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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

Jerath, Nivedita U.; Shy, Michael E.

Journal of clinical neurophysiology. Volume 34:Issue 6 (2017); pp 508-511 -- Wolters Kluwer

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Charcot–Marie–Tooth disease type 1C: Clinical and electrophysiological findings for the c.334G>a (p.Gly112Ser) Litaf/Simple mutation

Jerath, Nivedita U.; Shy, Michael E.

Muscle & nerve. Volume 56:Issue 6 (2017); pp 1092-1095 -- John Wiley & Sons

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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

Jerath, Nivedita U.; Shy, Michael E.

Journal of clinical neurophysiology. Volume 34:Issue 6 (2017) -- Wolters Kluwer

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A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States

Jerath, Nivedita U. et al.

Muscle & nerve. Volume 52:Issue 6 (2015); pp 1110-1113 -- John Wiley & Sons

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Charcot–marie–tooth disease type 1X in women: Electrodiagnostic findings

Jerath, Nivedita U. et al.

Muscle & nerve. Volume 54:Issue 4 (2016); pp 728-732 -- John Wiley & Sons

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Factors influencing aversion to specific electrodiagnostic studies

Jerath, Nivedita U. et al.

Brain and behavior. Volume 4:Issue 5 (2014, September); pp 698-702 -- Wiley Periodicals, Inc

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Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2‐p12) deletion

Jerath, Nivedita U. et al.

Muscle & nerve. Volume 52:Issue 5 (2015); pp 905-908 -- John Wiley & Sons

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Progressive Lower Extremity Weakness and Axonal Sensorimotor Polyneuropathy from a Mutation in KIF5A (c.611G>A;p.Arg204Gln)

Jerath, Nivedita U.; Grider, Tiffany; Shy, Michael E.

Case reports in genetics. Volume 2015 (2015) -- Hindawi

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Progressive Lower Extremity Weakness and Axonal Sensorimotor Polyneuropathy from a Mutation in KIF5A (c.611G>A;p.Arg204Gln)

Jerath, Nivedita U.; Grider, Tiffany; Shy, Michael E.

Case reports in genetics. Volume 2015 (2015) -- Hindawi

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Leptomeningeal transthyretin-type amyloidosis presenting as acute hydrocephalus and subarachnoid hemorrhage

Bevers, Matthew B. et al.

Elsevier Ltd -- 2016

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