Lindig T - Search Results

1

Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations.

Lindig T, Bender B, Hauser TK, Mang S, Schweikardt D, Klose U, Karle KN, Schüle R, Schöls L, Rattay TW. Lindig T, et al. J Neurol. 2015 Aug;262(8):1961-71. doi: 10.1007/s00415-015-7791-7. Epub 2015 Jun 9. J Neurol. 2015. PMID: 26050637

2

Diffusion tensor imaging of the spinal cord at 1.5 and 3.0 Tesla.

Rossi C, Boss A, Lindig TM, Martirosian P, Steidle G, Maetzler W, Claussen CD, Klose U, Schick F. Rossi C, et al. Among authors: lindig tm. Rofo. 2007 Mar;179(3):219-24. doi: 10.1055/s-2007-962832. Rofo. 2007. PMID: 17325991

3

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.

Schüle R, Schlipf N, Synofzik M, Klebe S, Klimpe S, Hehr U, Winner B, Lindig T, Dotzer A, Riess O, Winkler J, Schöls L, Bauer P. Schüle R, et al. Among authors: lindig t. J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1402-4. doi: 10.1136/jnnp.2008.167528. J Neurol Neurosurg Psychiatry. 2009. PMID: 19917823

4

Complex hyperkinetic movement disorders associated with POLG mutations.

Synofzik M, Schüle R, Schulte C, Krüger R, Lindig T, Schöls L, Asmus F. Synofzik M, et al. Among authors: lindig t. Mov Disord. 2010 Oct 30;25(14):2472-5. doi: 10.1002/mds.23307. Mov Disord. 2010. PMID: 20818669 No abstract available.

5

Restless legs and substantia nigra hypoechogenicity are common features in Friedreich's ataxia.

Synofzik M, Godau J, Lindig T, Schöls L, Berg D. Synofzik M, et al. Among authors: lindig t. Cerebellum. 2011 Mar;10(1):9-13. doi: 10.1007/s12311-010-0215-4. Cerebellum. 2011. PMID: 20865356

6

Transcranial sonography reveals cerebellar, nigral, and forebrain abnormalities in Friedreich's ataxia.

Synofzik M, Godau J, Lindig T, Schöls L, Berg D. Synofzik M, et al. Among authors: lindig t. Neurodegener Dis. 2011;8(6):470-5. doi: 10.1159/000327751. Epub 2011 Jun 9. Neurodegener Dis. 2011. PMID: 21659723

7

Acetazolamide-responsive exercise-induced episodic ataxia associated with a novel homozygous DARS2 mutation.

Synofzik M, Schicks J, Lindig T, Biskup S, Schmidt T, Hansel J, Lehmann-Horn F, Schöls L. Synofzik M, et al. Among authors: lindig t. J Med Genet. 2011 Oct;48(10):713-5. doi: 10.1136/jmg.2011.090282. Epub 2011 Jul 11. J Med Genet. 2011. PMID: 21749991

8

Friedreich ataxia: dysarthria profile and clinical data.

Brendel B, Ackermann H, Berg D, Lindig T, Schölderle T, Schöls L, Synofzik M, Ziegler W. Brendel B, et al. Among authors: lindig t. Cerebellum. 2013 Aug;12(4):475-84. doi: 10.1007/s12311-012-0440-0. Cerebellum. 2013. PMID: 23315038

9

Encephalopathic Susac's Syndrome associated with livedo racemosa in a young woman before the completion of family planning.

Engeholm M, Leo-Kottler B, Rempp H, Lindig T, Lerche H, Kleffner I, Henes M, Dihné M. Engeholm M, et al. Among authors: lindig t. BMC Neurol. 2013 Nov 25;13:185. doi: 10.1186/1471-2377-13-185. BMC Neurol. 2013. PMID: 24274741 Free PMC article.

10

Dominant spinal muscular atrophy due to BICD2: a novel mutation refines the phenotype.

Synofzik M, Martinez-Carrera LA, Lindig T, Schöls L, Wirth B. Synofzik M, et al. Among authors: lindig t. J Neurol Neurosurg Psychiatry. 2014 May;85(5):590-2. doi: 10.1136/jnnp-2013-306777. Epub 2013 Dec 11. J Neurol Neurosurg Psychiatry. 2014. PMID: 24336790 No abstract available.

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