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289 related items for PubMed ID: 18975527

  • 1. Agenesis of the corpus callosum in Turner's syndrome: report of a case and review of the literature.
    Lee YY, Hung J, Chang TY, Huang CC.
    Acta Neurol Taiwan; 2008 Sep; 17(3):194-8. PubMed ID: 18975527
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  • 4. Spectrum of corpus callosum agenesis.
    Sztriha L.
    Pediatr Neurol; 2005 Feb; 32(2):94-101. PubMed ID: 15664768
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  • 6. Pregnancy and the Turner syndrome.
    King CR, Magenis E, Bennett S.
    Obstet Gynecol; 1978 Nov; 52(5):617-24. PubMed ID: 724182
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  • 8. Halo nevus, rather than vitiligo, is a typical dermatologic finding of turner's syndrome: clinical, genetic, and immunogenetic study in 72 patients.
    Brazzelli V, Larizza D, Martinetti M, Martinoli S, Calcaterra V, De Silvestri A, Pandolfi R, Borroni G.
    J Am Acad Dermatol; 2004 Sep; 51(3):354-8. PubMed ID: 15337976
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  • 11. Agenesis of the corpus callosum: clinical and genetic study in 63 young patients.
    Bedeschi MF, Bonaglia MC, Grasso R, Pellegri A, Garghentino RR, Battaglia MA, Panarisi AM, Di Rocco M, Balottin U, Bresolin N, Bassi MT, Borgatti R.
    Pediatr Neurol; 2006 Mar; 34(3):186-93. PubMed ID: 16504787
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  • 12. [Heart malformations and vascular complications associated with Turner's syndrome. Prospective study of 26 patients].
    Douchin S, Rossignol AM, Klein SK, Siché JP, Baguet JP, Bost M.
    Arch Mal Coeur Vaiss; 2000 May; 93(5):565-70. PubMed ID: 10858854
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  • 13. [Prenatal MRI of corpus callosum agenesis. Study of 20 cases with neuropathological correlations].
    Brisse H, Sebag G, Fallet C, Elmaleh M, Garel C, Rossler L, Vuillard E, Oury JF, Hassan M.
    J Radiol; 1998 Jul; 79(7):659-66. PubMed ID: 9757293
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  • 14. Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation.
    Işik U, Başaran S, Dehgan T, Apak M.
    Pediatr Neurol; 2008 Jul; 39(1):55-7. PubMed ID: 18555175
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  • 15. Ivemark syndrome with agenesis of the corpus callosum: a case report with a review of the literature.
    Noack F, Sayk F, Ressel A, Berg C, Gembruch U, Reusche E.
    Prenat Diagn; 2002 Nov; 22(11):1011-5. PubMed ID: 12424766
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  • 16. Agenesis of the corpus callosum: a study of the frequency of associated malformations.
    Parrish ML, Roessmann U, Levinsohn MW.
    Ann Neurol; 1979 Oct; 6(4):349-54. PubMed ID: 554524
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  • 17. Seckel syndrome with asymptomatic tonsillar herniation and congenital mirror movements.
    Thapa R, Mukherjee K.
    J Child Neurol; 2010 Feb; 25(2):231-3. PubMed ID: 19372093
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  • 18. Delayed diagnoses of Turner's syndrome: proposed guidelines for change.
    Sävendahl L, Davenport ML.
    J Pediatr; 2000 Oct; 137(4):455-9. PubMed ID: 11035820
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  • 19. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
    Aykut A, Cogulu O, Ekmekci AY, Ozkinay F.
    Genet Couns; 2008 Oct; 19(2):237-40. PubMed ID: 18618999
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  • 20. Cirrhosis in Turner's syndrome: case report and literature review.
    Idilman R, De Maria N, Colantoni A, Kugelmas M, Van Thiel DH.
    Eur J Gastroenterol Hepatol; 2000 Jun; 12(6):707-9. PubMed ID: 10912494
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