Biological material for the repair of connective tissue defects comprising mesenchymal stem cells and hyaluronic acid derivative von BRUDER SCOTT PHILIP, MOSKOWITZ ROLAND, SOLCHAGA LUIS A, KADIYALA SUDHAKAR, CALLEGARO LANFRANCO, CAPLAN ARNOLD I, ABATANGELO GIOVANNI, BARRY FRANCIS PETER, MURPHY JOSEPHINE MARY, YOO JUNG U, FINK DAVID JORDAN, YOUNG RANDELL G

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Biological material for the repair of connective tissue defects comprising mesenchymal stem cells and hyaluronic acid derivative von Abatangelo, Giovanni, Callegaro, Lanfranco, Young, Randell G, Murphy, Josephine Mary, Fink, David Jordan, Bruder, Scott Philip, Barry, Francis Peter, Kadiyala, Sudhakar, Caplan, Arnold I, Moskowitz, Roland, Yoo, Jung U, Solchaga, Luis A

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A method of making a collagen strenghtened cellulosic sheet von HUGHES KENNETH EUGENE, MASTERSON DAVID CHRIS, BRODY RICHARD SIMON, PICKETT GORDON EUGENE, METZ BARBARA ANN, FINK DAVID JORDAN, GEMMER PAUL MICHAEL

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The diagnosis and management of anaphylaxis practice parameter: 2010 Update von Lieberman, Phillip, MD, Nicklas, Richard A., MD, Oppenheimer, John, MD, Kemp, Stephen F., MD, Lang, David M., MD, Bernstein, David I., MD, Bernstein, Jonathan A., MD, Burks, A. Wesley, MD, Feldweg, Anna M., MD, Fink, Jordan N., MD, Greenberger, Paul A., MD, Golden, David B.K., MD, James, John M., MD, Ledford, Dennis K., MD, Sheffer, Albert L., MD, Blessing-Moore, Joann, MD, Cox, Linda, MD, Khan, David A., MD, Lang, David, MD, Portnoy, Jay M., MD, Randolph, Christopher, MD, Schuller, Diane E., MD, Spector, Sheldon L., MD, Tilles, Stephen, MD, Wallace, Dana, MD

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Csnk1a1 inhibition has p53-dependent therapeutic efficacy in acute myeloid leukemia von Järås, Marcus, Miller, Peter G, Chu, Lisa P, Puram, Rishi V, Fink, Emma C, Schneider, Rebekka K, Al-Shahrour, Fatima, Peña, Pablo, Breyfogle, L Jordan, Hartwell, Kimberly A, McConkey, Marie E, Cowley, Glenn S, Root, David E, Kharas, Michael G, Mullally, Ann, Ebert, Benjamin L

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The diagnosis and management of anaphylaxis: An updated practice parameter von Lieberman, Phillip, Kemp, Stephen F., Oppenheimer, John, Lang, David M., Bernstein, I. Leonard, Nicklas, Richard A., Anderson, John A., Bernstein, David I., Bernstein, Jonathan A., Fink, Jordan N., Greenberger, Paul A., Ledford, Dennis K., Li, James, Sheffer, Albert L., Solensky, Roland, Wolf, Bruce L., Blessing-Moore, Joann, Khan, David A., Lee, Rufus E., Portnoy, Jay M., Schuller, Diane E., Spector, Sheldon L., Tilles, Stephen A.

