Rezultaty - William Allen
- Rezultaty 1 - 20 Rezultaty od 20
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The History and Epidemiology of Syphilis. od William Allen Pusey
Wydane 1933Artigo -
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NEUROTIC EXCORIATIONS WITH REPORT OF CASES od William Allen Pusey
Wydane 1920Artigo -
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Artificial Intelligence-Driven Analysis Identifies Anterior Cruciate Ligament Reconstruction, Hip Arthroscopy and Femoroacetabular Impingement Syndrome, and Shoulder Instability as... od Henry B. G. Baird, William Allen, María‐Trinidad Gallegos, Cody Ashy, Harris S. Slone, W. Michael Pullen
Wydane 2025Revisão -
12
WS(2) Nanotubes, 2D Nanomeshes, and 2D In-Plane Films through One Single Chemical Vapor Deposition Route od Liu, Zichen, Murphy, Alexander William Allen, Kuppe, Christian, Hooper, David Charles, Valev, Ventsislav Kolev, Ilie, Adelina
Wydane 2019Text -
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Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures od Stephen R. Williams, Sureni V. Mullegama, Jill A. Rosenfeld, Aditi I Dagli, Eli Hatchwell, William Allen, Charles A. Williams, Sarah H. Elsea
Wydane 2009Artigo -
14
Loss-of-function mutations in the human <i>GLI2</i> gene are associated with pituitary anomalies and holoprosencephaly-like features od Erich Roessler, Yangzhu Du, José L. Mullor, Esther Casas, William Allen, Gabriele Gillessen‐Kaesbach, Elizabeth Roeder, Jeffrey E. Ming, Ariel Ruiz i Altaba, Maximilian Muenke
Wydane 2003Artigo -
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HOW TO MAKE A DOCTOR: AN UNUSUAL SYMPOSIUM ON THE ESSENTIALS OF MEDICAL EDUCATION od Wilbur, Ray Lyman, Pusey, William Allen, Strickler, David A., Colwell, N. P., Zapffe, Frederick C., Rodman, J. S., Ophuls, William, Schmitt, L. S., Phillips, Percy T., Magan, Percy T., Musgrave, William Everett
Wydane 1925Text -
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NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease od Paige Martin, Yu Kigoshi-Tansho, Roger B. Sher, Gianina Ravenscroft, Jennifer E. Stauffer, Rajesh Kumar, Ryo Yonashiro, Tina Müller, Christopher Griffith, William Allen, Davut Pehli̇van, Tamar Harel, Martin Zenker, Denise Howting, Denny Schanze, Eissa Faqeih, Naif A. M. Almontashiri, Reza Maroofian, Henry Houlden, Neda Mazaheri, Hamid Galehdari, Ganka Douglas, Jennifer E. Posey, Monique M. Ryan, James R. Lupski, Nigel G. Laing, Claudio A.P. Joazeiro, Gregory A. Cox
Wydane 2020Artigo -
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Comparing Outcomes with Bone Marrow or Peripheral Blood Stem Cells as Graft Source for Matched Sibling Transplants in Severe Aplastic Anemia across Different Economic Regions od Kumar, Rajat, Kimura, Fumihiko, Ahn, Kwang Woo, Hu, Zhen-Huan, Kuwatsuka, Yachiyo, Klein, John P., Pasquini, Marcelo, Miyamura, Koichi, Kato, Koji, Yoshimi, Ayami, Inamoto, Yoshihiro, Ichinohe, Tatsuo, Wood, William Allen, Wirk, Baldeep, Seftel, Matthew, Rowlings, Philip, Marks, David I, Schultz, Kirk R., Gupta, Vikas, Dedeken, Laurence, George, Biju, Cahn, Jean-Yves, Szer, Jeff, Lee, Jong Wook, Ho, Aloysius YL, Fasth, Anders, Hahn, Theresa, Khera, Nandita, Dalal, Jignesh, Bonfim, Carmem, Aljurf, Mahmoud, Atsuta, Yoshiko, Saber, Wael
