Gärtner J - Search Results

1

Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus-Merzbacher disease.

Stumpf SK, Berghoff SA, Trevisiol A, Spieth L, Düking T, Schneider LV, Schlaphoff L, Dreha-Kulaczewski S, Bley A, Burfeind D, Kusch K, Mitkovski M, Ruhwedel T, Guder P, Röhse H, Denecke J, Gärtner J, Möbius W, Nave KA, Saher G. Stumpf SK, et al. Among authors: gartner j. Acta Neuropathol. 2019 Oct;138(4):673-674. doi: 10.1007/s00401-019-02064-2. Epub 2019 Sep 3. Acta Neuropathol. 2019. PMID: 31482207 Free PMC article.

2

Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI.

Dreha-Kulaczewski S, Dechent P, Helms G, Frahm J, Gärtner J, Brockmann K. Dreha-Kulaczewski S, et al. Among authors: gartner j. Neuroradiology. 2006 Dec;48(12):893-8. doi: 10.1007/s00234-006-0148-2. Epub 2006 Sep 30. Neuroradiology. 2006. PMID: 17013586

3

Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS study.

Dreha-Kulaczewski SF, Dechent P, Finsterbusch J, Brockmann K, Gärtner J, Frahm J, Hanefeld FA. Dreha-Kulaczewski SF, et al. Among authors: gartner j. Pediatr Res. 2008 Apr;63(4):444-9. doi: 10.1203/01.pdr.0000304934.90198.25. Pediatr Res. 2008. PMID: 18356755

4

Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations.

Brockmann K, Dreha-Kulaczewski S, Dechent P, Bönnemann C, Helms G, Kyllerman M, Brück W, Frahm J, Huehne K, Gärtner J, Rautenstrauss B. Brockmann K, et al. Among authors: gartner j. J Neurol. 2008 Jul;255(7):1049-58. doi: 10.1007/s00415-008-0847-1. Epub 2008 Apr 21. J Neurol. 2008. PMID: 18425620 Free article.

5

Serial proton MR spectroscopy and diffusion tensor imaging in infantile Balo's concentric sclerosis.

Dreha-Kulaczewski SF, Helms G, Dechent P, Hofer S, Gärtner J, Frahm J. Dreha-Kulaczewski SF, et al. Among authors: gartner j. Neuroradiology. 2009 Feb;51(2):113-21. doi: 10.1007/s00234-008-0470-y. Epub 2008 Oct 29. Neuroradiology. 2009. PMID: 18958461 Free PMC article.

6

Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.

Kohlschütter A, Bley A, Brockmann K, Gärtner J, Krägeloh-Mann I, Rolfs A, Schöls L. Kohlschütter A, et al. Among authors: gartner j. Brain Dev. 2010 Feb;32(2):82-9. doi: 10.1016/j.braindev.2009.03.014. Epub 2009 May 7. Brain Dev. 2010. PMID: 19427149 Review.

7

Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism.

Steinfeld R, Grapp M, Kraetzner R, Dreha-Kulaczewski S, Helms G, Dechent P, Wevers R, Grosso S, Gärtner J. Steinfeld R, et al. Among authors: gartner j. Am J Hum Genet. 2009 Sep;85(3):354-63. doi: 10.1016/j.ajhg.2009.08.005. Am J Hum Genet. 2009. PMID: 19732866 Free PMC article.

8

Unilateral dilation of virchow-robin spaces in early childhood.

Brockmann K, Gröschel S, Dreha-Kulaczewski S, Reinhardt K, Gärtner J, Dechent P. Brockmann K, et al. Among authors: gartner j. Neuropediatrics. 2009 Oct;40(5):234-8. doi: 10.1055/s-0029-1246158. Epub 2010 Mar 10. Neuropediatrics. 2009. PMID: 20221960

9

Assessment of myelination in hypomyelinating disorders by quantitative MRI.

Dreha-Kulaczewski SF, Brockmann K, Henneke M, Dechent P, Wilken B, Gärtner J, Helms G. Dreha-Kulaczewski SF, et al. Among authors: gartner j. J Magn Reson Imaging. 2012 Dec;36(6):1329-38. doi: 10.1002/jmri.23774. Epub 2012 Aug 21. J Magn Reson Imaging. 2012. PMID: 22911904

10

Pediatric onset multiple sclerosis: McDonald criteria 2010 and the contribution of spinal cord MRI.

Hummel HM, Brück W, Dreha-Kulaczewski S, Gärtner J, Wuerfel J. Hummel HM, et al. Among authors: gartner j. Mult Scler. 2013 Sep;19(10):1330-5. doi: 10.1177/1352458513493033. Epub 2013 Jul 4. Mult Scler. 2013. PMID: 23828866

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