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Somatic point mutation calling in low cellularity tumors von Kassahn, Karin S, Holmes, Oliver, Nones, Katia, Patch, Ann-Marie, Miller, David K, Christ, Angelika N, Harliwong, Ivon, Bruxner, Timothy J, Xu, Qinying, Anderson, Matthew, Wood, Scott, Leonard, Conrad, Taylor, Darrin, Newell, Felicity, Song, Sarah, Idrisoglu, Senel, Nourse, Craig, Nourbakhsh, Ehsan, Manning, Suzanne, Wani, Shivangi, Steptoe, Anita, Pajic, Marina, Cowley, Mark J, Pinese, Mark, Chang, David K, Gill, Anthony J, Johns, Amber L, Wu, Jianmin, Wilson, Peter J, Fink, Lynn, Biankin, Andrew V, Waddell, Nicola, Grimmond, Sean M, Pearson, John V

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A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative von Schoch, Kelly, Spillmann, Rebecca, Tan, Queenie K.-G., McConkie-Rosell, Allyn, Jiang, Yong-Hui, Goldstein, David B., Adams, David R., Allard, Patrick, Ashley, Euan A., Bacino, Carlos A., Beggs, Alan H., Birch, Camille L., Bonner, Devon, Boone, Braden E., Brown, Donna M., Chen, Shan, Coakley, Terra R., Cogan, Joy D., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., Davidson, Jean M., Dayal, Jyoti G., Dell’Angelica, Esteban C., Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Draper, David D., Dries, Annika M., Eckstein, David J., Emrick, Lisa T., Enns, Gregory M., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Fisher, Paul G., Fogel, Brent L., Friedman, Noah D., Gahl, William A., Goldstein, David B., Gourdine, Jean-Philippe F., Haendel, Melissa, Handley, Lori H., Krasnewich, Donna M., Krier, Joel B., Lazar, Jozef, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, Martin, Martin G., McConkie-Rosell, Allyn, McCormack, Colleen E., Might, Matthew, Morimoto, Marie, Mulvihill, John J., Murphy, Jennifer L., Muzny, Donna M., Nehrebecky, Michele E., Nelson, Stan F., Newberry, J. Scott, Newman, John H., Nicholas, Sarah K., Pallais, J. Carl, Palmer, Christina GS, Parker, Neil H., Phillips, John A., Postlethwait, John H., Reuter, Chloe M., Sampson, Jacinda B., Scott, Daryl A., Sharma, Prashant, Shashi, Vandana, Silverman, Edwin K., Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walsh, Chris A., Wan, Jijun, Wangler, Michael F., Ward, Patricia A., Wheeler, Matthew T., Wolfe, Lynne A., Worthey, Elizabeth A., Yamamoto, Shinya, Yang, Yaping, Yu, Guoyun, Zhao, Chunli, Zheng, Allison

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Genetic sharing and heritability of paediatric age of onset autoimmune diseases von Li, Yun R., Zhao, Sihai D., Li, Jin, Bradfield, Jonathan P., Mohebnasab, Maede, Steel, Laura, Kobie, Julie, Abrams, Debra J., Mentch, Frank D., Glessner, Joseph T., Guo, Yiran, Wei, Zhi, Connolly, John J., Cardinale, Christopher J., Bakay, Marina, Li, Dong, Maggadottir, S. Melkorka, Thomas, Kelly A., Qui, Haijun, Chiavacci, Rosetta M., Kim, Cecilia E., Wang, Fengxiang, Snyder, James, Flatø, Berit, Førre, Øystein, Denson, Lee A., Thompson, Susan D., Becker, Mara L., Guthery, Stephen L., Latiano, Anna, Perez, Elena, Resnick, Elena, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Silverberg, Mark S., Lie, Benedicte A., Punaro, Marilynn, Russell, Richard K., Wilson, David C., Dubinsky, Marla C., Monos, Dimitri S., Annese, Vito, Munro, Jane E., Wise, Carol, Chapel, Helen, Cunningham-Rundles, Charlotte, Orange, Jordan S., Behrens, Edward M., Sullivan, Kathleen E., Kugathasan, Subra, Griffiths, Anne M., Satsangi, Jack, Grant, Struan F. A., Sleiman, Patrick M. A., Finkel, Terri H., Polychronakos, Constantin, Baldassano, Robert N., Luning Prak, Eline T., Ellis, Justine A., Li, Hongzhe, Keating, Brendan J., Hakonarson, Hakon

