G B Landwehrmeyer
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Explore the profile of G B Landwehrmeyer including associated specialties, affiliations and a list of published articles.
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58
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2945
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Recent Articles
1.
Muhlback A, Lindenberg K, Saft C, Priller J, Landwehrmeyer G
Nervenarzt
. 2020 Mar;
91(4):303-311.
PMID: 32179957
In Germany at least 8000 and probably up to ca. 14,000 people currently suffer from clinically manifest Huntington's disease (HD). In addition, an estimated 24,000 Germans carry the HD mutation...
2.
Sussmuth S, Muller V, Geitner C, Landwehrmeyer G, Iff S, Gemperli A, et al.
J Neurol
. 2015 Apr;
262(6):1533-40.
PMID: 25904208
The causes of weight loss in Huntington's disease (HD) are not entirely clear. The aim was to identify risk factors that are associated with a loss of metabolically active tissues,...
3.
Wolf R, Sambataro F, Vasic N, Depping M, Thomann P, Landwehrmeyer G, et al.
Psychol Med
. 2014 Jul;
44(15):3341-56.
PMID: 25066491
Background: Functional magnetic resonance imaging (fMRI) of multiple neural networks during the brain's 'resting state' could facilitate biomarker development in patients with Huntington's disease (HD) and may provide new insights...
4.
Sprengelmeyer R, Orth M, Muller H, Wolf R, Gron G, Depping M, et al.
Psychol Med
. 2013 Oct;
44(9):1867-78.
PMID: 24093462
Background: Depressive symptoms are prominent psychopathological features of Huntington's disease (HD), making a negative impact on social functioning and well-being. Method: We compared the frequencies of a history of depression,...
5.
Lee J, Ramos E, Lee J, Gillis T, Mysore J, Hayden M, et al.
Neurology
. 2012 Feb;
78(10):690-5.
PMID: 22323755
Objective: Age at onset of diagnostic motor manifestations in Huntington disease (HD) is strongly correlated with an expanded CAG trinucleotide repeat. The length of the normal CAG repeat allele has...
6.
Kassubek J, Pinkhardt E, Dietmaier A, Ludolph A, Landwehrmeyer G, Huppertz H
AJNR Am J Neuroradiol
. 2011 Jun;
32(7):1328-32.
PMID: 21680653
Background And Purpose: The atrophy of the caudate is considered the hallmark of HD-associated neurodegeneration and has high potential as a biomarker in structural MR imaging. This study aimed at...
7.
Orth M, Handley O, Schwenke C, Dunnett S, Wild E, Tabrizi S, et al.
J Neurol Neurosurg Psychiatry
. 2010 Nov;
82(12):1409-12.
PMID: 21097549
No abstract available.
8.
Bechtel N, Scahill R, Rosas H, Acharya T, van den Bogaard S, Jauffret C, et al.
Neurology
. 2010 Nov;
75(24):2150-60.
PMID: 21068430
Objective: Motor signs are functionally disabling features of Huntington disease. Characteristic motor signs define disease manifestation. Their severity and onset are assessed by the Total Motor Score of the Unified...
9.
Maier C, Baron R, Tolle T, Binder A, Birbaumer N, Birklein F, et al.
Pain
. 2010 Jul;
150(3):439-450.
PMID: 20627413
Neuropathic pain is accompanied by both positive and negative sensory signs. To explore the spectrum of sensory abnormalities, 1236 patients with a clinical diagnosis of neuropathic pain were assessed by...
10.
Aziz N, Jurgens C, Landwehrmeyer G, van Roon-Mom W, van Ommen G, Stijnen T, et al.
Neurology
. 2009 Sep;
73(16):1280-5.
PMID: 19776381
Objective: Huntington disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG repeat expansion in the HD gene (HTT). We aimed to assess whether interaction between CAG repeat...