N. Mitrović

发表

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.

H. Lerche, P. Iaizzo, F. Lehmann-Horn, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type II.

H. Lerche, F. Lehmann-Horn, K. Jurkat-Rott, 2002, Brain : a journal of neurology.

Roleinfast inactivation oftheIV/S4-S5 loopofthehuman muscle Naechannel probedbycysteine mutagenesis

H. Lerche, N. Mitrović, U. Pika-Hartlaub, 2011 .

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions

F. Bretschneider, H. Lerche, O. Steinlein, 1999, Annals of neurology.

Chapter 8 Sodium channelopathies in skeletal muscle and brain

H. Lerche, F. Lehmann-Horn, K. Jurkat-Rott, 2002 .

Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man

H. Lerche, F. Lehmann-Horn, N. Mitrović, 2001, The European journal of neuroscience.

A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro

H. Lerche, N. Mitrović, Alexi K. Alekov, 2000, The Journal of physiology.

Mechanism of voltage-dependent gating in skeletal muscle chloride channels.

A. George, A. Rosenbohm, C. Fahlke, 1996, Biophysical journal.

An aspartic acid residue important for voltage-dependent gating of human muscle chloride channels

A. George, C. Fahlke, Ming Zhou, 1995, Neuron.

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III‐IV linker.

H. Lerche, N. Mitrović, T. Weiss, 1993, The Journal of physiology.

Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V

B. Mohammadi, R. Dengler, F. Lehmann-Horn, 2003, The Journal of physiology.

Sodium and calcium channelopathies of sarcolemma: Periodic paralyses, paramyotonia congenita and potassium-aggravated myotonia

H. Lerche, N. Mitrović, 2000 .

Paramyotonia congenita: The R1448P Na+ channel mutation in adult human skeletal muscle

H. Lerche, V. Dubowitz, F. Lehmann-Horn, 1996, Annals of neurology.

A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivity

H. Lerche, F. Lehmann-Horn, N. Mitrović, 1997, Neurology.

Mutant channels contribute <50% to Na+ current in paramyotonia congenita muscle.

H. Lerche, F. Lehmann-Horn, R. Rüdel, 1999, Brain : a journal of neurology.

Hyperglycaemic hypoxia alters after‐potential and fast K+ conductance of rat axons by cytoplasmic acidification.

P. Grafe, N. Mitrović, S. Quasthoff, 1993, The Journal of physiology.

Role in fast inactivation of conserved amino acids in the IV/S4-S5 loop of the human muscle Na+ channel

H. Lerche, F. Lehmann-Horn, N. Mitrović, 1996, Neuroscience Letters.

A human muscle Na+ channel mutation in the voltage sensor IV/S4 affects channel block by the pentapeptide KIFMK

H. Lerche, F. Lehmann-Horn, N. Mitrović, 1999, The Journal of physiology.

Screening for α-synuclein immunoreactive neuronal inclusions in the hippocampus allows identification of atypical MSA (FTLD-synuclein)

S. Weis, P. Liberski, G. Kovacs, 2015, Acta Neuropathologica.

Sodium channel inactivation kinetics of rat sensory and motor nerve fibres and their modulation by glutathione

P. Grafe, N. Mitrović, S. Quasthoff, 2004, Pflügers Archiv.

Role in fast inactivation of the IV/S4–S5 loop of the human muscle Na+ channel probed by cysteine mutagenesis

H. Lerche, F. Lehmann-Horn, N. Mitrović, 1997, The Journal of physiology.

Teaching course: ion channelopathies in neurology

H. Lerche, F. Lehmann-Horn, K. Jurkat-Rott, 1999, Journal of Neurology.

Glutathione accelerates sodium channel inactivation in excised rat axonal membrane patches

P. Grafe, M. Strupp, N. Mitrović, 2004, Pflügers Archiv.

Impaired slow inactivation due to a polymorphism and substitutions of Ser-906 in the II-III loop of the human Nav1.4 channel

F. Lehmann-Horn, K. Jurkat-Rott, N. Mitrović, 2003, Pflügers Archiv.

Erratum: Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current (Proceedings of National Academy of Sciences of the United States of America (Aug. 15, 2000) 97(17) (9549-9554))

Paul A. Iaizzo, Holger Lerche, Bertrand Fontaine, 2000 .

Role of Domain 4 in Sodium Channel Slow Inactivation

R. Horn, A. George, N. Mitrović, 2000, The Journal of general physiology.

Independent Versus Coupled Inactivation in Sodium Channels

R. Horn, A. George, N. Mitrović, 1998, The Journal of general physiology.

Independent Versus Coupled Inactivation in Sodium Channels

R. Horn, A. George, N. Mitrović, 1998, The Journal of general physiology.

Two mutations in the IV/S4-S5 segment of the human skeletal muscle Na+ channel disrupt fast and enhance slow inactivation

H. Lerche, F. Lehmann-Horn, N. Mitrović, 2001, Neuroscience Letters.

Effects of temperature and mexiletine on the F1473S Na+ channel mutation causing paramyotonia congenita

Frank Lehmann-Horn, F. Lehmann-Horn, F. Deymeer, 1998, Pflügers Archiv.

Different effects of mexiletine on two mutant sodium channels causing paramyotonia congenita and hyperkalemic periodic paralysis

B. Mohammadi, K. Weckbecker, T. Mansuroglu, 2000, Neuromuscular Disorders.