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655 results

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Page 1
Genetic and neuroradiological heterogeneity of double cortex syndrome.
Gleeson JG, Luo RF, Grant PE, Guerrini R, Huttenlocher PR, Berg MJ, Ricci S, Cusmai R, Wheless JW, Berkovic S, Scheffer I, Dobyns WB, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Ann Neurol. 2000 Feb;47(2):265-9. Ann Neurol. 2000. PMID: 10665503
Molecular genetics of human microcephaly.
Mochida GH, Walsh CA. Mochida GH, et al. Among authors: walsh ca. Curr Opin Neurol. 2001 Apr;14(2):151-6. doi: 10.1097/00019052-200104000-00003. Curr Opin Neurol. 2001. PMID: 11262728 Review.
ASPM is a major determinant of cerebral cortical size.
Bond J, Roberts E, Mochida GH, Hampshire DJ, Scott S, Askham JM, Springell K, Mahadevan M, Crow YJ, Markham AF, Walsh CA, Woods CG. Bond J, et al. Among authors: walsh ca. Nat Genet. 2002 Oct;32(2):316-20. doi: 10.1038/ng995. Epub 2002 Sep 23. Nat Genet. 2002. PMID: 12355089
Periventricular heterotopia associated with chromosome 5p anomalies.
Sheen VL, Wheless JW, Bodell A, Braverman E, Cotter PD, Rauen KA, Glenn O, Weisiger K, Packman S, Walsh CA, Sherr EH. Sheen VL, et al. Among authors: walsh ca. Neurology. 2003 Mar 25;60(6):1033-6. doi: 10.1212/01.wnl.0000052689.03214.61. Neurology. 2003. PMID: 12654978
Autosomal recessive form of periventricular heterotopia.
Sheen VL, Topçu M, Berkovic S, Yalnizoglu D, Blatt I, Bodell A, Hill RS, Ganesh VS, Cherry TJ, Shugart YY, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Neurology. 2003 Apr 8;60(7):1108-12. doi: 10.1212/01.wnl.0000055898.00349.02. Neurology. 2003. PMID: 12682315
Protein-truncating mutations in ASPM cause variable reduction in brain size.
Bond J, Scott S, Hampshire DJ, Springell K, Corry P, Abramowicz MJ, Mochida GH, Hennekam RC, Maher ER, Fryns JP, Alswaid A, Jafri H, Rashid Y, Mubaidin A, Walsh CA, Roberts E, Woods CG. Bond J, et al. Among authors: walsh ca. Am J Hum Genet. 2003 Nov;73(5):1170-7. doi: 10.1086/379085. Epub 2003 Oct 21. Am J Hum Genet. 2003. PMID: 14574646 Free PMC article.
655 results