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Journal Abstract Search

152 related items for PubMed ID: 31285160

  • 21.
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  • 22. Co-occurrence of rhabdomyosarcoma and Mowat-Wilson syndrome: is there a connection?
    Rogac M, Kitanovski L, Writzl K.
    Clin Dysmorphol; 2017 Jul; 26(3):185-186. PubMed ID: 28230647
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  • 23. Submucosal Supernumerary Smooth Muscle Coat: A Common Histologic Finding in Mowat-Wilson Syndrome With or Without Hirschsprung Disease.
    Suchi M, Calkins CM, Chogle A, Bond JS, Kapur RP.
    Pediatr Dev Pathol; 2020 Jul; 23(5):372-379. PubMed ID: 32469269
    [Abstract] [Full Text] [Related]

  • 24. Mowat-Wilson syndrome: neurological and molecular study in seven patients.
    Paz JA, Kim CA, Goossens M, Giurgea I, Marques-Dias MJ.
    Arq Neuropsiquiatr; 2015 Jan; 73(1):12-7. PubMed ID: 25608121
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  • 25. [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
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  • 26.
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  • 27. Ocular phenotype of Mowat-Wilson syndrome in the first reported Cypriot patients: an under-recognized association.
    Tanteles GA, Christophidou-Anastasiadou V.
    Clin Dysmorphol; 2014 Jan 02; 23(1):20-23. PubMed ID: 24263623
    [No Abstract] [Full Text] [Related]

  • 28. The Role of ZEB2 in Human CD8 T Lymphocytes: Clinical and Cellular Immune Profiling in Mowat-Wilson Syndrome.
    Frith K, Munier CML, Hastings L, Mowat D, Wilson M, Seddiki N, Macintosh R, Kelleher AD, Gray P, Zaunders JJ.
    Int J Mol Sci; 2021 May 18; 22(10):. PubMed ID: 34070208
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  • 29. Incidental finding of pulmonary arterial sling during patent ductus arteriosus surgery in a patient with Mowat-Wilson syndrome.
    Cano Sierra JD, Mestra CF, Ronderos Dumit MA.
    Cardiol Young; 2018 Aug 18; 28(8):1074-1076. PubMed ID: 29954473
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  • 30.
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  • 31. Sleep polygraphy in Angelman syndrome.
    Miano S, Bruni O, Leuzzi V, Elia M, Verrillo E, Ferri R.
    Clin Neurophysiol; 2004 Apr 18; 115(4):938-45. PubMed ID: 15003776
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  • 32. Vagus nerve stimulation for drug-resistant epilepsy in a patient with Mowat-Wilson syndrome.
    Benedetti-Isaac JC, Torres-Zambrano M, Alcalá-Cerra G, Gutiérrez-Paternina JJ.
    Neurol India; 2013 Apr 18; 61(3):306-7. PubMed ID: 23860154
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  • 35. 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 18; 167(7):1587-92. PubMed ID: 25899569
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  • 38. 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 18; 19(6):691-700. PubMed ID: 27831545
    [Abstract] [Full Text] [Related]

  • 39. 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 18; 11(7):889-893. PubMed ID: 38650363
    [No Abstract] [Full Text] [Related]

  • 40. A case of Mowat-Wilson syndrome caused by a truncating mutation within exon 8 of the ZEB2 gene.
    Meral C, Malbora B, Celikel F, Aydemir G, Süleymanoğlu S, Zollino M, Derbent M.
    Turk J Pediatr; 2012 Jul 18; 54(5):523-7. PubMed ID: 23427518
    [Abstract] [Full Text] [Related]

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