Search Results - Haviv, Ami

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  1. 1
    A-to-I RNA editing occurs at over a hundred million genomic sites, located in a majority of human genes

    A-to-I RNA editing occurs at over a hundred million genomic sites, located in a majority of human genes by Bazak, Lily, Haviv, Ami, Barak, Michal, Jacob-Hirsch, Jasmine, Deng, Patricia, Zhang, Rui, Isaacs, Farren J, Rechavi, Gideon, Li, Jin Billy, Eisenberg, Eli, Levanon, Erez Y

    Published in Genome research
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  2. 2
    Microcephaly Thin Corpus Callosum Intellectual Disability Syndrome Caused by Mutated TAF2

    Microcephaly Thin Corpus Callosum Intellectual Disability Syndrome Caused by Mutated TAF2 by Hellman-Aharony, Shlomit, MSc, Smirin-Yosef, Pola, MSc, Halevy, Ayelet, MD, Pasmanik-Chor, Metsada, PhD, Yeheskel, Adva, MSc, Har-Zahav, Adi, MSc, Maya, Idit, MD, Straussberg, Rachel, MD, Dahary, Dvir, MSc, Haviv, Ami, PhD, Shohat, Mordechai, MD, Basel-Vanagaite, Lina, MD, PhD

    Published in Pediatric neurology
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  3. 3
    Biallelic SZT2 Mutations Cause Infantile Encephalopathy with Epilepsy and Dysmorphic Corpus Callosum

    Biallelic SZT2 Mutations Cause Infantile Encephalopathy with Epilepsy and Dysmorphic Corpus Callosum by Basel-Vanagaite, Lina, Hershkovitz, Tova, Heyman, Eli, Raspall-Chaure, Miquel, Kakar, Naseebullah, Smirin-Yosef, Pola, Vila-Pueyo, Marta, Kornreich, Liora, Thiele, Holger, Bode, Harald, Lagovsky, Irina, Dahary, Dvir, Haviv, Ami, Hubshman, Monika Weisz, Pasmanik-Chor, Metsada, Nürnberg, Peter, Gothelf, Doron, Kubisch, Christian, Shohat, Mordechai, Macaya, Alfons, Borck, Guntram

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  4. 4
    Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene

    Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene by Blumkin, Lubov, Halevy, Ayelet, Ben-Ami-Raichman, Dominique, Dahari, Dvir, Haviv, Ami, Sarit, Cohen, Lev, Dorit, van der Knaap, Marjo S., Lerman-Sagie, Tally, Leshinsky-Silver, Esther

    Published in Neurogenetics
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  5. 5
    Reply to: The many faces of TUBB4A mutations

    Reply to: The many faces of TUBB4A mutations by Blumkin, Lubov, Halevy, Ayelet, Ben-Ami-Raichman, Dominique, Dahari, Dvir, Haviv, Ami, Sarit, Cohen, Lev, Dorit, van der Knaap, Marjo S., Lerman-Sagie, Tally, Leshinsky-Silver, Esther

    Published in Neurogenetics
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  6. 6
    Erratum to: Expansion of the spectrum of TUBB4A-related disorders: A new phenotype associated with a novel mutation in the TUBB4A gene

    Erratum to: Expansion of the spectrum of TUBB4A-related disorders: A new phenotype associated with a novel mutation in the TUBB4A gene by Blumkin, Lubov, Halevy, Ayelet, Ben-Ami-Raichman, Dominique, Dahari, Dvir, Haviv, Ami, Sarit, Cohen, Lev, Dorit, van der Knaap, Marjo S., Lerman-Sagie, Tally, Leshinsky-Silver, Esther

    Published in Neurogenetics
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  7. 7
    Towards a Diagrammatic Analogue of the Reshetikhin-Turaev Link Invariants

    Towards a Diagrammatic Analogue of the Reshetikhin-Turaev Link Invariants by Haviv, Ami

    Published in arXiv.org
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  8. 8
    The Duistermaat-Heckman Measure for the Coadjoint Orbits of Compact Semisimple Lie Groups

    The Duistermaat-Heckman Measure for the Coadjoint Orbits of Compact Semisimple Lie Groups by Haviv, Ami

    Published in arXiv.org
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  9. 9
    Once-Weekly Somapacitan vs Daily GH in Children With GH Deficiency: Results From a Randomized Phase 2 Trial

    Once-Weekly Somapacitan vs Daily GH in Children With GH Deficiency: Results From a Randomized Phase 2 Trial by Sävendahl, Lars, Battelino, Tadej, Brod, Meryl, Højby Rasmussen, Michael, Horikawa, Reiko, Juul, Rasmus Vestergaard, Saenger, Paul

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  10. 10
    Effect of enoxaparin on homocysteine concentration in warfarin-treated patients

    Effect of enoxaparin on homocysteine concentration in warfarin-treated patients by Haviv, Y, Lubetsky, A, Sela, BA, Ezra, D, Olchovsky, D

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