Pseudoaneurysm of the uterine artery von Zimon, Alison E, Hwang, Joseph K, Principe, David L, Bahado-Singh, Ray O

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Aging and reproductive potential in women von Fitzgerald, C, Zimon, A E, Jones, E E

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Association of Hepatosplenic Schistosomiasis with HLA-DQB10201 von Secor, W. Evan, del Corral, Helena, dos Reis, Mitermayer G., Ramos, Eduardo A. G., Zimon, Alison E., Matos, E. Peixoto, Reis, Eliana A. G., do Carmo, Theomira M. A., Hirayama, Kenji, David, Roberta A., David, John R., Harn, Donald A.

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Risk of death in pregnancy achieved through oocyte donation in patients with Turner syndrome: a national survey von Karnis, Megan Freebury, Zimon, Alison Elizabeth, Lalwani, Sasmira Indru, Timmreck, Lorna Smink, Klipstein, Sigal, Reindollar, Richard Henry

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Association of Hepatosplenic Schistosomiasis with HLA-DQBl0201 von Secor, W. Evan, del Corral, Helena, dos Rels, Mitermayer G., Ramos, Eduardo A. G., Zimon, Alison E., Matos, E. Peixoto, Reis, Eliana A. G., do Carmo, Theomira M. A., Hirayama, Kenji, David, Roberta A., David, John R., Harn, Donald A.

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Embryo donation: Survey of in-vitro fertilization (IVF) patients and randomized trial of complimentary counseling von Zimon, Alison E, Shepard, Donald S, Prottas, Jeffrey, Rooney, Kristin L, Ungerleider, Jeanie, Halasa-Rappel, Yara A, Sakkas, Denny, Oskowitz, Selwyn P

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Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy von Ylikallio, Emil, Pöyhönen, Rosanna, Zimon, Magdalena, De Vriendt, Els, Hilander, Taru, Paetau, Anders, Jordanova, Albena, Lönnqvist, Tuula, Tyynismaa, Henna

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Genetic spectrum of hereditary neuropathies with onset in the first year of life von Baets, Jonathan, Deconinck, Tine, De Vriendt, Els, Zimo, Magdalena, Yperzeele, Laetitia, Van Hoorenbeeck, Kim, Peeters, Kristien, Spiegel, Ronen, Parman, Yesim, Ceulemans, Berten, Van Bogaert, Patrick, Pou-Serradell, Adolf, Bernert, Günther, Dinopoulos, Argirios, Auer-Grumbach, Michaela, Sallinen, Satu-Leena, Fabrizi, Gian Maria, Pauly, Fernand, Van den Bergh, Peter, Bilir, Birdal, Battaloglu, Esra, Madrid, Ricardo E., Kabzi ska, Dagmara, Kochanski, Andrzej, Topaloglu, Haluk, Miller, Geoffrey, Jordanova, Albena, Timmerman, Vincent, De Jonghe, Peter

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Dominant GDAP1 mutations cause predominantly mild CMT phenotypes von ZIMON, M, BAETS, J, GUELLY, C, HUBER, N, DE VRIENDT, E, TIMMERMAN, V, SUTER, U, PETRUSEWICZ, I. Hausmanowa, NIEMANN, A, KOCHANSKI, A, DE JONGHE, P, JORDANOVA, A, FABRIZI, G. M, JAAKKOLA, E, KABZINSKA, D, PILCH, J, SCHINDLER, A. B, CORNBLATH, D. R, FISCHBECK, K. H, AUER-GRUMBACH, M

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Efficient Adaptive Stochastic Collocation Strategies for Advection–Diffusion Problems with Uncertain Inputs von Kent, Benjamin M., Powell, Catherine E., Silvester, David J., Zimoń, Małgorzata J.

