Search Results - Dorit Lev

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  1. 1
    The fetal cerebellum. Pitfalls in diagnosis and management

    The fetal cerebellum. Pitfalls in diagnosis and management by G. Malinger, Dorit Lev, Tally Lerman‐Sagie

    Published 2009
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  2. 2
    Sonographic developmental milestones of the fetal cerebral cortex: a longitudinal study

    Sonographic developmental milestones of the fetal cerebral cortex: a longitudinal study by Bina Cohen-Sacher, Tally Lerman‐Sagie, Dorit Lev, G. Malinger

    Published 2006
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  3. 3
    Developmental outcome of isolated fetal microcephaly

    Developmental outcome of isolated fetal microcephaly by Shiri Stoler-Poria, Dorit Lev, Avraham Schweiger, T. Lerman‐Sagie, G. Malinger

    Published 2010
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  4. 4
    A normal second‐trimester ultrasound does not exclude intracranial structural pathology

    A normal second‐trimester ultrasound does not exclude intracranial structural pathology by G. Malinger, Tally Lerman‐Sagie, Nathan Watemberg, Siegfried Rotmensch, Dorit Lev, Marek Glezerman

    Published 2002
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  5. 5
    Differential diagnosis in fetuses with absent septum pellucidum

    Differential diagnosis in fetuses with absent septum pellucidum by G. Malinger, Dorit Lev, Dvora Kidron, Fernando Martínez Heredia, R. Hershkovitz, Tally Lerman‐Sagie

    Published 2004
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  6. 6
    Fetal brain imaging: a comparison between magnetic resonance imaging and dedicated neurosonography

    Fetal brain imaging: a comparison between magnetic resonance imaging and dedicated neurosonography by G. Malinger, Liat Ben‐Sira, Dorit Lev, Zahi Ben-Aroya, Devora Kidron, Tally Lerman‐Sagie

    Published 2004
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  7. 7
    Prenatal diagnosis of malformations of cortical development by dedicated neurosonography

    Prenatal diagnosis of malformations of cortical development by dedicated neurosonography by G. Malinger, Debora Kidron, Letizia Schreiber, Liat Ben‐Sira, Chen Hoffmann, Dorit Lev, T. Lerman‐Sagie

    Published 2007
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  8. 8
    Fetal optic nerve sheath measurement as a non‐invasive tool for assessment of increased intracranial pressure

    Fetal optic nerve sheath measurement as a non‐invasive tool for assessment of increased intracranial pressure by Karina Krajden Haratz, Fernando Nuez Viñals, Dorit Lev, Hagit Feit, Liat Ben‐Sira, Tally Lerman‐Sagie, G. Malinger

    Published 2011
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  9. 9
    Mutations of the Thyroid Hormone Transporter MCT8 Cause Prenatal Brain Damage and Persistent Hypomyelination

    Mutations of the Thyroid Hormone Transporter MCT8 Cause Prenatal Brain Damage and Persistent Hypomyelination by Daniela López-Espíndola, Carmen Morales-Bastos, Carmen Grijota-Martínez, Xiao-Hui Liao, Dorit Lev, Ella Sugo, Charles F. Verge, Samuel Refetoff, Juan Bernal, Ana Guadaño‐Ferraz

    Published 2014
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  10. 10
    Megalencephaly‐capillary malformation (MCAP) and megalencephaly‐polydactyly‐polymicrogyria‐hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis

    Megalencephaly‐capillary malformation (MCAP) and megalencephaly‐polydactyly‐polymicrogyria‐hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abn... by Ghayda Mirzaa, Robert L. Conway, Karen W. Gripp, Tally Lerman‐Sagie, Dawn H. Siegel, Linda S. deVries, Dorit Lev, Nancy Kramer, Elizabeth Hopkins, John M. Graham, William B. Dobyns

    Published 2012
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  11. 11
    OC21.02: Brainstem malformations in severe fetal ventriculomegaly

    OC21.02: Brainstem malformations in severe fetal ventriculomegaly by Karina Krajden Haratz, Z. Leibovitz, P.S. Oliveira, G. Malinger, Antônio Fernandes Moron, L. Gindes, Dorit Lev, M. Tamarkin, Y. Shalev, Nili Raz, Lotem Dafna, J. Har‐Toov, Andrea Poretti, T. Lerman‐Sagie

    Published 2018
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  12. 12
    Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy

    Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy by Orly Agamy, Bruria Ben Zeev, Dorit Lev, Barak Marcus, Dina Fine, Dan Su, Ginat Narkis, Rivka Ofir, Chen Hoffmann, Esther Leshinsky‐Silver, Hagit Flusser, Sara Sivan, Dieter Söll, Tally Lerman‐Sagie, Ohad S. Birk

    Published 2010
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  13. 13
    Association Between Osteosarcoma and Deleterious Mutations in the RECQL4 Gene in Rothmund-Thomson Syndrome

    Association Between Osteosarcoma and Deleterious Mutations in the RECQL4 Gene in Rothmund-Thomson Syndrome by Liangliang Wang, Anu Gannavarapu, Claudia A. Kozinetz, Moise L. Levy, Richard A. Lewis, Murali Chintagumpala, R. Ruiz-Maldanado, José Contreras‐Ruiz, Christopher Cunniff, Robert P. Erickson, Dorit Lev, Maureen Rogers, Elaine H. Zackai, Sharon E. Plon

    Published 2003
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  14. 14
    Prediction of microcephaly at birth using three reference ranges for fetal head circumference: can we improve prenatal diagnosis?