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Needs and Opportunities for Research in Hypersensitivity Pneumonitis von Fink, Jordan N, Ortega, Hector G, Reynolds, Herbert Y, Cormier, Yvon F, Fan, Leland L, Franks, Teri J, Kreiss, Kathleen, Kunkel, Steven, Lynch, David, Quirce, Santiago, Rose, Cecile, Schleimer, Robert P, Schuyler, Mark R, Selman, Moises, Trout, Douglas, Yoshizawa, Yasuyuki

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Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes von Phillips, Jennifer B., Lanza, Denise G., Jain, Mahim, Raman, Vandana, Chitayat, David, Chinn, Ivan K., Bertuch, Alison A., Bamshad, Michael, Savarirayan, Ravi, Doddapaneni, Harsha, Muzny, Donna, Gibbs, Richard A., Rosenfeld, Jill A., Postlethwait, John, Beaudet, Arthur L., Ranza, Emmanuelle, Cormier-Daire, Valérie, Orange, Jordan S., Allard, Patrick, Barseghyan, Hayk, Batzli, Gabriel F., Beggs, Alan H., Bellen, Hugo J., Bernstein, Jonathan A., Bick, David P., Briere, Lauren C., Brokamp, Elly, Brush, Matthew, Coakley, Terra R., Cope, Heidi, Davidson, Jean M., Dayal, Jyoti G., Dhar, Shweta U., Dipple, Katrina M., Dorrani, Naghmeh, Duncan, Laura, Emrick, Lisa T., Eng, Christine M., Enns, Gregory M., Fisher, Paul G., Friedman, Noah D., Gahl, William A., Glanton, Emily, Goldman, Alica M., Gourdine, Jean-Philippe F., Groden, Catherine A., Haendel, Melissa, Hamid, Rizwan, High, Frances, Huang, Yong, Karaviti, Lefkothea, Kohler, Jennefer N., Krasnewich, Donna M., Korrick, Susan, Krier, Joel B., Kyle, Jennifer E., Lau, C. Christopher, Lee, Hane, Loo, Sandra K., Loscalzo, Joseph, Martin, Martin G., Martínez-Agosto, Julian A., Marwaha, Shruti, McCormack, Colleen E., McCray, Alexa T., Metz, Thomas O., Murdock, David R., Newberry, J. Scott, Nicholas, Sarah K., Palmer, Christina G.S., Papp, Jeanette C., Phillips, John A., Posey, Jennifer E., Pusey, Barbara N., Sampson, Jacinda B., Shakachite, Lisa, Signer, Rebecca, Silverman, Edwin K., Spillmann, Rebecca C., Stoler, Joan M., Stong, Nicholas, Sweetser, David A., Tan, Queenie K.-G., Tran, Alyssa A., Vogel, Tiphanie P., Wahl, Colleen E., Wangler, Michael F., Waters, Katrina M., Westerfield, Monte, Wise, Anastasia L., Yang, John, Yang, Yaping, Yoon, Amanda J., Zastrow, Diane B., Zhao, Chunli, Offiah, Amaka C., Carey, John C., Bacino, Carlos A., Campeau, Philippe M., Lee, Brendan

