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Results: 1-17 |
Results: 17
Enhanced inactivation and acceleration of activation of the sodium channelassociated with epilepsy in man
Authors: Alekov, AK Rahman, M Mitrovic, N Lehmann-Horn, F Lerche, H
Citation: Ak. Alekov et al., Enhanced inactivation and acceleration of activation of the sodium channelassociated with epilepsy in man, EUR J NEURO, 13(11), 2001, pp. 2171-2176
Two mutations in the IV/S4-S5 segment of the human skeletal muscle Na+ channel disrupt fast and enhance slow inactivation
Authors: Alekov, AK Peter, WG Mitrovic, N Lehmann-Horn, F Lerche, H
Citation: Ak. Alekov et al., Two mutations in the IV/S4-S5 segment of the human skeletal muscle Na+ channel disrupt fast and enhance slow inactivation, NEUROSCI L, 306(3), 2001, pp. 173-176
Ion channels and epilepsy
Authors: Lerche, H Jurkat-Rott, K Lehmann-Horn, F
Citation: H. Lerche et al., Ion channels and epilepsy, AM J MED G, 106(2), 2001, pp. 146-159
Generalized epilepsy with febrile seizures plus - Further heterogeneity ina large family
Authors: Lerche, H Weber, YG Baier, H Jurkat-Rott, K de Camargo, OK Ludolph, AC Bode, H Lehmann-Horn, F
Citation: H. Lerche et al., Generalized epilepsy with febrile seizures plus - Further heterogeneity ina large family, NEUROLOGY, 57(7), 2001, pp. 1191-1198
Formation of a novel colored product during the Maillard reaction of D-glucose
Authors: Knerr, T Lerche, H Pischetsrieder, M Severin, T
Citation: T. Knerr et al., Formation of a novel colored product during the Maillard reaction of D-glucose, J AGR FOOD, 49(4), 2001, pp. 1966-1970
Different effects of mexiletine on two mutant sodium channels causing paramyotonia congenita and hyperkalemic periodic paralysis
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
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current (vol 97, pg 9549, 2000)
Authors: Jurkat-Rott, K Mitrovic, N Hang, C Kouzmekine, A Iaizzo, P Herzog, J Lerche, H Nicole, S Vale-Santos, J Chauveau, D Fontaine, B Lehmann-Horn, F
Citation: K. Jurkat-rott et al., Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current (vol 97, pg 9549, 2000), P NAS US, 97(21), 2000, pp. 11673-11673
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
Authors: Jurkat-Rott, K Mitrovic, N Hang, C Kouzmekine, A Iaizzo, P Herzog, J Lerche, H Nicole, S Vale-Santos, J Chauveau, D Fontaine, B Lehmann-Horn, F
Citation: K. Jurkat-rott et al., Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current, P NAS US, 97(17), 2000, pp. 9549-9554
A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro
Authors: Alekov, AK Rahman, MM Mitrovic, N Lehmann-Horn, F Lerche, H
Citation: Ak. Alekov et al., A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro, J PHYSL LON, 529(3), 2000, pp. 533-539
Formation of tetrahydro-beta-carbolines and beta-carbolines during the reaction of L-tryptophan with D-glucose
Authors: Ronner, B Lerche, H Bergmuller, W Freilinger, C Severin, T Pischetsrieder, M
Citation: B. Ronner et al., Formation of tetrahydro-beta-carbolines and beta-carbolines during the reaction of L-tryptophan with D-glucose, J AGR FOOD, 48(6), 2000, pp. 2111-2116
Sodium and calcium channelopathies of sarcolemma: periodic paralyses, paramyotonia congenita and potassium-aggravated myotonia
Authors: Mitrovic, N Lerche, H
Citation: N. Mitrovic et H. Lerche, Sodium and calcium channelopathies of sarcolemma: periodic paralyses, paramyotonia congenita and potassium-aggravated myotonia, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 3-32
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
Authors: Lerche, H Biervert, C Alekov, AK Schleithoff, L Lindner, M Klingler, W Bretschneider, F Mitrovic, N Jurkat-Rott, K Bode, H Lehmann-Horn, F Steinlein, OK
Citation: H. Lerche et al., A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions, ANN NEUROL, 46(3), 1999, pp. 305-312
Teaching course: ion channelopathies in neurology
Authors: Jurkat-Rott, K Lerche, H Mitrovic, N Lehmann-Horn, F
Citation: K. Jurkat-rott et al., Teaching course: ion channelopathies in neurology, J NEUROL, 246(9), 1999, pp. 758-763
On identification of Na+ channel gating schemes using moving-average filtered hidden Markov models
Authors: Michalek, S Lerche, H Wagner, M Mitrovic, N Schiebe, M Lehmann-Horn, F Timmer, J
Citation: S. Michalek et al., On identification of Na+ channel gating schemes using moving-average filtered hidden Markov models, EUR BIOPHYS, 28(7), 1999, pp. 605-609
Two novel triterpenoids from the stemwood of Herrania cuatrecasana
Authors: Wiedemann, B Lerche, H Lotter, H Neszmelyi, A Wagner, H Muller, AA
Citation: B. Wiedemann et al., Two novel triterpenoids from the stemwood of Herrania cuatrecasana, PHYTOCHEM, 52(2), 1999, pp. 333-337
A human muscle Na+ channel mutation in the voltage sensor IV/S4 affects channel block by the pentapeptide KIFMK
Authors: Peter, W Mitrovic, N Schiebe, M Lehmann-Horn, F Lerche, H
Citation: W. Peter et al., A human muscle Na+ channel mutation in the voltage sensor IV/S4 affects channel block by the pentapeptide KIFMK, J PHYSL LON, 518(1), 1999, pp. 13-22
Mutant channels contribute < 50% to Na+ current in paramyotonia congenita muscle
Authors: Mitrovic, N George, AL Rudel, R Lehmann-Horn, F Lerche, H
Citation: N. Mitrovic et al., Mutant channels contribute < 50% to Na+ current in paramyotonia congenita muscle, BRAIN, 122, 1999, pp. 1085-1092
Risultati: 1-17 |