Reimann J - Search Results

1

Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls.

Reimann J, Lehmann D, Hardy SA, Falkous G, Knowles CV, Jones RL, Kunz WS, Taylor RW, Kornblum C. Reimann J, et al. Neurol Genet. 2017 Apr 5;3(3):e147. doi: 10.1212/NXG.0000000000000147. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28396884 Free PMC article. No abstract available.

2

Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy.

Schröder R, Kunz WS, Rouan F, Pfendner E, Tolksdorf K, Kappes-Horn K, Altenschmidt-Mehring M, Knoblich R, van der Ven PF, Reimann J, Fürst DO, Blümcke I, Vielhaber S, Zillikens D, Eming S, Klockgether T, Uitto J, Wiche G, Rolfs A. Schröder R, et al. Among authors: reimann j. J Neuropathol Exp Neurol. 2002 Jun;61(6):520-30. doi: 10.1093/jnen/61.6.520. J Neuropathol Exp Neurol. 2002. PMID: 12071635

3

Mitochondrial dysfunction in myofibrillar myopathy.

Reimann J, Kunz WS, Vielhaber S, Kappes-Horn K, Schröder R. Reimann J, et al. Neuropathol Appl Neurobiol. 2003 Feb;29(1):45-51. doi: 10.1046/j.1365-2990.2003.00428.x. Neuropathol Appl Neurobiol. 2003. PMID: 12581339

4

On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.

Schröder R, Goudeau B, Simon MC, Fischer D, Eggermann T, Clemen CS, Li Z, Reimann J, Xue Z, Rudnik-Schöneborn S, Zerres K, van der Ven PF, Fürst DO, Kunz WS, Vicart P. Schröder R, et al. Among authors: reimann j. Hum Mol Genet. 2003 Mar 15;12(6):657-69. doi: 10.1093/hmg/ddg060. Hum Mol Genet. 2003. PMID: 12620971

5

Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study.

Kesper K, Kornblum C, Reimann J, Lutterbey G, Schröder R, Wattjes MP. Kesper K, et al. Among authors: reimann j. Acta Neurol Scand. 2009 Aug;120(2):111-8. doi: 10.1111/j.1600-0404.2008.01129.x. Epub 2008 Dec 22. Acta Neurol Scand. 2009. PMID: 19154541

6

Endplate destruction due to maternal antibodies in arthrogryposis multiplex congenita.

Reimann J, Jacobson L, Vincent A, Kornblum C. Reimann J, et al. Neurology. 2009 Nov 24;73(21):1806-8. doi: 10.1212/WNL.0b013e3181c34a65. Neurology. 2009. PMID: 19933984 No abstract available.

7

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

Kornblum C, Lutterbey GG, Czermin B, Reimann J, von Kleist-Retzow JC, Jurkat-Rott K, Wattjes MP. Kornblum C, et al. Among authors: reimann j. Acta Neurol Scand. 2010 Feb;121(2):131-5. doi: 10.1111/j.1600-0404.2009.01228.x. Epub 2009 Dec 28. Acta Neurol Scand. 2010. PMID: 20047568

8

Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery.

Niehusmann P, Surges R, von Wrede RD, Elger CE, Wellmer J, Reimann J, Urbach H, Vielhaber S, Bien CG, Kunz WS. Niehusmann P, et al. Among authors: reimann j. Epilepsy Behav. 2011 Jan;20(1):38-43. doi: 10.1016/j.yebeh.2010.11.008. Epub 2010 Dec 9. Epilepsy Behav. 2011. PMID: 21145289

9

Myopathy and neuropathy with pipestem capillaries and vascular activated complement deposition.

Reimann J, Kornblum C, Tolksdorf K, Brück W, van Landeghem FK. Reimann J, et al. Neurology. 2011 Jul 26;77(4):401-3. doi: 10.1212/WNL.0b013e3182267bb1. Epub 2011 Jul 13. Neurology. 2011. PMID: 21753180 No abstract available.

10

ZASPopathy with childhood-onset distal myopathy.

Strach K, Reimann J, Thomas D, Naehle CP, Kress W, Kornblum C. Strach K, et al. Among authors: reimann j. J Neurol. 2012 Jul;259(7):1494-6. doi: 10.1007/s00415-012-6543-1. Epub 2012 May 23. J Neurol. 2012. PMID: 22619057

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