Baloh RW - Search Results

1

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.

Jen JC, Chan WM, Bosley TM, Wan J, Carr JR, Rüb U, Shattuck D, Salamon G, Kudo LC, Ou J, Lin DD, Salih MA, Kansu T, Al Dhalaan H, Al Zayed Z, MacDonald DB, Stigsby B, Plaitakis A, Dretakis EK, Gottlob I, Pieh C, Traboulsi EI, Wang Q, Wang L, Andrews C, Yamada K, Demer JL, Karim S, Alger JR, Geschwind DH, Deller T, Sicotte NL, Nelson SF, Baloh RW, Engle EC. Jen JC, et al. Among authors: baloh rw. Science. 2004 Jun 4;304(5676):1509-13. doi: 10.1126/science.1096437. Epub 2004 Apr 22. Science. 2004. PMID: 15105459 Free PMC article.

2

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

3

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.

4

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: baloh rw. Hum Mutat. 2004 Dec;24(6):536. doi: 10.1002/humu.9295. Hum Mutat. 2004. PMID: 15532032

5

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

6

Familial episodic ataxia: a model for migrainous vertigo.

Jen JC, Baloh RW. Jen JC, et al. Among authors: baloh rw. Ann N Y Acad Sci. 2009 May;1164:252-6. doi: 10.1111/j.1749-6632.2008.03723.x. Ann N Y Acad Sci. 2009. PMID: 19645908

7

Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations.

Kerber KA, Jen JC, Perlman S, Baloh RW. Kerber KA, et al. Among authors: baloh rw. J Neurol Sci. 2005 Nov 15;238(1-2):41-5. doi: 10.1016/j.jns.2005.06.006. Epub 2005 Aug 16. J Neurol Sci. 2005. PMID: 16109427 Review.

8

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.

Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF. Lee H, et al. Among authors: baloh rw. Hum Mol Genet. 2006 Jan 15;15(2):251-8. doi: 10.1093/hmg/ddi441. Epub 2005 Dec 5. Hum Mol Genet. 2006. PMID: 16330481

9

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

10

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

Lee H, Jen JC, Cha YH, Nelson SF, Baloh RW. Lee H, et al. Among authors: baloh rw. Headache. 2008 Nov-Dec;48(10):1460-7. doi: 10.1111/j.1526-4610.2007.01002.x. Epub 2007 Dec 11. Headache. 2008. PMID: 18081823 Free PMC article.

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