Pongratz D - Search Results

1

Localization of transforming growth factor beta in association with neuromuscular junctions in adult human muscle.

Toepfer M, Fischer P, Abicht A, Lochmüller H, Pongratz D, Müller-Felber W. Toepfer M, et al. Among authors: pongratz d. Cell Mol Neurobiol. 1999 Apr;19(2):297-300. doi: 10.1023/a:1006989530148. Cell Mol Neurobiol. 1999. PMID: 10081612

2

A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome.

Abicht A, Stucka R, Schmidt C, Briguet A, Höpfner S, Song IH, Pongratz D, Müller-Felber W, Ruegg MA, Lochmüller H. Abicht A, et al. Among authors: pongratz d. Brain. 2002 May;125(Pt 5):1005-13. doi: 10.1093/brain/awf095. Brain. 2002. PMID: 11960891

3

Myofibrillogenesis in primary tissue cultures of adult human skeletal muscle: expression of desmin, titin, and nebulin.

Behr T, Fischer P, Müller-Felber W, Schmidt-Achert M, Pongratz D. Behr T, et al. Among authors: pongratz d. Clin Investig. 1994 Jan;72(2):150-5. doi: 10.1007/BF00184594. Clin Investig. 1994. PMID: 8186663

4

Congenital myasthenic syndromes: clinical and genetic analysis of 18 patients.

Abicht A, Müller-Felber W, Fischer P, Jakob I, Kürz L, Rudel R, Mortier W, Pongratz D, Lochmüller H. Abicht A, et al. Among authors: pongratz d. Eur J Med Res. 1997 Dec 31;2(12):515-22. Eur J Med Res. 1997. PMID: 9498929

5

Tenascin is a useful marker in the diagnosis of inflammatory myopathies.

Müller-Felber W, Toepfer M, Müller T, Müller-Höcker J, Fischer P, Lochmüller H, Pongratz D. Müller-Felber W, et al. Among authors: pongratz d. Eur J Med Res. 1998 Jun 17;3(6):281-7. Eur J Med Res. 1998. PMID: 9620889

6

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

7

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. Among authors: pongratz d. Neuromuscul Disord. 2003 Dec;13(10):830-4. doi: 10.1016/s0960-8966(03)00140-8. Neuromuscul Disord. 2003. PMID: 14678807

8

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

9

Marinesco Sjögren syndrome with rhabdomyolysis. A new subtype of the disease.

Müller-Felber W, Zafiriou D, Scheck R, Pätzke I, Toepfer M, Pongratz DE, Walther U. Müller-Felber W, et al. Among authors: pongratz de. Neuropediatrics. 1998 Apr;29(2):97-101. doi: 10.1055/s-2007-973542. Neuropediatrics. 1998. PMID: 9638664

10

Exercise-induced myalgia in hypothyroidism.

Lochmüller H, Reimers CD, Fischer P, Heuss D, Müller-Höcker J, Pongratz DE. Lochmüller H, et al. Among authors: pongratz de. Clin Investig. 1993 Dec;71(12):999-1001. doi: 10.1007/BF00180031. Clin Investig. 1993. PMID: 8124059

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