Walsh CA - Search Results

1

Disorders of Microtubule Function in Neurons: Imaging Correlates.

Mutch CA, Poduri A, Sahin M, Barry B, Walsh CA, Barkovich AJ. Mutch CA, et al. Among authors: walsh ca. AJNR Am J Neuroradiol. 2016 Mar;37(3):528-35. doi: 10.3174/ajnr.A4552. Epub 2015 Nov 12. AJNR Am J Neuroradiol. 2016. PMID: 26564436 Free PMC article.

2

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME. Pilz DT, et al. Among authors: walsh ca. Hum Mol Genet. 1998 Dec;7(13):2029-37. doi: 10.1093/hmg/7.13.2029. Hum Mol Genet. 1998. PMID: 9817918

3

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly.

Dobyns WB, Truwit CL, Ross ME, Matsumoto N, Pilz DT, Ledbetter DH, Gleeson JG, Walsh CA, Barkovich AJ. Dobyns WB, et al. Among authors: walsh ca. Neurology. 1999 Jul 22;53(2):270-7. doi: 10.1212/wnl.53.2.270. Neurology. 1999. PMID: 10430413

4

Callosal agenesis with cyst: a better understanding and new classification.

Barkovich AJ, Simon EM, Walsh CA. Barkovich AJ, et al. Among authors: walsh ca. Neurology. 2001 Jan 23;56(2):220-7. doi: 10.1212/wnl.56.2.220. Neurology. 2001. PMID: 11160959

5

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: walsh ca. Ann Neurol. 2003 May;53(5):596-606. doi: 10.1002/ana.10520. Ann Neurol. 2003. PMID: 12730993

6

G protein-coupled receptor-dependent development of human frontal cortex.

Piao X, Hill RS, Bodell A, Chang BS, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Ross ME, Michaud JL, Déscarie JC, Barkovich AJ, Walsh CA. Piao X, et al. Among authors: walsh ca. Science. 2004 Mar 26;303(5666):2033-6. doi: 10.1126/science.1092780. Science. 2004. PMID: 15044805

7

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.

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. Among authors: walsh ca. Ann Neurol. 2005 Nov;58(5):680-7. doi: 10.1002/ana.20616. Ann Neurol. 2005. PMID: 16240336

9

A familial syndrome of unilateral polymicrogyria affecting the right hemisphere.

Chang BS, Apse KA, Caraballo R, Cross JH, Mclellan A, Jacobson RD, Valente KD, Barkovich AJ, Walsh CA. Chang BS, et al. Among authors: walsh ca. Neurology. 2006 Jan 10;66(1):133-5. doi: 10.1212/01.wnl.0000191393.06679.e9. Neurology. 2006. PMID: 16401865

10

An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation.

Rajab A, Yoo SY, Abdulgalil A, Kathiri S, Ahmed R, Mochida GH, Bodell A, Barkovich AJ, Walsh CA. Rajab A, et al. Among authors: walsh ca. Am J Med Genet A. 2006 Jul 15;140(14):1504-10. doi: 10.1002/ajmg.a.31288. Am J Med Genet A. 2006. PMID: 16761294 Free PMC article.

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