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Journal Abstract Search

288 related items for PubMed ID: 24282181

  • 1. Mowat-Wilson syndrome: deafness in the first Egyptian case who was conceived by intracytoplasmic sperm injection.
    Abdalla EM, Zayed LH.
    J Child Neurol; 2014 Dec; 29(12):NP168-70. PubMed ID: 24282181
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  • 4. ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome.
    Ghoumid J, Drevillon L, Alavi-Naini SM, Bondurand N, Rio M, Briand-Suleau A, Nasser M, Goodwin L, Raymond P, Yanicostas C, Goossens M, Lyonnet S, Mowat D, Amiel J, Soussi-Yanicostas N, Giurgea I.
    Hum Mol Genet; 2013 Jul 01; 22(13):2652-61. PubMed ID: 23466526
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  • 7. The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
    Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N.
    Am J Med Genet A; 2014 Aug 01; 164A(8):1899-908. PubMed ID: 24715670
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  • 11. Polymicrogyria in a 10-month-old boy with Mowat-Wilson syndrome.
    Murray SB, Spangler BB, Helm BM, Vergano SS.
    Am J Med Genet A; 2015 Oct 01; 167A(10):2402-5. PubMed ID: 26012591
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  • 14. [Mowat-Wilson syndrome: a report of three Danish cases].
    Nissen KB, Søndergaard C, Thelle T, Møller RS.
    Ugeskr Laeger; 2011 Sep 05; 173(36):2199-200. PubMed ID: 21893004
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  • 18. Mowat-Wilson syndrome: the first report of an association with central nervous system tumors.
    Valera ET, Ferraz ST, Brassesco MS, Zhen X, Shen Y, dos Santos AC, Neder L, Oliveira RS, Scrideli CA, Tone LG.
    Childs Nerv Syst; 2013 Dec 05; 29(12):2151-5. PubMed ID: 24092421
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  • 20. Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants.
    Nardello R, Fontana A, Mangano GD, Efthymiou S, Salpietro V, Houlden H, Mangano S.
    Epileptic Disord; 2020 Feb 01; 22(1):111-115. PubMed ID: 32031527
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