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Items: 39

1.

Parsing rooms: the role of the PPA and RSC in perceiving object relations and spatial layout.

Bilalić M, Lindig T, Turella L.

Brain Struct Funct. 2019 Sep;224(7):2505-2524. doi: 10.1007/s00429-019-01901-0. Epub 2019 Jul 17.

2.

T1ρ-based dynamic glucose-enhanced (DGEρ) MRI at 3 T: method development and early clinical experience in the human brain.

Herz K, Lindig T, Deshmane A, Schittenhelm J, Skardelly M, Bender B, Ernemann U, Scheffler K, Zaiss M.

Magn Reson Med. 2019 Nov;82(5):1832-1847. doi: 10.1002/mrm.27857. Epub 2019 Jun 23.

PMID:
31231853
3.

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

Rattay TW, Lindig T, Baets J, Smets K, Deconinck T, Söhn AS, Hörtnagel K, Eckstein KN, Wiethoff S, Reichbauer J, Döbler-Neumann M, Krägeloh-Mann I, Auer-Grumbach M, Plecko B, Münchau A, Wilken B, Janauschek M, Giese AK, De Bleecker JL, Ortibus E, Debyser M, Lopez de Munain A, Pujol A, Bassi MT, D'Angelo MG, De Jonghe P, Züchner S, Bauer P, Schöls L, Schüle R.

Brain. 2019 Jun 1;142(6):1561-1572. doi: 10.1093/brain/awz102.

PMID:
31135052
4.

DeepCEST: 9.4 T Chemical exchange saturation transfer MRI contrast predicted from 3 T data - a proof of concept study.

Zaiss M, Deshmane A, Schuppert M, Herz K, Glang F, Ehses P, Lindig T, Bender B, Ernemann U, Scheffler K.

Magn Reson Med. 2019 Jun;81(6):3901-3914. doi: 10.1002/mrm.27690. Epub 2019 Feb 25.

PMID:
30803000
5.

Pattern of Cerebellar Atrophy in Friedreich's Ataxia-Using the SUIT Template.

Lindig T, Bender B, Kumar VJ, Hauser TK, Grodd W, Brendel B, Just J, Synofzik M, Klose U, Scheffler K, Ernemann U, Schöls L.

Cerebellum. 2019 Jun;18(3):435-447. doi: 10.1007/s12311-019-1008-z.

PMID:
30771164
6.

Possible artifacts in dynamic CEST MRI due to motion and field alterations.

Zaiss M, Herz K, Deshmane A, Kim M, Golay X, Lindig T, Bender B, Ernemann U, Scheffler K.

J Magn Reson. 2019 Jan;298:16-22. doi: 10.1016/j.jmr.2018.11.002. Epub 2018 Nov 13.

7.

3D gradient echo snapshot CEST MRI with low power saturation for human studies at 3T.

Deshmane A, Zaiss M, Lindig T, Herz K, Schuppert M, Gandhi C, Bender B, Ernemann U, Scheffler K.

Magn Reson Med. 2019 Apr;81(4):2412-2423. doi: 10.1002/mrm.27569. Epub 2018 Nov 15.

8.

Systematic Assessment of Multispectral Voxel-Based Morphometry in Previously MRI-Negative Focal Epilepsy.

Kotikalapudi R, Martin P, Marquetand J, Lindig T, Bender B, Focke NK.

AJNR Am J Neuroradiol. 2018 Nov;39(11):2014-2021. doi: 10.3174/ajnr.A5809. Epub 2018 Oct 18.

9.

Brain-Area Specific White Matter Hyperintensities: Associations to Falls in Parkinson's Disease.

Ciliz M, Sartor J, Lindig T, Pilotto A, Schäffer E, Weiss M, Scheltens P, Becker S, Hobert MA, Berg D, Liepelt-Scarfone I, Maetzler W.

J Parkinsons Dis. 2018;8(3):455-462. doi: 10.3233/JPD-181351.

PMID:
30040742
10.

Chemical exchange saturation transfer MRI contrast in the human brain at 9.4 T.

Zaiss M, Schuppert M, Deshmane A, Herz K, Ehses P, Füllbier L, Lindig T, Bender B, Ernemann U, Scheffler K.

Neuroimage. 2018 Oct 1;179:144-155. doi: 10.1016/j.neuroimage.2018.06.026. Epub 2018 Jun 15.

PMID:
29894826
11.

Corrigendum: White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease.

