R37 NS35129/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2003	1
2004	2
2005	4
2006	6
2007	5
2009	2
2010	1
2011	1
2013	2
2024	0

1

Barkovich AJ. Barkovich AJ. Neuroradiology. 2010 Jun;52(6):479-87. doi: 10.1007/s00234-009-0644-2. Epub 2010 Mar 3. Neuroradiology. 2010. PMID: 20198472 Free PMC article. Review.

2

A developmental and genetic classification for midbrain-hindbrain malformations.

Barkovich AJ, Millen KJ, Dobyns WB. Barkovich AJ, et al. Brain. 2009 Dec;132(Pt 12):3199-230. doi: 10.1093/brain/awp247. Brain. 2009. PMID: 19933510 Free PMC article. Review.

3

Mapping form and function in the human brain: the emerging field of functional neuroimaging in cortical malformations.

Chang BS, Walsh CA. Chang BS, et al. Epilepsy Behav. 2003 Dec;4(6):618-25. doi: 10.1016/j.yebeh.2003.09.006. Epilepsy Behav. 2003. PMID: 14698694 Review.

4

Complication begets clarification in classification.

Barkovich J. Barkovich J. Brain. 2013 Feb;136(Pt 2):368-73. doi: 10.1093/brain/awt001. Brain. 2013. PMID: 23413256 Free PMC article. No abstract available.

5

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

6

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.

Parrini E, Ramazzotti A, Dobyns WB, Mei D, Moro F, Veggiotti P, Marini C, Brilstra EH, Dalla Bernardina B, Goodwin L, Bodell A, Jones MC, Nangeroni M, Palmeri S, Said E, Sander JW, Striano P, Takahashi Y, Van Maldergem L, Leonardi G, Wright M, Walsh CA, Guerrini R. Parrini E, et al. Brain. 2006 Jul;129(Pt 7):1892-906. doi: 10.1093/brain/awl125. Epub 2006 May 9. Brain. 2006. PMID: 16684786

7

Genomic and evolutionary analyses of asymmetrically expressed genes in human fetal left and right cerebral cortex.

Sun T, Collura RV, Ruvolo M, Walsh CA. Sun T, et al. Cereb Cortex. 2006 Jul;16 Suppl 1:i18-25. doi: 10.1093/cercor/bhk026. Cereb Cortex. 2006. PMID: 16766703

8

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes.

Piao X, Chang BS, Bodell A, Woods K, Benzeev B, Topcu M, Guerrini R, Goldberg-Stern H, Sztriha L, Dobyns WB, Barkovich AJ, Walsh CA. Piao X, et al. Ann Neurol. 2005 Nov;58(5):680-7. doi: 10.1002/ana.20616. Ann Neurol. 2005. PMID: 16240336

9

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia.

Chang BS, Ly J, Appignani B, Bodell A, Apse KA, Ravenscroft RS, Sheen VL, Doherty MJ, Hackney DB, O'Connor M, Galaburda AM, Walsh CA. Chang BS, et al. Neurology. 2005 Mar 8;64(5):799-803. doi: 10.1212/01.WNL.0000152874.57180.AF. Neurology. 2005. PMID: 15753412

10

Disease-associated mutations affect GPR56 protein trafficking and cell surface expression.

Jin Z, Tietjen I, Bu L, Liu-Yesucevitz L, Gaur SK, Walsh CA, Piao X. Jin Z, et al. Hum Mol Genet. 2007 Aug 15;16(16):1972-85. doi: 10.1093/hmg/ddm144. Epub 2007 Jun 18. Hum Mol Genet. 2007. PMID: 17576745

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