Baloh RW - Search Results

1

Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene).

Baloh RH, Jen JC, Kim G, Baloh RW. Baloh RH, et al. Among authors: baloh rw. Neurology. 2004 May 25;62(10):1905-6. doi: 10.1212/01.wnl.0000125287.98456.23. Neurology. 2004. PMID: 15159512 No abstract available.

2

Genetics of episodic ataxia.

Jen JC, Baloh RW. Jen JC, et al. Among authors: baloh rw. Adv Neurol. 2002;89:459-61. Adv Neurol. 2002. PMID: 11968470 Review. No abstract available.

3

No mutations in CACNA1A and ATP1A2 in probands with common types of migraine.

Jen JC, Kim GW, Dudding KA, Baloh RW. Jen JC, et al. Among authors: baloh rw. Arch Neurol. 2004 Jun;61(6):926-8. doi: 10.1001/archneur.61.6.926. Arch Neurol. 2004. PMID: 15210532

4

Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene.

Jen J, Baloh RH, Ishiyama A, Baloh RW. Jen J, et al. Among authors: baloh rh, baloh rw. J Neurol Sci. 2005 Oct 15;237(1-2):21-4. doi: 10.1016/j.jns.2005.05.003. J Neurol Sci. 2005. PMID: 15992829

5

A new episodic ataxia syndrome with linkage to chromosome 19q13.

Kerber KA, Jen JC, Lee H, Nelson SF, Baloh RW. Kerber KA, et al. Among authors: baloh rw. Arch Neurol. 2007 May;64(5):749-52. doi: 10.1001/archneur.64.5.749. Arch Neurol. 2007. PMID: 17502476

6

Progressive cerebellar ataxia with variable episodic symptoms--phenotypic diversity of R1668W CACNA1A mutation.

Marti S, Baloh RW, Jen JC, Straumann D, Jung HH. Marti S, et al. Among authors: baloh rw. Eur Neurol. 2008;60(1):16-20. doi: 10.1159/000127974. Epub 2008 Apr 25. Eur Neurol. 2008. PMID: 18437043 Free article.

7

Nonconsensus intronic mutations cause episodic ataxia.

Wan J, Carr JR, Baloh RW, Jen JC. Wan J, et al. Among authors: baloh rw. Ann Neurol. 2005 Jan;57(1):131-5. doi: 10.1002/ana.20343. Ann Neurol. 2005. PMID: 15622542

8

Neurotological findings in a family with episodic ataxia.

Sasaki O, Jen JC, Baloh RW, Kim GW, Isawa M, Usami S. Sasaki O, et al. Among authors: baloh rw. J Neurol. 2003 Mar;250(3):373-5. doi: 10.1007/s00415-003-0994-3. J Neurol. 2003. PMID: 12749331 No abstract available.

9

Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2.

Wan J, Mamsa H, Johnston JL, Spriggs EL, Singer HS, Zee DS, Al-Bayati AR, Baloh RW, Jen JC; CINCH Investigators. Wan J, et al. Among authors: baloh rw. Front Neurol. 2011 Sep 9;2:51. doi: 10.3389/fneur.2011.00051. eCollection 2011. Front Neurol. 2011. PMID: 21927611 Free PMC article.

10

Genetics of familial episodic vertigo and ataxia.

Baloh RW, Jen JC. Baloh RW, et al. Ann N Y Acad Sci. 2002 Apr;956:338-45. doi: 10.1111/j.1749-6632.2002.tb02832.x. Ann N Y Acad Sci. 2002. PMID: 11960817

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