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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 29258970)

  • 1. 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; 19(4):481-485. PubMed ID: 29258970
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat-Wilson syndrome.
    Hu Y; Peng Q; Ma K; Li S; Rao C; Zhong B; Lu X
    J Clin Lab Anal; 2020 Sep; 34(9):e23413. PubMed ID: 32519765
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
    Ivanovski I; Djuric O; Caraffi SG; Santodirocco D; Pollazzon M; Rosato S; Cordelli DM; Abdalla E; Accorsi P; Adam MP; Ajmone PF; Badura-Stronka M; Baldo C; Baldi M; Bayat A; Bigoni S; Bonvicini F; Breckpot J; Callewaert B; Cocchi G; Cuturilo G; De Brasi D; Devriendt K; Dinulos MB; Hjortshøj TD; Epifanio R; Faravelli F; Fiumara A; Formisano D; Giordano L; Grasso M; Grønborg S; Iodice A; Iughetti L; Kuburovic V; Kutkowska-Kazmierczak A; Lacombe D; Lo Rizzo C; Luchetti A; Malbora B; Mammi I; Mari F; Montorsi G; Moutton S; Møller RS; Muschke P; Nielsen JEK; Obersztyn E; Pantaleoni C; Pellicciari A; Pisanti MA; Prpic I; Poch-Olive ML; Raviglione F; Renieri A; Ricci E; Rivieri F; Santen GW; Savasta S; Scarano G; Schanze I; Selicorni A; Silengo M; Smigiel R; Spaccini L; Sorge G; Szczaluba K; Tarani L; Tone LG; Toutain A; Trimouille A; Valera ET; Vergano SS; Zanotta N; Zenker M; Conidi A; Zollino M; Rauch A; Zweier C; Garavelli L
    Genet Med; 2018 Sep; 20(9):965-975. PubMed ID: 29300384
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 161A(2):273-84. PubMed ID: 23322667
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prenatal diagnosis of a fetus with Mowat-Wilson syndrome].
    Hu R; Luo X; Li Y; Lu J; Huang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1203-1205. PubMed ID: 31813148
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neuropathology of Mowat-Wilson Syndrome.
    Conces MR; Hughes A; Pierson CR
    Pediatr Dev Pathol; 2020 Aug; 23(4):322-325. PubMed ID: 32252596
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [No Abstract]   [Full Text] [Related]  

  • 15. Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome.
    Jakubiak A; Szczałuba K; Badura-Stronka M; Kutkowska-Kaźmierczak A; Jakubiuk-Tomaszuk A; Chilarska T; Pilch J; Braun-Walicka N; Castaneda J; Wołyńska K; Wiśniewska M; Kugaudo M; Bielecka M; Pesz K; Wierzba J; Latos-Bieleńska A; Obersztyn E; Krajewska-Walasek M; Śmigiel R
    J Appl Genet; 2021 Sep; 62(3):477-485. PubMed ID: 33982229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mowat-Wilson syndrome detected by using high resolution microarray.
    Park JY; Cho EH; Lee EH; Kang YS; Jun KR; Hur YJ
    Gene; 2013 Dec; 532(2):307-9. PubMed ID: 24029077
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mowat-Wilson syndrome: a report of three Danish cases].
    Nissen KB; Søndergaard C; Thelle T; Møller RS
    Ugeskr Laeger; 2011 Sep; 173(36):2199-200. PubMed ID: 21893004
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencing.
    Babkina N; Deignan JL; Lee H; Vilain E; Sankar R; Giurgea I; Mowat D; Graham JM
    Eur J Med Genet; 2016 Feb; 59(2):70-4. PubMed ID: 26721324
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 24(1):61-8. PubMed ID: 23610866
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.