Authors:
Font, M
Feliubadalo, L
Estivill, X
Nunes, V
Golomb, E
Kreiss, Y
Pras, E
Bisceglia, L
d'Adamo, AP
Zelante, L
Gasparini, P
Bassi, MT
George, AL
Manzoni, M
Riboni, M
Ballabio, A
Borsani, G
Reig, N
Fernandez, E
Zorzano, A
Bertran, J
Palacin, M
Citation: M. Font et al., Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria, HUM MOL GEN, 10(4), 2001, pp. 305-316
Citation: L. Bianchi et al., Expression of a CIC chloride channel in Caenorhabditis elegans gamma-aminobutyric acid-ergic neurons, NEUROSCI L, 299(3), 2001, pp. 177-180
Authors:
Schneider, E
Knoll, AG
Carmeliet, E
Fozzard, HA
Hiraoka, M
Janse, J
Ogawa, S
Roden, DM
Rosen, MR
Rudy, Y
Schwartz, PJ
Matteo, S
Camm, AJ
Antzelevitch, C
Boyden, PA
Catterall, WA
Fishman, GI
George, AL
Izumo, S
Jalife, J
January, CT
Kleber, AG
Marban, E
Marks, AR
Spooner, PM
Waldo, AL
Weiss, JM
Zipes, DP
Citation: E. Schneider et al., New approaches to antiarrhythmic therapy - Emerging therapeutic applications of the cell biology of cardiac arrhythmias, EUR HEART J, 22(23), 2001, pp. 2148-2163
Authors:
Plaster, NM
Tawil, R
Tristani-Firouzi, M
Canun, S
Bendahhou, S
Tsunoda, A
Donaldson, MR
Iannaccone, ST
Brunt, E
Barohn, R
Clark, J
Deymeer, F
George, AL
Fish, FA
Hahn, A
Nitu, A
Ozdemir, C
Serdaroglu, P
Subramony, SH
Wolfe, G
Fu, YH
Ptacek, LJ
Citation: Nm. Plaster et al., Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome, CELL, 105(4), 2001, pp. 511-519
Authors:
Desaphy, JF
De Luca, A
Tortorella, P
De Vito, D
George, AL
Camerino, DC
Citation: Jf. Desaphy et al., Gating of myotonic Na channel mutants defines the response to mexiletine and a potent derivative, NEUROLOGY, 57(10), 2001, pp. 1849-1857
Citation: Ar. Tapper et Al. George, Location and orientation of minK within the I-Ks potassium channel complex, J BIOL CHEM, 276(41), 2001, pp. 38249-38254
Authors:
Carmeliet, E
Fozzard, HA
Hiraoka, M
Janse, MJ
Ogawa, S
Roden, DM
Rosen, MR
Rudy, Y
Schwartz, PJ
Matteo, PS
Antzelevitch, C
Boyden, PA
Catterall, WA
Fishman, GI
George, AL
Izumo, S
Jalife, J
January, CT
Kleber, AG
Marban, E
Marks, AR
Spooner, PM
Waldo, AL
Weiss, JM
Zipes, DLP
Citation: E. Carmeliet et al., New approaches to antiarrhythmic therapy, part I - Emerging therapeutic applications of the cell biology of cardiac arrhythmias, CIRCULATION, 104(23), 2001, pp. 2865-2873
Authors:
Viswanathan, PC
Bezzina, CR
George, AL
Roden, DM
Wilde, AAM
Balser, JR
Citation: Pc. Viswanathan et al., Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes, CIRCULATION, 104(10), 2001, pp. 1200-1205
Authors:
Spooner, PM
Albert, C
Benjamin, EJ
Boineau, R
Elston, RC
George, AL
Jouven, X
Kuller, LH
MacCluer, JW
Marban, E
Muller, JE
Schwartz, PJ
Siscovick, DS
Tracy, RP
Zareba, W
Zipes, DP
Citation: Pm. Spooner et al., Sudden cardiac death, genes, and arrhythmogenesis - Consideration of new population and mechanistic approaches from a National Heart, Lung, and BloodInstitute Workshop, part II, CIRCULATION, 103(20), 2001, pp. 2447-2452
Authors:
Spooner, PM
Albert, C
Benjamin, EJ
Boineau, R
Elston, RC
George, AL
Jouven, X
Kuller, LH
MacCluer, JW
Marban, E
Muller, JE
Schwartz, PJ
Siscovick, DS
Tracy, RP
Zareba, W
Zipes, DP
Citation: Pm. Spooner et al., Sudden cardiac death, genes, and arrhythmogenesis - Consideration of new population and mechanistic approaches from a national heart, lung, and bloodinstitute workshop, part I, CIRCULATION, 103(19), 2001, pp. 2361-2364
Authors:
Wallace, RH
Scheffer, IE
Barnett, S
Richards, M
Dibbens, L
Desai, RR
Lerman-Sagie, T
Lev, D
Mazarib, A
Brand, N
Ben-Zeev, B
Goikhman, I
Singh, R
Kremmidiotis, G
Gardner, A
Sutherland, GR
George, AL
Mulley, JC
Berkovic, SF
Citation: Rh. Wallace et al., Neuronal sodium-channel alpha 1-subunit mutations in generalized epilepsy with febrile seizures plus, AM J HU GEN, 68(4), 2001, pp. 859-865
Authors:
Weckbecker, K
Wurz, A
Mohammadi, B
Mansuroglu, T
George, AL
Lerche, H
Dengler, R
Lehmann-Horn, F
Mitrovic, N
Citation: K. Weckbecker et al., Different effects of mexiletine on two mutant sodium channels causing paramyotonia congenita and hyperkalemic periodic paralysis, NEUROMUSC D, 10(1), 2000, pp. 31-39
Citation: Al. George et S. Hebert, Forefronts in nephrology: Ion channelopathies: Hereditary dysfunction of ion channels - Skytop, Pennsylvania, USA - October 28-31, 1998 - Introduction, KIDNEY INT, 57(3), 2000, pp. 761-765