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Journal Abstract Search

160 related items for PubMed ID: 24092421

  • 1. 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; 29(12):2151-5. PubMed ID: 24092421
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS).
    Moore SW, Fieggen K, Honey E, Zaahl M.
    J Pediatr Surg; 2016 Feb; 51(2):268-71. PubMed ID: 26852091
    [Abstract] [Full Text] [Related]

  • 4. 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; 167A(10):2402-5. PubMed ID: 26012591
    [Abstract] [Full Text] [Related]

  • 5. Mowat-Wilson syndrome in a Chinese population: A case series.
    Ho S, Luk HM, Chung BH, Fung JL, Mak HH, Lo IFM.
    Am J Med Genet A; 2020 Jun; 182(6):1336-1341. PubMed ID: 32196960
    [Abstract] [Full Text] [Related]

  • 6. A new finding in a patient with Mowat Wilson syndrome: peripupillary atrophy and gingival hypertrophy.
    Kiraz A, Aldemir O, Karabulut Y, Turan C, Dundar M.
    Genet Couns; 2013 Jun; 24(1):61-8. PubMed ID: 23610866
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. Sleep disturbance in Mowat-Wilson syndrome.
    Evans E, Mowat D, Wilson M, Einfeld S.
    Am J Med Genet A; 2016 Mar 01; 170(3):654-60. PubMed ID: 26686679
    [Abstract] [Full Text] [Related]

  • 9. Difficult airway in Mowat-Wilson syndrome.
    Packiasabapathy S, Chandiran R, Batra RK, Agarwala S.
    J Clin Anesth; 2016 Nov 01; 34():151-3. PubMed ID: 27687363
    [Abstract] [Full Text] [Related]

  • 10. ZEB2 gene mutation and duplication of 22q11.23 in Mowat-Wilson syndrome.
    Buraniqi E, Moodley M.
    J Child Neurol; 2015 Jan 01; 30(1):32-6. PubMed ID: 25028418
    [Abstract] [Full Text] [Related]

  • 11. CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases.
    Wenger TL, Harr M, Ricciardi S, Bhoj E, Santani A, Adam MP, Barnett SS, Ganetzky R, McDonald-McGinn DM, Battaglia D, Bigoni S, Selicorni A, Sorge G, Monica MD, Mari F, Andreucci E, Romano S, Cocchi G, Savasta S, Malbora B, Marangi G, Garavelli L, Zollino M, Zackai EH.
    Am J Med Genet A; 2014 Oct 01; 164A(10):2557-66. PubMed ID: 25123255
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Hirschsprung's disease in children with Mowat-Wilson syndrome.
    Coyle D, Puri P.
    Pediatr Surg Int; 2015 Aug 01; 31(8):711-7. PubMed ID: 26156877
    [Abstract] [Full Text] [Related]

  • 14. Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndrome.
    Bourchany A, Giurgea I, Thevenon J, Goldenberg A, Morin G, Bremond-Gignac D, Paillot C, Lafontaine PO, Thouvenin D, Massy J, Duncombe A, Thauvin-Robinet C, Masurel-Paulet A, Chehadeh SE, Huet F, Bron A, Creuzot-Garcher C, Lyonnet S, Faivre L.
    Am J Med Genet A; 2015 Jul 01; 167(7):1587-92. PubMed ID: 25899569
    [Abstract] [Full Text] [Related]

  • 15. Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome.
    Jakubiak A, Szczałuba K, Badura-Stronka M, Kutkowska-Kaźmierczak A, Jakubiuk-Tomaszuk A, Chilarska T, Pilch J, Braun-Walicka N, Castaneda J, Wołyńska K, Wiśniewska M, Kugaudo M, Bielecka M, Pesz K, Wierzba J, Latos-Bieleńska A, Obersztyn E, Krajewska-Walasek M, Śmigiel R.
    J Appl Genet; 2021 Sep 01; 62(3):477-485. PubMed ID: 33982229
    [Abstract] [Full Text] [Related]

  • 16. Co-occurrence of rhabdomyosarcoma and Mowat-Wilson syndrome: is there a connection?
    Rogac M, Kitanovski L, Writzl K.
    Clin Dysmorphol; 2017 Jul 01; 26(3):185-186. PubMed ID: 28230647
    [No Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

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  • 19. Neuropathology of Mowat-Wilson Syndrome.
    Conces MR, Hughes A, Pierson CR.
    Pediatr Dev Pathol; 2020 Aug 01; 23(4):322-325. PubMed ID: 32252596
    [Abstract] [Full Text] [Related]

  • 20. [Clinical and genetic features of Mowat-Wilson syndrome: an analysis of 3 cases].
    Wang H, Yan YC, Li Q, Zhang Z, Xiao P, Yuan XY, Li L, Jiang Q.
    Zhongguo Dang Dai Er Ke Za Zhi; 2019 May 01; 21(5):468-473. PubMed ID: 31104665
    [Abstract] [Full Text] [Related]

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