Katalog der Deutschen Nationalbibliothek

Go to:

Knowledge Web

Person
Person

Person

Frank Lehmann-Horn (1948-2018)

Arzt

Name

Frank Lehmann-Horn

Time

1948-2018 (Date of birth and death)

Place

Michlbach (Geburtsort)
Ulm (Wirkungsort)
Deutschland

Gender

männlich

Profession

Arzt (characteristic profession)
Neurowissenschaftler
Hochschullehrer

Variant

Frank Lehmann- Horn

Topic

Personen zu Medizin, Tiermedizin

Further information

Direktor des Instituts für Angewandte Physiologie der Universität Ulm 1992-2010, Direktor Division of Neurophysiology, Universität Ulm 2010-2016

Source

Landesbibliographie Baden-Württemberg

Record type

Person

GND-Identifier

172221145

Record ID

172221145

Involved in

show all

Therapie und Verlauf neurologischer Erkrankungen

Correction to: Preclinical pharmacological in vitro investigations on low chloride conductance myotonia: effects of potassium regulation

Preclinical pharmacological in vitro investigations on low chloride conductance myotonia: effects of potassium regulation

Paxilline prevents the onset of myotonic stiffness in pharmacologically induced myotonia: a preclinical investigation

Paxilline Prevents the Onset of Myotonic Stiffness in Pharmacologically Induced Myotonia: A Preclinical Investigation

Strength and muscle structure preserved during long-term therapy in a patient with hypokalemic periodic paralysis (Cav1.1-R1239G)

Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 Mutation

NaV1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibers

Myotone Dystrophien, nicht dystrophe Myotonien und periodische Paralysen

Myotone Dystrophien, nicht dystrophe Myotonien und periodische Paralysen

Therapie und Verlauf neurologischer Erkrankungen

Therapie und Verlauf neurologischer Erkrankungen

Therapie und Verlauf neurologischer Erkrankungen

Hypermetabolism in B–lymphocytes from malignant hyperthermia susceptible individuals

Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre study

Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre study

A G301R Na+/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

Lečenie zabolevanij nervnoj sistemy

A G301R Na+/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

Neurologia, diagnostyka i leczenie : 75 tabel

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

Periodic paralysis: Understanding channelopathies

Neurologische Therapie : mit 75 Tabellen

Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval

Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

Therapieschemata Neurologie

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17

Enhancement of K+ conductance improves in vitro the contraction force of skeletal muscle in hypokalemic periodic paralysis

Therapieschemata Neurologie

Cromakalim (BRL 34915) restores in vitro the membrane potential of depolarized human skeletal muscle fibres

Adynamia episodica hereditaria with myotonia: A non-inactivating sodium current and the effect of extracellular pH

Über die Wirkung von Amphotericin B auf die Warmblüter-Muskelzellmembran : Elektrophysiologische Untersuchungen am Rattenzwerchfell
Please note

The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link:

DNB portal