Nelson SF - Search Results

1

Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p.

Baloh RW, Yue Q, Furman JM, Nelson SF. Baloh RW, et al. Among authors: nelson sf. Ann Neurol. 1997 Jan;41(1):8-16. doi: 10.1002/ana.410410105. Ann Neurol. 1997. PMID: 9005860

2

Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).

Jen J, Cohen AH, Yue Q, Stout JT, Vinters HV, Nelson S, Baloh RW. Jen J, et al. Neurology. 1997 Nov;49(5):1322-30. doi: 10.1212/wnl.49.5.1322. Neurology. 1997. PMID: 9371916

3

A novel mutation in KCNA1 causes episodic ataxia without myokymia.

Lee H, Wang H, Jen JC, Sabatti C, Baloh RW, Nelson SF. Lee H, et al. Among authors: nelson sf. Hum Mutat. 2004 Dec;24(6):536. doi: 10.1002/humu.9295. Hum Mutat. 2004. PMID: 15532032

4

Familial migraine with vertigo and essential tremor.

Baloh RW, Foster CA, Yue Q, Nelson SF. Baloh RW, et al. Among authors: nelson sf. Neurology. 1996 Feb;46(2):458-60. doi: 10.1212/wnl.46.2.458. Neurology. 1996. PMID: 8614512

5

Progressive ataxia due to a missense mutation in a calcium-channel gene.

Yue Q, Jen JC, Nelson SF, Baloh RW. Yue Q, et al. Among authors: nelson sf. Am J Hum Genet. 1997 Nov;61(5):1078-87. doi: 10.1086/301613. Am J Hum Genet. 1997. PMID: 9345107 Free PMC article.

6

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia.

Yue Q, Jen JC, Thwe MM, Nelson SF, Baloh RW. Yue Q, et al. Among authors: nelson sf. Am J Med Genet. 1998 May 26;77(4):298-301. doi: 10.1002/(sici)1096-8628(19980526)77:4<298::aid-ajmg9>3.0.co;2-j. Am J Med Genet. 1998. PMID: 9600739

7

Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia.

Jen JC, Yue Q, Karrim J, Nelson SF, Baloh RW. Jen JC, et al. Among authors: nelson sf. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):565-8. doi: 10.1136/jnnp.65.4.565. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771787 Free PMC article.

8

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia.

Jen J, Yue Q, Nelson SF, Yu H, Litt M, Nutt J, Baloh RW. Jen J, et al. Among authors: nelson sf. Neurology. 1999 Jul 13;53(1):34-7. doi: 10.1212/wnl.53.1.34. Neurology. 1999. PMID: 10408533

9

Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25.

Jen J, Coulin CJ, Bosley TM, Salih MA, Sabatti C, Nelson SF, Baloh RW. Jen J, et al. Among authors: nelson sf. Neurology. 2002 Aug 13;59(3):432-5. doi: 10.1212/wnl.59.3.432. Neurology. 2002. PMID: 12177379

10

Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy.

Jen JC, Wang H, Lee H, Sabatti C, Trent R, Hannigan I, Brantberg K, Halmagyi GM, Nelson SF, Baloh RW. Jen JC, et al. Among authors: nelson sf. Neurology. 2004 Dec 28;63(12):2376-9. doi: 10.1212/01.wnl.0000149498.79541.49. Neurology. 2004. PMID: 15623703

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