, Berdal, Ariane, Stoetzel, Corinne, Manière, Marie Cécile, Dollfus, Hélène, Bloch-Zupan, Agnès

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Association between Pseudomonas aeruginosa positive water samples and healthcare-associated cases. Nine-year study at one university hospital von Lefebvre, Annick, MD, Bertrand, Xavier, MD, PhD, Quantin, Catherine, MD, PhD, Vanhems, Philippe, MD, PhD, Lucet, Jean-Christophe, MD, PhD, Nuemi, Gilles, MD, PhD, Astruc, Karine, MD, Chavanet, Pascal, MD, PhD, Aho-Glélé, Ludwig S., MD

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The Arecibo Legacy Fast ALFA Survey. II. Results of Precursor Observations von Giovanelli, Riccardo, Haynes, Martha P, Kent, Brian R, Perillat, Philip, Catinella, Barbara, Hoffman, G. Lyle, Momjian, Emmanuel, Rosenberg, Jessica L, Saintonge, Amelie, Spekkens, Kristine, Stierwalt, Sabrina, Brosch, Noah, Masters, Karen L, Springob, Christopher M, Karachentsev, Igor D, Karachentseva, Valentina E, Koopmann, Rebecca A, Muller, Erik, van Driel, Wim, van Zee, Liese

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Development and application of first Sc-44-labeled Affibody molecule von Honarvar, H., Muller, C., van der Meulen, N., Cohrs, S., Westerlund, Kristina, Eriksson Karlström, Amelie, Schibli, R., Tolmachev, V.

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Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities von Cali, Elisa, Suri, Mohnish, Scala, Marcello, Ferla, Matteo P, Alavi, Shahryar, Faqeih, Eissa Ali, Bijlsma, Emilia K, Wigby, Kristen M, Baralle, Diana, Mehrjardi, Mohammad YV, Schwab, Jennifer, Platzer, Konrad, Steindl, Katharina, Hashem, Mais, Jones, Marilyn, Niyazov, Dmitriy M, Jacober, Jennifer, Littlejohn, Rebecca Okashah, Weis, Denisa, Zadeh, Neda, Rodan, Lance, Goldenberg, Alice, Lecoquierre, François, Dutra-Clarke, Marina, Horvath, Gabriella, Young, Dana, Orenstein, Naama, Bawazeer, Shahad, Vulto-van Silfhout, Anneke T, Herenger, Yvan, Dehghani, Mohammadreza, Seyedhassani, Seyed Mohammad, Bahreini, Amir, Nasab, Mahya E, Ercan-Sencicek, A Gulhan, Firoozfar, Zahra, Movahedinia, Mojtaba, Efthymiou, Stephanie, Striano, Pasquale, Karimiani, Ehsan Ghayoor, Salpietro, Vincenzo, Taylor, Jenny C, Redman, Melody, Stegmann, Alexander PA, Laner, Andreas, Abdel-Salam, Ghada, Li, Megan, Bengala, Mario, Müller, Amelie Johanna, Digilio, Maria C, Rauch, Anita, Gunel, Murat, Titheradge, Hannah, Schweitzer, Daniela N, Kraus, Alison, Valenzuela, Irene, McLean, Scott D, Phornphutkul, Chanika, Salih, Mustafa, Begtrup, Amber, Schnur, Rhonda E, Torti, Erin, Haack, Tobias B, Prada, Carlos E, Alkuraya, Fowzan S, Houlden, Henry, Maroofian, Reza

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