Christopher Jon Klein, MD, MS

  • 4959 Citations
  • 40 Scopus h-Index
1991 …2019
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  • 14 Similar Profiles
Polyneuropathies Medicine & Life Sciences
Mutation Medicine & Life Sciences
Immunotherapy Medicine & Life Sciences
Peripheral Nervous System Diseases Medicine & Life Sciences
Autoantibodies Medicine & Life Sciences
Neural Conduction Medicine & Life Sciences
Autoimmunity Medicine & Life Sciences
Immunoglobulin G Medicine & Life Sciences

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Projects 2009 2014

Hereditary Sensory and Autonomic Neuropathies
Hearing Loss

Research Output 1991 2019

Amphiphysin-IgG autoimmune neuropathy: A recognizable clinicopathologic syndrome

Dubey, D., Jitprapaikulsan, J., Bi, H., Do Campo, R. V., McKeon, A., Pittock, S. J., Engelstad, J. K., Mills, J. R. & Klein, C. J., Nov 12 2019, In : Neurology. 93, 20, p. e1873-e1880

Research output: Contribution to journalArticle

Immunoglobulin G

Autoimmune gait disturbance accompanying adaptor protein-3B2-IgG

Honorat, J. A., Lopez-Chiriboga, A. S., Kryzer, T. J., Komorowski, L., Scharf, M., Hinson, S. R., Lennon, V. A., Pittock, S. J., Klein, C. J. & McKeon, A., Sep 3 2019, In : Neurology. 93, 10, p. e954-e963

Research output: Contribution to journalArticle

Open Access
Immunoglobulin G
Western Blotting
Cerebellar Ataxia

DNA methylation patterns in human iPSC-derived sensory neuronal differentiation

Ankam, S., Rovini, A., Baheti, S., Hrstka, R., Wu, Y., Schmidt, K., Wang, H., Madigan, N., Koenig, L. S., Stelzig, K., Resch, Z., Klein, C. J., Sun, Z. & Staff, N. P., Jan 1 2019, In : Epigenetics.

Research output: Contribution to journalArticle

Sensory Receptor Cells
DNA Methylation
Induced Pluripotent Stem Cells
Peripheral Nervous System

Embolized Spinal Dural AV Fistula Repairs Syringomyelia and Polyradiculopathy

Pinto, M. V., Cloft, H. & Klein, C. J., Sep 2019, In : Mayo Clinic proceedings. 94, 9, p. 1904-1906 3 p.

Research output: Contribution to journalLetter

Open Access

Mitochondrial cerebellar ataxia, renal failure, neuropathy, and encephalopathy (MCARNE)

Ng, P. S., Pinto, M. V., Neff, J. L., Hasadsri, L., Highsmith, W. E. J., Fidler, M. E., Gavrilova, R. M. & Klein, C. J., Apr 1 2019, In : Neurology: Genetics. 5, 2, e314.

Research output: Contribution to journalArticle

Open Access
MELAS Syndrome
NADH Dehydrogenase
Cerebellar Ataxia
Brain Diseases
Missense Mutation