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Archives of Neurology|July 11, 2007
Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkleRobert H Baloh, Ezequiel Salavaggione, Jeffrey Milbrandt, et al.Current Opinion in Neurology|August 7, 2018
Stem cell transplantation for amyotrophic lateral sclerosisRobert H Baloh, Jonathan D Glass, Clive N SvendsenMuscle & Nerve|February 15, 2007
Frequent atrophic groups with mixed-type myofibers is distinctive to motor neuron syndromesRobert H Baloh, Wojtek Rakowicz, Robert Gardner, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 12, 2007
Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutationsRobert H Baloh, Robert E Schmidt, Alan Pestronk, et al.Structure (London, England : 1993)|June 13, 2006
Structure of artemin complexed with its receptor GFRalpha3: convergent recognition of glial cell line-derived neurotrophic factorsXinquan Wang, Robert H Baloh, Jeffrey Milbrandt, et al.Journal of the Neurological Sciences|July 5, 2005
Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 geneJoanna Jen, Robert H Baloh, Akira Ishiyama, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 22, 2009
Transgenic mice expressing the Nmnat1 protein manifest robust delay in axonal degeneration in vivoYo Sasaki, Bhupinder P S Vohra, Robert H Baloh, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 26, 2010
Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complexAlbert Misko, Sirui Jiang, Iga Wegorzewska, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 24, 2012
Mitofusin2 mutations disrupt axonal mitochondrial positioning and promote axon degenerationAlbert L Misko, Yo Sasaki, Elizabeth Tuck, et al.Proceedings of the National Academy of Sciences of the United States of America|October 17, 2009
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degenerationIga Wegorzewska, Shaughn Bell, Nigel J Cairns, et al.Pageof 9