Acellular human amniotic fluid protects the ischemic-reperfused rat myocardium von Lee, Young Sook, Javan, Hadi, Reems, Jo-Anna, Li, Ling, Lusty, Jessica, Schaaf, Christine I, Pierce, Jan, Phillips, John D, Selzman, Craig H

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Executive Summary: Official American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America Clinical Practice Guidelines: Treatment of D... von Nahid, Payam, Dorman, Susan E, Alipanah, Narges, Barry, Pennan M, Brozek, Jan L, Cattamanchi, Adithya, Chaisson, Lelia H, Chaisson, Richard E, Daley, Charles L, Grzemska, Malgosia, Higashi, Julie M, Ho, Christine S, Hopewell, Philip C, Keshavjee, Salmaan A, Lienhardt, Christian, Menzies, Richard, Merrifield, Cynthia, Narita, Masahiro, O'Brien, Rick, Peloquin, Charles A, Raftery, Ann, Saukkonen, Jussi, Schaaf, H Simon, Sotgiu, Giovanni, Starke, Jeffrey R, Migliori, Giovanni Battista, Vernon, Andrew

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Official American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America Clinical Practice Guidelines: Treatment of Drug-Susceptible Tub... von Nahid, Payam, Dorman, Susan E, Alipanah, Narges, Barry, Pennan M, Brozek, Jan L, Cattamanchi, Adithya, Chaisson, Lelia H, Chaisson, Richard E, Daley, Charles L, Grzemska, Malgosia, Higashi, Julie M, Ho, Christine S, Hopewell, Philip C, Keshavjee, Salmaan A, Lienhardt, Christian, Menzies, Richard, Merrifield, Cynthia, Narita, Masahiro, O'Brien, Rick, Peloquin, Charles A, Raftery, Ann, Saukkonen, Jussi, Schaaf, H Simon, Sotgiu, Giovanni, Starke, Jeffrey R, Migliori, Giovanni Battista, Vernon, Andrew

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Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations von Wang, Xia, Charng, Wu-Lin, Chen, Chun-An, Rosenfeld, Jill A, Al Shamsi, Aisha, Al-Gazali, Lihadh, McGuire, Marianne, Mew, Nicholas Ah, Arnold, Georgianne L, Qu, Chunjing, Ding, Yan, Muzny, Donna M, Gibbs, Richard A, Eng, Christine M, Walkiewicz, Magdalena, Xia, Fan, Plon, Sharon E, Lupski, James R, Schaaf, Christian P, Yang, Yaping

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GestaltMatcher facilitates rare disease matching using facial phenotype descriptors von Hsieh, Tzung-Chien, Bar-Haim, Aviram, Moosa, Shahida, Ehmke, Nadja, Gripp, Karen W., Pantel, Jean Tori, Danyel, Magdalena, Mensah, Martin Atta, Horn, Denise, Rosnev, Stanislav, Fleischer, Nicole, Bonini, Guilherme, Hustinx, Alexander, Schmid, Alexander, Knaus, Alexej, Javanmardi, Behnam, Klinkhammer, Hannah, Lesmann, Hellen, Sivalingam, Sugirthan, Kamphans, Tom, Meiswinkel, Wolfgang, Ebstein, Frédéric, Krüger, Elke, Küry, Sébastien, Bézieau, Stéphane, Schmidt, Axel, Peters, Sophia, Engels, Hartmut, Mangold, Elisabeth, Kreiß, Martina, Cremer, Kirsten, Perne, Claudia, Betz, Regina C., Bender, Tim, Grundmann-Hauser, Kathrin, Haack, Tobias B., Wagner, Matias, Brunet, Theresa, Bentzen, Heidi Beate, Averdunk, Luisa, Coetzer, Kimberly Christine, Lyon, Gholson J., Spielmann, Malte, Schaaf, Christian P., Mundlos, Stefan, Nöthen, Markus M., Krawitz, Peter M.

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Lessons learned from additional research analyses of unsolved clinical exome cases von Eldomery, Mohammad K, Coban-Akdemir, Zeynep, Harel, Tamar, Rosenfeld, Jill A, Gambin, Tomasz, Stray-Pedersen, Asbjørg, Küry, Sébastien, Mercier, Sandra, Lessel, Davor, Denecke, Jonas, Wiszniewski, Wojciech, Penney, Samantha, Liu, Pengfei, Bi, Weimin, Lalani, Seema R, Schaaf, Christian P, Wangler, Michael F, Bacino, Carlos A, Lewis, Richard Alan, Potocki, Lorraine, Graham, Brett H, Belmont, John W, Scaglia, Fernando, Orange, Jordan S, Jhangiani, Shalini N, Chiang, Theodore, Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M, Xia, Fan, Beaudet, Arthur L, Boerwinkle, Eric, Eng, Christine M, Plon, Sharon E, Sutton, V Reid, Gibbs, Richard A, Posey, Jennifer E, Yang, Yaping, Lupski, James R

