Walsh CA - Search Results

1

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.

Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA. Ferland RJ, et al. Among authors: walsh ca. J Comp Neurol. 2003 May 26;460(2):266-79. doi: 10.1002/cne.10654. J Comp Neurol. 2003. PMID: 12687690

2

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

3

Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation.

Chang BS, Piao X, Giannini C, Cascino GD, Scheffer I, Woods CG, Topcu M, Tezcan K, Bodell A, Leventer RJ, Barkovich AJ, Grant PE, Walsh CA. Chang BS, et al. Among authors: walsh ca. Neurology. 2004 May 25;62(10):1722-8. doi: 10.1212/01.wnl.0000125187.52952.e9. Neurology. 2004. PMID: 15159468 Review.

4

Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus.

Sheen VL, Basel-Vanagaite L, Goodman JR, Scheffer IE, Bodell A, Ganesh VS, Ravenscroft R, Hill RS, Cherry TJ, Shugart YY, Barkovich J, Straussberg R, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Brain Dev. 2004 Aug;26(5):326-34. doi: 10.1016/j.braindev.2003.09.004. Brain Dev. 2004. PMID: 15165674

5

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, Walsh CA. Ferland RJ, et al. Among authors: walsh ca. Nat Genet. 2004 Sep;36(9):1008-13. doi: 10.1038/ng1419. Epub 2004 Aug 22. Nat Genet. 2004. PMID: 15322546

6

Expression of Cux-1 and Cux-2 in the subventricular zone and upper layers II-IV of the cerebral cortex.

Nieto M, Monuki ES, Tang H, Imitola J, Haubst N, Khoury SJ, Cunningham J, Gotz M, Walsh CA. Nieto M, et al. Among authors: walsh ca. J Comp Neurol. 2004 Nov 8;479(2):168-80. doi: 10.1002/cne.20322. J Comp Neurol. 2004. PMID: 15452856

7

Early asymmetry of gene transcription in embryonic human left and right cerebral cortex.

Sun T, Patoine C, Abu-Khalil A, Visvader J, Sum E, Cherry TJ, Orkin SH, Geschwind DH, Walsh CA. Sun T, et al. Among authors: walsh ca. Science. 2005 Jun 17;308(5729):1794-8. doi: 10.1126/science.1110324. Epub 2005 May 12. Science. 2005. PMID: 15894532 Free PMC article.

8

Characterization of Rho-GDIgamma and Rho-GDIalpha mRNA in the developing and mature brain with an analysis of mice with targeted deletions of Rho-GDIgamma.

Ferland RJ, Li X, Buhlmann JE, Bu X, Walsh CA, Lim B. Ferland RJ, et al. Among authors: walsh ca. Brain Res. 2005 Aug 23;1054(1):9-21. doi: 10.1016/j.brainres.2005.04.088. Brain Res. 2005. PMID: 16054116

9

Overlapping expression of ARFGEF2 and Filamin A in the neuroependymal lining of the lateral ventricles: insights into the cause of periventricular heterotopia.

Lu J, Tiao G, Folkerth R, Hecht J, Walsh C, Sheen V. Lu J, et al. J Comp Neurol. 2006 Jan 20;494(3):476-84. doi: 10.1002/cne.20806. J Comp Neurol. 2006. PMID: 16320251

10

Neocortical neuronal arrangement in Miller Dieker syndrome.

Sheen VL, Ferland RJ, Neal J, Harney M, Hill RS, Banham A, Brown P, Chenn A, Corbo J, Hecht J, Folkerth R, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Acta Neuropathol. 2006 May;111(5):489-96. doi: 10.1007/s00401-005-0010-3. Epub 2006 Feb 3. Acta Neuropathol. 2006. PMID: 16456669

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