E M Wicklein
Overview
Explore the profile of E M Wicklein including associated specialties, affiliations and a list of published articles.
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9
Citations
181
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Recent Articles
1.
Langdon D, Benedict R, Wicklein E, Beckmann K, Fredrikson S
Eur Neurol
. 2013 May;
69(6):346-51.
PMID: 23635720
Objective: To assess the Multiple Sclerosis Neuropsychological Questionnaire (MSNQ) in patients with clinically isolated syndrome (CIS). Methods: 130 European CIS patients and 60 relatives completed the MSNQ. Results: The mean...
2.
Pfeiffer G, Wicklein E, Ratusinski T, Schmitt L, Kunze K
J Neurol Neurosurg Psychiatry
. 2001 Mar;
70(4):548-50.
PMID: 11254787
Objectives: Charcot-Marie-Tooth disease type I (CMT1) is a hereditary sensorimotor neuropathy causing variable degrees of handicap. The risk for relevant disability in respect to genetic counselling is unknown. An attempt...
3.
Bonne G, Mercuri E, Muchir A, Urtizberea A, Becane H, Recan D, et al.
Ann Neurol
. 2000 Aug;
48(2):170-80.
PMID: 10939567
Emery-Dreifuss muscular dystrophy (EDMD) is characterized by early contractures of the elbows and Achilles tendons, slowly progressive muscle wasting and weakness, and life-threatening cardiomyopathy with conduction blocks. We recently identified...
4.
Pfeiffer G, Wicklein E, Wittig K
Clin Neurophysiol
. 2000 Jul;
111(8):1388-94.
PMID: 10904219
Objectives: To resolve the discrepancy between conduction block criteria derived from healthy controls and stricter criteria suggested by computer simulation of interphase cancellation through altered motor units. Methods: An EMG...
5.
Kubisch C, Wicklein E, Jentsch T
Hum Mutat
. 1998 Jun;
12(1):27-32.
PMID: 9633816
McArdle disease is a rare autosomal recessive disorder of the muscle glycogen metabolism caused by mutations in the muscle glycogen phosphorylase gene. Until now, a total number of 11 different...
6.
Wicklein E, Pfeiffer G, Yuki N, Hartard C, Kunze K
J Neurol Sci
. 1997 Dec;
151(2):227-9.
PMID: 9349681
Sensitization with GD1b has been shown to cause sensory neuropathy in rabbit. A patient with chronic sensory-dominant polyneuropathy who had IgM antibody specifically to GD1b has been reported previously. This...
7.
Wicklein E, Orth U, Gal A, Kunze K
J Neurol Neurosurg Psychiatry
. 1997 Nov;
63(3):379-81.
PMID: 9328258
A small family with sensorimotor neuropathy of dominant inheritance was examined. All three affected members were female. They had unusually severe symptoms and pronounced reduction of motor nerve conduction velocities...
8.
Wicklein E, Pfeiffer G, Ratusinski T, Kunze K
Nervenarzt
. 1997 Apr;
68(4):358-62.
PMID: 9273468
Molecular genetic research on Charcot-Marie-Tooth 1 syndrome (CMT 1) progresses rapidly, still obviously no cure is available for affected individuals. Our aim was to investigate current management in clinical CMT...
9.