Lindig T - Search Results

1

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

2

Comparison of three clinical rating scales in Friedreich ataxia (FRDA).

Bürk K, Mälzig U, Wolf S, Heck S, Dimitriadis K, Schmitz-Hübsch T, Hering S, Lindig TM, Haug V, Timmann D, Degen I, Kruse B, Dörr JM, Ratzka S, Ivo A, Schöls L, Boesch S, Klockgether T, Klopstock T, Schulz JB. Bürk K, et al. Among authors: lindig tm. Mov Disord. 2009 Sep 15;24(12):1779-84. doi: 10.1002/mds.22660. Mov Disord. 2009. PMID: 19562766

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

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

6

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

7

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

8

Teaching neuroimages: hypomyelinating leukodystrophy with hypodontia due to POLR3B: look into a leukodystrophy's mouth.

Synofzik M, Bernard G, Lindig T, Gburek-Augustat J. Synofzik M, et al. Among authors: lindig t. Neurology. 2013 Nov 5;81(19):e145. doi: 10.1212/01.wnl.0000435300.64776.7e. Neurology. 2013. PMID: 24190003 Free PMC article.

9

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.

10

X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation.

Synofzik M, Müller vom Hagen J, Haack TB, Wilhelm C, Lindig T, Beck-Wödl S, Nabuurs SB, van Kuilenburg AB, de Brouwer AP, Schöls L. Synofzik M, et al. Among authors: lindig t. Orphanet J Rare Dis. 2014 Feb 14;9:24. doi: 10.1186/1750-1172-9-24. Orphanet J Rare Dis. 2014. PMID: 24528855 Free PMC article.

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