Schlotter-Weigel B - Search Results

1

A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation.

Krause S, Schlotter-Weigel B, Walter MC, Najmabadi H, Wiendl H, Müller-Höcker J, Müller-Felber W, Pongratz D, Lochmüller H. Krause S, et al. Neuromuscul Disord. 2003 Dec;13(10):830-4. doi: 10.1016/s0960-8966(03)00140-8. Neuromuscul Disord. 2003. PMID: 14678807

2

[Polyneuropathy--Case report].

Schlotter-Weigel B, Pongratz DE. Schlotter-Weigel B, et al. Dtsch Med Wochenschr. 2002 Oct 4;127(40):2071. doi: 10.1055/s-2002-34515. Dtsch Med Wochenschr. 2002. PMID: 12373639 German. No abstract available.

3

[Polyneuropathy--diagnostic].

Schlotter-Weigel B, Pongratz DE. Schlotter-Weigel B, et al. Dtsch Med Wochenschr. 2002 Oct 4;127(40):2072-5. doi: 10.1055/s-2002-34529. Dtsch Med Wochenschr. 2002. PMID: 12373640 Review. German. No abstract available.

4

[Polyneuropathy--treatment].

Schlotter-Weigel B, Pongratz DE. Schlotter-Weigel B, et al. Dtsch Med Wochenschr. 2002 Oct 4;127(40):2076-8. doi: 10.1055/s-2002-34517. Dtsch Med Wochenschr. 2002. PMID: 12373641 Review. German. No abstract available.

5

Successful treatment of muscle sarcoidosis with thalidomide.

Walter MC, Lochmüller H, Schlotter-Weigel B, Meindl T, Müller-Felber W. Walter MC, et al. Acta Myol. 2003 May;22(1):22-5. Acta Myol. 2003. PMID: 12966701

6

The long-term outcome of anti-Jo-1-positive inflammatory myopathies.

Späth M, Schröder M, Schlotter-Weigel B, Walter MC, Hautmann H, Leinsinger G, Pongratz D, Müller-Felber W. Späth M, et al. J Neurol. 2004 Jul;251(7):859-64. doi: 10.1007/s00415-004-0449-5. J Neurol. 2004. PMID: 15258790

7

Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood.

Walter MC, Dekomien G, Schlotter-Weigel B, Reilich P, Pongratz D, Müller-Felber W, Epplen JT, Huebner A, Lochmüller H. Walter MC, et al. Acta Myol. 2004 May;23(1):1-5. Acta Myol. 2004. PMID: 15298081

8

Phenotypes of the N88S Berardinelli-Seip congenital lipodystrophy 2 mutation.

Auer-Grumbach M, Schlotter-Weigel B, Lochmüller H, Strobl-Wildemann G, Auer-Grumbach P, Fischer R, Offenbacher H, Zwick EB, Robl T, Hartl G, Hartung HP, Wagner K, Windpassinger C; Austrian Peripheral Neuropathy Study Group. Auer-Grumbach M, et al. Ann Neurol. 2005 Mar;57(3):415-24. doi: 10.1002/ana.20410. Ann Neurol. 2005. PMID: 15732094

9

Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy.

Müller JS, Piko H, Schoser BG, Schlotter-Weigel B, Reilich P, Gürster S, Born C, Karcagi V, Pongratz D, Lochmüller H, Walter MC. Müller JS, et al. Neuromuscul Disord. 2006 Jul;16(7):432-6. doi: 10.1016/j.nmd.2006.04.006. Epub 2006 May 26. Neuromuscul Disord. 2006. PMID: 16730439

10

Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients.

Müller-Felber W, Horvath R, Gempel K, Podskarbi T, Shin Y, Pongratz D, Walter MC, Baethmann M, Schlotter-Weigel B, Lochmüller H, Schoser B. Müller-Felber W, et al. Neuromuscul Disord. 2007 Oct;17(9-10):698-706. doi: 10.1016/j.nmd.2007.06.002. Epub 2007 Jul 23. Neuromuscul Disord. 2007. PMID: 17643989

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