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In-depth mutational analyses of colorectal neuroendocrine carcinomas with adenoma or adenocarcinoma components von Woischke, Christine, Schaaf, Christian W, Yang, Hui-Min, Vieth, Michael, Veits, Lothar, Geddert, Helene, Märkl, Bruno, Stömmer, Peter, Schaeffer, David F, Frölich, Matthias, Blum, Helmut, Vosberg, Sebastian, Greif, Philipp A, Jung, Andreas, Kirchner, Thomas, Horst, David

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Clinical and molecular characterization of de novo loss of function variants in HNRNPU von Leduc, Magalie S., Chao, Hsiao‐Tuan, Qu, Chunjing, Walkiewicz, Magdalena, Xiao, Rui, Magoulas, Pilar, Pan, Shujuan, Beuten, Joke, He, Weimin, Bernstein, Jonathan A., Schaaf, Christian P., Scaglia, Fernando, Eng, Christine M., Yang, Yaping

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Producing food from CO2 using microorganisms: Lots to do, little to lose von Minden, Steven, Grünberger, Alexander, van der Schaaf, Ulrike, Neumann, Anke, Rösch, Christine, Sauer, Jörg, Kaster, Anne-Kristin

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Reanalysis of Clinical Exome Sequencing Data von Liu, Pengfei, Meng, Linyan, Normand, Elizabeth A, Xia, Fan, Song, Xiaofei, Ghazi, Andrew, Rosenfeld, Jill, Magoulas, Pilar L, Braxton, Alicia, Ward, Patricia, Dai, Hongzheng, Yuan, Bo, Bi, Weimin, Xiao, Rui, Wang, Xia, Chiang, Theodore, Vetrini, Francesco, He, Weimin, Cheng, Hanyin, Dong, Jie, Gijavanekar, Charul, Benke, Paul J, Bernstein, Jonathan A, Eble, Tanya, Eroglu, Yasemen, Erwin, Deanna, Escobar, Luis, Gibson, James B, Gripp, Karen, Kleppe, Soledad, Koenig, Mary K, Lewis, Andrea M, Natowicz, Marvin, Mancias, Pedro, Minor, LaKeesha, Scaglia, Fernando, Schaaf, Christian P, Streff, Haley, Vernon, Hilary, Uhles, Crescenda L, Zackai, Elaine H, Wu, Nan, Sutton, V. Reid, Beaudet, Arthur L, Muzny, Donna, Gibbs, Richard A, Posey, Jennifer E, Lalani, Seema, Shaw, Chad, Eng, Christine M, Lupski, James R, Yang, Yaping

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Measurement of preferences with self-explicated approaches: A classification and merge of trade-off- and non-trade-off-based evaluation types von Schlereth, Christian, Eckert, Christine, Schaaf, René, Skiera, Bernd

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Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits von Yuan, Bo, Schulze, Katharina V, Assia Batzir, Nurit, Sinson, Jefferson, Dai, Hongzheng, Zhu, Wenmiao, Bocanegra, Francia, Fong, Chin-To, Holder, Jimmy, Nguyen, Joanne, Schaaf, Christian P, Yang, Yaping, Bi, Weimin, Eng, Christine, Shaw, Chad, Lupski, James R, Liu, Pengfei

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Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies von Yuan, Bo, Neira, Juanita, Pehlivan, Davut, Santiago-Sim, Teresa, Song, Xiaofei, Rosenfeld, Jill, Posey, Jennifer E., Patel, Vipulkumar, Jin, Weihong, Adam, Margaret P., Baple, Emma L., Dean, John, Fong, Chin-To, Hickey, Scott E., Hudgins, Louanne, Leon, Eyby, Madan-Khetarpal, Suneeta, Rawlins, Lettie, Rustad, Cecilie F., Stray-Pedersen, Asbjørg, Tveten, Kristian, Wenger, Olivia, Diaz, Jullianne, Jenkins, Laura, Martin, Laura, McGuire, Marianne, Pietryga, Marguerite, Ramsdell, Linda, Slattery, Leah, Abid, Farida, Bertuch, Alison A., Grange, Dorothy, Immken, LaDonna, Schaaf, Christian P., Van Esch, Hilde, Bi, Weimin, Cheung, Sau Wai, Breman, Amy M., Smith, Janice L., Shaw, Chad, Crosby, Andrew H., Eng, Christine, Yang, Yaping, Lupski, James R., Xiao, Rui, Liu, Pengfei

