Bornemann A - Search Results

1

Gain and loss of extracellular molecules in sporadic inclusion body myositis and polymyositis--a proteomics-based study.

Doppler K, Lindner A, Schütz W, Schütz M, Bornemann A. Doppler K, et al. Among authors: bornemann a. Brain Pathol. 2012 Jan;22(1):32-40. doi: 10.1111/j.1750-3639.2011.00510.x. Epub 2011 Aug 16. Brain Pathol. 2012. PMID: 21672074 Free PMC article.

2

Basement membrane remodelling and segmental fibrosis in sporadic inclusion body myositis.

Doppler K, Mittelbronn M, Lindner A, Bornemann A. Doppler K, et al. Among authors: bornemann a. Neuromuscul Disord. 2009 Jun;19(6):406-11. doi: 10.1016/j.nmd.2009.04.011. Epub 2009 May 26. Neuromuscul Disord. 2009. PMID: 19473842

3

Invasive fibroblasts: fundamental difference between sporadic inclusion body myositis and polymyositis.

Doppler K, Pantazis G, Mack A, Bornemann A. Doppler K, et al. Among authors: bornemann a. Muscle Nerve. 2014 Feb;49(2):175-80. doi: 10.1002/mus.23898. Muscle Nerve. 2014. PMID: 23649793

4

Myogenesis in human denervated muscle biopsies.

Doppler K, Mittelbronn M, Bornemann A. Doppler K, et al. Among authors: bornemann a. Muscle Nerve. 2008 Jan;37(1):79-83. doi: 10.1002/mus.20902. Muscle Nerve. 2008. PMID: 17912750

5

[Myositides].

Bornemann A, Heitmann S, Lindner A. Bornemann A, et al. Pathologe. 2009 Sep;30(5):352-6. doi: 10.1007/s00292-009-1167-7. Pathologe. 2009. PMID: 19618187 Review. German.

6

Myofiber degeneration in autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) (LGMD1B).

Mittelbronn M, Hanisch F, Gleichmann M, Stötter M, Korinthenberg R, Wehnert M, Bonne G, Rudnik-Schöneborn S, Bornemann A. Mittelbronn M, et al. Among authors: bornemann a. Brain Pathol. 2006 Oct;16(4):266-72. doi: 10.1111/j.1750-3639.2006.00028.x. Brain Pathol. 2006. PMID: 17107595 Free PMC article.

7

Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian family.

Stober A, Aleo A, Kuhl V, Bornemann A, Walter MC, Lochmüller H, Lindner A, Krause S. Stober A, et al. Among authors: bornemann a. Neuromuscul Disord. 2010 May;20(5):335-6. doi: 10.1016/j.nmd.2010.02.013. Epub 2010 Mar 25. Neuromuscul Disord. 2010. PMID: 20346669

8

Diagnostic protein expression in human muscle biopsies.

Bornemann A, Anderson LV. Bornemann A, et al. Brain Pathol. 2000 Apr;10(2):193-214. doi: 10.1111/j.1750-3639.2000.tb00254.x. Brain Pathol. 2000. PMID: 10764040 Free PMC article. Review.

9

July 2003: 62-year-old female with progressive muscular weakness.

Bornemann A, Bohl J, Schneider HM, Goebel HH, Schmidt PF, Gherardi RK. Bornemann A, et al. Brain Pathol. 2004 Jan;14(1):109-10, 115. doi: 10.1111/j.1750-3639.2004.tb00504.x. Brain Pathol. 2004. PMID: 14997943 Free PMC article.

10

Myonuclear degeneration in LMNA null mice.

Mittelbronn M, Sullivan T, Stewart CL, Bornemann A. Mittelbronn M, et al. Among authors: bornemann a. Brain Pathol. 2008 Jul;18(3):338-43. doi: 10.1111/j.1750-3639.2008.00123.x. Epub 2008 Mar 26. Brain Pathol. 2008. PMID: 18371185 Free PMC article.

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