Wydane 2016Text -
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De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies od Konrad Platzer, Heinrich Sticht, Stacey L. Edwards, William Allen, Kaitlin M. Angione, Maria Teresa Bonati, Campbell K. Brasington, Megan T. Cho, Laurie Demmer, Tzipora C. Falik‐Zaccai, Candace Gamble, Yorck Hellenbroich, Maria Iascone, Fernando Kok, Sonal Mahida, Hanna Mandel, Thorsten Marquardt, Kirsty McWalter, Bianca Panis, Alexander Pepler, Hailey Pinz, Luiza Ramos, Deepali N. Shinde, Constance Smith‐Hicks, Alexander P.A. Stegmann, Petra Stöbe, Constance T. R. M. Stumpel, Carolyn M. Wilson, Johannes R. Lemke, Nataliya Di Donato, Kenneth G. Miller, Rami Abou Jamra
Wydane 2019Artigo -
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Scoring System Prognostic of Outcome in Patients Undergoing Allogeneic Hematopoietic Cell Transplantation for Myelodysplastic Syndrome od Shaffer, Brian C., Ahn, Kwang Woo, Hu, Zhen-Huan, Nishihori, Taiga, Malone, Adriana K., Valcárcel, David, Grunwald, Michael R., Bacher, Ulrike, Hamilton, Betty, Kharfan-Dabaja, Mohamed A., Saad, Ayman, Cutler, Corey, Warlick, Erica, Reshef, Ran, Wirk, Baldeep Mona, Sabloff, Mitchell, Fasan, Omotayo, Gerds, Aaron, Marks, David, Olsson, Richard, Wood, William Allen, Costa, Luciano J., Miller, Alan M., Cortes, Jorge, Daly, Andrew, Kindwall-Keller, Tamila L., Kamble, Rammurti, Rizzieri, David A., Cahn, Jean-Yves, Gale, Robert Peter, William, Basem, Litzow, Mark, Wiernik, Peter H., Liesveld, Jane, Savani, Bipin N., Vij, Ravi, Ustun, Celalettin, Copelan, Edward, Popat, Uday, Kalaycio, Matt, Maziarz, Richard, Alyea, Edwin, Sobecks, Ron, Pavletic, Steven, Tallman, Martin, Saber, Wael
Wydane 2016Text -
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Mutations in TOP3A Cause a Bloom Syndrome-like Disorder od Carol-Anne Martin, Kata Sarlós, Clare V. Logan, Roshan Singh Thakur, David Parry, Anna H. Bizard, Andrea Leitch, Louise Cleal, Nadia Shaukat Ali, Mohammed Al‐Owain, William Allen, Janine Altmüller, Miriam Aza‐Carmona, Bushra A.Y. Barakat, Jimena Barraza‐García, Amber Begtrup, Massimo Bogliolo, Megan T. Cho, Jaime Cruz‐Rojo, Hassan Ali Mundi Dhahrabi, Nursel Elçioğlu, Gráinne S. Gorman, Rebekah Jobling, Ian Kesterton, Yoshihito Kishita, Masakazu Kohda, Polona Le Quesne Stabej, Asam Jassim Malallah, Peter Nürnberg, Akira Ohtake, Yasushi Okazaki, Roser Pujol, Marı́a José Ramı́rez, Anya Revah‐Politi, Masaru Shimura, Paul E. Stevens, Robert W. Taylor, Lesley Turner, Hywel Williams, Carolyn M. Wilson, Gökhan Yigit, Laura Zahavich, Fowzan S. Alkuraya, Jordi Surrallés, Alejandro Iglesias, Kei Murayama, Bernd Wollnik, Mehul Dattani, Karen E. Heath, Ian D. Hickson, Andrew P. Jackson
Wydane 2018Artigo
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