Grant PE - Search Results

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: grant pe. Ann Neurol. 2000 Feb;47(2):265-9. Ann Neurol. 2000. PMID: 10665503

2

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA. Hong SE, et al. Among authors: grant pe. Nat Genet. 2000 Sep;26(1):93-6. doi: 10.1038/79246. Nat Genet. 2000. PMID: 10973257

3

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

Piao X, Basel-Vanagaite L, Straussberg R, Grant PE, Pugh EW, Doheny K, Doan B, Hong SE, Shugart YY, Walsh CA. Piao X, et al. Among authors: grant pe. Am J Hum Genet. 2002 Apr;70(4):1028-33. doi: 10.1086/339552. Epub 2002 Feb 13. Am J Hum Genet. 2002. PMID: 11845408 Free PMC article.

4

Diffusion-weighted images in neonatal cerebral hypoxic-ischemic injury.

Takeoka M, Soman TB, Yoshii A, Caviness VS Jr, Gonzalez RG, Grant PE, Krishnamoorthy KS. Takeoka M, et al. Among authors: grant pe. Pediatr Neurol. 2002 Apr;26(4):274-81. doi: 10.1016/s0887-8994(01)00403-9. Pediatr Neurol. 2002. PMID: 11992754

5

Abnormal cortical development shown by 3D MRI in Prader-Willi syndrome.

Yoshii A, Krishnamoorthy KS, Grant PE. Yoshii A, et al. Among authors: grant pe. Neurology. 2002 Aug 27;59(4):644-5. doi: 10.1212/wnl.59.4.644. Neurology. 2002. PMID: 12196672 No abstract available.

6

Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16.

Chang BS, Piao X, Bodell A, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Grant PE, Barkovich AJ, Walsh CA. Chang BS, et al. Among authors: grant pe. Ann Neurol. 2003 May;53(5):596-606. doi: 10.1002/ana.10520. Ann Neurol. 2003. PMID: 12730993

7

A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21.

Rajab A, Mochida GH, Hill A, Ganesh V, Bodell A, Riaz A, Grant PE, Shugart YY, Walsh CA. Rajab A, et al. Among authors: grant pe. Neurology. 2003 May 27;60(10):1664-7. doi: 10.1212/01.wnl.0000068548.58498.41. Neurology. 2003. PMID: 12771259

8

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA. Sheen VL, et al. Among authors: grant pe. Nat Genet. 2004 Jan;36(1):69-76. doi: 10.1038/ng1276. Epub 2003 Nov 30. Nat Genet. 2004. PMID: 14647276

9

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: grant pe. Neurology. 2004 May 25;62(10):1722-8. doi: 10.1212/01.wnl.0000125187.52952.e9. Neurology. 2004. PMID: 15159468 Review.

10

Clinical correlates in an experimental model of repetitive mild brain injury.

Mannix R, Meehan WP, Mandeville J, Grant PE, Gray T, Berglass J, Zhang J, Bryant J, Rezaie S, Chung JY, Peters NV, Lee C, Tien LW, Kaplan DL, Feany M, Whalen M. Mannix R, et al. Among authors: grant pe. Ann Neurol. 2013 Jul;74(1):65-75. doi: 10.1002/ana.23858. Epub 2013 Aug 6. Ann Neurol. 2013. PMID: 23922306 Free PMC article.

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