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Journal Abstract Search

149 related items for PubMed ID: 24265573

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  • 2. Cerebellar vermis hypoplasia in a case of cri-du-chat syndrome.
    De Michele G, Presta M, Di Salle F, Serra L, Mazzaccara A, Della Rocca G, Ambrosio G, Filla A.
    Acta Neurol (Napoli); 1993 Apr; 15(2):92-6. PubMed ID: 8328329
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  • 4. Pontine hypoplasia in cri-du-chat syndrome: alterations in diffusion tensor imaging.
    Corrêa DG, Ventura N, Gasparetto EL.
    Childs Nerv Syst; 2017 Aug; 33(8):1241-1242. PubMed ID: 28676976
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  • 5. Prenatal diagnosis of cri du chat syndrome with encephalocele.
    Bakkum JN, Watson WJ, Johansen KL, Brost BC.
    Am J Perinatol; 2005 Oct; 22(7):351-2. PubMed ID: 16215919
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  • 7. Peters anomaly in cri-du-chat syndrome.
    Hope WC, Cordovez JA, Capasso JE, Hammersmith KM, Eagle RC, Lall-Trail J, Levin AV.
    J AAPOS; 2015 Jun; 19(3):277-9. PubMed ID: 26059676
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  • 8. Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.
    Villa R, Fergnani VGC, Silipigni R, Guerneri S, Cinnante C, Guala A, Danesino C, Scola E, Conte G, Fumagalli M, Gangi S, Colombo L, Picciolini O, Ajmone PF, Accogli A, Madia F, Tassano E, Scala M, Capra V, Srour M, Spaccini L, Righini A, Greco D, Castiglia L, Romano C, Bedeschi MF.
    Eur J Paediatr Neurol; 2020 Sep; 28():110-119. PubMed ID: 32800423
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  • 9. Progressive scoliosis in cri-du-chat syndrome over a 20-year follow-up period: a case report.
    Saito N, Ebara S, Fukushima Y, Wakui K, Takaoka K.
    Spine (Phila Pa 1976); 2001 Apr 01; 26(7):835-7. PubMed ID: 11295909
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  • 10. The association between Cri du chat syndrome and dental anomalies.
    Hall C, Hallett K, Manton D.
    J Dent Child (Chic); 2014 Apr 01; 81(3):171-7. PubMed ID: 25514263
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  • 12. Selective pontine hypoplasia: a possible common feature in 5p monosomy syndrome.
    Kato Z, Kondo N, Kato H, Morita H, Teramoto T, Miyamoto K, Shimizu K.
    Brain Dev; 2011 Sep 01; 33(8):702-3. PubMed ID: 21145676
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  • 15. Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition.
    Kjaer I, Niebuhr E.
    Am J Med Genet; 1999 Jan 01; 82(1):6-14. PubMed ID: 9916835
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  • 17. [Brain MRI Findings of the Cri-Du-Chat Syndrome: A Case Report and Summary].
    Choi JS, Yoo EA, Choi JO, Kim SJ.
    Taehan Yongsang Uihakhoe Chi; 2020 Jul 01; 81(4):979-984. PubMed ID: 36238176
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  • 19. Prenatal diagnosis of cri-du-chat syndrome: importance of ultrasonographical markers.
    Teoh XH, Tan TY, Chow KK, Lee IW.
    Singapore Med J; 2009 May 01; 50(5):e181-4. PubMed ID: 19495505
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