Infertility and uterine contour von Nickerson, Charles W.

Volltext

Gonorrhea Amnionitis von NICKERSON, CHARLES W.

Volltext

Amniotic sac dystocia in twins von Nickerson, C W

Volltext

Assessing Medical Practices through PSRO Cooperative Studies: An Evaluation of Cesarean Births in Nine PSRO Areas von Jessee, William F., Nickerson, C. W., Grant, William S.

Volltext

Laceration of Umbilical Artery and Abruptio Placentae Secondary to Amniocentesis von JAMES, J DONALD, NICKERSON, CHARLES W.

Volltext

Vaginal arteriovenous fistula von Barnett, Jewell M., Nickerson, Charles W.

Volltext

Recurrent Pseudotumor Cerebri in Pregnancy: Report of 2 Cases von NICKERSON, CHARLES W., KIRK, ROBERT F.

Volltext

Surgical Blood Loss and Preoperative Estrogen in the Premenopausal Patient von NICKERSON, CHARLES W., LEE, JAMES H.

Volltext

Evolution and Clinical Pathologic Correlations of De Novo Donor‐Specific HLA Antibody Post Kidney Transplant von Wiebe, C., Gibson, I. W., Blydt‐Hansen, T. D., Karpinski, M., Ho, J., Storsley, L. J., Goldberg, A., Birk, P. E., Rush, D. N., Nickerson, P. W.

Volltext

Class II HLA Epitope Matching—A Strategy to Minimize De Novo Donor‐Specific Antibody Development and Improve Outcomes von Wiebe, C., Pochinco, D., Blydt‐Hansen, T. D., Ho, J., Birk, P. E., Karpinski, M., Goldberg, A., Storsley, L. J., Gibson, I. W., Rush, D. N., Nickerson, P. W.

Volltext

Entanglement distillation between solid-state quantum network nodes von Kalb, N., Reiserer, A. A., Humphreys, P. C., Bakermans, J. J. W., Kamerling, S. J., Nickerson, N. H., Benjamin, S. C., Twitchen, D. J., Markham, M., Hanson, R.

Volltext

The Synergistic Effect of Class II HLA Epitope‐Mismatch and Nonadherence on Acute Rejection and Graft Survival von Wiebe, C., Nevins, T. E., Robiner, W. N., Thomas, W., Matas, A. J., Nickerson, P. W.

Volltext

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA von Turner, Tychele N., Hormozdiari, Fereydoun, Duyzend, Michael H., McClymont, Sarah A., Hook, Paul W., Iossifov, Ivan, Raja, Archana, Baker, Carl, Hoekzema, Kendra, Stessman, Holly A., Zody, Michael C., Nelson, Bradley J., Huddleston, John, Sandstrom, Richard, Smith, Joshua D., Hanna, David, Swanson, James M., Faustman, Elaine M., Bamshad, Michael J., Stamatoyannopoulos, John, Nickerson, Deborah A., McCallion, Andrew S., Darnell, Robert, Eichler, Evan E.

Volltext

Rates and Determinants of Progression to Graft Failure in Kidney Allograft Recipients With De Novo Donor‐Specific Antibody von Wiebe, C., Gibson, I. W., Blydt‐Hansen, T. D., Pochinco, D., Birk, P. E., Ho, J., Karpinski, M., Goldberg, A., Storsley, L., Rush, D. N., Nickerson, P. W.

Volltext

Recurrent Gain-of-Function Mutation in PRKG1 Causes Thoracic Aortic Aneurysms and Acute Aortic Dissections von Guo, Dong-chuan, Regalado, Ellen, Casteel, Darren E., Santos-Cortez, Regie L., Gong, Limin, Kim, Jeong Joo, Dyack, Sarah, Horne, S. Gabrielle, Chang, Guijuan, Jondeau, Guillaume, Boileau, Catherine, Coselli, Joseph S., Li, Zhenyu, Leal, Suzanne M., Shendure, Jay, Rieder, Mark J., Bamshad, Michael J., Nickerson, Deborah A., Kim, Choel, Milewicz, Dianna M.

Volltext

Evaluation of C1q Status and Titer of De Novo Donor‐Specific Antibodies as Predictors of Allograft Survival von Wiebe, C., Gareau, A. J., Pochinco, D., Gibson, I. W., Ho, J., Birk, P. E., Blydt‐Hansen, T., Karpinski, M., Goldberg, A., Storsley, L., Rush, D. N., Nickerson, P. W.

Volltext

Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders von Guo, Hui, Bettella, Elisa, Marcogliese, Paul C., Zhao, Rongjuan, Andrews, Jonathan C., Nowakowski, Tomasz J., Gillentine, Madelyn A., Hoekzema, Kendra, Wang, Tianyun, Wu, Huidan, Jangam, Sharayu, Liu, Cenying, Ni, Hailun, Willemsen, Marjolein H., van Bon, Bregje W., Rinne, Tuula, Stevens, Servi J. C., Kleefstra, Tjitske, Brunner, Han G., Yntema, Helger G., Long, Min, Zhao, Wenjing, Hu, Zhengmao, Colson, Cindy, Richard, Nicolas, Schwartz, Charles E., Romano, Corrado, Castiglia, Lucia, Bottitta, Maria, Dhar, Shweta U., Erwin, Deanna J., Emrick, Lisa, Keren, Boris, Afenjar, Alexandra, Zhu, Baosheng, Bai, Bing, Stankiewicz, Pawel, Herman, Kristin, Mercimek-Andrews, Saadet, Juusola, Jane, Wilfert, Amy B., Abou Jamra, Rami, Büttner, Benjamin, Mefford, Heather C., Muir, Alison M., Scheffer, Ingrid E., Regan, Brigid M., Malone, Stephen, Gecz, Jozef, Cobben, Jan, Weiss, Marjan M., Waisfisz, Quinten, Bijlsma, Emilia K., Hoffer, Mariëtte J. V., Ruivenkamp, Claudia A. L., Sartori, Stefano, Xia, Fan, Rosenfeld, Jill A., Bernier, Raphael A., Wangler, Michael F., Yamamoto, Shinya, Xia, Kun, Stegmann, Alexander P. A., Bellen, Hugo J., Murgia, Alessandra, Eichler, Evan E.

Volltext

GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome von LaCroix, Amy J., Stabley, Deborah, Sahraoui, Rebecca, Adam, Margaret P., Mehaffey, Michele, Kernan, Kelly, Myers, Candace T., Fagerstrom, Carrie, Anadiotis, George, Akkari, Yassmine M., Robbins, Katherine M., Gripp, Karen W., Baratela, Wagner A.R., Bober, Michael B., Duker, Angela L., Doherty, Dan, Dempsey, Jennifer C., Miller, Daniel G., Kircher, Martin, Bamshad, Michael J., Nickerson, Deborah A., Mefford, Heather C., Sol-Church, Katia

Volltext

Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia von Horani, Amjad, Druley, Todd E, Zariwala, Maimoona A, Patel, Anand C, Levinson, Benjamin T, Van Arendonk, Laura G, Thornton, Katherine C, Giacalone, Joe C, Albee, Alison J, Wilson, Kate S, Turner, Emily H, Nickerson, Deborah A, Shendure, Jay, Bayly, Philip V, Leigh, Margaret W, Knowles, Michael R, Brody, Steven L, Dutcher, Susan K, Ferkol, Thomas W

Volltext

Microbial Responses to Microgravity and Other Low-Shear Environments von Nickerson, Cheryl A., Ott, C. Mark, Wilson, James W., Ramamurthy, Rajee, Pierson, Duane L.

Volltext