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

133 related items for PubMed ID: 38650363

  • 61.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 62. Severe clinical course of Hirschsprung disease in a Mowat-Wilson syndrome patient.
    Smigiel R, Szafranska A, Czyzewska M, Rauch A, Zweier Ch, Patkowski D.
    J Appl Genet; 2010; 51(1):111-3. PubMed ID: 20145308
    [Abstract] [Full Text] [Related]

  • 63.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 64. Paroxysmal dystonic choreoathetosis in a patient with familial ataxia.
    Mayeux R, Fahn S.
    Neurology; 1982 Oct; 32(10):1184-6. PubMed ID: 6889704
    [Abstract] [Full Text] [Related]

  • 65. Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study.
    Di Pisa V, Provini F, Ubertiello S, Bonetti S, Ricci E, Ivanovski I, Caraffi SG, Giordano L, Accorsi P, Savasta S, Raviglione F, Boni A, Grioni D, Graziano C, Garavelli L, Cordelli DM.
    Sleep Med; 2019 Sep; 61():44-51. PubMed ID: 31285160
    [Abstract] [Full Text] [Related]

  • 66.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 67.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 68. Mowat Wilson syndrome and Hirschsprung disease: a retrospective study on functional outcomes.
    Dagorno C, Pio L, Capri Y, Ali L, Giurgea I, Qoshe L, Morcrette G, Julien-Marsollier F, Sommet J, Chomton M, Berrebi D, Bonnard A.
    Pediatr Surg Int; 2020 Nov; 36(11):1309-1315. PubMed ID: 32980962
    [Abstract] [Full Text] [Related]

  • 69. Mowat-Wilson syndrome: Case report.
    Wójcik-Niklewska B, Filipek E.
    Medicine (Baltimore); 2024 Jul 19; 103(29):e39082. PubMed ID: 39029032
    [Abstract] [Full Text] [Related]

  • 70.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 71. Novel Alu insertion in the ZEB2 gene causing Mowat-Wilson syndrome.
    Barington M, Bak M, Kjartansdóttir KR, Hansen TVO, Birkedal U, Østergaard E, Hove HB.
    Am J Med Genet A; 2024 Aug 19; 194(8):e63581. PubMed ID: 38600862
    [Abstract] [Full Text] [Related]

  • 72.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 73. Choreoathetosis of genetic origin.
    Gordon N.
    Dev Med Child Neurol; 1980 Aug 19; 22(4):521-4. PubMed ID: 7409344
    [No Abstract] [Full Text] [Related]

  • 74. ZEB2, the Mowat-Wilson Syndrome Transcription Factor: Confirmations, Novel Functions, and Continuing Surprises.
    Birkhoff JC, Huylebroeck D, Conidi A.
    Genes (Basel); 2021 Jul 03; 12(7):. PubMed ID: 34356053
    [Abstract] [Full Text] [Related]

  • 75.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 76. Neurological Phenotype of Mowat-Wilson Syndrome.
    Cordelli DM, Di Pisa V, Fetta A, Garavelli L, Maltoni L, Soliani L, Ricci E.
    Genes (Basel); 2021 Jun 27; 12(7):. PubMed ID: 34199024
    [Abstract] [Full Text] [Related]

  • 77. Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.
    Cordelli DM, Garavelli L, Savasta S, Guerra A, Pellicciari A, Giordano L, Bonetti S, Cecconi I, Wischmeijer A, Seri M, Rosato S, Gelmini C, Della Giustina E, Ferrari AR, Zanotta N, Epifanio R, Grioni D, Malbora B, Mammi I, Mari F, Buoni S, Mostardini R, Grosso S, Pantaleoni C, Doz M, Poch-Olivé ML, Rivieri F, Sorge G, Simonte G, Licata F, Tarani L, Terazzi E, Mazzanti L, Cerruti Mainardi P, Boni A, Faravelli F, Grasso M, Bianchi P, Zollino M, Franzoni E.
    Am J Med Genet A; 2013 Feb 27; 161A(2):273-84. PubMed ID: 23322667
    [Abstract] [Full Text] [Related]

  • 78. Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development.
    Cui S, Erlichman J, Russo P, Haber BA, Matthews RP.
    J Pediatr Gastroenterol Nutr; 2011 Mar 27; 52(3):339-44. PubMed ID: 21336163
    [Abstract] [Full Text] [Related]

  • 79. Autosomal dominant paroxysmal kinesigenic choreoathetosis: a clinical and genetic study of two families.
    Picard F, Tassin J, Vidailhet M, Marescaux C, Picard F, Agid Y, Brice A.
    J Neurol Neurosurg Psychiatry; 1998 Dec 27; 65(6):955-6. PubMed ID: 9854993
    [No Abstract] [Full Text] [Related]

  • 80. ZEB2, a new candidate gene for asplenia.
    Pons L, Dupuis-Girod S, Cordier MP, Edery P, Rossi M.
    Orphanet J Rare Dis; 2014 Jan 08; 9():2. PubMed ID: 24401652
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.