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Journal Abstract Search

230 related items for PubMed ID: 31321886

  • 21. A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.
    Kilic E, Cetinkaya A, Utine GE, Boduroğlu K.
    J Child Neurol; 2016 Jun; 31(7):913-7. PubMed ID: 26809768
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  • 22. [Analysis of a case with Mowat-Wilson syndrome caused by ZEB2 gene variant].
    Ma J, Liu Y, Zhang K, Lyu Y, Gao M, Wang D, Gai Z, Liu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May 10; 37(5):539-542. PubMed ID: 32335881
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  • 23. 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 10; 182(6):1336-1341. PubMed ID: 32196960
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  • 26. [Analysis of a case with Mowat-Wilson syndrome due to nonsense variant of ZEB2 gene].
    She M, Zhao Z, Shi P, Gao S, Kong X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Aug 10; 39(8):889-892. PubMed ID: 35929943
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  • 27. Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.
    Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR.
    Genet Med; 2017 Jun 10; 19(6):691-700. PubMed ID: 27831545
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  • 28. De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.
    Takagi T, Nishizaki Y, Matsui F, Wakamatsu N, Higashi Y.
    Hum Mol Genet; 2015 Nov 15; 24(22):6390-402. PubMed ID: 26319231
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  • 32. 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 Nov 15; 24(1):61-8. PubMed ID: 23610866
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  • 35. Mowat-Wilson syndrome: growth charts.
    Ivanovski I, Djuric O, Broccoli S, Caraffi SG, Accorsi P, Adam MP, Avela K, Badura-Stronka M, Bayat A, Clayton-Smith J, Cocco I, Cordelli DM, Cuturilo G, Di Pisa V, Dupont Garcia J, Gastaldi R, Giordano L, Guala A, Hoei-Hansen C, Inaba M, Iodice A, Nielsen JEK, Kuburovic V, Lazalde-Medina B, Malbora B, Mizuno S, Moldovan O, Møller RS, Muschke P, Otelli V, Pantaleoni C, Piscopo C, Poch-Olive ML, Prpic I, Marín Reina P, Raviglione F, Ricci E, Scarano E, Simonte G, Smigiel R, Tanteles G, Tarani L, Trimouille A, Valera ET, Schrier Vergano S, Writzl K, Callewaert B, Savasta S, Street ME, Iughetti L, Bernasconi S, Giorgi Rossi P, Garavelli L.
    Orphanet J Rare Dis; 2020 Jun 15; 15(1):151. PubMed ID: 32539836
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  • 36. Clinical utility gene card for: Mowat-Wilson syndrome.
    Zollino M, Garavelli L, Rauch A.
    Eur J Hum Genet; 2011 Aug 15; 19(8):. PubMed ID: 21343952
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  • 37. Atypical Mowat-Wilson Syndrome: Dystonia, Choreoathetosis and Cognitive Features.
    Nou-Fontanet L, Martí-Sánchez L, Martorell L, Casas J, Ortigoza-Escobar JD.
    Mov Disord Clin Pract; 2024 Jul 15; 11(7):889-893. PubMed ID: 38650363
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  • 38. [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 15; 21(5):468-473. PubMed ID: 31104665
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