Nivedita U Jerath

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Late onset CMT2A in a Family with an MFN2 Variant: c.2222T>G (p.Leu741Trp).

Kwo Wei David Ho, Hsin-Pin Lin, Nivedita U Jerath, 2019, Journal of neuromuscular diseases.

A neuropathy‐associated kinesin KIF1A mutation hyper‐stabilizes the motor‐neck interaction during the ATPase cycle

N. Hirokawa, S. Zuchner, M. Shy, 2022, The EMBO journal.

Long-term efficacy and safety of eculizumab in Japanese patients with generalized myasthenia gravis: A subgroup analysis of the REGAIN open-label extension study

P. van Damme, M. Benatar, F. Piehl, 2019, Journal of the Neurological Sciences.

Teaching NeuroImages: Intraneural ganglion cyst of the tibial nerve

C. Reddy, B. Miller, Joseph J. Chen, 2014, Neurology.

Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease

S. Züchner, Michael A. Gonzalez, S. Brandner, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

Options in treating trigeminal neuralgia: Experience with 195 patients

M. Holland, Mark C. Smith, T. Moritani, 2016, Clinical Neurology and Neurosurgery.

Neuroleukemiosis: an unusual cause of peripheral neuropathy

C. Reddy, K. Amrami, K. Begna, 2012, Leukemia & lymphoma.

Quantitative Imaging Analysis of FDG PET/CT Imaging for Detection of Central Neurolymphomatosis in a Case of Recurrent Diffuse B-Cell Lymphoma.

M. Graham, F. Shaikh, O. Awan, 2015, Cureus.

F wave, A wave, H reflex, and blink reflex.

J. Kimura, Nivedita U Jerath, 2019, Handbook of clinical neurology.

‘Minimal symptom expression’ in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab

P. van Damme, M. Benatar, F. Piehl, 2020, Journal of Neurology.

Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges

T. Crawford, M. Shy, T. Heiman-Patterson, 2018, Muscle & nerve.

Eculizumab improves fatigue in refractory generalized myasthenia gravis

K. Patra, P. van Damme, M. Benatar, 2019, Quality of Life Research.

V144D Mutation of SPTLC1 Can Present with Both Painful and Painless Phenotypes in Hereditary Sensory and Autonomic Neuropathies Type I

Kwo Wei David Ho, Nivedita U Jerath, 2018, Case reports in genetics.

Three‐dimensional volumetric computed tomographic scoring as an objective outcome measure for chronic rhinosinusitis: clinical correlations and comparison to Lund‐Mackay scoring

Cynthia H McCollough, Lifeng Yu, John Lane, 2013, International forum of allergy & rhinology.

Epidural Spinal Cord Stimulation: A Novel Therapy in the Treatment of Restless Legs Syndrome.

Oliver E. Flouty, C. Reddy, M. Holland, 2016, World neurosurgery.

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

D. Mcguone, M. Bevers, P. Musolino, 2016, Journal of Clinical Neuroscience.

Hereditary motor and sensory neuropathies: Understanding molecular pathogenesis could lead to future treatment strategies.

M. Shy, N. Jerath, Nivedita U Jerath, 2015, Biochimica et biophysica acta.

Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation

Michael A. Gonzalez, T. Chou, S. Zuchner, 2015, Case reports in genetics.

Charcot–Marie–Tooth Disease Type 1A: Influence of Body Mass Index on Nerve Conduction Studies and on the Charcot–Marie–Tooth Examination Score

M. Shy, Nivedita U Jerath, 2017, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

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

C. Reddy, L. Gutmann, M. Shy, 2016, Muscle & nerve.

Factors influencing aversion to specific electrodiagnostic studies

C. Reddy, E. Aul, A. Swenson, 2014, Brain and behavior.

Mild Late-Onset Sensory Neuropathy Associated with Heterozygous Missense GDAP1 Variants

N. Jerath, Nivedita U Jerath, 2022, Case reports in medicine.

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

M. Shy, T. Grider, L. Gutmann, 2015, Muscle & nerve.

T118M Variant of PMP22 Gene Presents with Painful Peripheral Neuropathy and Varying Charcot-Marie-Tooth Features: A Case Series and Review of the Literature

Kwo Wei David Ho, Nivedita U Jerath, 2018, Case reports in genetics.

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

M. Shy, N. Jerath, Nivedita U Jerath, 2017, Journal of neuromuscular diseases.

Gender differences in presenting signs and symptoms of acute ischemic stroke: a population-based study.

C. Reddy, Robert D. Brown, W. D. Freeman, 2011, Gender medicine.

Dorsal Root Ganglion Stimulation as a Potentially Effective Treatment for Painful Hereditary and Idiopathic Axonal Polyneuropathy: A Retrospective Case Series

Kwo Wei David Ho, T. Rempe, A. Antony, 2020, Neuromodulation : journal of the International Neuromodulation Society.

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

Nivedita U Jerath, 2019, Case reports in genetics.

Treating Epilepsy in the Setting of Medical Comorbidities

M. Granner, Dronacharya Lamichhane, Madhu Jasti, 2014, Current Treatment Options in Neurology.

Prolongation of F-wave minimal latency: a sensitive predictor of polyneuropathy

C. Reddy, E. Aul, A. Swenson, 2015, The International journal of neuroscience.

Gender differences in presenting signs and symptoms of acute ischemic stroke: a population-based study.

C. Reddy, Robert D. Brown, W. D. Freeman, 2011, Gender medicine.