Výsledky vyhledávání - Yuval Yaron

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  1. 1
    The implications of non-invasive prenatal testing failures: a review of an under-discussed phenomenon

    The implications of non-invasive prenatal testing failures: a review of an under-discussed phenomenon Autor Yuval Yaron

    Vydáno 2016
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  2. 2
    Difficult or repeated sequential embryo transfers do not adversely affect in-vitro fertilization pregnancy rates or outcome

    Difficult or repeated sequential embryo transfers do not adversely affect in-vitro fertilization pregnancy rates or outcome Autor Ilan Tur-Kaspa, Yuval Yaron, David Bider, Jacob Levron, Adrian Shulman, Dor J

    Vydáno 1998
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  3. 3
    High prevalence of the prothrombin gene mutation in women with intrauterine growth retardation, abruptio placentae and second trimester loss

    High prevalence of the prothrombin gene mutation in women with intrauterine growth retardation, abruptio placentae and second trimester loss Autor Michael J. Kupferminc, Hava Peri, Eti Zwang, Yuval Yaron, Igal Wolman, Amiram Eldor

    Vydáno 2000
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  4. 4
    Endometrial receptivity: the age-related decline in pregnancy rates and the effect of ovarian function

    Endometrial receptivity: the age-related decline in pregnancy rates and the effect of ovarian function Autor Yuval Yaron, Amnon Botchan, Ami Amit, Abraham Kogosowski, Israel Yovel, Joseph B. Lessing

    Vydáno 1993
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  5. 5
    An evidence-based scoring system for prioritizing mosaic aneuploid embryos following preimplantation genetic screening

    An evidence-based scoring system for prioritizing mosaic aneuploid embryos following preimplantation genetic screening Autor Francesca Romana Grati, Gloria Gallazzi, Lara Branca, Federico Maggi, Giuseppe Simoni, Yuval Yaron

    Vydáno 2018
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  6. 6
    Circulating autoimmune antibodies may be responsible for implantation failure in in vitro fertilization

    Circulating autoimmune antibodies may be responsible for implantation failure in in vitro fertilization Autor Eli Geva, Yuval Yaron, Joseph B. Lessing, Israel Yovel, Nurit Vardinon, Michael Burke, Ami Amit

    Vydáno 1994
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  7. 7
    Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potential

    Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potential Autor Shiri Barbash‐Hazan, Tsvia Frumkin, Mira Malcov, Yuval Yaron, Tania Cohen, Foad Azem, Ami Amit, Dalit Ben‐Yosef

    Vydáno 2008
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  8. 8
    Prednisone and Aspirin Improve Pregnancy Rate in Patients with Reproductive Failure and Autoimmune Antibodies: A Prospective Study

    Prednisone and Aspirin Improve Pregnancy Rate in Patients with Reproductive Failure and Autoimmune Antibodies: A Prospective Study Autor Eli Geva, Ami Amit, Liat Lerner‐Geva, Yuval Yaron, Yair Daniel, Tamar Schwartz, Foad Azem, Israel Yovel, Joseph B. Lessing

    Vydáno 2000
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  9. 9
    Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos

    Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos Autor Rachel Eiges, Achia Urbach, Mira Malcov, Tsvia Frumkin, Tamar Schwartz, Ami Amit, Yuval Yaron, Amir Eden, Ofra Yanuka, Nissim Benvenisty, Dalit Ben‐Yosef

    Vydáno 2007
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  10. 10
    Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog

    Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog Autor Ashley M Byrnes, Lemuel Racacho, Allison Grimsey, Louanne Hudgins, Andrea Kwan, Michel Sangalli, Alexa Kidd, Yuval Yaron, YL Lau, Sarah M. Nikkel, Dennis E. Bulman

    Vydáno 2009
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  11. 11
    International Society for Prenatal Diagnosis Position Statement: cell free (cf)<scp>DNA</scp> screening for Down syndrome in multiple pregnancies

    International Society for Prenatal Diagnosis Position Statement: cell free (cf)<scp>DNA</scp> screening for Down syndrome in multiple pregnancies Autor Glenn E. Palomaki, Rossa W. K. Chiu, Mark D. Pertile, Erik A. Sistermans, Yuval Yaron, Joris Vermeesch, Neeta L. Vora, Robert G. Best, Louise Wilkins‐Haug

    Vydáno 2020
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  12. 12
    Aneuploidy screening: a position statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, January 2011

    Aneuploidy screening: a position statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, January 2011 Autor Peter Benn, A. Borrell, Jenny Crossley, Howard Cuckle, Lorraine Dugoff, Susan J. Gross, Jo-Ann Johnson, Ron Maymon, Anthony Odibo, Peter C. J. I. Schielen, Kevin Spencer, Dave Wright, Yuval Yaron

    Vydáno 2011
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  13. 13
    A Novel Founder Mutation in the RNASEL Gene, 471delAAAG, Is Associated with Prostate Cancer in Ashkenazi Jews

