Stoltenburg G - Search Results

1

Successful treatment of extracranially metastasized pineal gland germinoma with high-dose methotrexate.

Fietz T, Thiel E, Baldus C, Blau IW, Stoltenburg G, Knauf WU. Fietz T, et al. Among authors: stoltenburg g. Ann Oncol. 2002 Oct;13(10):1681-5. doi: 10.1093/annonc/mdf276. Ann Oncol. 2002. PMID: 12377660 Free article.

2

Hemosiderin deposits in chronic graft-vs.-host disease related myopathy.

Schmidt-Hieber M, Okuducu AF, Stoltenburg G, Mackert BM, Benzian N, Thiel E, Blau IW. Schmidt-Hieber M, et al. Among authors: stoltenburg g. Eur J Haematol. 2005 Dec;75(6):522-6. doi: 10.1111/j.1600-0609.2005.00548.x. Eur J Haematol. 2005. PMID: 16313267

3

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

4

[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.

5

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

6

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

7

Pseudo-Popeye syndrome: extramedullary plasmacytoma manifesting in skeletal muscle.

Schneider I, Müller T, Stoltenburg G, Holzhausen HJ, Mawrin C, Hanisch F. Schneider I, et al. Among authors: stoltenburg g. Neurology. 2014 Feb 11;82(6):544-5. doi: 10.1212/WNL.0000000000000099. Neurology. 2014. PMID: 24514010 No abstract available.

8

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

9

Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathy.

Schneider I, Stoltenburg G, Deschauer M, Winterholler M, Hanisch F. Schneider I, et al. Among authors: stoltenburg g. Acta Myol. 2014 May;33(1):19-21. Acta Myol. 2014. PMID: 24843231 Free PMC article.

10

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

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