Pongratz D - 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. Among authors: pongratz d. 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. Among authors: pongratz d. Neurology. 2000 Dec 12;55(11):1748-51. doi: 10.1212/wnl.55.11.1748. Neurology. 2000. PMID: 11113239 Clinical Trial.

3

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. Among authors: pongratz de. Clin Neuropathol. 1993 Jul-Aug;12(4):211-4. Clin Neuropathol. 1993. PMID: 8403631

4

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. Among authors: pongratz d. Clin Investig. 1993 Feb;71(2):109-14. doi: 10.1007/BF00179990. Clin Investig. 1993. PMID: 8096411

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. Among authors: pongratz d. 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. Among authors: pongratz d. 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. Among authors: pongratz d. 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

Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL.

Mayer M, Straube A, Bruening R, Uttner I, Pongratz D, Gasser T, Dichgans M, Müller-Höcker J. Mayer M, et al. Among authors: pongratz d. J Neurol. 1999 Jul;246(7):526-32. doi: 10.1007/s004150050398. J Neurol. 1999. PMID: 10463351

9

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. Among authors: pongratz d. Neuromuscul Disord. 2001 Jan;11(1):88-92. doi: 10.1016/s0960-8966(00)00161-9. Neuromuscul Disord. 2001. PMID: 11166170 No abstract available.

10

Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis.

Müller-Felber W, Ansevin CF, Ricker K, Müller-Jenssen A, Töpfer M, Goebel HH, Pongratz DE. Müller-Felber W, et al. Among authors: pongratz de. Neuromuscul Disord. 1999 Dec;9(8):604-7. doi: 10.1016/s0960-8966(99)00065-6. Neuromuscul Disord. 1999. PMID: 10619721

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