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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

288 related items for PubMed ID: 24282181

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  • 25. 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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  • 26. 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; 149A(3):417-26. PubMed ID: 19215041
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  • 27. Mowat-Wilson syndrome.
    Garavelli L, Mainardi PC.
    Orphanet J Rare Dis; 2007 Oct 24; 2():42. PubMed ID: 17958891
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  • 28. 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 24; 28(8):1074-1076. PubMed ID: 29954473
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  • 29. 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 24; 19(6):691-700. PubMed ID: 27831545
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  • 31. "Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene.
    Zweier C, Albrecht B, Mitulla B, Behrens R, Beese M, Gillessen-Kaesbach G, Rott HD, Rauch A.
    Am J Med Genet; 2002 Mar 15; 108(3):177-81. PubMed ID: 11891681
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  • 32. 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 15; 73(1):12-7. PubMed ID: 25608121
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  • 33. Mowat-Wilson syndrome.
    Mowat DR, Wilson MJ, Goossens M.
    J Med Genet; 2003 May 15; 40(5):305-10. PubMed ID: 12746390
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  • 34. [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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  • 35. Fetal diagnosis of Mowat-Wilson syndrome by whole exome sequencing.
    Evans CA, Pinner J, Chan CY, Bowyer L, Mowat D, Buckley MF, Roscioli T.
    Am J Med Genet A; 2019 Oct 15; 179(10):2152-2157. PubMed ID: 31321886
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  • 36. Mowat-Wilson syndrome: the first clinical and molecular report of an indonesian patient.
    Mundhofir FE, Yntema HG, van der Burgt I, Hamel BC, Faradz SM, van Bon BW.
    Case Rep Genet; 2012 Oct 15; 2012():949507. PubMed ID: 23243526
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  • 37. 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
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  • 39. Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome.
    Teraishi M, Takaishi M, Nakajima K, Ikeda M, Higashi Y, Shimoda S, Asada Y, Hijikata A, Ohara O, Hiraki Y, Mizuno S, Fukada T, Furukawa T, Wakamatsu N, Sano S.
    Sci Rep; 2017 Apr 19; 7():46565. PubMed ID: 28422173
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