Spauschus A - Search Results

1

Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1.

Rea R, Spauschus A, Eunson LH, Hanna MG, Kullmann DM. Rea R, et al. Among authors: spauschus a. J Physiol. 2002 Jan 1;538(Pt 1):5-23. doi: 10.1113/jphysiol.2001.013242. J Physiol. 2002. PMID: 11773313 Free PMC article.

2

Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy.

Spauschus A, Eunson L, Hanna MG, Kullmann DM. Spauschus A, et al. Ann N Y Acad Sci. 1999 Apr 30;868:442-6. doi: 10.1111/j.1749-6632.1999.tb11310.x. Ann N Y Acad Sci. 1999. PMID: 10414318 No abstract available.

3

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.

Eunson LH, Rea R, Zuberi SM, Youroukos S, Panayiotopoulos CP, Liguori R, Avoni P, McWilliam RC, Stephenson JB, Hanna MG, Kullmann DM, Spauschus A. Eunson LH, et al. Among authors: spauschus a. Ann Neurol. 2000 Oct;48(4):647-56. Ann Neurol. 2000. PMID: 11026449

4

The inherited episodic ataxias: how well do we understand the disease mechanisms?

Kullmann DM, Rea R, Spauschus A, Jouvenceau A. Kullmann DM, et al. Among authors: spauschus a. Neuroscientist. 2001 Feb;7(1):80-8. doi: 10.1177/107385840100700111. Neuroscientist. 2001. PMID: 11486347 Review.

5

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.

Jouvenceau A, Eunson LH, Spauschus A, Ramesh V, Zuberi SM, Kullmann DM, Hanna MG. Jouvenceau A, et al. Among authors: spauschus a. Lancet. 2001 Sep 8;358(9284):801-7. doi: 10.1016/S0140-6736(01)05971-2. Lancet. 2001. PMID: 11564488

6

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

Zuberi SM, Eunson LH, Spauschus A, De Silva R, Tolmie J, Wood NW, McWilliam RC, Stephenson JB, Kullmann DM, Hanna MG. Zuberi SM, et al. Among authors: spauschus a. Brain. 1999 May;122 ( Pt 5):817-25. doi: 10.1093/brain/122.5.817. Brain. 1999. PMID: 10355668

7

The origin of ocular microtremor in man.

Spauschus A, Marsden J, Halliday DM, Rosenberg JR, Brown P. Spauschus A, et al. Exp Brain Res. 1999 Jun;126(4):556-62. doi: 10.1007/s002210050764. Exp Brain Res. 1999. PMID: 10422719

8

Potassium channel dysfunction and depolarized resting membrane potential in a cell model of SCA3.

Jeub M, Herbst M, Spauschus A, Fleischer H, Klockgether T, Wuellner U, Evert BO. Jeub M, et al. Among authors: spauschus a. Exp Neurol. 2006 Sep;201(1):182-92. doi: 10.1016/j.expneurol.2006.03.029. Epub 2006 Jun 12. Exp Neurol. 2006. PMID: 16765348

9

The molecular biology of the autosomal-dominant cerebellar ataxias.

Klockgether T, Wüllner U, Spauschus A, Evert B. Klockgether T, et al. Among authors: spauschus a. Mov Disord. 2000 Jul;15(4):604-12. doi: 10.1002/1531-8257(200007)15:4<604::aid-mds1004>3.0.co;2-k. Mov Disord. 2000. PMID: 10928570 Review.

10

Subunit interactions in the assembly of neuronal Kir3.0 inwardly rectifying K+ channels.

Wischmeyer E, Döring F, Wischmeyer E, Spauschus A, Thomzig A, Veh R, Karschin A. Wischmeyer E, et al. Among authors: spauschus a. Mol Cell Neurosci. 1997;9(3):194-206. doi: 10.1006/mcne.1997.0614. Mol Cell Neurosci. 1997. PMID: 9245502

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