Armstrong D - Search Results

1

CMT4A: identification of a Hispanic GDAP1 founder mutation.

Boerkoel CF, Takashima H, Nakagawa M, Izumo S, Armstrong D, Butler I, Mancias P, Papasozomenos SC, Stern LZ, Lupski JR. Boerkoel CF, et al. Among authors: armstrong d. Ann Neurol. 2003 Mar;53(3):400-5. doi: 10.1002/ana.10505. Ann Neurol. 2003. PMID: 12601710

2

Disturbance of muscle fiber differentiation in congenital hypomyelinating neuropathy caused by a novel myelin protein zero mutation.

Szigeti K, Saifi GM, Armstrong D, Belmont JW, Miller G, Lupski JR. Szigeti K, et al. Among authors: armstrong d. Ann Neurol. 2003 Sep;54(3):398-402. doi: 10.1002/ana.10681. Ann Neurol. 2003. PMID: 12953275

3

Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy.

Takashima H, Boerkoel CF, John J, Saifi GM, Salih MA, Armstrong D, Mao Y, Quiocho FA, Roa BB, Nakagawa M, Stockton DW, Lupski JR. Takashima H, et al. Among authors: armstrong d. Nat Genet. 2002 Oct;32(2):267-72. doi: 10.1038/ng987. Epub 2002 Sep 16. Nat Genet. 2002. PMID: 12244316

4

Expression patterns of cytochrome P4501B1 (Cyp1b1) in FVB/N mouse eyes.

Bejjani BA, Xu L, Armstrong D, Lupski JR, Reneker LW. Bejjani BA, et al. Among authors: armstrong d. Exp Eye Res. 2002 Sep;75(3):249-57. Exp Eye Res. 2002. PMID: 12384088

5

Neuropathology of Rett syndrome.

Armstrong DD. Armstrong DD. J Child Neurol. 2005 Sep;20(9):747-53. doi: 10.1177/08830738050200090901. J Child Neurol. 2005. PMID: 16225830 Review.

6

Pathologic basis of the symptomatic epilepsies in childhood.

Armstrong DD, Mizrahi EM. Armstrong DD, et al. J Child Neurol. 1998 Aug;13(8):361-71. doi: 10.1177/088307389801300801. J Child Neurol. 1998. PMID: 9721890 Review.

7

Presence of filamin in the astrocytic inclusions of Aicardi syndrome.

Van den Veyver IB, Panichkul PP, Antalffy BA, Sun Y, Hunter JV, Armstrong DD. Van den Veyver IB, et al. Among authors: armstrong dd. Pediatr Neurol. 2004 Jan;30(1):7-15. doi: 10.1016/s0887-8994(03)00311-4. Pediatr Neurol. 2004. PMID: 14738943 Review.

8

The neurological mutant quaking(viable) is Parkin deficient.

Lorenzetti D, Antalffy B, Vogel H, Noveroske J, Armstrong D, Justice M. Lorenzetti D, et al. Among authors: armstrong d. Mamm Genome. 2004 Mar;15(3):210-7. doi: 10.1007/s00335-003-2333-5. Mamm Genome. 2004. PMID: 15014970

9

Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain.

Armstrong DD, Deguchi K, Antallfy B. Armstrong DD, et al. J Child Neurol. 2003 Oct;18(10):683-7. doi: 10.1177/08830738030180100601. J Child Neurol. 2003. PMID: 14649549

10

Selective dendritic alterations in the cortex of Rett syndrome.

Armstrong D, Dunn JK, Antalffy B, Trivedi R. Armstrong D, et al. J Neuropathol Exp Neurol. 1995 Mar;54(2):195-201. doi: 10.1097/00005072-199503000-00006. J Neuropathol Exp Neurol. 1995. PMID: 7876888

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