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Items: 1 to 20 of 411

1.

Clinical usefulness of FDG-PET/CT for identification of abnormal extra-cardiac foci in patients with infective endocarditis.

Holle SLK, Andersen MH, Klein CF, Bruun NE, Tønder N, Haarmark C, Loft A, Høilund-Carlsen PF, Bundgaard H, Iversen KK.

Int J Cardiovasc Imaging. 2020 Feb 14. doi: 10.1007/s10554-020-01787-8. [Epub ahead of print]

PMID:
32060776
2.

Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?

Bally JF, Breen DP, Schaake S, Trinh J, Rakovic A, Klein C, Lang AE.

Parkinsonism Relat Disord. 2020 Jan 30;71:44-45. doi: 10.1016/j.parkreldis.2020.01.017. [Epub ahead of print]

PMID:
32018151
3.

LRRK2 in Parkinson disease: challenges of clinical trials.

Tolosa E, Vila M, Klein C, Rascol O.

Nat Rev Neurol. 2020 Feb;16(2):97-107. doi: 10.1038/s41582-019-0301-2. Epub 2020 Jan 24. Review.

PMID:
31980808
4.

Needle in a Haystack: The Common Can Inform the Rare in Restless Legs Syndrome.

Trinh J, Klein C.

Ann Neurol. 2020 Feb;87(2):172-174. doi: 10.1002/ana.25663. Epub 2020 Jan 11. No abstract available.

PMID:
31926030
5.

The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci.

Germer EL, Imhoff S, Vilariño-Güell C, Kasten M, Seibler P, Brüggemann N; International Parkinson’s Disease Genomics Consortium, Klein C, Trinh J.

Front Neurol. 2019 Dec 13;10:1284. doi: 10.3389/fneur.2019.01284. eCollection 2019.

6.

Essential phenotypes of NOTCH2NLC-related repeat expansion disorder.

Westenberger A, Klein C.

Brain. 2020 Jan 1;143(1):5-8. doi: 10.1093/brain/awz404. No abstract available.

PMID:
31886491
7.

Risk of spread in adult-onset isolated focal dystonia: a prospective international cohort study.

Berman BD, Groth CL, Sillau SH, Pirio Richardson S, Norris SA, Junker J, Brüggemann N, Agarwal P, Barbano RL, Espay AJ, Vizcarra JA, Klein C, Bäumer T, Loens S, Reich SG, Vidailhet M, Bonnet C, Roze E, Jinnah HA, Perlmutter JS.

J Neurol Neurosurg Psychiatry. 2020 Mar;91(3):314-320. doi: 10.1136/jnnp-2019-321794. Epub 2019 Dec 17.

8.

'Atypical' Parkinson's disease - genetic.

Weissbach A, Wittke C, Kasten M, Klein C.

Int Rev Neurobiol. 2019;149:207-235. doi: 10.1016/bs.irn.2019.10.011. Epub 2019 Nov 25.

PMID:
31779813
9.

Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants.

Vulinovic F, Krajka V, Hausrat TJ, Seibler P, Alvarez-Fischer D, Madoev H, Park JS, Kumar KR, Sue CM, Lohmann K, Kneussel M, Klein C, Rakovic A.

Hum Mutat. 2019 Dec;40(12):2444. doi: 10.1002/humu.23913. Epub 2019 Nov 4. No abstract available.

PMID:
31758849
10.

Osteoclast imbalance in primary familial brain calcification: evidence for its role in brain calcification.

Schiemenz C, Westenberger A, Tanzer K, Grütz K, Borsche M, Mahlke G, Schaake S, Rakovic A, Aherrahrou Z, Erdmann J, Klein C, Alvarez-Fischer D.

Brain. 2020 Jan 1;143(1):e1. doi: 10.1093/brain/awz351. No abstract available.

PMID:
31754706
11.

Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment.

Trinh J, Imhoff S, Dulovic-Mahlow M, Kandaswamy KK, Tadic V, Schäfer J, Dobricic V, Nolte A, Werber M, Rolfs A, Münchau A, Klein C, Lohmann K, Brüggemann N.

