Rezultati - Hagit Flusser

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  1. 1
    Sleep Disturbances and Sensory Sensitivities Co-Vary in a Longitudinal Manner in Pre-School Children with Autism Spectrum Disorders

    Sleep Disturbances and Sensory Sensitivities Co-Vary in a Longitudinal Manner in Pre-School Children with Autism Spectrum Disorders od Liora Manelis‐Baram, Gal Meiri, Michal Ilan, Michal Faroy, Analya Michaelovski, Hagit Flusser, Idan Menashe, Ilan Dinstein

    Izdano 2021
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  2. 2
    The desmosterolosis phenotype: spasticity, microcephaly and micrognathia with agenesis of corpus callosum and loss of white matter

    The desmosterolosis phenotype: spasticity, microcephaly and micrognathia with agenesis of corpus callosum and loss of white matter od Jenny Zolotushko, Hagit Flusser, Barak Markus, Ilan Shelef, Yshaia Langer, Maura Heverin, Ingemar Björkhem, Sara Sivan, Ohad S. Birk

    Izdano 2011
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  3. 3
    Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish

    Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish od Yonatan Perez, Reut Bar-Yaacov, Rotem Kadir, Ohad Wormser, Ilan Shelef, Ohad S. Birk, Hagit Flusser, Ramon Y. Birnbaum

    Izdano 2019
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  4. 4
    A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta

    A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta od Michael Volodarsky, Barak Markus, Idan Cohen, Orna Staretz‐Chacham, Hagit Flusser, Daniella Landau, Ilan Shelef, Yshaia Langer, Ohad S. Birk

    Izdano 2013
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  5. 5
    Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation

    Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation od Yonatan Perez, Libe Gradstein, Hagit Flusser, Barak Markus, Idan Cohen, Yshaia Langer, Mira Marcus, Tova Lifshitz, Rotem Kadir, Ohad S. Birk

    Izdano 2013
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  6. 6
    Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ

    Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ od Ortal Barel, Zamir Shorer, Hagit Flusser, Rivka Ofir, Ginat Narkis, Gal Finer, Hanah Shalev, A El Nasasra, Ann Saada, Ohad S. Birk

    Izdano 2008
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  7. 7
    PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy

    PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy od Shareef Khateeb, Hagit Flusser, Rivka Ofir, Ilan Shelef, Ginat Narkis, Gideon Vardi, Zamir Shorer, Rachel Lévy, Aharon Galil, Khalil Elbedour, Ohad S. Birk

    Izdano 2006
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  8. 8
    Early diagnosis of autism in the community is associated with marked improvement in social symptoms within 1–2 years

    Early diagnosis of autism in the community is associated with marked improvement in social symptoms within 1–2 years od Nitzan Gabbay-Dizdar, Michal Ilan, Gal Meiri, Michal Faroy, Analya Michaelovski, Hagit Flusser, Idan Menashe, Judah Koller, Ditza A. Zachor, Ilan Dinstein

    Izdano 2021
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  9. 9
    Sleep disturbances are associated with specific sensory sensitivities in children with autism

    Sleep disturbances are associated with specific sensory sensitivities in children with autism od Orna Tzischinsky, Gal Meiri, Liora Manelis, Asif Bar‐Sinai, Hagit Flusser, Analya Michaelovski, Orit Zivan, Michal Ilan, Michal Faroy, Idan Menashe, Ilan Dinstein

    Izdano 2018
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  10. 10
    Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation

    Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation od Miora Feinstein, Barak Markus, Iris Noyman, Hannah Shalev, Hagit Flusser, Ilan Shelef, Keren Liani-Leibson, Zamir Shorer, Idan Cohen, Shareef Khateeb, Sara Sivan, Ohad S. Birk

    Izdano 2010
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  11. 11
    Brief Report: The Negev Hospital-University-Based (HUB) Autism Database

    Brief Report: The Negev Hospital-University-Based (HUB) Autism Database od Gal Meiri, Ilan Dinstein, Analya Michaelowski, Hagit Flusser, Michal Ilan, Michal Faroy, Asif Bar‐Sinai, Liora Manelis, Dana Stolowicz, Lili Lea Yosef, Nadav Davidovitch, Hava M. Golan, Shosh Arbelle, Idan Menashe

    Izdano 2017
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  12. 12
    Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy

    Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy od 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

    Izdano 2010
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  13. 13
    SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome

    SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome od Ohad Wormser, Libe Gradstein, Yuval Yogev, Yonatan Perez, Rotem Kadir, Inna Goliand, Yair Sadka, Saad El Riati, Hagit Flusser, Dikla Nachmias, Ruth Birk, Muhamad Iraqi, Einat Kadar, Roni Gat, Max Drabkin, Daniel Halpérin, Amir Horev, Sara Sivan, Uri Abdu, Natalie Elia, Ohad S. Birk

    Izdano 2019
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