Skip to main content

H Houlden

First name:
H
Last name:
Houlden
Alg, V., Ke, X., Grieve, J., Bonner, S., Walsh, D., Bulters, D., … Study, I. G. and O. S. H. (2018). Association of functional MMP-2 gene variant with intracranial aneurysms: case-control genetic association study and meta-analysis. British Journal of Neurosurgery, 1-5. https://doi.org/10.1080/02688697.2018.1427213 (Original work published 2018)
Wiethoff, S., O’Connor, E., Haridy, N., Nethisinghe, S., Wood, N., Giunti, P., … Houlden, H. (2018). Sequencing analysis of the SCA6 CAG expansion excludes an influence of repeat interruptions on disease onset. Journal of Neurology, Neurosurgery, and Psychiatry. https://doi.org/10.1136/jnnp-2017-317253 (Original work published 2018)
Hufnagel, R., Arno, G., Hein, N., Hersheson, J., Prasad, M., Anderson, Y., … Ahmed, Z. (2015). Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes. Journal of Medical Genetics, 52(2), 85-94. https://doi.org/10.1136/jmedgenet-2014-102856