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Items: 4


ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia.

Bouwkamp CG, Afawi Z, Fattal-Valevski A, Krabbendam IE, Rivetti S, Masalha R, Quadri M, Breedveld GJ, Mandel H, Tailakh MA, Beverloo HB, Stevanin G, Brice A, van IJcken WFJ, Vernooij MW, Dolga AM, de Vrij FMS, Bonifati V, Kushner SA.

Neurol Genet. 2018 Mar 21;4(2):e223. doi: 10.1212/NXG.0000000000000223. eCollection 2018 Apr.


Mitochondrial Ca2+-activated K+ channels and their role in cell life and death pathways.

Krabbendam IE, Honrath B, Culmsee C, Dolga AM.

Cell Calcium. 2018 Jan;69:101-111. doi: 10.1016/j.ceca.2017.07.005. Epub 2017 Jul 22. Review.


Fibril polymorphism affects immobilized non-amyloid flanking domains of huntingtin exon1 rather than its polyglutamine core.

Lin HK, Boatz JC, Krabbendam IE, Kodali R, Hou Z, Wetzel R, Dolga AM, Poirier MA, van der Wel PCA.

Nat Commun. 2017 May 24;8:15462. doi: 10.1038/ncomms15462.


Small conductance Ca2+-activated K+ channels in the plasma membrane, mitochondria and the ER: Pharmacology and implications in neuronal diseases.

Honrath B, Krabbendam IE, Culmsee C, Dolga AM.

Neurochem Int. 2017 Oct;109:13-23. doi: 10.1016/j.neuint.2017.05.005. Epub 2017 May 13. Review.


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