    A Novel Founder Mutation in the RNASEL Gene, 471delAAAG, Is Associated with Prostate Cancer in Ashkenazi Jews Autor Hanna Rennert, Dani Bercovich, Ayala Hubert, Dvora Abeliovich, Uri Rozovsky, Anat Bar‐Shira, С. А. Соловьёв, Letizia Schreiber, Haim Matzkin, Gad Rennert, Luna Kadouri, Tamar Peretz, Yuval Yaron, Avi Orr‐Urtreger

    Vydáno 2002
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  14. 14
    Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies

    Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies Autor Yuval Yaron, Vered Ofen Glassner, Adi Mory, Noa Zunz Henig, Alina Kurolap, Anat Bar Shira, D. Brabbing Goldstein, Daphna Marom, Liat Ben‐Sira, Hagit Baris Feldman, G. Malinger, Karina Krajden Haratz, Adi Reches

    Vydáno 2022
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  15. 15
    Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

    Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis Autor Peter Benn, Antoni Borell, Rossa W. K. Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte H. W. Faas, Susan J. Gross, Jo‐Ann Johnson, Ron Maymon, Mary E. Norton, Anthony Odibo, Peter C. J. I. Schielen, Kevin Spencer, Tianhua Huang, Dave Wright, Yuval Yaron

    Vydáno 2013
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  16. 16
    Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature

    Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature Autor Bert Callewaert, Bart Loeys, Anna Ficcadenti, Sascha Vermeer, Magnus Landgren, Hester Y. Kroes, Yuval Yaron, Michael Pope, Nicola Foulds, Odile Boute, Francisco Galán, Helen Kingston, Nathalie Van der Aa, Iratxe Salcedo, Mariëlle E.M. Swinkels, Carina Wallgren‐Pettersson, Orazio Gabrielli, Julie De Backer, Paul Coucke, Anne M. De Paepe

    Vydáno 2008
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  17. 17
    Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

    Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes Autor Enza Maria Valente, Clare V. Logan, Soumaya Mougou-Zerelli, Jeong Ho Lee, Jennifer L. Silhavy, Francesco Brancati, Miriam Iannicelli, Lorena Travaglini, Sveva Romani, Barbara Illi, Matthew Adams, Katarzyna Szymańska, Annalisa Mazzotta, Ji Eun Lee, Jerlyn C. Tolentino, Dominika Swistun, Carmelo Salpietro, Carmelo Fede, Stacey Gabriel, Carsten Russ, Kristian Cibulskis, Carrie Sougnez, Friedhelm Hildebrandt, Edgar A. Otto, Susanne Held, Bill H. Diplas, Erica E. Davis, Mario Mikula, Charles M. Strom, Bruria Ben‐Zeev, Dorit Lev, T. Sagie, Marina Michelson, Yuval Yaron, Amanda Krause, Eugen Boltshauser, Nadia Elkhartoufi, J. Roume, Stavit A. Shalev, Arnold Münnich, Sophie Saunier, Chris F. Inglehearn, Ali Saâd, Adila Al‐Kindy, Sophie Thomas, Michel Vekemans, Bruno Dallapiccola, Nicholas Katsanis, Colin A. Johnson, Tania Attié‐Bitach, Joseph G. Gleeson

    Vydáno 2010
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  18. 18
    Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

    Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease Autor Daniel G. Calame, Tianyu Guo, Chen Wang, Lillian Garrett, Angad Jolly, Moez Dawood, Alina Kurolap, Noa Zunz Henig, Jawid M. Fatih, Isabella Herman, Haowei Du, Tadahiro Mitani, Lore Becker, Birgit Rathkolb, Raffaele Gerlini, Claudia Seisenberger, Susan Marschall, Jill V. Hunter, Amanda Gerard, Alexis R. Heidlebaugh, Thomas D. Challman, Rebecca C. Spillmann, Shalini N. Jhangiani, Zeynep Coban‐Akdemir, Seema R. Lalani, Lingxiao Liu, Anya Revah‐Politi, Alejandro Iglesias, Edwin R. Guzman, Evan H. Baugh, Nathalie Boddaert, Sophie Rondeau, Clothide Ormieres, Giulia Barcia, Queenie K.‐G. Tan, Isabelle Thiffault, Tomi Pastinen, Kazim A. Sheikh, Suur Biliciler, Davide Mei, Federico Melani, Vandana Shashi, Yuval Yaron, Mary Steele, Emma Wakeling, Elsebet Østergaard, Lusine Nazaryan‐Petersen, Francisca Millan, Teresa Santiago‐Sim, Julien Thévenon, Ange‐Line Bruel, Christel Thauvin‐Robinet, Denny Popp, Konrad Platzer, Paweł Gawliński, Wojciech Wiszniewski, Dana Marafi, Davut Pehli̇van, Jennifer E. Posey, Richard A. Gibbs, Valérie Gailus‐Durner, Renzo Guerrini, Helmut Fuchs, Martin Hrabě de Angelis, Sabine M. Hölter, Hoi‐Hung Cheung, Shen Gu, James R. Lupski

    Vydáno 2023
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