Vanderver AL - Search Results

1

Isolated cranial nerve enhancement in metachromatic leukodystrophy.

Singh RK, Leshner RT, Kadom N, Vanderver AL. Singh RK, et al. Among authors: vanderver al. Pediatr Neurol. 2009 May;40(5):380-2. doi: 10.1016/j.pediatrneurol.2008.11.015. Pediatr Neurol. 2009. PMID: 19380076 Free PMC article.

2

Tools for diagnosis of leukodystrophies and other disorders presenting with white matter disease.

Vanderver A. Vanderver A. Curr Neurol Neurosci Rep. 2005 Mar;5(2):110-8. doi: 10.1007/s11910-005-0008-1. Curr Neurol Neurosci Rep. 2005. PMID: 15743548 Review.

3

Genetic and clinical heterogeneity in eIF2B-related disorder.

Maletkovic J, Schiffmann R, Gorospe JR, Gordon ES, Mintz M, Hoffman EP, Alper G, Lynch DR, Singhal BS, Harding C, Amartino H, Brown CM, Chan A, Renaud D, Geraghty M, Jensen L, Senbil N, Kadom N, Nazarian J, Yuanjian Feng, Zuyi Wang, Hartka T, Morizono H, Vanderver A. Maletkovic J, et al. J Child Neurol. 2008 Feb;23(2):205-15. doi: 10.1177/0883073807308705. J Child Neurol. 2008. PMID: 18263758

4

Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder.

Vanderver A, Hathout Y, Maletkovic J, Gordon ES, Mintz M, Timmons M, Hoffman EP, Horzinski L, Niel F, Fogli A, Boespflug-Tanguy O, Schiffmann R. Vanderver A, et al. Neurology. 2008 Jun 3;70(23):2226-32. doi: 10.1212/01.wnl.0000313857.54398.0e. Neurology. 2008. PMID: 18519871 Free PMC article.

5

New-onset afebrile seizures in infants: role of neuroimaging.

Hsieh DT, Chang T, Tsuchida TN, Vezina LG, Vanderver A, Siedel J, Brown K, Berl MM, Stephens S, Zeitchick A, Gaillard WD. Hsieh DT, et al. Neurology. 2010 Jan 12;74(2):150-6. doi: 10.1212/WNL.0b013e3181c91847. Neurology. 2010. PMID: 20065250 Free PMC article.

6

Magnetic resonance imaging pattern recognition in hypomyelinating disorders.

Steenweg ME, Vanderver A, Blaser S, Bizzi A, de Koning TJ, Mancini GM, van Wieringen WN, Barkhof F, Wolf NI, van der Knaap MS. Steenweg ME, et al. Brain. 2010 Oct;133(10):2971-82. doi: 10.1093/brain/awq257. Brain. 2010. PMID: 20881161 Free PMC article.

7

Focal central white matter lesions in Alexander disease.

Barreau P, Prust MJ, Crane J, Loewenstein J, Kadom N, Vanderver A. Barreau P, et al. J Child Neurol. 2011 Nov;26(11):1422-4. doi: 10.1177/0883073811405381. Epub 2011 May 13. J Child Neurol. 2011. PMID: 21572052 Free PMC article.

8

MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.

Ah Mew N, Loewenstein JB, Kadom N, Lichter-Konecki U, Gropman AL, Martin JM, Vanderver A. Ah Mew N, et al. Among authors: vanderver a. Pediatr Neurol. 2011 Jul;45(1):57-9. doi: 10.1016/j.pediatrneurol.2011.02.003. Pediatr Neurol. 2011. PMID: 21723463 Free PMC article.

9

Relative incidence of inherited white matter disorders in childhood to acquired pediatric demyelinating disorders.

Vanderver A, Hussey H, Schmidt JL, Pastor W, Hoffman HJ. Vanderver A, et al. Semin Pediatr Neurol. 2012 Dec;19(4):219-23. doi: 10.1016/j.spen.2012.10.001. Semin Pediatr Neurol. 2012. PMID: 23245555 Free PMC article.

10

Elevation of proinflammatory cytokines in patients with Aicardi-Goutières syndrome.

Takanohashi A, Prust M, Wang J, Gordish-Dressman H, Bloom M, Rice GI, Schmidt JL, Crow YJ, Lebon P, Kuijpers TW, Nagaraju K, Vanderver A. Takanohashi A, et al. Neurology. 2013 Mar 12;80(11):997-1002. doi: 10.1212/WNL.0b013e3182872694. Epub 2013 Feb 13. Neurology. 2013. PMID: 23408864 Free PMC article.

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