Stoltenburg G - Search Results

1

Protracted course of juvenile ceroid lipofuscinosis associated with a novel CLN3 mutation (p.Y199X).

Sarpong A, Schottmann G, Rüther K, Stoltenburg G, Kohlschütter A, Hübner C, Schuelke M. Sarpong A, et al. Among authors: stoltenburg g. Clin Genet. 2009 Jul;76(1):38-45. doi: 10.1111/j.1399-0004.2009.01179.x. Epub 2009 May 21. Clin Genet. 2009. PMID: 19489875

2

Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation.

Schuelke M, Bakker M, Stoltenburg G, Sperner J, von Moers A. Schuelke M, et al. Among authors: stoltenburg g. Ann Neurol. 1998 Oct;44(4):700-4. doi: 10.1002/ana.410440420. Ann Neurol. 1998. PMID: 9778273

3

Arthrogryposis multiplex with deafness, inguinal hernias, and early death: a family report of a probably autosomal recessive trait.

Tiemann C, Bührer C, Burwinkel B, Wirtenberger M, Hoehn T, Hübner C, van Landeghem FK, Stoltenburg G, Obladen M. Tiemann C, et al. Among authors: stoltenburg g. Am J Med Genet A. 2005 Aug 30;137(2):125-9. doi: 10.1002/ajmg.a.30860. Am J Med Genet A. 2005. PMID: 16059941

4

Polyglucosan myopathy and functional characterization of a novel GYG1 mutation.

Hedberg-Oldfors C, Mensch A, Visuttijai K, Stoltenburg G, Stoevesandt D, Kraya T, Oldfors A, Zierz S. Hedberg-Oldfors C, et al. Among authors: stoltenburg g. Acta Neurol Scand. 2018 Mar;137(3):308-315. doi: 10.1111/ane.12865. Epub 2017 Nov 15. Acta Neurol Scand. 2018. PMID: 29143313

5

Unusual manifestations in two cases of necrotizing myopathy associated with SRP-antibodies.

Hanisch F, Müller T, Stoltenburg G, Zierz S. Hanisch F, et al. Among authors: stoltenburg g. Clin Neurol Neurosurg. 2012 Sep;114(7):1104-6. doi: 10.1016/j.clineuro.2011.12.055. Epub 2012 Feb 3. Clin Neurol Neurosurg. 2012. PMID: 22306424

6

Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations.

Hanisch F, Müller T, Dietz A, Bitoun M, Kress W, Weis J, Stoltenburg G, Zierz S. Hanisch F, et al. Among authors: stoltenburg g. J Neurol. 2011 Jun;258(6):1085-90. doi: 10.1007/s00415-010-5889-5. Epub 2011 Jan 9. J Neurol. 2011. PMID: 21221624

7

[Muscular dystrophy due to mutations in anoctamin 5: clinical and molecular genetic findings].

Deschauer M, Joshi PR, Gläser D, Hanisch F, Stoltenburg G, Zierz S. Deschauer M, et al. Among authors: stoltenburg g. Nervenarzt. 2011 Dec;82(12):1596-603. doi: 10.1007/s00115-011-3325-4. Nervenarzt. 2011. PMID: 21739273 German.

8

[Treatability of sporadic late onset nemaline myopathy].

Hanisch F, Schneider I, Müller T, Romeike BF, Stoltenburg G, Holzhausen HJ, Zierz S. Hanisch F, et al. Among authors: stoltenburg g. Nervenarzt. 2013 Aug;84(8):955-61. doi: 10.1007/s00115-013-3825-5. Nervenarzt. 2013. PMID: 23836301 Review. German.

9

Sialylation and muscle performance: sialic acid is a marker of muscle ageing.

Hanisch F, Weidemann W, Großmann M, Joshi PR, Holzhausen HJ, Stoltenburg G, Weis J, Zierz S, Horstkorte R. Hanisch F, et al. Among authors: stoltenburg g. PLoS One. 2013 Dec 11;8(12):e80520. doi: 10.1371/journal.pone.0080520. eCollection 2013. PLoS One. 2013. PMID: 24349002 Free PMC article.

10

Unusual manifestations in two cases of necrotizing myopathy associated with SRP antibodies.

Hanisch F, Müller T, Stoltenburg G, Zierz S. Hanisch F, et al. Among authors: stoltenburg g. Rheumatol Int. 2013 May;33(5):1371-2. doi: 10.1007/s00296-011-2311-2. Epub 2011 Dec 27. Rheumatol Int. 2013. PMID: 22200810 No abstract available.

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