Search Results - "Jurkat-Rott K"

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Monogene Ionenkanalerkrankungen der Skelettmuskulatur.

Alternate Title: Monogenic channelopathies of the skeletal muscle.

Authors: Lehmann-Horn, F. Jurkat-Rott, K.

Source: Medizinische Genetik. Dec2013, Vol. 25 Issue 4, p454-461. 8p.

Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita.

Authors: Kornblum, C. Lutterbey, G. G. Czermin, B. et al.

Source: Acta Neurologica Scandinavica. Feb2010, Vol. 121 Issue 2, p131-135. 5p. 2 Black and White Photographs, 1 Diagram.

Subjects: Myotonia congenita, Medical imaging systems, Neuromuscular diseases, Hypertrophy, Muscle diseases

Nanotechnology for neuronal ion channels.

Authors: Lehmann-Horn F Jurkat-Rott K Lehmann-Horn, F et al.

Source: Journal of Neurology, Neurosurgery & Psychiatry. Nov2003, Vol. 74 Issue 11, p1466-1475. 10p. 1 Black and White Photograph, 4 Diagrams, 1 Chart, 4 Graphs.

Muskuläre Kanalopathien.

Alternate Title: Muscle channelopathies.

Authors: Jurkat-Rott, K. Lerche, H. Lehmann-Horn, F.

Source: Der Nervenarzt. Apr2011, Vol. 82 Issue 4, p511-521. 11p. 1 Color Photograph, 2 Diagrams, 2 Charts.

EFNS task force on molecular diagnosis of neurologic disorders Guidelines for the molecular diagnosis of inherited neurologic diseases Second of two parts.

Authors: Gasser, T. Dichgans, M. Finsterer, J. et al.

Source: European Journal of Neurology. Sep2001, Vol. 8 Issue 5, p407-424. 18p. 2 Diagrams, 2 Charts.

Subjects: Neurological disorders, Muscle diseases, Molecular diagnosis

S45-4 Periodic paralysis

Authors: Jurkat-Rott, K. Lehmann-Horn, F.

Source: Clinical Neurophysiology. Oct2010 Supplement 1, Vol. 121, pS65-S65. 1p.

Acetazolamide-responsive episodic ataxia type 2, migraine, and diarrhoea due to a CACNA1A gene mutation.

Authors: Zafeiriou DI Jurkat-Rott K Vargiami E et al.

Source: Developmental Medicine & Child Neurology. Jan2007 Supplement 108, Vol. 49, p32-32. 1p.

Nonanesthetic malignant hyperthermia.

Authors: Lehmann-Horn F Klingler W Jurkat-Rott K

Source: Anesthesiology. 2011 Nov, Vol. 115 Issue 5, p915-917. 3p.

In vitro muscle contracture investigations on the malignant hyperthermia like episodes in myotonia congenita.

Authors: HOPPE, K. LEHMANN‐HORN, F. CHAIKLIENG, S. et al.

Source: Acta Anaesthesiologica Scandinavica. Sep2013, Vol. 57 Issue 8, p1017-1023. 7p. 1 Black and White Photograph, 1 Chart, 3 Graphs.

Recent advances in the diagnosis of malignant hyperthermia susceptibility: How confident can we be of genetic testing?

Authors: Robinson, R L Anetseder, M J Brancadoro, V et al.

Source: European Journal of Human Genetics. Apr2003, Vol. 11 Issue 4, p342. 7p.

Myopathy as the first symptom of hypokalemic periodic paralysis -- case report of a girl from a Polish family with CACNA1S (R1239G) mutation.

Authors: Winczewska-Wiktor, A. Steinborn, B. Lehman-Horn, F. et al.

Source: Advances in Medical Sciences (De Gruyter Open). 2007 Supplement, Vol. 52, p155-157. 3p.

Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na v1.4 cause periodic paralysis.

Authors: Fan, C. Mao, N. Lehmann‐Horn, F. et al.

Source: Clinical Genetics. Jun2017, Vol. 91 Issue 6, p859-867. 10p. 1 Diagram, 2 Charts, 3 Graphs.

S44-5 Chloride and sodium channel myotonias

Authors: Lehmann-Horn, F. Deymeer, F. Jurkat-Rott, K.

Source: Clinical Neurophysiology. Oct2010 Supplement 1, Vol. 121, pS64-S64. 1p.

Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individuals.

Authors: Charles, G. Zheng, C. Lehmann-Horn, F. et al.

Source: Journal of Neurology. Oct2013, Vol. 260 Issue 10, p2606-2613. 8p.

Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degeneration.

Authors: Weber, M.-A. Nagel, A. Wolf, M. et al.

Source: Journal of Neurology. Nov2012, Vol. 259 Issue 11, p2385-2392. 8p. 1 Black and White Photograph, 3 Charts.

135. Electrophysiological decrement and transient weakness in myotonic syndromes

Authors: Matur, Z. Ciftci, F.D. Kara, B. et al.

Source: Clinical Neurophysiology. Jun2012, Vol. 123 Issue 6, pe55-e55. 1p.

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

Authors: Hoppe K Sartorius T Chaiklieng S et al.

Source: Frontiers in physiology [Front Physiol] 2020 Nov 23; Vol. 11, pp. 533946. Date of Electronic Publication: 2020 Nov 23 (Print Publication: 2020).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101549006 Publication Model: eCollection Cited Medium: Print ISSN: 1664-042X (Print) Linking ISSN: 1664042X NLM ISO Abbreviation: Front Physiol Subsets: PubMed not MEDLINE

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

Authors: Hoppe K Chaiklieng S Lehmann-Horn F et al.

Source: Pflugers Archiv : European journal of physiology [Pflugers Arch] 2020 Oct; Vol. 472 (10), pp. 1533.

Publication Type: Published Erratum

Journal Info: Publisher: Springer Country of Publication: Germany NLM ID: 0154720 Publication Model: Print Cited Medium: Internet ISSN: 1432-2013 (Electronic) Linking ISSN: 00316768 NLM ISO Abbreviation: Pflugers Arch Subsets: MEDLINE; PubMed not MEDLINE