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Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
de Vries B, Mamsa H, Stam AH, Wan J, Bakker SL, Vanmolkot KR, Haan J, Terwindt GM, Boon EM, Howard BD, Frants RR, Baloh RW, Ferrari MD, Jen JC, van den Maagdenberg AM. de Vries B, et al. Among authors: jen jc. Arch Neurol. 2009 Jan;66(1):97-101. doi: 10.1001/archneurol.2008.535. Arch Neurol. 2009. PMID: 19139306
Familial migraine with vertigo: no mutations found in CACNA1A.
Kim JS, Yue Q, Jen JC, Nelson SF, Baloh RW. Kim JS, et al. Among authors: jen jc. Am J Med Genet. 1998 Sep 1;79(2):148-51. doi: 10.1002/(sici)1096-8628(19980901)79:2<148::aid-ajmg11>3.0.co;2-j. Am J Med Genet. 1998. PMID: 9741473
Oculomotor phenotypes in autosomal dominant ataxias.
Buttner N, Geschwind D, Jen JC, Perlman S, Pulst SM, Baloh RW. Buttner N, et al. Among authors: jen jc. Arch Neurol. 1998 Oct;55(10):1353-7. doi: 10.1001/archneur.55.10.1353. Arch Neurol. 1998. PMID: 9779665
Familial benign recurrent vertigo.
Oh AK, Lee H, Jen JC, Corona S, Jacobson KM, Baloh RW. Oh AK, et al. Among authors: jen jc. Am J Med Genet. 2001 May 15;100(4):287-91. doi: 10.1002/ajmg.1294. Am J Med Genet. 2001. PMID: 11343320
Genetics of familial episodic vertigo and ataxia.
Baloh RW, Jen JC. Baloh RW, et al. Among authors: jen jc. 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
91 results