Lindig T - Search Results

1

Proof of principle for the clinical use of a CE-certified automatic imaging analysis tool in rare diseases studying hereditary spastic paraplegia type 4 (SPG4).

Lindig T, Bender B, Bürkle E, Kumar V, Ernemann U, Schöls L, Rattay TW. Lindig T, et al. Sci Rep. 2022 Dec 21;12(1):22075. doi: 10.1038/s41598-022-25545-z. Sci Rep. 2022. PMID: 36543827 Free PMC article.

2

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

3

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.

4

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

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

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.

9

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.

10

Motor protein mutations cause a new form of hereditary spastic paraplegia.

Caballero Oteyza A, Battaloğlu E, Ocek L, Lindig T, Reichbauer J, Rebelo AP, Gonzalez MA, Zorlu Y, Ozes B, Timmann D, Bender B, Woehlke G, Züchner S, Schöls L, Schüle R. Caballero Oteyza A, et al. Among authors: lindig t. Neurology. 2014 Jun 3;82(22):2007-16. doi: 10.1212/WNL.0000000000000479. Epub 2014 May 7. Neurology. 2014. PMID: 24808017 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

63 results

Search Page