Sartor J, Bettecken K, Bernhard FP, Hofmann M, Gladow T, Lindig T, Ciliz M, Ten Kate M, Geritz J, Heinzel S, Benedictus M, Scheltens P, Hobert MA, Maetzler W.

Front Aging Neurosci. 2017 Oct 17;9:342. doi: 10.3389/fnagi.2017.00342. eCollection 2017.

12.

White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease.

Sartor J, Bettecken K, Bernhard FP, Hofmann M, Gladow T, Lindig T, Ciliz M, Ten Kate M, Geritz J, Heinzel S, Benedictus M, Scheltens P, Hobert MA, Maetzler W.

Front Aging Neurosci. 2017 Jun 30;9:213. doi: 10.3389/fnagi.2017.00213. eCollection 2017. Erratum in: Front Aging Neurosci. 2017 Oct 17;9:342.

13.

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.

Minnerop M, Kurzwelly D, Wagner H, Soehn AS, Reichbauer J, Tao F, Rattay TW, Peitz M, Rehbach K, Giorgetti A, Pyle A, Thiele H, Altmüller J, Timmann D, Karaca I, Lennarz M, Baets J, Hengel H, Synofzik M, Atasu B, Feely S, Kennerson M, Stendel C, Lindig T, Gonzalez MA, Stirnberg R, Sturm M, Roeske S, Jung J, Bauer P, Lohmann E, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Carloni P, Brüstle O, Klopstock T, Mathews KD, Shy ME, de Jonghe P, Chinnery PF, Horvath R, Kohlhase J, Schmitt I, Wolf M, Greschus S, Amunts K, Maier W, Schöls L, Nürnberg P, Zuchner S, Klockgether T, Ramirez A, Schüle R.

Brain. 2017 Jun 1;140(6):1561-1578. doi: 10.1093/brain/awx095. Erratum in: Brain. 2017 Dec 9;:.

14.

Evaluation of multimodal segmentation based on 3D T1-, T2- and FLAIR-weighted images - the difficulty of choosing.

Lindig T, Kotikalapudi R, Schweikardt D, Martin P, Bender F, Klose U, Ernemann U, Focke NK, Bender B.

Neuroimage. 2018 Apr 15;170:210-221. doi: 10.1016/j.neuroimage.2017.02.016. Epub 2017 Feb 7.

PMID:
28188918
15.

[MR-imaging findings in Epstein-Barr virus encephalitis].

Lindig T, Bender B, Heckl S, Nägele T, Ioanoviciu SD, Horger M.

Rofo. 2016 Oct;188(10):899-903. Epub 2016 Sep 27. German. No abstract available.

PMID:
27677103
16.

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.

J Neurol. 2015 Aug;262(8):1961-71. doi: 10.1007/s00415-015-7791-7. Epub 2015 Jun 9.

PMID:
26050637
17.

Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta.

Garbes L, Kim K, Rieß A, Hoyer-Kuhn H, Beleggia F, Bevot A, Kim MJ, Huh YH, Kweon HS, Savarirayan R, Amor D, Kakadia PM, Lindig T, Kagan KO, Becker J, Boyadjiev SA, Wollnik B, Semler O, Bohlander SK, Kim J, Netzer C.

Am J Hum Genet. 2015 Mar 5;96(3):432-9. doi: 10.1016/j.ajhg.2015.01.002. Epub 2015 Feb 12.

18.

The Faces in Radiological Images: Fusiform Face Area Supports Radiological Expertise.

Bilalic M, Grottenthaler T, Nägele T, Lindig T.

Cereb Cortex. 2016 Mar;26(3):1004-1014. doi: 10.1093/cercor/bhu272. Epub 2014 Dec 1.

PMID:
25452573
19.

[MR-imaging of focal cortical dysplasia].

Bender B, Rona S, Focke N, Reimold M, Lindig T, Horger M.

Rofo. 2014 Nov;186(11):987-90. doi: 10.1055/s-0034-1369334. Epub 2014 Oct 23. German. No abstract available.

PMID:
25340568
20.

Comparing speech characteristics in spinocerebellar ataxias type 3 and type 6 with Friedreich ataxia.

Brendel B, Synofzik M, Ackermann H, Lindig T, Schölderle T, Schöls L, Ziegler W.

J Neurol. 2015 Jan;262(1):21-6. doi: 10.1007/s00415-014-7511-8. Epub 2014 Sep 30.

PMID:
25267338
21.