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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype von Pena, Loren D.M., Hempel, Maja, McLaughlin, Heather M., Cho, Megan, Stong, Nicholas, Shuss, Christine M., Burrage, Lindsay C., Dhar, Shweta U., Emrick, Lisa T., Graham, Brett H., Lalani, Seema R., Lewis, Richard A., Posey, Jennifer E., Hanchard, Neil A., Mercedes, Alejandro E., Wangler, Michael F., Muzny, Donna M., Ward, Patricia A., Ramoni, Rachel B., McCray, Alexa T., Mazur, Paul, Splinter, Kimberly, Esteves, Cecilia, Jiang, Yong-hui, Pena, Loren D.M., McConkie-Rosell, Allyn, Schoch, Kelly, Spillmann, Rebecca C., Goldstein, David B., Loscalzo, Joseph, Rodan, Lance H., Walsh, Chris A., Cooper, Cynthia M., Donnell-Fink, Laurel A., Krieg, Elizabeth L., Lincoln, Sharyn A., Worthey, Elizabeth A., Lazar, Joe, Handley, Lori H., Newberry, J. Scott, Schroeder, Molly C., Brown, Donna M., Levy, Shawn E., Dorset, Dan C., Jones, Angela L., Manolio, Teri A., Wise, Anastasia L., Eckstein, David J., Krasnewich, Donna M., Loomis, Carson R., Iglesias, Brenda, Martin, Casey, Koeller, David M., Ashley, Euan A., Zornio, Patricia A., Nelson, Stan F., Palmer, Christina G.S., Allard, Patrick, Dell Angelica, Esteban C., Lee, Hane, Papp, Jeanette C., Dorrani, Naghmeh, Draper, David D., Estwick, Tyra, Gahl, William A., Gartner, Valerie, Godfrey, Rena A., Goheen, Mitchell, Johnston, Jean M., Latham, Lea, Macnamara, Ellen F., Maduro, Valerie V., Malicdan, May V., McCarty, Alexandra J., Murphy, Jennifer L., Novacic, Donna, Pusey, Barbara N., Sadozai, Sarah, Schaffer, Katherine E., Sharma, Prashant, Soldatos, Ariane G., Tifft, Cynthia J., Tolman, Nathanial J., Toro, Camilo, Wahl, Colleen E., Weech, Alec A., Yu, Guoyun, Hamid, Rizwan, Bellet, Jane S., Keels, Martha Ann, El-Dairi, Maysantoine, Stumpel, Constance T.R.M., Klinkenberg, Sylvia, Oberndorff, Karin, Petrovski, Slavé, Kuismin, Outi, Korpi-Heikkilä, Satu, Kurki, Mitja I., Hoischen, Alexander, Goldstein, David B.

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Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases von Pena, Loren D M, Jiang, Yong-Hui, Schoch, Kelly, Spillmann, Rebecca C, Walley, Nicole, Stong, Nicholas, Rapisardo Horn, Sarah, Sullivan, Jennifer A, McConkie-Rosell, Allyn, Kansagra, Sujay, Smith, Edward C, El-Dairi, Mays, Bellet, Jane, Keels, Martha Ann, Jasien, Joan, Kranz, Peter G, Noel, Richard, Nagaraj, Shashi K, Lark, Robert K, Wechsler, Daniel S G, del Gaudio, Daniela, Leung, Marco L, Hendon, Laura G, Parker, Collette C, Jones, Kelly L, Goldstein, David B, Shashi, Vandana

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Immune response among patients exposed to molds von Edmondson, David A, Barrios, Christy S, Brasel, Trevor L, Straus, David C, Kurup, Viswanath P, Fink, Jordan N

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Immune Modulation: New Treatment for Heart Failure von Lancaster, Jordan J, Grijalva, Ambar, Fink, John, Benson, David, Ref, Jacob, Fox, Kathryn, Mangiola, Massimo, Pandey, Amitabh C, Zile, Michael R, Mann, Douglas L, Perin, Emerson C, Singh, Sonal, Moukabary, Talal, Koevary, Jennifer W, Goldman, Steven