J Neurol. 2019 Dec 5. doi: 10.1007/s00415-019-09640-2. [Epub ahead of print]

PMID:
31745726
12.

Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's disease.

Dulovic-Mahlow M, Lukomska A, Diaw SH, Balck A, Borsche M, Grütz K, Lenz I, Rudolph F, Lohmann K, Klein C, Seibler P.

Stem Cell Res. 2019 Dec;41:101629. doi: 10.1016/j.scr.2019.101629. Epub 2019 Oct 19.

13.

Impaired serine metabolism complements LRRK2-G2019S pathogenicity in PD patients.

Nickels SL, Walter J, Bolognin S, Gérard D, Jaeger C, Qing X, Tisserand J, Jarazo J, Hemmer K, Harms A, Halder R, Lucarelli P, Berger E, Antony PMA, Glaab E, Hankemeier T, Klein C, Sauter T, Sinkkonen L, Schwamborn JC.

Parkinsonism Relat Disord. 2019 Oct;67:48-55. doi: 10.1016/j.parkreldis.2019.09.018. Epub 2019 Sep 19.

14.

Nomenclature of Genetically Determined Myoclonus Syndromes: Recommendations of the International Parkinson and Movement Disorder Society Task Force.

van der Veen S, Zutt R, Klein C, Marras C, Berkovic SF, Caviness JN, Shibasaki H, de Koning TJ, Tijssen MAJ.

Mov Disord. 2019 Nov;34(11):1602-1613. doi: 10.1002/mds.27828. Epub 2019 Oct 4. Review.

15.

Risky behaviors and Parkinson disease: A mendelian randomization study.

Grover S, Lill CM, Kasten M, Klein C, Del Greco M F, König IR.

Neurology. 2019 Oct 8;93(15):e1412-e1424. doi: 10.1212/WNL.0000000000008245. Epub 2019 Sep 16.

PMID:
31527283
16.

Imaging gradual neurodegeneration in a basal ganglia model disease.

Hanssen H, Prasuhn J, Heldmann M, Diesta CC, Domingo A, Göttlich M, Blood AJ, Rosales RL, Jamora RDG, Münte TF, Klein C, Brüggemann N.

Ann Neurol. 2019 Oct;86(4):517-526. doi: 10.1002/ana.25566. Epub 2019 Aug 23.

PMID:
31376168
17.

The sooner, the later - Delayed diagnosis in Parkinson's disease due to Parkin mutations.

Borsche M, Balck A, Kasten M, Lohmann K, Klein C, Brüggemann N.

Parkinsonism Relat Disord. 2019 Aug;65:284-285. doi: 10.1016/j.parkreldis.2019.06.020. Epub 2019 Jun 23.

PMID:
31255538
18.

[Model for personalized diagnostics and treatment in neurology-German Academy for Rare Neurological Diseases].

Münchau A, Schöls L, Klein C, Graessner H.

Nervenarzt. 2019 Aug;90(8):796-803. doi: 10.1007/s00115-019-0750-2. Review. German.

PMID:
31243508
19.

Discordance in monozygotic Parkinson's disease twins - continuum or dichotomy?

Balck A, Borsche M, Kasten M, Lohmann K, Seibler P, Brüggemann N, Klein C.

Ann Clin Transl Neurol. 2019 May 2;6(6):1102-1105. doi: 10.1002/acn3.775. eCollection 2019 Jun.

20.

Increased Risk of Ischemic Stroke After Treatment of Infective Endocarditis: A Danish, Nationwide, Propensity Score-Matched Cohort Study.

Klein CF, Gørtz S, Wohlfahrt J, Nørgaard Munch T, Melbye M, Bundgaard H, Iversen KK.

Clin Infect Dis. 2019 Apr 27. pii: ciz320. doi: 10.1093/cid/ciz320. [Epub ahead of print]

PMID:
31198927

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