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Journal Abstract Search

248 related items for PubMed ID: 21403111

  • 21. Perisylvian polymicrogyria, infantile spasms and arthrogryposis: the severe end of the spectrum of congenital bilateral perisylvian polymicrogyria.
    De Coene A, Van Coster R, Verhelst H.
    Eur J Paediatr Neurol; 2010 May; 14(3):270-3. PubMed ID: 19559633
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  • 22. [Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing].
    Bahi-Buisson N, Boddaert N, Saillour Y, Souville I, Poirier K, Léger PL, Castelnau L, Plouin P, Carion N, Beldjord C, Chelly J.
    Rev Neurol (Paris); 2008 Dec; 164(12):995-1009. PubMed ID: 18808783
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  • 23. Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown.
    Saillour Y, Broix L, Bruel-Jungerman E, Lebrun N, Muraca G, Rucci J, Poirier K, Belvindrah R, Francis F, Chelly J.
    Hum Mol Genet; 2014 Mar 15; 23(6):1516-26. PubMed ID: 24179174
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  • 24. TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
    Yokoi S, Ishihara N, Miya F, Tsutsumi M, Yanagihara I, Fujita N, Yamamoto H, Kato M, Okamoto N, Tsunoda T, Yamasaki M, Kanemura Y, Kosaki K, Kojima S, Saitoh S, Kurahashi H, Natsume J.
    Sci Rep; 2015 Oct 23; 5():15165. PubMed ID: 26493046
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  • 27. Tubulin genes and malformations of cortical development.
    Romaniello R, Arrigoni F, Fry AE, Bassi MT, Rees MI, Borgatti R, Pilz DT, Cushion TD.
    Eur J Med Genet; 2018 Dec 23; 61(12):744-754. PubMed ID: 30016746
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  • 28. Auditory processing disorder in perisylvian syndrome.
    Boscariol M, Garcia VL, Guimarães CA, Montenegro MA, Hage SR, Cendes F, Guerreiro MM.
    Brain Dev; 2010 Apr 23; 32(4):299-304. PubMed ID: 19410403
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  • 29. TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation.
    Myers KA, Bello-Espinosa LE, Kherani A, Wei XC, Innes AM.
    Pediatr Neurol; 2015 Nov 23; 53(5):442-4. PubMed ID: 26294046
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  • 31. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G, Verdú-Pérez A, de Castro-De Castro P.
    Rev Neurol; 2015 Nov 23; 48(4):188-90. PubMed ID: 19226486
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  • 32. Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway.
    Tian G, Jaglin XH, Keays DA, Francis F, Chelly J, Cowan NJ.
    Hum Mol Genet; 2010 Sep 15; 19(18):3599-613. PubMed ID: 20603323
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  • 34. Diffuse malformations of cortical development.
    Bahi-Buisson N, Guerrini R.
    Handb Clin Neurol; 2013 Sep 15; 111():653-65. PubMed ID: 23622213
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  • 36. A case of TUBA1A mutation presenting with lissencephaly and Hirschsprung disease.
    Hikita N, Hattori H, Kato M, Sakuma S, Morotomi Y, Ishida H, Seto T, Tanaka K, Shimono T, Shintaku H, Tokuhara D.
    Brain Dev; 2014 Feb 15; 36(2):159-62. PubMed ID: 23528852
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  • 38. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.
    Gerkes EH, Hordijk R, Dijkhuizen T, Sival DA, Meiners LC, Sikkema-Raddatz B, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2010 Feb 15; 53(5):344-6. PubMed ID: 20553986
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  • 39. Lissencephaly with marked ventricular dilation, agenesis of corpus callosum, and cerebellar hypoplasia caused by TUBA1A mutation.
    Okumura A, Hayashi M, Tsurui H, Yamakawa Y, Abe S, Kudo T, Suzuki R, Shimizu T, Shimojima K, Yamamoto T.
    Brain Dev; 2013 Mar 15; 35(3):274-9. PubMed ID: 22633752
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  • 40. Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development.
    Aksel Kiliçarslan Ö, Ataman E, Gürsoy S, Gürbüz G, Ünalp A, Gençpinar P, Olgaç Dündar N, Edizer S, Ülgenalp A, Giray Bozkaya Ö.
    Turk J Med Sci; 2020 Oct 22; 50(6):1573-1579. PubMed ID: 32718119
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