Kullmann DM - Search Results

1

Basket to Purkinje Cell Inhibitory Ephaptic Coupling Is Abolished in Episodic Ataxia Type 1.

Martin HGS, Kullmann DM. Martin HGS, et al. Among authors: kullmann dm. Cells. 2023 May 13;12(10):1382. doi: 10.3390/cells12101382. Cells. 2023. PMID: 37408217 Free PMC article.

2

Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.

Imbrici P, Jaffe SL, Eunson LH, Davies NP, Herd C, Robertson R, Kullmann DM, Hanna MG. Imbrici P, et al. Among authors: kullmann dm. Brain. 2004 Dec;127(Pt 12):2682-92. doi: 10.1093/brain/awh301. Epub 2004 Oct 13. Brain. 2004. PMID: 15483044

3

Episodic ataxia type 1: a neuronal potassium channelopathy.

Rajakulendran S, Schorge S, Kullmann DM, Hanna MG. Rajakulendran S, et al. Among authors: kullmann dm. Neurotherapeutics. 2007 Apr;4(2):258-66. doi: 10.1016/j.nurt.2007.01.010. Neurotherapeutics. 2007. PMID: 17395136 Free article. Review.

4

Episodic ataxia type 1 mutations differentially affect neuronal excitability and transmitter release.

Heeroma JH, Henneberger C, Rajakulendran S, Hanna MG, Schorge S, Kullmann DM. Heeroma JH, et al. Among authors: kullmann dm. Dis Model Mech. 2009 Nov-Dec;2(11-12):612-9. doi: 10.1242/dmm.003582. Epub 2009 Sep 24. Dis Model Mech. 2009. PMID: 19779067 Free PMC article.

5

Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.

Rajakulendran S, Graves TD, Labrum RW, Kotzadimitriou D, Eunson L, Davis MB, Davies R, Wood NW, Kullmann DM, Hanna MG, Schorge S. Rajakulendran S, et al. Among authors: kullmann dm. J Physiol. 2010 Jun 1;588(Pt 11):1905-13. doi: 10.1113/jphysiol.2009.186437. Epub 2010 Feb 15. J Physiol. 2010. PMID: 20156848 Free PMC article.

6

Nerve excitability studies characterize Kv1.1 fast potassium channel dysfunction in patients with episodic ataxia type 1.

Tomlinson SE, Tan SV, Kullmann DM, Griggs RC, Burke D, Hanna MG, Bostock H. Tomlinson SE, et al. Among authors: kullmann dm. Brain. 2010 Dec;133(Pt 12):3530-40. doi: 10.1093/brain/awq318. Epub 2010 Nov 23. Brain. 2010. PMID: 21106501 Free PMC article.

7

Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1.

Tomlinson SE, Rajakulendran S, Tan SV, Graves TD, Bamiou DE, Labrum RW, Burke D, Sue CM, Giunti P, Schorge S, Kullmann DM, Hanna MG. Tomlinson SE, et al. Among authors: kullmann dm. J Neurol Neurosurg Psychiatry. 2013 Oct;84(10):1107-12. doi: 10.1136/jnnp-2012-304131. Epub 2013 Jan 24. J Neurol Neurosurg Psychiatry. 2013. PMID: 23349320 Free PMC article.

8

Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2.

Graves TD, Imbrici P, Kors EE, Terwindt GM, Eunson LH, Frants RR, Haan J, Ferrari MD, Goadsby PJ, Hanna MG, van den Maagdenberg AM, Kullmann DM. Graves TD, et al. Among authors: kullmann dm. Neurobiol Dis. 2008 Oct;32(1):10-5. doi: 10.1016/j.nbd.2008.06.002. Epub 2008 Jun 19. Neurobiol Dis. 2008. PMID: 18606230

9

Dysfunction of the Ca(V)2.1 calcium channel in cerebellar ataxias.

Rajakulendran S, Schorge S, Kullmann DM, Hanna MG. Rajakulendran S, et al. Among authors: kullmann dm. F1000 Biol Rep. 2010 Jan 18;2:4. doi: 10.3410/B2-4. F1000 Biol Rep. 2010. PMID: 20948794 Free PMC article.

10

In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2.

Tomlinson SE, Tan SV, Burke D, Labrum RW, Haworth A, Gibbons VS, Sweeney MG, Griggs RC, Kullmann DM, Bostock H, Hanna MG. Tomlinson SE, et al. Among authors: kullmann dm. Brain. 2016 Feb;139(Pt 2):380-91. doi: 10.1093/brain/awv380. Brain. 2016. PMID: 26912519 Free PMC article.

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