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Journal Abstract Search

398 related items for PubMed ID: 23322667

  • 1.
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  • 2. Sleep disturbance in Mowat-Wilson syndrome.
    Evans E, Mowat D, Wilson M, Einfeld S.
    Am J Med Genet A; 2016 Mar; 170(3):654-60. PubMed ID: 26686679
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  • 3. 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; 164A(8):1899-908. PubMed ID: 24715670
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  • 5. Mowat-Wilson syndrome.
    Garavelli L, Mainardi PC.
    Orphanet J Rare Dis; 2007 Oct 24; 2():42. PubMed ID: 17958891
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  • 7. Mowat-Wilson syndrome presenting with fever-associated seizures.
    Seo SE, Kim SH, Lee ST, Choi JR, Lee JS, Kim HD, Kang HC.
    Epileptic Disord; 2017 Dec 01; 19(4):481-485. PubMed ID: 29258970
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  • 8. Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS).
    Moore SW, Fieggen K, Honey E, Zaahl M.
    J Pediatr Surg; 2016 Feb 01; 51(2):268-71. PubMed ID: 26852091
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  • 10. [Clinical features of epilepsy in 5 children with Mowat-Wilson syndrome].
    Ju Y, Ji TY.
    Zhonghua Er Ke Za Zhi; 2022 Jun 02; 60(6):578-582. PubMed ID: 35658366
    [Abstract] [Full Text] [Related]

  • 11. The behavioral phenotype of Mowat-Wilson syndrome.
    Evans E, Einfeld S, Mowat D, Taffe J, Tonge B, Wilson M.
    Am J Med Genet A; 2012 Feb 02; 158A(2):358-66. PubMed ID: 22246645
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  • 13. Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencing.
    Babkina N, Deignan JL, Lee H, Vilain E, Sankar R, Giurgea I, Mowat D, Graham JM.
    Eur J Med Genet; 2016 Feb 02; 59(2):70-4. PubMed ID: 26721324
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  • 14. Mowat Wilson syndrome and Hirschsprung disease: a retrospective study on functional outcomes.
    Dagorno C, Pio L, Capri Y, Ali L, Giurgea I, Qoshe L, Morcrette G, Julien-Marsollier F, Sommet J, Chomton M, Berrebi D, Bonnard A.
    Pediatr Surg Int; 2020 Nov 02; 36(11):1309-1315. PubMed ID: 32980962
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  • 16. 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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  • 20. A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.
    Kilic E, Cetinkaya A, Utine GE, Boduroğlu K.
    J Child Neurol; 2016 Jun 01; 31(7):913-7. PubMed ID: 26809768
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