Berg D - Search Results

1

Cognitive decline in Parkinson's disease: the impact of the motor phenotype on cognition.

Wojtala J, Heber IA, Neuser P, Heller J, Kalbe E, Rehberg SP, Storch A, Linse K, Schneider C, Gräber S, Berg D, Dams J, Balzer-Geldsetzer M, Hilker-Roggendorf R, Oberschmidt C, Baudrexel S, Witt K, Schmidt N, Deuschl G, Mollenhauer B, Trenkwalder C, Liepelt-Scarfone I, Spottke A, Roeske S, Wüllner U, Wittchen HU, Riedel O, Dodel R, Schulz JB, Reetz K. Wojtala J, et al. Among authors: berg d. J Neurol Neurosurg Psychiatry. 2019 Feb;90(2):171-179. doi: 10.1136/jnnp-2018-319008. Epub 2018 Oct 8. J Neurol Neurosurg Psychiatry. 2019. PMID: 30297519

2

Relationship of substantia nigra echogenicity and motor function in elderly subjects.

Berg D, Siefker C, Ruprecht-Dörfler P, Becker G. Berg D, et al. Neurology. 2001 Jan 9;56(1):13-7. doi: 10.1212/wnl.56.1.13. Neurology. 2001. PMID: 11148229

3

Therapeutic strategies for Parkinson's disease based on data derived from genetic research.

Riess O, Berg D, Krüger R, Schulz JB. Riess O, et al. Among authors: berg d. J Neurol. 2003 Feb;250 Suppl 1:I3-10. doi: 10.1007/s00415-003-1101-3. J Neurol. 2003. PMID: 12761628 Review.

4

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.

Hering R, Petrovic S, Mietz EM, Holzmann C, Berg D, Bauer P, Woitalla D, Müller T, Berger K, Krüger R, Riess O. Hering R, et al. Among authors: berg d. Neurology. 2004 Apr 13;62(7):1231-2. doi: 10.1212/01.wnl.0000118285.18383.90. Neurology. 2004. PMID: 15079038 No abstract available.

5

Differentiation of Parkinson's disease and atypical parkinsonian syndromes by transcranial ultrasound.

Behnke S, Berg D, Naumann M, Becker G. Behnke S, et al. Among authors: berg d. J Neurol Neurosurg Psychiatry. 2005 Mar;76(3):423-5. doi: 10.1136/jnnp.2004.049221. J Neurol Neurosurg Psychiatry. 2005. PMID: 15716540 Free PMC article. Clinical Trial.

6

Multiple regions of alpha-synuclein are associated with Parkinson's disease.

Mueller JC, Fuchs J, Hofer A, Zimprich A, Lichtner P, Illig T, Berg D, Wüllner U, Meitinger T, Gasser T. Mueller JC, et al. Among authors: berg d. Ann Neurol. 2005 Apr;57(4):535-41. doi: 10.1002/ana.20438. Ann Neurol. 2005. PMID: 15786467

7

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.

Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, Gasser T, Wszolek Z, Müller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, Krüger R. Strauss KM, et al. Among authors: berg d. Hum Mol Genet. 2005 Aug 1;14(15):2099-111. doi: 10.1093/hmg/ddi215. Epub 2005 Jun 16. Hum Mol Genet. 2005. PMID: 15961413

8

Common variants of LRRK2 are not associated with sporadic Parkinson's disease.

Biskup S, Mueller JC, Sharma M, Lichtner P, Zimprich A, Berg D, Wüllner U, Illig T, Meitinger T, Gasser T. Biskup S, et al. Among authors: berg d. Ann Neurol. 2005 Dec;58(6):905-8. doi: 10.1002/ana.20664. Ann Neurol. 2005. PMID: 16254973

9

Comprehensive association analysis of the NOS2A gene with Parkinson disease.

Schulte C, Sharma M, Mueller JC, Lichtner P, Prestel J, Berg D, Gasser T. Schulte C, et al. Among authors: berg d. Neurology. 2006 Dec 12;67(11):2080-2. doi: 10.1212/01.wnl.0000247672.41736.bd. Neurology. 2006. PMID: 17159127

10

The proteasomal subunit S6 ATPase is a novel synphilin-1 interacting protein--implications for Parkinson's disease.

Marx FP, Soehn AS, Berg D, Melle C, Schiesling C, Lang M, Kautzmann S, Strauss KM, Franck T, Engelender S, Pahnke J, Dawson S, von Eggeling F, Schulz JB, Riess O, Krüger R. Marx FP, et al. Among authors: berg d. FASEB J. 2007 Jun;21(8):1759-67. doi: 10.1096/fj.06-6734com. Epub 2007 Feb 27. FASEB J. 2007. PMID: 17327361

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