News & Publications for:

Matthew Harms

Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age

Posted on July 25, 2013

Eschbach, J., Sinniger, J., Bouitbir, J., Fergani, A., Schlagowski, A.-I., Zoll, J., Geny, B., René, F., Larmet, Y., Marion, V., Baloh, R.H., Harms, M.B., Shy, M.E., Messadeq, N., Weydt, P., Loeffler, J.-P., Ludolph, A.C., Dupuis, L.; Neurobiology of Disease Volume 58, October 2013, Pages 220-230 Read More

Posted in: Neurogenetics, Publications Faculty:

Cramps and small-fiber neuropathy

Posted on July 11, 2013

Lopate, G., Streif, E., Harms, M., Weihl, C., Pestronk, A.; Muscle and Nerve 2013 Read More

Posted in: HPAN, Neurodegeneration, Neurogenetics, Publications Faculty: , ,

Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis

Posted on June 26, 2013

Harms, M.B., Cady, J., Zaidman, C., Cooper, P., Bali, T., Allred, P., Cruchaga, C., Baughn, M., Libby, R.T., Pestronk, A., Goate, A., Ravits, J., Baloh, R.H.; (2013) Neurobiology of Aging, 34 (9), pp. 2234.e13-e19. Read More

Posted in: HPAN, Neurogenetics, Publications Faculty: , , ,

C9orf72 hexanucleotide repeat expansions in clinical alzheimer disease

Posted on June 19, 2013

Harms, M., Benitez, B.A., Cairns, N., Cooper, B., Cooper, P., Mayo, K., Carrell, D., Faber, K., Williamson, J.g , Bird, T.h , Diaz-Arrastia, R.i , Foroud, T.M.f , Boeve, B.F.j , Graff-Radford, N.R., Mayeux, R., Chakraverty, S., Goate, A.M., Cruchaga, C.;(2013) JAMA Neurology, 70 (6), pp. 736-741. Read More

Posted in: HPAN, Neurogenetics, Publications Faculty: , , ,

Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy

Posted on May 4, 2012

Harms MB, Sommerville RB, Allred P, Bell S, Ma D, Cooper P, Lopate G, Pestronk A, Weihl CC, Baloh RH (2012). Ann Neurol, 71(3):407-16 Read More

Posted in: Neurodegeneration, Neurogenetics, Pilot Projects, Publications Faculty: , ,