Nivedita U Jerath

5PUBLICATIONS
0CO-AUTHORS
Gene mappingMolecular evolutionMedical infection agents (incl. prions)Autonomic nervous systemProsthetics and orthotics
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Publications (5)

|Jun 03, 2022
Mild Late-Onset Sensory Neuropathy Associated with Heterozygous Missense GDAP1 Variants.

Nivedita U Jerath

|Nov 06, 2019
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

|Jan 25, 2019
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

|Nov 14, 2018
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

|Dec 09, 2017
Survey of the functional priorities in patients with disability due to neuromuscular disorders.

Nivedita U Jerath, Kevin Simoens, Dylan Mann

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