Intravesical Foreign Body and Vesicovaginal Fistula: A Rare Complication of a Neglected Pessary von Grody, M. H. T., Nyirjesy, P., Chatwani, A.

Volltext

Over-the-counter and alternative medicines in the treatment of chronic vaginal symptoms von Nyirjesy, Paul, Weitz, M. Velma, Grody, M.H. Terry, Lorber, Bennett

Volltext

Chronic fungal vaginitis: The value of cultures von Nyirjesy, Paul, Seeney, Sueny M., Terry Grody, Marvin H., Jordan, Carol A., Buckley, Helen R.

Volltext

A comparison of abdominal and vaginal hysterectomy for the large uterus von Harmanli, O.H., Gentzler, C.K., Byun, S., Dandolu, V., Grody, M.H.T.

Volltext

Paraurethral fascial sling urethropexy and vaginal paravaginal defects cystopexy in the correction of urethrovesical prolapse von Grody, M. H. T., Nyirjesy, P., Kelley, L. M., Millar, M. L.

Volltext

The Bonney test : A reassessment. Discussion von MIYAZAKI, F. S, GRODY, M. H. T

Volltext

Propelled lavage in the reduction of postoperative infection in vaginal reconstructive surgery von GRODY, M. H. T, NYIRJESY, P, PADMAVATHY TUMMALA

Volltext

Long-term analysis of the surgical management of pelvic support defects. Discussion von PORGES, R. F, SMILEN, S. W, ELKINS, T. E, GRODY, M. H. T

Volltext

NOAA operational hydrological products derived from the advanced microwave sounding unit von Ferraro, R.R., Fuzhong Weng, Grody, N.C., Limin Zhao, Huan Meng, Cezar Kongoli, Pellegrino, P., Shuang Qiu, Dean, C.

Volltext

Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells von Goyal, Yogesh, Busch, Gianna T., Pillai, Maalavika, Li, Jingxin, Boe, Ryan H., Grody, Emanuelle I., Chelvanambi, Manoj, Dardani, Ian P., Emert, Benjamin, Bodkin, Nicholas, Braun, Jonas, Fingerman, Dylan, Kaur, Amanpreet, Jain, Naveen, Ravindran, Pavithran T., Mellis, Ian A., Kiani, Karun, Alicea, Gretchen M., Fane, Mitchell E., Ahmed, Syeda Subia, Li, Haiyin, Chen, Yeqing, Chai, Cedric, Kaster, Jessica, Witt, Russell G., Lazcano, Rossana, Ingram, Davis R., Johnson, Sarah B., Wani, Khalida, Dunagin, Margaret C., Lazar, Alexander J., Weeraratna, Ashani T., Wargo, Jennifer A., Herlyn, Meenhard, Raj, Arjun

Volltext

Massively parallel base editing to map variant effects in human hematopoiesis von Martin-Rufino, Jorge D., Castano, Nicole, Pang, Michael, Grody, Emanuelle I., Joubran, Samantha, Caulier, Alexis, Wahlster, Lara, Li, Tongqing, Qiu, Xiaojie, Riera-Escandell, Anna Maria, Newby, Gregory A., Al’Khafaji, Aziz, Chaudhary, Santosh, Black, Susan, Weng, Chen, Munson, Glen, Liu, David R., Wlodarski, Marcin W., Sims, Kacie, Oakley, Jamie H., Fasano, Ross M., Xavier, Ramnik J., Lander, Eric S., Klein, Daryl E., Sankaran, Vijay G.

Volltext

A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders von Ngo, Kathie J., Rexach, Jessica E., Lee, Hane, Petty, Lauren E., Perlman, Susan, Valera, Juliana M., Deignan, Joshua L., Mao, Yuanming, Aker, Mamdouh, Posey, Jennifer E., Jhangiani, Shalini N., Coban‐Akdemir, Zeynep H., Boerwinkle, Eric, Muzny, Donna, Nelson, Alexandra B., Hassin‐Baer, Sharon, Poke, Gemma, Neas, Katherine, Geschwind, Michael D., Grody, Wayne W., Gibbs, Richard, Geschwind, Daniel H., Lupski, James R., Below, Jennifer E., Nelson, Stanley F., Fogel, Brent L.

Volltext

High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects von Zodanu, Gloria K E, Hwang, John H, Mehta, Zubin, Sisniega, Carlos, Barsegian, Alexander, Kang, Xuedong, Biniwale, Reshma, Si, Ming-Sing, Satou, Gary M, Halnon, Nancy, Ucla Congenital Heart Defect BioCore Faculty, Grody, Wayne W, Van Arsdell, Glen S, Nelson, Stanley F, Touma, Marlin

Volltext

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction von Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

Volltext

Arginases I and II: do their functions overlap? von Cederbaum, Stephen D, Yu, Hong, Grody, Wayne W, Kern, Rita M, Yoo, Paul, Iyer, Ramaswamy K

Volltext

Mouse Model for Human Arginase Deficiency von Iyer, Ramaswamy K., Yoo, Paul K., Kern, Rita M., Rozengurt, Nora, Tsoa, Rosemarie, O'Brien, William E., Yu, Hong, Grody, Wayne W., Cederbaum, Stephen D.

Volltext

Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology von Schrijver, Iris, Aziz, Nazneen, Farkas, Daniel H, Furtado, Manohar, Gonzalez, Andrea Ferreira, Greiner, Timothy C, Grody, Wayne W, Hambuch, Tina, Kalman, Lisa, Kant, Jeffrey A, Klein, Roger D, Leonard, Debra G B, Lubin, Ira M, Mao, Rong, Nagan, Narasimhan, Pratt, Victoria M, Sobel, Mark E, Voelkerding, Karl V, Gibson, Jane S

Volltext

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants von Fu, Wenqing, O’Connor, Timothy D., Jun, Goo, Kang, Hyun Min, Abecasis, Goncalo, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Altshuler, David, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., NHLBI Exome Sequencing Project, Akey, Joshua M.

Volltext

Collagen content of nonsupport tissue in pelvic organ prolapse and stress urinary incontinence von Wong, Michael Y, Harmanli, Ozgur H, Agar, Mehmet, Dandolu, Vani, Grody, M.H.Terry

Volltext

TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome von Boileau, Catherine, Guo, Dong-Chuan, Hanna, Nadine, Regalado, Ellen S, Detaint, Delphine, Gong, Limin, Varret, Mathilde, Prakash, Siddharth K, Li, Alexander H, d'Indy, Hyacintha, Braverman, Alan C, Grandchamp, Bernard, Kwartler, Callie S, Gouya, Laurent, Santos-Cortez, Regie Lyn P, Abifadel, Marianne, Leal, Suzanne M, Muti, Christine, Shendure, Jay, Gross, Marie-Sylvie, Rieder, Mark J, Vahanian, Alec, Nickerson, Deborah A, Michel, Jean Baptiste, Jondeau, Guillaume, Milewicz, Dianna M

Volltext