These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

246 related items for PubMed ID: 26012591

  • 1. 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]

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

  • 3. 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; 158A(2):358-66. PubMed ID: 22246645
    [Abstract] [Full Text] [Related]

  • 4. 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; 164A(10):2557-66. PubMed ID: 25123255
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

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

  • 7. 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]

  • 8. 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; 167(7):1587-92. PubMed ID: 25899569
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Clinical utility gene card for: Mowat-Wilson syndrome.
    Zollino M, Garavelli L, Rauch A.
    Eur J Hum Genet; 2011 Aug 01; 19(8):. PubMed ID: 21343952
    [No Abstract] [Full Text] [Related]

  • 11. [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
    [Abstract] [Full Text] [Related]

  • 12. Mowat-Wilson syndrome associated with craniosynostosis.
    Hartill VL, Pendlebury M, Hobson E.
    Clin Dysmorphol; 2014 Jan 05; 23(1):16-19. PubMed ID: 24300291
    [No Abstract] [Full Text] [Related]

  • 13. Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
    Ariss M, Natan K, Friedman N, Traboulsi EI.
    Ophthalmic Genet; 2012 Sep 05; 33(3):159-60. PubMed ID: 22486326
    [Abstract] [Full Text] [Related]

  • 14. Mowat-Wilson syndrome.
    Mowat DR, Wilson MJ, Goossens M.
    J Med Genet; 2003 May 05; 40(5):305-10. PubMed ID: 12746390
    [Abstract] [Full Text] [Related]

  • 15. Recurrence of Mowat-Wilson syndrome in siblings with the same proven mutation.
    McGaughran J, Sinnott S, Dastot-Le Moal F, Wilson M, Mowat D, Sutton B, Goossens M.
    Am J Med Genet A; 2005 Sep 01; 137A(3):302-4. PubMed ID: 16088920
    [Abstract] [Full Text] [Related]

  • 16. A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype.
    Heinritz W, Zweier C, Froster UG, Strenge S, Kujat A, Syrbe S, Rauch A, Schuster V.
    Am J Med Genet A; 2006 Jun 01; 140(11):1223-7. PubMed ID: 16688751
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
    Garavelli L, Zollino M, Mainardi PC, Gurrieri F, Rivieri F, Soli F, Verri R, Albertini E, Favaron E, Zignani M, Orteschi D, Bianchi P, Faravelli F, Forzano F, Seri M, Wischmeijer A, Turchetti D, Pompilii E, Gnoli M, Cocchi G, Mazzanti L, Bergamaschi R, De Brasi D, Sperandeo MP, Mari F, Uliana V, Mostardini R, Cecconi M, Grasso M, Sassi S, Sebastio G, Renieri A, Silengo M, Bernasconi S, Wakamatsu N, Neri G.
    Am J Med Genet A; 2009 Mar 01; 149A(3):417-26. PubMed ID: 19215041
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.
    Spaggiari E, Baumann C, Alison M, Oury JF, Belarbi N, Dupont C, Guimiot F, Delezoide AL.
    Eur J Med Genet; 2013 Jun 01; 56(6):297-300. PubMed ID: 23523603
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.