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Office
201 N Park Ave
Ste 301
Apopka, FL 32703Phone+1 407-614-0528Fax+1 407-614-0529
Education & Training
- University of Iowa Hospitals and ClinicsFellowship, Neuromuscular Medicine (Neurology), 2013
- University of IowaM.S., Translational Biomedicine, 2016
- University of Iowa Hospitals and ClinicsFellowship, Clinical Neurophysiology, 2012 - 2013
- Brigham and Women's Hospital/Massachusetts General Hospital/Harvard Medical SchoolResidency, Neurology, 2009 - 2012
- University of Iowa Hospitals and ClinicsResidency, Neurology, 2008 - 2012
- Ascension Illinois/Saint FrancisInternship, Internal Medicine, 2008 - 2009
- Mayo Clinic College of MedicineClass of 2008
- Harvard UniversityBA, Economics, 1999 - 2003
- Harvard UniversityB.A., Economics, 2003
Certifications & Licensure
- FL State Medical License 2017 - 2025
- IA State Medical License 2012 - 2017
- MA State Medical License 2009 - 2012
- IL State Medical License 2008 - 2009
- American Board of Psychiatry and Neurology Neurology
- American Board of Psychiatry and Neurology Neuromuscular Medicine
Awards, Honors, & Recognition
- Making a Difference Award University of Iowa, 2015-2016
- MDA Conference Best Poster Prize 2014
- Second Place Award for Poster, Carrel-Krusen Neuromuscular Symposium 2014
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Publications & Presentations
PubMed
- Two Cases of Periodic Paralysis Associated With MCM3AP Variants.Tatsuya Oishi, Jennifer Pagano, Cody Sellers, Nivedita U Jerath
Journal of Clinical Neuromuscular Disease. 2023-09-01 - 11 citationsA neuropathy-associated kinesin KIF1A mutation hyper-stabilizes the motor-neck interaction during the ATPase cycle.Manatsu Morikawa, Nivedita U Jerath, Tadayuki Ogawa, Momo Morikawa, Yosuke Tanaka
The EMBO Journal. 2022-03-01 - Mild Late-Onset Sensory Neuropathy Associated with Heterozygous Missense GDAP1 Variants.Nivedita U Jerath
Case Reports in Medicine. 2022-01-01
Journal Articles
- Dorsal Root Ganglion Stimulation As a Potentially Effective Treatment for Painful Hereditary and Idiopathic Axonal Polyneuropathy: A Retrospective Case SeriesWei Ho KD, Rempe T, Jerath N.U., Anthony AB, Neuromodulation: Technology at the Neural Interface, 1/1/2019
- V144D mutation of SPTLC1 can present with both painful and painless phenotypes in hereditary sensory and autonomic neuropathies type IWei Ho KD, Jerath N.U., Case Reports in Genetics, 1/1/2018
- Charcot Marie Tooth Disease type 4C: Novel Mutations, Clinical Presentations, and Diagnostic Challenges of an Atypical CMTJerath N.U., Mankodi A, Crawford TO, Grunseich C, Baloui H, Nnamdi-Emeratom C, Schindler AB, Heiman-Patterson T, Chrast R, and Shy ME, Muscle Nerve, 1/1/2018
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Books/Book Chapters
Abstracts/Posters
- Presentation of SPTLC1 mutation and electrophysiological data in CMT2.Jerath N.U., Peripheral Nerve Society Conference, Baltimore, MD, 1/1/2018
- Presentation of CMT1C cohort of patients and CMT 4C case series.Jerath N.U., Peripheral Nerve Society Conference, Sitges, Spain, 1/1/2017
- Preliminary Data on Driving Ability in CMT 1A patients.Jerath N.U., Clinical Research for Rare Diseases; Peripheral Nerve Society Conference, Quebec, Canada, 2015; Washington, DC, 2016, 1/1/2016
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Lectures
- Updates on CMT.Tampa, FL; Atlanta, GA - 1/1/2018
- Challenging Neuromuscular Case.Mayo Clinic-Jacksonville - 1/1/2018
- CMT X Electrodiagnostic Findings in Women.Washington, DC - 1/1/2015
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Press Mentions
- As ALS Research Booms, One Treatment Center Finds Itself in the SpotlightDecember 24th, 2023
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