    Prediction of microcephaly at birth using three reference ranges for fetal head circumference: can we improve prenatal diagnosis? by Z. Leibovitz, Etty Daniel‐Spiegel, G. Malinger, Karina Krajden Haratz, M. Tamarkin, L. Gindes, Letizia Schreiber, Liat Ben‐Sira, Dorit Lev, I. Shapiro, H. Bakry, B. Weizman, A. Zreik, S. Egenburg, Ayala Arad, R. Tepper, Debora Kidron, Tally Lerman‐Sagie

    Published 2015
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  15. 15
    <i><scp>GRIN</scp>1</i> mutations cause encephalopathy with infantile‐onset epilepsy, and hyperkinetic and stereotyped movement disorders

    <i><scp>GRIN</scp>1</i> mutations cause encephalopathy with infantile‐onset epilepsy, and hyperkinetic and stereotyped movement disorders by Chihiro Ohba, Masaaki Shiina, Jun Tohyama, Kazuhiro Haginoya, Tally Lerman‐Sagie, Nobuhiko Okamoto, Lubov Blumkin, Dorit Lev, Souichi Mukaida, Fumihito Nozaki, Mitsugu Uematsu, Akira Onuma, Hirofumi Kodera, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Fumiaki Tanaka, Mitsuhiro Kato, Kazuhiro Ogata, Hirotomo Saitsu, Naomichi Matsumoto

    Published 2015
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  16. 16
    Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus

    Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus by Robyn H. Wallace, Ingrid E. Scheffer, Shaun Barnett, M. Richards, Leanne M. Dibbens, R. Desai, Tally Lerman‐Sagie, Dorit Lev, Aziz Mazarib, Nathan Brand, Bruria Ben‐Zeev, Igor Goikhman, Rita Singh, Gabriel Kremmidiotis, Alison Gardner, G.R. Sutherland, Alfred L. George, John C. Mulley, Samuel F. Berkovic

    Published 2001
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  17. 17
    Central 22q11.2 deletions

    Central 22q11.2 deletions by Patrick Rump, Nicole de Leeuw, Anthonie J. van Essen, Corien C. Verschuuren‐Bemelmans, Hermine E. Veenstra‐Knol, Mariëlle E.M. Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, William Reardon, Sonja de Munnik, Mariken Ruiter, Ayala Frumkin, Dorit Lev, Christina Evers, Birgit Sikkema‐Raddatz, Trijnie Dijkhuizen, Conny M.A. van Ravenswaaij‐Arts

    Published 2014
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  18. 18
    Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

    Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families by Zippora Brownstein, Lilach M. Friedman, Hashem Shahin, Varda Oron‐Karni, Nitzan Kol, Amal Abu Rayyan, Thomas Parzefall, Dorit Lev, Stavit A. Shalev, Moshe Frydman, Bella Davidov, Mordechai Shohat, Michele Rahile, Sari Lieberman, Ephrat Levy‐Lahad, Ming K. Lee, Noam Shomron, Mary‐Claire King, Tom Walsh, Moien Kanaan, Karen B. Avraham

    Published 2011
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  19. 19
    De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy

    De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy by Sahar Esmaeeli Nieh, Maura R.Z. Madou, Minhajuddin Sirajuddin, Brieana Fregeau, Dianalee McKnight, Katrina W. Lexa, Jonathan B. Strober, Christine G. Spaeth, Barbara Hallinan, Nizar Smaoui, John Pappas, Thomas Andrew Burrow, Marie McDonald, Mariam Latibashvili, Esther Leshinsky‐Silver, Dorit Lev, Luba Blumkin, Ronald D. Vale, A. James Barkovich, Elliott H. Sherr

    Published 2015
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  20. 20
    Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy

    Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy by Hirofumi Kodera, Mitsuhiro Kato, Alex S. Nord, Tom Walsh, Ming Lee, Gaku Yamanaka, Jun Tohyama, Kazuyuki Nakamura, Eiji Nakagawa, Tae Ikeda, Bruria Ben‐Zeev, Dorit Lev, Tally Lerman‐Sagie, Rachel Straussberg, Saori Tanabe, Kazutoshi Ueda, Masano Amamoto, Sayaka Ohta, Yutaka Nonoda, Kiyomi Nishiyama, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Kiyoshi Hayasaka, Mary‐Claire King, Naomichi Matsumoto, Hirotomo Saitsu

    Published 2013
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