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Results: 1-6 |
Results: 6

Authors: Jouvenceau, A Eunson, LH Spauschus, A Ramesh, V Zuberi, SM Kullmann, DM Hanna, MG
Citation: A. Jouvenceau et al., Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel, LANCET, 358(9284), 2001, pp. 801-807

Authors: Zuberi, SM Hanna, MG
Citation: Sm. Zuberi et Mg. Hanna, Ion channels and neurology, ARCH DIS CH, 84(3), 2001, pp. 277-280

Authors: Phillips, HA Favre, I Kirkpatrick, M Zuberi, SM Goudie, D Heron, SE Scheffer, IE Sutherland, GR Berkovic, SF Bertrand, D Mulley, JC
Citation: Ha. Phillips et al., CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy, AM J HU GEN, 68(1), 2001, pp. 225-231

Authors: Eunson, LH Rea, R Zuberi, SM Youroukos, S Panayiotopoulos, CP Liguori, R Avoni, P McWilliam, RC Stephenson, JBP Hanna, MG Kullmann, DM Spauschus, A
Citation: Lh. Eunson et al., Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability, ANN NEUROL, 48(4), 2000, pp. 647-656

Authors: Zuberi, SM Matta, N Nawaz, S Stephenson, JB McWilliam, RC Hollman, A
Citation: Sm. Zuberi et al., Muscle ultrasound in the assessment of suspected neuromuscular disease in childhood, NEUROMUSC D, 9(4), 1999, pp. 203-207

Authors: Zuberi, SM Eunson, LH Spauschus, A De Silva, R Tolmie, J Wood, NW McWilliam, RC Stephenson, JPB Kullmann, DM Hanna, MG
Citation: Sm. Zuberi et al., A novel mutation in the human voltage-gated potassium channel gene (Kv1.1)associates with episodic ataxia type 1 and sometimes with partial epilepsy, BRAIN, 122, 1999, pp. 817-825
Risultati: 1-6 |