NiveditaUberoiJerathMD

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 Sep 1
• 9 citations
  A 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, Michael E Shy, Stephan Zuchner, Nobutaka Hirokawa> ;The EMBO Journal. 2022 Mar 1
• Mild Late-Onset Sensory Neuropathy Associated with Heterozygous Missense GDAP1 Variants.
  Nivedita U Jerath> ;Case Reports in Medicine. 2022 Jan 1
• 4 citations
  Dorsal Root Ganglion Stimulation as a Potentially Effective Treatment for Painful Hereditary and Idiopathic Axonal Polyneuropathy: A Retrospective Case Series.
  Kwo Wei David Ho, Torge Rempe, Nivedita U. Jerath, Ajay Antony> ;Neuromodulation. 2020 Feb 1
• 5 citations
  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> ;Case Reports in Genetics. 2019 Oct 9
• 4 citations
  Survey of the functional priorities in patients with disability due to neuromuscular disorders.
  Nivedita U. Jerath, Kevin J. Simoens, Dylan Mann, Steph Kollasch, Nicole M. Grosland, Karim A Malik, Chandan G Reddy> ;Disability and Rehabilitation. Assistive Technology. 2019 Feb 1
• 19 citations
  F wave, A wave, H reflex, and blink reflex.
  Nivedita U. Jerath, Jun Kimura> ;Handbook of Clinical Neurology. 2019 Jan 1
• 2 citations
  Late onset CMT2A in a Family with an MFN2 Variant: c.2222T>G (p.Leu741Trp).
  Hsin-Pin Lin, Kwo Wei David Ho, Nivedita U. Jerath> ;Journal of Neuromuscular Diseases. 2019 Jan 1
• 4 citations
  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> ;Case Reports in Genetics. 2018 Dec 25
• 6 citations
  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> ;Case Reports in Genetics. 2018 Oct 18
• 10 citations
  Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges
  Nivedita U. Jerath, Ami Mankodi, Thomas O. Crawford, Christopher Grunseich, Hasna Baloui, Chioma Nnamdi-Emeratom, Alice B. Schindler, Terry Heiman-Patterson, Roman Chr...> ;Muscle & Nerve. 2018 May 1
• 1 citations
  Asymmetric Ataxia, Depression, Memory Loss, Epilepsy, and Axonal Neuropathy Associated with A Heterozygous DNA Polymerase Gamma Variant of Uncertain Significance, c137...
  Nivedita U. Jerath, Michael E. Shy> ;Journal of Neuromuscular Diseases. 2017 Dec 20
• 2 citations
  Charcot-Marie-Tooth Disease Type 1A: Influence of Body Mass Index on Nerve Conduction Studies and on the Charcot-Marie-Tooth Examination Score.
  Nivedita U. Jerath, Michael E. Shy> ;Journal of Clinical Neurophysiology. 2017 Nov 1
• 29 citations
  Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease.
  Alejandro Horga, Matilde Laura, Zane Jaunmuktane, Nivedita U. Jerath, Michael A. Gonzalez, James M. Polke, Roy Poh, Julian Blake, Yo Tsen Liu, Sarah Wiethoff, Conceiçã...> ;Journal of Neurology, Neurosurgery, and Psychiatry. 2017 May 13
• 6 citations
  Charcot–Marie–Tooth disease type 1C: Clinical and electrophysiological findings for the c.334G>a (p.Gly112Ser) LITAF/SIMPLE mutation
  Nivedita U. Jerath, Michael E. Shy> ;Muscle & Nerve. 2017 Apr 1
• 26 citations
  Options in treating trigeminal neuralgia: Experience with 195 patients.
  Patrick W. Hitchon, Marshall T. Holland, Jennifer Noeller, Mark C. Smith, Toshio Moritani, Nivedita U. Jerath, Wenzhuan He> ;Clinical Neurology and Neurosurgery. 2016 Oct 1
• 12 citations
  Epidural Spinal Cord Stimulation: A Novel Therapy in the Treatment of Restless Legs Syndrome
  Marshall T. Holland, Leigh A. Rettenmaier, Oliver E. Flouty, Teri Thomsen, Nivedita U. Jerath, Chandan G. Reddy> ;World Neurosurgery. 2016 Aug 1
• 4 citations
  Leptomeningeal transthyretin-type amyloidosis presenting as acute hydrocephalus and subarachnoid hemorrhage.