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A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay von Schoch, Kelly, Meng, Linyan, Szelinger, Szabolcs, Liston, Eriskay, Scaglia, Fernando, Rosenfeld, Jill A., Deardorff, Matthew A., Akdemir, Zeynep Coban, Jasien, Joan, Kansagra, Sujay, Freedman, Sharon, Bale, Sherri, Nelson, Stanley F., Lee, Hane, Dorrani, Naghmeh, Nelson, Stanley F., Lee, Hane, Vilain, Eric, Kantarci, Sibel, Dorrani, Naghmeh, Mullegama, Sureni, Kang, Sung-Hae, Bacino, Carlos A., Balasubramanyam, Ashok, Craigen, William J., Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Lewis, Richard A., Moretti, Paolo M., Orange, Jordan S., Potocki, Lorraine, Rosenfeld, Jill A., Wangler, Michael F., Yamamoto, Shinya, Muzny, Donna M., Yang, Yaping, Gropman, Andrea L., Goldstein, David B., Schoch, Kelly, Walley, Nicole M., Beggs, Alan H., Krier, Joel B., Loscalzo, Joseph, Walsh, Chris A., Esteves, Cecilia, Holm, Ingrid A., Kohane, Isaac S., Mazur, Paul, McCray, Alexa T., Might, Matthew, Splinter, Kimberly, Brown, Donna M., Dorset, Dan C., Jones, Angela L., Lazar, Jozef, Newberry, J. Scott, Schroeder, Molly C., Strong, Kimberly A., Dayal, Jyoti G., Loomis, Carson R., Mulvihill, John J., Wise, Anastasia L., Haendel, Melissa, Kyle, Jennifer E., Webb-Robertson, Bobbie-Jo M., Kohler, Jennefer N., Herzog, Matthew R., Nelson, Stan F., Palmer, Christina G.S., Papp, Jeanette C., Adams, Christopher J., Burke, Elizabeth A., Chao, Katherine R., Davids, Mariska, Frost, Kate, Gartner, Valerie, Gordon, Mary “Gracie” G., Groden, Catherine A., Hardee, Isabel, Johnston, Jean M., Latham, Lea, Lau, C. Christopher, Maduro, Valerie V., Pusey, Barbara N., Sadozai, Sarah, Schaffer, Katherine E., Sharma, Prashant, Thomas, Sara P., Valivullah, Zaheer M., Wahl, Colleen E., Weech, Alec A., Westerfield, Monte, Bican, Anna, Phillips, John A., Robertson, Amy K., Xiao, Rui, Posey, Jennifer E., Wangler, Michael F., Shashi, Vandana

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The Incidence and Associated Risk Factors of Thoracolumbar Epidural Hematoma following Adult Trauma von Verma, Ravi, Ricart-Hoffiz, Pedro A., Fineberg, Steven J., Fink, Kyle Y., Patel, Neel, Gross, Jordan M., Lucas, Paul A., Lo, Yungtai, Asprinio, David, Amorosa, Louis F.

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111 - The Incidence and Associated Risk Factors of Thoracolumbar Epidural Hematoma following Adult Trauma von Verma, Ravi, Ricart-Hoffiz, Pedro A., Fineberg, Steven J., Fink, Kyle Y., Patel, Neel, Gross, Jordan M., Lucas, Paul A., Lo, Yungtai, Asprinio, David, Amorosa, Louis F.

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Allergy and “toxic mold syndrome” von Edmondson, David A., Nordness, Mark E., Zacharisen, Michael C., Kurup, Viswanath P., Fink, Jordan N.

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Technology-enabled assessments to enhance multiple sclerosis clinical care and research von Macaron, Gabrielle, Moss, Brandon P., Li, Hong, Baldassari, Laura E., Rao, Stephen M., Schindler, David, Alberts, Jay L., Weber, Malory, Ayers, Malissa, Bethoux, François, Boissy, Adrienne, Chizmadia, Desiree, Conway, Devon S., Fink, Charlene, Fox, Robert J., Gales, Shauna, Green, Bethany, Hara-Cleaver, Claire, Jordan, Neal, Mahajan, Kedar R., McGinley, Marisa P., Miller, Deborah M., Namey, Marie, Rae-Grant, Alexander, Rensel, Mary, Young, Hilary, Willis, Mary A., Ontaneda, Daniel, Cohen, Jeffrey A., Bermel, Robert A.

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