Hereditary motor and sensory neuropathies: Understanding molecular pathogenesis could lead to future treatment strategies von Jerath, Nivedita U., Shy, Michael E.

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A neuropathy‐associated kinesin KIF1A mutation hyper‐stabilizes the motor‐neck interaction during the ATPase cycle von Morikawa, Manatsu, Jerath, Nivedita U, Ogawa, Tadayuki, Morikawa, Momo, Tanaka, Yosuke, Shy, Michael E, Zuchner, Stephan, Hirokawa, Nobutaka

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Mild Late-Onset Sensory Neuropathy Associated with Heterozygous Missense GDAP1 Variants von Jerath, Nivedita U.

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Epidural spinal cord stimulation: A novel therapy in the treatment of restless legs syndrome von Holland, Marshall T., MD, Rettenmaier, Leigh A, Flouty, Oliver E., MD, Thomsen, Teri R., MD, Jerath, Nivedita U., MD, Reddy, Chandan G., MD

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V144D Mutation of SPTLC1 Can Present with Both Painful and Painless Phenotypes in Hereditary Sensory and Autonomic Neuropathies Type I von Ho, Kwo Wei David, Jerath, Nivedita U.

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T118M Variant of PMP22 Gene Presents with Painful Peripheral Neuropathy and Varying Charcot-Marie-Tooth Features: A Case Series and Review of the Literature von Ho, Kwo Wei David, Jerath, Nivedita U.

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A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States von Jerath, Nivedita U., Shy, Michael E., Grider, Tiffany, Gutmann, Ludwig

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Charcot–Marie–Tooth disease type 1C: Clinical and electrophysiological findings for the c.334G>a (p.Gly112Ser) Litaf/Simple mutation von Jerath, Nivedita U., Shy, Michael E.

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Gender Differences in Presenting Signs and Symptoms of Acute Ischemic Stroke: A Population-Based Study von Jerath, Nivedita U., MD, Reddy, Chandan, MD, Freeman, W. David, MD, Jerath, Aarti U., MD, MA, Brown, Robert D., MD, MPH

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Resolving a Multi-Generational Neuromuscular Mystery in a Family Presenting with a Variable Scapuloperoneal Syndrome in a c.464G>A, p.Arg155His VCP Mutation von Jerath, Nivedita U.

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Charcot–Marie–Tooth Disease Type 1A: Influence of Body Mass Index on Nerve Conduction Studies and on the Charcot–Marie–Tooth Examination Score von Jerath, Nivedita U, Shy, Michael E

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Charcot-marie-tooth disease type 1X in women: Electrodiagnostic findings von Jerath, Nivedita U., Gutmann, Laurie, Reddy, Chandan G., Shy, Michael E.

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Progressive Lower Extremity Weakness and Axonal Sensorimotor Polyneuropathy from a Mutation in KIF5A (c.611G>A;p.Arg204Gln) von Jerath, Nivedita U., Shy, Michael E., Grider, Tiffany

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Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges von Jerath, Nivedita U., Mankodi, Ami, Crawford, Thomas O., Grunseich, Christopher, Baloui, Hasna, Nnamdi‐Emeratom, Chioma, Schindler, Alice B., Heiman‐Patterson, Terry, Chrast, Roman, Shy, Michael E.

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Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2-p12) deletion von Jerath, Nivedita U., Kamholz, John, Grider, Tiffany, Harper, Amy, Swenson, Andrea, Shy, Michael E.

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Teaching NeuroImages: Intraneural ganglion cyst of the tibial nerve von Jerath, Nivedita U, Chen, Joseph J, Miller, Benjamin J, Reddy, Chandan G

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Leptomeningeal transthyretin-type amyloidosis presenting as acute hydrocephalus and subarachnoid hemorrhage von Bevers, Matthew B, McGuone, Declan, Jerath, Nivedita U, Musolino, Patricia L

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Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation von Swenson, Andrea, Zuchner, Stephan, Grider, Tiffany, Chou, Tsui-Fen, Weihl, Conrad C., Shy, Michael E., Moore, Steven A., Crockett, Cameron D., Jerath, Nivedita U., Gonzalez, Michael A.

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Asymmetric Ataxia, Depression, Memory Loss, Epilepsy, and Axonal Neuropathy Associated with A Heterozygous DNA Polymerase Gamma Variant of Uncertain Significance, c1370G>a (R457Q) von Jerath, Nivedita U., Shy, Michael E.

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Driving Simulator Performance in Charcot-Marie-Tooth Disease Type 1A von Jerath, Nivedita U., Aksan, Nazan, Dawson, Jeffrey D., Rizzo, Matthew, Uc, Ergun Y., Shy, Michael E.

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