F. Lehmann‐Horn - Concepedia

Author

F. Lehmann‐Horn

Also Known As

F Lehmann-Horn, F. LEHMANN-HORN, F. LEHMANN‐HORN, F. Lehmann-Horn, F. Lehmann‐Horn, F. Lehmann–Horn, Franck Lehmann-Horn

Publications

4.5K

Citations

H-Index

100

Concepts

All Affiliations

Universität Ulm Technical University of Munich University College Cork University of Würzburg Universität Hamburg

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	32	2.2K
2	Health Sciences	11	11	798
3	Engineering	3	3	243
4	Natural Sciences	2	2	87
5	Education	1	1	13

F. Lehmann‐Horn

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) Sophie Nicole, Claire-Sophie Davoine, Haluk Topaloğlu, Nature Genetics Schwartz-jampel SyndromeSurgical PathologyHistopathologyMajor ProteoglycanPathology	2000	296
In vitro contracture test for diagnosis of malignant hyperthermia following the protocol of the European MH Group: Results of testing patients surviving fulminant MH and unrelated low‐risk subjects Helle Ørding, Virginia Brancadoro, Santolo Cozzolino, Acta Anaesthesiologica Scandinavica	1997	295
Proximal myotonic myopathy K. Ricker, Manuela C. Koch, F. Lehmann‐Horn, Neurology Neuromusculoskeletal DisorderChannelopathiesMendelian DisorderGenetic DisorderGenetics	1994	253
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families B. Fontaine, J. Vale-Santos, K Jurkat-Rott, Nature Genetics Health SciencesCytogeneticsEuropean FamiliesGeneticsPhysiology	1994	234
Active fascial contractility: Fascia may be able to contract in a smooth muscle-like manner and thereby influence musculoskeletal dynamics Robert Schleip, Werner Klingler, F. Lehmann‐Horn Medical Hypotheses MechanobiologySmooth Muscle-like MannerFascial RepairMuscle FunctionKinesiology	2005	218
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias Michael Strupp, R. Kalla, Christine Adrion, Neurology	2011	204
Localization of the gene encoding the α<sub>2</sub>/δ-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families David Iles, F. Lehmann‐Horn, Stephen W. Scherer, Human Molecular Genetics Muscle FunctionSignal TransductionMolecular PhysiologySkeletal MuscleGenetic Disorder	1994	166
Variability of familial hemiplegic migraine with novel A1A2 Na <sup>+</sup> /K <sup>+</sup> -ATPase variants Karin Jurkat‐Rott, Tobias Freilinger, Jens P. Dreier, Neurology	2004	159
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions Holger Lerche, Christian Biervert, Alexi K. Alekov, Annals of Neurology Family MembersGeneticsNeurotransmitterNeurotransmissionSocial Sciences	1999	137
Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2 Yvonne Weber, Robert Roebling, Jan Kassubek, Neurology	2010	128

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