Kullmann DM - Search Results

1

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.

Gardiner AR, Bhatia KP, Stamelou M, Dale RC, Kurian MA, Schneider SA, Wali GM, Counihan T, Schapira AH, Spacey SD, Valente EM, Silveira-Moriyama L, Teive HA, Raskin S, Sander JW, Lees A, Warner T, Kullmann DM, Wood NW, Hanna M, Houlden H. Gardiner AR, et al. Among authors: kullmann dm. Neurology. 2012 Nov 20;79(21):2115-21. doi: 10.1212/WNL.0b013e3182752c5a. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077024 Free PMC article.

2

Neurological disorders caused by inherited ion-channel mutations.

Kullmann DM, Hanna MG. Kullmann DM, et al. Lancet Neurol. 2002 Jul;1(3):157-66. doi: 10.1016/s1474-4422(02)00071-6. Lancet Neurol. 2002. PMID: 12849484 Review.

3

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

4

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.

5

Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita.

Fialho D, Kullmann DM, Hanna MG, Schorge S. Fialho D, et al. Among authors: kullmann dm. Neuromuscul Disord. 2008 Nov;18(11):869-72. doi: 10.1016/j.nmd.2008.07.004. Epub 2008 Sep 23. Neuromuscul Disord. 2008. PMID: 18815035

6

Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivo.

Tomlinson SE, Hanna MG, Kullmann DM, Tan SV, Burke D. Tomlinson SE, et al. Among authors: kullmann dm. Clin Neurophysiol. 2009 Oct;120(10):1768-76. doi: 10.1016/j.clinph.2009.07.003. Epub 2009 Sep 5. Clin Neurophysiol. 2009. PMID: 19734086 Review.

7

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.

8

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.

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

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.

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