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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 1 |
1999 | 1 |
2001 | 3 |
2004 | 1 |
2005 | 1 |
2024 | 0 |
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Ataxia and calcium channels: what a headache!
Arch Neurol. 2001 Feb;58(2):179-80. doi: 10.1001/archneur.58.2.179.
Arch Neurol. 2001.
PMID: 11176954
No abstract available.
Calcium channelopathies in the central nervous system.
Jen J.
Jen J.
Curr Opin Neurobiol. 1999 Jun;9(3):274-80. doi: 10.1016/s0959-4388(99)80040-3.
Curr Opin Neurobiol. 1999.
PMID: 10395579
Review.
Item in Clipboard
Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
Jen J, Wan J, Graves M, Yu H, Mock AF, Coulin CJ, Kim G, Yue Q, Papazian DM, Baloh RW.
Jen J, et al.
Neurology. 2001 Nov 27;57(10):1843-8. doi: 10.1212/wnl.57.10.1843.
Neurology. 2001.
PMID: 11723274
Item in Clipboard
CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kinetics.
Wan J, Khanna R, Sandusky M, Papazian DM, Jen JC, Baloh RW.
Wan J, et al.
Neurology. 2005 Jun 28;64(12):2090-7. doi: 10.1212/01.WNL.0000167409.59089.C0.
Neurology. 2005.
PMID: 15985579
Item in Clipboard
Inferring articulation and recognizing gestures from acoustics with a neural network trained on x-ray microbeam data.
Papcun G, Hochberg J, Thomas TR, Laroche F, Zacks J, Levy S.
Papcun G, et al.
J Acoust Soc Am. 1992 Aug;92(2 Pt 1):688-700. doi: 10.1121/1.403994.
J Acoust Soc Am. 1992.
PMID: 1506525
Item in Clipboard
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.
Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR.
Ophoff RA, et al.
Am J Hum Genet. 2001 Aug;69(2):447-53. doi: 10.1086/321975. Epub 2001 Jun 28.
Am J Hum Genet. 2001.
PMID: 11438888
Free PMC article.
Item in Clipboard
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.
Science. 2004 Jun 4;304(5676):1509-13. doi: 10.1126/science.1096437. Epub 2004 Apr 22.
Science. 2004.
PMID: 15105459
Free PMC article.
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