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Items: 4

1.

Genetic dosage compensation via co-occurrence of PMP22 duplication and PMP22 deletion.

Hirt N, Eggermann K, Hyrenbach S, Lambeck J, Busche A, Fischer J, Rudnik-Schöneborn S, Gaspar H.

Neurology. 2015 Apr 14;84(15):1605-6. doi: 10.1212/WNL.0000000000001470. Epub 2015 Mar 20. No abstract available.

PMID:
25795643
2.

No association of the -105 promoter polymorphism of the selenoprotein S encoding gene SEPS1 with cerebrovascular disease.

Hyrenbach S, Pezzini A, del Zotto E, Giossi A, Lichy C, Kloss M, Werner I, Padovani A, Brandt T, Grond-Ginsbach C.

Eur J Neurol. 2007 Oct;14(10):1173-5.

PMID:
17880573
3.

MTHFR 677TT genotype increases the risk for cervical artery dissections.

Kloss M, Wiest T, Hyrenbach S, Werner I, Arnold ML, Lichy C, Grond-Ginsbach C.

J Neurol Neurosurg Psychiatry. 2006 Aug;77(8):951-2.

4.

Genetic analysis of familial connective tissue alterations associated with cervical artery dissections suggests locus heterogeneity.

Wiest T, Hyrenbach S, Bambul P, Erker B, Pezzini A, Hausser I, Arnold ML, Martin JJ, Engelter S, Lyrer P, Busse O, Brandt T, Grond-Ginsbach C.

Stroke. 2006 Jul;37(7):1697-702. Epub 2006 May 25.

PMID:
16728685

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