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European lipodystrophy registry: background and structure von von Schnurbein, Julia, Adams, Claire, Akinci, Baris, Ceccarini, Giovanni, D'Apice, Maria Rosaria, Gambineri, Alessandra, Hennekam, Raoul C M, Jeru, Isabelle, Lattanzi, Giovanna, Miehle, Konstanze, Nagel, Gabriele, Novelli, Giuseppe, Santini, Ferruccio, Santos Silva, Ermelinda, Savage, David B, Sbraccia, Paolo, Schaaf, Jannik, Sorkina, Ekaterina, Tanteles, George, Vantyghem, Marie-Christine, Vatier, Camille, Vigouroux, Corinne, Vorona, Elena, Araújo-Vilar, David, Wabitsch, Martin

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De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive von Tokita, Mari J., Braxton, Alicia A., Shao, Yunru, Lewis, Andrea M., Vincent, Marie, Küry, Sébastien, Besnard, Thomas, Isidor, Bertrand, Latypova, Xénia, Bézieau, Stéphane, Liu, Pengfei, Motter, Connie S., Melver, Catherine Ward, Robin, Nathaniel H., Infante, Elena M., McGuire, Marianne, El-Gharbawy, Areeg, Littlejohn, Rebecca O., McLean, Scott D., Bi, Weimin, Bacino, Carlos A., Lalani, Seema R., Scott, Daryl A., Eng, Christine M., Yang, Yaping, Schaaf, Christian P., Walkiewicz, Magdalena A.

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New 2-in-1 Polyelectrolyte Step-by-Step Film Buildup without Solution Alternation: From PEDOT-PSS to Polyelectrolyte Complexes von de Saint-Aubin, Christine, Hemmerlé, Joseph, Boulmedais, Fouzia, Vallat, Marie-France, Nardin, Michel, Schaaf, Pierre

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Alpha-Toxin Contributes to Biofilm Formation among Staphylococcus aureus Wound Isolates von Anderson, Michele J, Schaaf, Emily, Breshears, Laura M, Wallis, Heidi W, Johnson, James R, Tkaczyk, Christine, Sellman, Bret R, Sun, Jisun, Peterson, Marnie L

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Mutations in PURA Cause Profound Neonatal Hypotonia, Seizures, and Encephalopathy in 5q31.3 Microdeletion Syndrome von Lalani, Seema R., Zhang, Jing, Schaaf, Christian P., Brown, Chester W., Magoulas, Pilar, Tsai, Anne Chun-Hui, El-Gharbawy, Areeg, Wierenga, Klaas J., Bartholomew, Dennis, Fong, Chin-To, Barbaro-Dieber, Tina, Kukolich, Mary K., Burrage, Lindsay C., Austin, Elise, Keller, Kory, Pastore, Matthew, Fernandez, Fabio, Lotze, Timothy, Wilfong, Angus, Purcarin, Gabriela, Zhu, Wenmiao, Craigen, William J., McGuire, Marianne, Jain, Mahim, Cooney, Erin, Azamian, Mahshid, Bainbridge, Matthew N., Muzny, Donna M., Boerwinkle, Eric, Person, Richard E., Niu, Zhiyv, Eng, Christine M., Lupski, James R., Gibbs, Richard A., Beaudet, Arthur L., Yang, Yaping, Wang, Meng C., Xia, Fan

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Phenotypic characterization of seven individuals with Marbach–Schaaf neurodevelopmental syndrome von Marbach, Felix, Lipska‐Ziętkiewicz, Beata S., Knurowska, Agata, Michaud, Vincent, Margot, Henri, Lespinasse, James, Tran Mau Them, Frédéric, Coubes, Christine, Park, Joohyun, Grosch, Sarah, Roggia, Cristiana, Grasshoff, Ute, Kalsner, Louisa, Denommé‐Pichon, Anne‐Sophie, Afenjar, Alexandra, Héron, Bénédicte, Keren, Boris, Caro, Pilar, Schaaf, Christian P.

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Sequential organ failure assessment score is an excellent operationalization of disease severity of adult patients with hospitalized community acquired pneumonia - results from the... von Ahnert, Peter, Creutz, Petra, Horn, Katrin, Schwarzenberger, Fabian, Kiehntopf, Michael, Hossain, Hamid, Bauer, Michael, Brunkhorst, Frank Martin, Reinhart, Konrad, Völker, Uwe, Chakraborty, Trinad, Witzenrath, Martin, Löffler, Markus, Suttorp, Norbert, Scholz, Markus

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