Bodell A[Author] - Search Results

Year	Number of Results
1994	1
1996	1
2003	5
2004	6
2005	5
2006	5
2007	4
2008	1
2009	1
2010	1
2012	1
2013	2
2014	2
2015	2
2024	0

1

Post-encystment/established immunity in cystic echinococcosis: is it really that simple?

Rogan MT, Bodell AJ, Craig PS. Rogan MT, et al. Among authors: bodell aj. Parasite Immunol. 2015 Jan;37(1):1-9. doi: 10.1111/pim.12149. Parasite Immunol. 2015. PMID: 25283301 Review.

2

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

3

Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndrome.

Currier SC, Lee CK, Chang BS, Bodell AL, Pai GS, Job L, Lagae LG, Al-Gazali LI, Eyaid WM, Enns G, Dobyns WB, Walsh CA. Currier SC, et al. Among authors: bodell al. Am J Med Genet A. 2005 Feb 15;133A(1):53-7. doi: 10.1002/ajmg.a.30487. Am J Med Genet A. 2005. PMID: 15637732

4

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: bodell a. Ann Neurol. 2005 Nov;58(5):680-7. doi: 10.1002/ana.20616. Ann Neurol. 2005. PMID: 16240336

5

A structural basis for reading fluency: white matter defects in a genetic brain malformation.

Chang BS, Katzir T, Liu T, Corriveau K, Barzillai M, Apse KA, Bodell A, Hackney D, Alsop D, Wong ST, Walsh CA. Chang BS, et al. Among authors: bodell a. Neurology. 2007 Dec 4;69(23):2146-54. doi: 10.1212/01.wnl.0000286365.41070.54. Neurology. 2007. PMID: 18056578

6

A molecular and ecological analysis of the trematode Plagiorchis elegans in the wood mouse Apodemus sylvaticus from a periaquatic ecosystem in the UK.

Boyce K, Hide G, Craig PS, Reynolds C, Hussain M, Bodell AJ, Bradshaw H, Pickles A, Rogan MT. Boyce K, et al. Among authors: bodell aj. J Helminthol. 2014 Sep;88(3):310-20. doi: 10.1017/S0022149X13000199. Epub 2013 Apr 19. J Helminthol. 2014. PMID: 23597061

7

Comprehensive EMX2 genotyping of a large schizencephaly case series.

Tietjen I, Bodell A, Apse K, Mendonza AM, Chang BS, Shaw GM, Barkovich AJ, Lammer EJ, Walsh CA. Tietjen I, et al. Among authors: bodell a. Am J Med Genet A. 2007 Jun 15;143A(12):1313-6. doi: 10.1002/ajmg.a.31767. Am J Med Genet A. 2007. PMID: 17506092

8

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.

Sheen VL, Jansen A, Chen MH, Parrini E, Morgan T, Ravenscroft R, Ganesh V, Underwood T, Wiley J, Leventer R, Vaid RR, Ruiz DE, Hutchins GM, Menasha J, Willner J, Geng Y, Gripp KW, Nicholson L, Berry-Kravis E, Bodell A, Apse K, Hill RS, Dubeau F, Andermann F, Barkovich J, Andermann E, Shugart YY, Thomas P, Viri M, Veggiotti P, Robertson S, Guerrini R, Walsh CA. Sheen VL, et al. Among authors: bodell a. Neurology. 2005 Jan 25;64(2):254-62. doi: 10.1212/01.WNL.0000149512.79621.DF. Neurology. 2005. PMID: 15668422

9

A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly.

Mochida GH, Mahajnah M, Hill AD, Basel-Vanagaite L, Gleason D, Hill RS, Bodell A, Crosier M, Straussberg R, Walsh CA. Mochida GH, et al. Among authors: bodell a. Am J Hum Genet. 2009 Dec;85(6):897-902. doi: 10.1016/j.ajhg.2009.10.027. Am J Hum Genet. 2009. PMID: 20004763 Free PMC article.

10

Desbuquois syndrome: clinical, radiographic, and morphologic characterization.

Shohat M, Lachman R, Gruber HE, Hsia YE, Golbus MS, Witt DR, Bodell A, Bryke CR, Hogge WA, Rimoin DL. Shohat M, et al. Among authors: bodell a. Am J Med Genet. 1994 Aug 1;52(1):9-18. doi: 10.1002/ajmg.1320520104. Am J Med Genet. 1994. PMID: 7977470

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