Müller-Felber W - Search Results

1

Markedly different course of Friedreich's ataxia in sib pairs with similar GAA repeat expansions in the frataxin gene.

Klopstock T, Chahrokh-Zadeh S, Holinski-Feder E, Meindl A, Gasser T, Pongratz D, Müller-Felber W. Klopstock T, et al. Acta Neuropathol. 1999 Feb;97(2):139-42. doi: 10.1007/s004010050966. Acta Neuropathol. 1999. PMID: 9928824

2

A placebo-controlled crossover trial of creatine in mitochondrial diseases.

Klopstock T, Querner V, Schmidt F, Gekeler F, Walter M, Hartard M, Henning M, Gasser T, Pongratz D, Straube A, Dieterich M, Müller-Felber W. Klopstock T, et al. Neurology. 2000 Dec 12;55(11):1748-51. doi: 10.1212/wnl.55.11.1748. Neurology. 2000. PMID: 11113239 Clinical Trial.

3

The clinical spectrum of Friedreich's ataxia in German families showing linkage to the FRDA locus on chromosome 9.

Müller-Felber W, Rossmanith T, Spes C, Chamberlain S, Pongratz D, Deufel T. Müller-Felber W, et al. Clin Investig. 1993 Feb;71(2):109-14. doi: 10.1007/BF00179990. Clin Investig. 1993. PMID: 8096411

4

Skeletal muscle in children with congenital myotonic dystrophy in the first year of life.

Müller-Felber W, Schmidt-Achert M, Pongratz DE. Müller-Felber W, et al. Clin Neuropathol. 1993 Jul-Aug;12(4):211-4. Clin Neuropathol. 1993. PMID: 8403631

5

Neuromyotonia, myocloni, sensory neuropathy and cerebellar symptoms in a patient with antibodies to neuronal nucleoproteins (anti-Hu-antibodies).

Toepfer M, Schroeder M, Unger JW, Lochmüller H, Pongratz D, Müller-Felber W. Toepfer M, et al. Clin Neurol Neurosurg. 1999 Sep;101(3):207-9. doi: 10.1016/s0303-8467(99)00037-2. Clin Neurol Neurosurg. 1999. PMID: 10536910

6

Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study.

Walter MC, Lochmüller H, Reilich P, Klopstock T, Huber R, Hartard M, Hennig M, Pongratz D, Müller-Felber W. Walter MC, et al. Neurology. 2000 May 9;54(9):1848-50. doi: 10.1212/wnl.54.9.1848. Neurology. 2000. PMID: 10802796 Clinical Trial.

7

Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited.

Schoser BG, Müller-Höcker J, Horvath R, Gempel K, Pongratz D, Lochmüller H, Müller-Felber W. Schoser BG, et al. Neuropathol Appl Neurobiol. 2007 Oct;33(5):544-59. doi: 10.1111/j.1365-2990.2007.00839.x. Epub 2007 Jun 15. Neuropathol Appl Neurobiol. 2007. PMID: 17573812

8

64th ENMC International Workshop: therapeutic approaches to dermatomyositis, polymyositis, and inclusion body myositis29-31 January 1999, Naarden, The Netherlands.

Müller-Felber W, Pongratz D, Reimers C. Müller-Felber W, et al. Neuromuscul Disord. 2001 Jan;11(1):88-92. doi: 10.1016/s0960-8966(00)00161-9. Neuromuscul Disord. 2001. PMID: 11166170 No abstract available.

9

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

10

[Diagnostic considerations in muscle pain.].

Müller-Felber W, Pongratz D. Müller-Felber W, et al. Schmerz. 1992 Sep;6(3):206-10. doi: 10.1007/BF02528604. Schmerz. 1992. PMID: 18415608 German.

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