F. Lehmann‐Horn - Concepedia

Author

F. Lehmann‐Horn

Universität Ulm

Also Known As

F Lehmann-Horn, F Lehmann‐Horn, F. LEHMANN-HORN, F. Lehmann-Horn, F. Lehmann‐Horn, Frank Lehmann-Horn

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Universität Ulm Technical University of Munich Ludwig-Maximilians-Universität München

About

F. Lehmann‐Horn is an author at Universität Ulm specializing in physiology, medicine, and electrophysiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	242
2	Health Sciences	4	4	105
3	Cell Biology	3	3	88
4	Engineering	1	1	33
5	Natural Sciences	1	1	18

F. Lehmann‐Horn

Publications

972

Citations

H-Index

Page 1

	Year	Citations
Fura-2 detected myoplasmic calcium and its correlation with contracture force in skeletal muscle from normal and malignant hyperthermia susceptible pigs P. A. Iaizzo, Werner Klein, F. Lehmann‐Horn Pflügers Archiv - European Journal of Physiology Animal PhysiologyMechanobiologyMuscle FunctionMuscle InjurySkeletal Muscle	1988	110
K(+)‐aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation. N Mitrovié, Alfred L. George, R Heine, The Journal of Physiology	1994	107
Different effects on gating of three myotonia‐causing mutations in the inactivation gate of the human muscle sodium channel. N Mitrovié, Alfred L. George, Holger Lerche, The Journal of Physiology	1995	100
Characteristics of Na+ channels and Cl‐ conductance in resealed muscle fibre segments from patients with myotonic dystrophy. Christian Franke, H. Hatt, Paul A. Iaizzo, The Journal of Physiology	1990	89
Paramyotonia congenita: The R1448P Na<sup>+</sup> channel mutation in adult human skeletal muscle Holger Lerche, Nenad Mitrović, Victor Dubowitz, Annals of Neurology	1996	86
A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivity Susanne Wagner, Holger Lerche, Nenad Mitrović, Neurology	1997	83
Cromakalim (BRL 34915) restores in vitro the membrane potential of depolarized human skeletal muscle fibres Andreas Spuler, F. Lehmann‐Horn, P. Grafe Naunyn-Schmiedeberg s Archives of Pharmacology Regenerative MedicineMembrane PotentialMuscle FunctionMolecular PhysiologySkeletal Muscle	1989	57
Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubes. I. Sipos, Karin Jurkat‐Rott, Cs Harasztosi, The Journal of Physiology	1995	55
The dominant chloride channel mutant G200R causing fluctuating myotonia: Clinical findings, electrophysiology, and channel pathology Susanne Wagner, Feza Deymeer, Lothar L. K�rz, Muscle & Nerve	1998	52
Acetazolamide-responsive exercise-induced episodic ataxia associated with a novel homozygous <i>DARS2</i> mutation: Figure 1 Matthis Synofzik, Julia Schicks, Tobias Lindig, Journal of Medical Genetics	2011	48

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