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Items: 8

1.

Analysis of blood-based gene expression in idiopathic Parkinson disease.

Shamir R, Klein C, Amar D, Vollstedt EJ, Bonin M, Usenovic M, Wong YC, Maver A, Poths S, Safer H, Corvol JC, Lesage S, Lavi O, Deuschl G, Kuhlenbaeumer G, Pawlack H, Ulitsky I, Kasten M, Riess O, Brice A, Peterlin B, Krainc D.

Neurology. 2017 Oct 17;89(16):1676-1683. doi: 10.1212/WNL.0000000000004516. Epub 2017 Sep 15.

PMID:
28916538
2.

Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases.

Craggs L, Taylor J, Slade JY, Chen A, Hagel C, Kuhlenbaeumer G, Borjesson-Hanson A, Viitanen M, Kalimo H, Deramecourt V, Oakley AE, Kalaria RN.

Neuropathol Appl Neurobiol. 2016 Feb;42(2):194-209. doi: 10.1111/nan.12248. Epub 2015 Jun 17.

3.

Identification of a novel risk variant in the FUS gene in essential tremor.

Kuhlenbaeumer G, Tan EK, Wu YR.

Neurology. 2014 Feb 4;82(5):461. doi: 10.1212/WNL.0000000000000073. No abstract available.

PMID:
24491973
4.

Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases.

Craggs LJ, Hagel C, Kuhlenbaeumer G, Borjesson-Hanson A, Andersen O, Viitanen M, Kalimo H, McLean CA, Slade JY, Hall RA, Oakley AE, Yamamoto Y, Deramecourt V, Kalaria RN.

Brain Pathol. 2013 Sep;23(5):547-57. doi: 10.1111/bpa.12041. Epub 2013 Mar 8.

PMID:
23387519
5.

Polymorphisms and noncardioembolic stroke in three case-control studies.

Luke MM, Berger K, Rowland CM, Catanese JJ, Tong CH, Ross DA, Garcia V, Kuhlenbaeumer G, Ringelstein EB, Pullinger CR, Malloy MJ, Deedwania P, Ellis SG, Kane JP, Devlin JJ, Lalouschek W, Mannhalter C.

Cerebrovasc Dis. 2012;33(1):80-5. doi: 10.1159/000333444. Epub 2011 Dec 1.

PMID:
22134093
6.

Genetic variants in the C-reactive protein gene are associated with microangiopathic ischemic stroke.

Kuhlenbaeumer G, Huge A, Berger K, Kessler C, Voelzke H, Funke H, Stoegbauer F, Stoll M, Ringelstein EB.

Cerebrovasc Dis. 2010;30(5):476-82. doi: 10.1159/000319021. Epub 2010 Aug 24.

PMID:
20733302
7.

Neurosonographical follow-up in patients with spontaneous cervical artery dissection.

Sengelhoff C, Nebelsieck J, Nassenstein I, Maintz D, Nabavi DG, Kuhlenbaeumer G, Ringelstein EB, Dittrich R.

Neurol Res. 2008 Sep;30(7):687-9. doi: 10.1179/174313208X319080.

PMID:
18826800
8.

Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA).

Kuhlenbaeumer G, Meuleman J, Schirmacher A, Stoegbauer F, Ringelstein EB, Wehnert M, Hoeltzenbein M, Broeckhoven CV, Timmerman V.

Ann Hum Genet. 1998 Sep;62(Pt 5):397-400.

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