Fischer D - Search Results

1

Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene.

Fischer D, Herasse M, Ferreiro A, Barragán-Campos HM, Chiras J, Viollet L, Maugenre S, Leroy JP, Monnier N, Lunardi J, Guicheney P, Fardeau M, Romero NB. Fischer D, et al. Neurology. 2006 Dec 26;67(12):2217-20. doi: 10.1212/01.wnl.0000249151.45200.71. Neurology. 2006. PMID: 17190947

2

Characterization of the muscle involvement in dynamin 2-related centronuclear myopathy.

Fischer D, Herasse M, Bitoun M, Barragán-Campos HM, Chiras J, Laforêt P, Fardeau M, Eymard B, Guicheney P, Romero NB. Fischer D, et al. Brain. 2006 Jun;129(Pt 6):1463-9. doi: 10.1093/brain/awl071. Epub 2006 Apr 3. Brain. 2006. PMID: 16585051

3

Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus.

Romero NB, Herasse M, Monnier N, Leroy JP, Fischer D, Ferreiro A, Viollet L, Eymard B, Laforêt P, Monges S, Lubieniecki F, Taratuto AL, Guicheney P, Lunardi J, Fardeau M. Romero NB, et al. Among authors: fischer d. Acta Myol. 2005 Oct;24(2):70-3. Acta Myol. 2005. PMID: 16550918 Review.

4

Distinct muscle imaging patterns in myofibrillar myopathies.

Fischer D, Kley RA, Strach K, Meyer C, Sommer T, Eger K, Rolfs A, Meyer W, Pou A, Pradas J, Heyer CM, Grossmann A, Huebner A, Kress W, Reimann J, Schröder R, Eymard B, Fardeau M, Udd B, Goldfarb L, Vorgerd M, Olivé M. Fischer D, et al. Neurology. 2008 Sep 2;71(10):758-65. doi: 10.1212/01.wnl.0000324927.28817.9b. Neurology. 2008. PMID: 18765652 Free PMC article.

5

Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene.

Olivé M, Armstrong J, Miralles F, Pou A, Fardeau M, Gonzalez L, Martínez F, Fischer D, Martínez Matos JA, Shatunov A, Goldfarb L, Ferrer I. Olivé M, et al. Among authors: fischer d. Neuromuscul Disord. 2007 Jun;17(6):443-50. doi: 10.1016/j.nmd.2007.02.009. Epub 2007 Apr 5. Neuromuscul Disord. 2007. PMID: 17418574 Free PMC article.

6

Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs.

Fischer D, Walter MC, Kesper K, Petersen JA, Aurino S, Nigro V, Kubisch C, Meindl T, Lochmüller H, Wilhelm K, Urbach H, Schröder R. Fischer D, et al. J Neurol. 2005 May;252(5):538-47. doi: 10.1007/s00415-005-0684-4. Epub 2005 Feb 23. J Neurol. 2005. PMID: 15726252

7

Jeub M, Bitoun M, Guicheney P, Kappes-Horn K, Strach K, Druschky KF, Weis J, Fischer D. Jeub M, et al. Among authors: fischer d. Clin Neuropathol. 2008 Nov-Dec;27(6):430-8. doi: 10.5414/npp27430. Clin Neuropathol. 2008. PMID: 19130742 Free article. Review.

8

Muscular involvement assessed by MRI correlates to motor function measurement values in oculopharyngeal muscular dystrophy.

Fischmann A, Gloor M, Fasler S, Haas T, Rodoni Wetzel R, Bieri O, Wetzel S, Heinimann K, Scheffler K, Fischer D. Fischmann A, et al. Among authors: fischer d. J Neurol. 2011 Jul;258(7):1333-40. doi: 10.1007/s00415-011-5937-9. Epub 2011 Feb 22. J Neurol. 2011. PMID: 21340522

9

Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P.

Walter MC, Reilich P, Huebner A, Fischer D, Schröder R, Vorgerd M, Kress W, Born C, Schoser BG, Krause KH, Klutzny U, Bulst S, Frey JR, Lochmüller H. Walter MC, et al. Among authors: fischer d. Brain. 2007 Jun;130(Pt 6):1485-96. doi: 10.1093/brain/awm039. Epub 2007 Apr 17. Brain. 2007. PMID: 17439987

10

Recent developments in muscle imaging of neuromuscular disorders.

Fischer D, Bonati U, Wattjes MP. Fischer D, et al. Curr Opin Neurol. 2016 Oct;29(5):614-20. doi: 10.1097/WCO.0000000000000364. Curr Opin Neurol. 2016. PMID: 27427989 Review.

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