von Moers A - Search Results

1

X-chromosomal (p21) muscular dystrophy and left ventricular diastolic and systolic function.

Brockmeier K, Schmitz L, von Moers A, Koch H, Vogel M, Bein G. Brockmeier K, et al. Among authors: von moers a. Pediatr Cardiol. 1998 Mar-Apr;19(2):139-44. doi: 10.1007/s002469900262. Pediatr Cardiol. 1998. PMID: 9565505

2

Serum levels of carboxyterminal propeptide of type I procollagen, aminoterminal propeptide of type III procollagen and laminin P1 in Duchenne muscular dystrophy.

von Moers A, Danne T, Möller P, Scheffner D. von Moers A, et al. Acta Paediatr. 1997 Apr;86(4):377-80. doi: 10.1111/j.1651-2227.1997.tb09026.x. Acta Paediatr. 1997. PMID: 9174223

3

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy.

Kerst B, Mennerich D, Schuelke M, Stoltenburg-Didinger G, von Moers A, Gossrau R, van Landeghem FK, Speer A, Braun T, Hübner C. Kerst B, et al. Among authors: von moers a. Neuromuscul Disord. 2000 Dec;10(8):572-7. doi: 10.1016/s0960-8966(00)00150-4. Neuromuscul Disord. 2000. PMID: 11053684

4

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy.

Sifringer M, Uhlenberg B, Lammel S, Hanke R, Neumann B, von Moers A, Koch I, Speer A. Sifringer M, et al. Among authors: von moers a. Hum Genet. 2004 Jan;114(2):149-56. doi: 10.1007/s00439-003-1041-2. Epub 2003 Nov 5. Hum Genet. 2004. PMID: 14600829

5

Cranial ultrasound findings in aspartoacylase deficiency (Canavan disease).

Bührer C, Bassir C, von Moers A, Sperner J, Michael T, Scheffner D, Kaufmann HJ. Bührer C, et al. Among authors: von moers a. Pediatr Radiol. 1993;23(5):395-7. doi: 10.1007/BF02011970. Pediatr Radiol. 1993. PMID: 8233699

6

Comparison of three immunoassays for diagnosing sensitization to latex in children with spina bifida.

Niggemann B, Michael T, von Moers A, Seidel U, Wahl R, Jacobsen L, Scheffer D, Wahn U. Niggemann B, et al. Among authors: von moers a. Pediatr Allergy Immunol. 1996 Nov;7(4):164-6. doi: 10.1111/j.1399-3038.1996.tb00126.x. Pediatr Allergy Immunol. 1996. PMID: 9151335

7

Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se.

Endesfelder S, Krahn A, Kreuzer KA, Lass U, Schmidt CA, Jahrmarkt C, von Moers A, Speer A. Endesfelder S, et al. Among authors: von moers a. J Mol Med (Berl). 2000;78(10):569-74. doi: 10.1007/s001090000153. J Mol Med (Berl). 2000. PMID: 11199330

8

Antisense oligonucleotides and short interfering RNAs silencing the cyclin-dependent kinase inhibitor p21 improve proliferation of Duchenne muscular dystrophy patients' primary skeletal myoblasts.

Endesfelder S, Kliche A, Lochmüller H, von Moers A, Speer A. Endesfelder S, et al. Among authors: von moers a. J Mol Med (Berl). 2005 Jan;83(1):64-71. doi: 10.1007/s00109-004-0607-3. Epub 2004 Nov 5. J Mol Med (Berl). 2005. PMID: 15536518

9

Increased mRNA expression of tissue inhibitors of metalloproteinase-1 and -2 in Duchenne muscular dystrophy.

von Moers A, Zwirner A, Reinhold A, Brückmann O, van Landeghem F, Stoltenburg-Didinger G, Schuppan D, Herbst H, Schuelke M. von Moers A, et al. Acta Neuropathol. 2005 Mar;109(3):285-93. doi: 10.1007/s00401-004-0941-0. Epub 2004 Dec 23. Acta Neuropathol. 2005. PMID: 15616792

10

Dystrophinopathy in a boy with Chediak-Higashi syndrome.

von Moers A, van Landeghem FK, Cohn RD, Baumgarten E, Bürger J, Stoltenburg-Didinger G. von Moers A, et al. Neuromuscul Disord. 1998 Oct;8(7):489-94. doi: 10.1016/s0960-8966(98)00062-5. Neuromuscul Disord. 1998. PMID: 9829279

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