Imaging features in conventional MRI, spectroscopy and diffusion weighted images of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS).

Bender B, Klose U, Lindig T, Biskup S, Nägele T, Schöls L, Karle KN.

J Neurol. 2014 Dec;261(12):2351-9. doi: 10.1007/s00415-014-7509-2. Epub 2014 Sep 20.

PMID:
25239393
22.

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.

Neurology. 2014 Jun 3;82(22):2007-16. doi: 10.1212/WNL.0000000000000479. Epub 2014 May 7.

23.

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.

Orphanet J Rare Dis. 2014 Feb 14;9:24. doi: 10.1186/1750-1172-9-24.

24.

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

Synofzik M, Martinez-Carrera LA, Lindig T, Schöls L, Wirth B.

J Neurol Neurosurg Psychiatry. 2014 May;85(5):590-2. doi: 10.1136/jnnp-2013-306777. Epub 2013 Dec 11. No abstract available.

PMID:
24336790
25.

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.

BMC Neurol. 2013 Nov 25;13:185. doi: 10.1186/1471-2377-13-185.

26.

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

Synofzik M, Bernard G, Lindig T, Gburek-Augustat J.

Neurology. 2013 Nov 5;81(19):e145. doi: 10.1212/01.wnl.0000435300.64776.7e.

27.

Friedreich ataxia: dysarthria profile and clinical data.

Brendel B, Ackermann H, Berg D, Lindig T, Schölderle T, Schöls L, Synofzik M, Ziegler W.

Cerebellum. 2013 Aug;12(4):475-84. doi: 10.1007/s12311-012-0440-0.

PMID:
23315038
28.

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.

J Med Genet. 2011 Oct;48(10):713-5. doi: 10.1136/jmg.2011.090282. Epub 2011 Jul 11.

PMID:
21749991
29.

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

Synofzik M, Godau J, Lindig T, Schöls L, Berg D.

Neurodegener Dis. 2011;8(6):470-5. doi: 10.1159/000327751. Epub 2011 Jun 9.

PMID:
21659723
30.

Functional neuroimaging of the oculomotor brainstem network in humans.

Linzenbold W, Lindig T, Himmelbach M.

Neuroimage. 2011 Aug 1;57(3):1116-23. doi: 10.1016/j.neuroimage.2011.05.052. Epub 2011 May 26.

PMID:
21640192
31.

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

Synofzik M, Godau J, Lindig T, Schöls L, Berg D.

Cerebellum. 2011 Mar;10(1):9-13. doi: 10.1007/s12311-010-0215-4.

PMID:
20865356
32.

Complex hyperkinetic movement disorders associated with POLG mutations.

Synofzik M, Schüle R, Schulte C, Krüger R, Lindig T, Schöls L, Asmus F.

Mov Disord. 2010 Oct 30;25(14):2472-5. doi: 10.1002/mds.23307. No abstract available.

PMID:
20818669
33.

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.

J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1402-4. doi: 10.1136/jnnp.2008.167528.

PMID:
19917823
34.

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.

Mov Disord. 2009 Sep 15;24(12):1779-84. doi: 10.1002/mds.22660.

PMID:
19562766
35.

Spiny versus stubby: 3D reconstruction of human myenteric (type I) neurons.

Lindig TM, Kumar V, Kikinis R, Pieper S, Schrödl F, Neuhuber WL, Brehmer A.

Histochem Cell Biol. 2009 Jan;131(1):1-12. doi: 10.1007/s00418-008-0505-9. Epub 2008 Sep 20.

36.

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.

Rofo. 2007 Mar;179(3):219-24.

PMID:
17325991
37.

Chemical coding of myenteric neurons with different axonal projection patterns in the porcine ileum.

Jungbauer C, Lindig TM, Schrödl F, Neuhuber W, Brehmer A.

J Anat. 2006 Dec;209(6):733-43.

38.

Morphology of enkephalin-immunoreactive myenteric neurons in the human gut.

Brehmer A, Lindig TM, Schrödl F, Neuhuber W, Ditterich D, Rexer M, Rupprecht H.

Histochem Cell Biol. 2005 Feb;123(2):131-8. Epub 2005 Mar 18.

PMID:
15776249
39.

Intracellular activities of Salmonella enterica in murine dendritic cells.

Jantsch J, Cheminay C, Chakravortty D, Lindig T, Hein J, Hensel M.

Cell Microbiol. 2003 Dec;5(12):933-45.

PMID:
14641178

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