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Embryo donation: Survey of in-vitro fertilization von Zimon, Alison E, Shepard, Donald S, Prottas, Jeffrey, Rooney, Kristin L, Ungerleider, Jeanie, Halasa-Rappel, Yara A, Sakkas, Denny, Oskowitz, Selwyn P

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S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC GENE von Colucci, S., Venturi, V., Nicole, F., Jové Solavera, D., Zimon, M., Richter‐Pechanska, P., Hernandez, G., Unal, S., Gumruk, F., Diaz‐Conradi, A., Romero‐Cortadellas, L., Ferrer‐Cortès, X., Olivella, M., Erlacher, M., Niemeyer, C., Wiesel, T., Pepperkok, R., Fleming, M. D., Kulozik, A. E., Sanchez, M., Muckenthaler, M. U.

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Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies von Zimoń, Magdalena, Baets, Jonathan, Auer-Grumbach, Michaela, Berciano, José, Garcia, Antonio, Lopez-Laso, Eduardo, Merlini, Luciano, Hilton-Jones, David, McEntagart, Meriel, Crosby, Andrew H., Barisic, Nina, Boltshauser, Eugen, Shaw, Christopher E., Landouré, Guida, Ludlow, Christy L., Gaudet, Rachelle, Houlden, Henry, Reilly, Mary M., Fischbeck, Kenneth H., Sumner, Charlotte J., Timmerman, Vincent, Jordanova, Albena, Jonghe, Peter De

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G.P.237 von Peeters, K, Litvinenko, I, Chamova, T, Asselbergh, B, Almeida-Souza, L, Geuens, T, Ydens, E, Zimon, M, Irobi, J, Vriendt, E. De, Winter, V. De, Ooms, T, Timmerman, V, Tournev, I, Jordanova, A

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Remdesivir Reduces Mortality in Hemato-Oncology Patients with COVID-19 von Aksak-Was, Bogusz Jan, Chober, Daniel, Serwin, Karol, Scheibe, Kaja, Niscigorska-Olsen, Jolanta, Niedzwiedz, Anna, Dobrowolska, Monika, Zybul, Katarzyna, Kubacka, Marta, Zimon, Agnieszka, Holda, Ewa, Miezynska-Kurtycz, Joanna, Gryczman, Marta, Jamro, Grzegorz, Szakola, Pawel, Parczewski, Milosz

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G.P.237: Autosomal-dominant spinal muscular atrophy due to mutations in BICD2 gene in Bulgarian patients von Peeters, K., Litvinenko, I., Chamova, T., Asselbergh, B., Almeida-Souza, L., Geuens, T., Ydens, E., Zimon, M., Irobi, J., Vriendt, E. De, Winter, V. De, Ooms, T., Timmerman, V., Tournev, I., Jordanova, A.

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OCENA LOGISTYKI MIEJSKIEJ W ZAKRESIE TRANSPORTU ZBIOROWEGO NA PRZYKŁADZIE TOMASZOWA MAZOWIECKIEGO I RZESZOWA von Zimon, Grzegorz, Gosik, Blanka

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Blastocyst versus day-3 embryo transfers: A comparison of fresh and thaw cycle cumulative outcomes von Zimon, Alison E, Witmyer, Jeannine, Reindollar, Richard H

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L239F founder mutation in GDAPI is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype von KABZINSKA, Dagmara, STRUGALSKA-CYNOWSKA, Halina, TIMMERMAN, Vincent, GUERGUELTCHEVA, Velina, TOURNEV, Ivailo, SARAFOV, Stayko, DE JONGHE, Peter, JORDANOVA, Albena, HAUSMANOWA-PETRUSEWICZ, Irena, KOCHANSKI, Andrzej, KOSTERA-PRUSZCZYK, Anna, RYNIEWICZ, Barbara, POSMYK, Renata, MIDRO, Alina, SEEMAN, Pavel, BARANKOVA, Lucia, ZIMON, Magdalena, BAETS, Jonathan

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A HIKER'S GUIDE TO ART OF THE CANADIAN ROCKIES. (2 nd edition) . Lisa Christensen A HIKER'S GUIDE TO THE ROCKY MOUNTAIN ART OF LAWREN HARRIS . Lisa Christensen von Zimon, Kathy E.

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