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Page 1
Oculomotor phenotypes in autosomal dominant ataxias.
Buttner N, Geschwind D, Jen JC, Perlman S, Pulst SM, Baloh RW. Buttner N, et al. Among authors: geschwind d. Arch Neurol. 1998 Oct;55(10):1353-7. doi: 10.1001/archneur.55.10.1353. Arch Neurol. 1998. PMID: 9779665
The SCA12 mutation as a rare cause of spinocerebellar ataxia.
Cholfin JA, Sobrido MJ, Perlman S, Pulst SM, Geschwind DH. Cholfin JA, et al. Among authors: geschwind dh. Arch Neurol. 2001 Nov;58(11):1833-5. doi: 10.1001/archneur.58.11.1833. Arch Neurol. 2001. PMID: 11708992
Ataxia and calcium channels: what a headache!
Jen J, Geschwind DH. Jen J, et al. Among authors: geschwind dh. Arch Neurol. 2001 Feb;58(2):179-80. doi: 10.1001/archneur.58.2.179. Arch Neurol. 2001. PMID: 11176954 No abstract available.
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: geschwind dh. Science. 2004 Jun 4;304(5676):1509-13. doi: 10.1126/science.1096437. Epub 2004 Apr 22. Science. 2004. PMID: 15105459 Free PMC article.
Inheritance of frontotemporal dementia.
Chow TW, Miller BL, Hayashi VN, Geschwind DH. Chow TW, et al. Among authors: geschwind dh. Arch Neurol. 1999 Jul;56(7):817-22. doi: 10.1001/archneur.56.7.817. Arch Neurol. 1999. PMID: 10404983 Free PMC article.
681 results