  Matthew B. Bevers, Nivedita U. Jerath, Patricia L. Musolino> ;Journal of Clinical Neuroscience. 2016 Jul 1
• 9 citations
  Charcot–marie–tooth disease type 1X in women: Electrodiagnostic findings
  Nivedita U. Jerath, Laurie Gutmann, Chandan G. Reddy, Michael E. Shy> ;Muscle & Nerve. 2016 Jul 4
• 19 citations
  A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States.
  Nivedita U. Jerath, Michael E. Shy, Tiffany Grider, Ludwig Gutmann> ;Muscle & Nerve. 2015 Dec 1
• Quantitative Imaging Analysis of FDG PET/CT Imaging for Detection of Central Neurolymphomatosis in a Case of Recurrent Diffuse B-Cell Lymphoma.
  Faiq Shaikh, Derek Savells, Omer A. Awan, Faisal Inayat, Ammar Chaudhry, Nivedita U. Jerath, Michael M. Graham> ;Cureus. 2015 Nov 13
• 4 citations
  Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2-p12) deletion.
  Nivedita U. Jerath, John Kamholz, Tiffany Grider, Amy Harper, Andrea Swenson, Michael E. Shy> ;Muscle & Nerve. 2015 Nov 1
• 4 citations
  Progressive Lower Extremity Weakness and Axonal Sensorimotor Polyneuropathy from a Mutation in KIF5A (c.611G>A;p.Arg204Gln).
  Nivedita U. Jerath, Tiffany Grider, Michael E. Shy> ;Case Reports in Genetics. 2015 Oct 12
• 8 citations
  Diagnostic Yield of FDG-PET/CT, MRI, and CSF Cytology in Non-Biopsiable Neurolymphomatosis as a Heralding Sign of Recurrent Non-Hodgkin's Lymphoma
  Faiq Shaikh, Aubrey C. Chan, Omer A. Awan, Nivedita U. Jerath, Chandan G. Reddy, Salman Khan, Michael M. Graham> ;Cureus. 2015 Sep 9
• 9 citations
  Prolongation of F-wave minimal latency: a sensitive predictor of polyneuropathy
  Nivedita U. Jerath, Edward A. Aul, Chandan G. Reddy, Hamid Azadeh, Andrea Swenson, Jun Kimura> ;The International Journal of Neuroscience. 2015 May 22
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Journal Articles

• Dorsal Root Ganglion Stimulation As a Potentially Effective Treatment for Painful Hereditary and Idiopathic Axonal Polyneuropathy: A Retrospective Case Series  
  Wei Ho KD, Rempe T, Jerath N.U., Anthony AB, Neuromodulation: Technology at the Neural Interface, 1/1/2019
• T118M variant of PMP22 gene presents with painful peripheral neuropathy and varying Charcot-Marie-Tooth features � a case series and review of the literature  
  Wei 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 CMT  
  Jerath 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
• V144D mutation of SPTLC1 can present with both painful and painless phenotypes in hereditary sensory and autonomic neuropathies type I  
  Wei Ho KD, Jerath N.U., Case Reports in Genetics, 1/1/2018
• Survey of the functional priorities in patients with disability due to neuromuscular disorders  
  Jerath N.U., Simoens K, Mann D, Kollasch S, Grosland N, Malik KA and Reddy CG, Disability and Rehabilitation: Assistive Technology, 1/1/2017
• Charcot-Marie-Tooth Disease Type 1A: Influence of Body Mass Index on Nerve Conduction Studies and on the Charcot-Marie-Tooth Examination Score  
  Jerath, N.U. and Shy ME, J Clin Neurophysiol, 1/1/2017
• Genetic and clinical characteristics of NEFL-related Charcot-MarieTooth disease  
  Horga, A., Laura, M., Jaunmuktane, Z., Jerath, N. U., Gonzalez, M. A., Polke, J. M., . . . Reilly, M. M., J Neurol Neurosurg Psychiatry, 1/1/2017
• Asymmetric Ataxia, Depression, Memory Loss, Epilepsy, and Axonal Neuropathy Associated with A Heterozygous DNA Polymerase Gamma Variant of Uncertain Significance, c137...  
  Jerath N.U., Shy ME, Journal of Neuromuscular Diseases, 1/1/2017
• Charcot-Marie-Tooth disease type 1C: Clinical and electrophysiological findings for the c334G>a (pGly112Ser) LITAF/SIMPLE mutation  
  Jerath, N.U., Shy, ME, Muscle Nerve, 1/1/2017
• Leptomeningeal transthyretin-type amyloidosis presenting as acute hydrocephalus and subarachnoid hemorrhage  
  Bevers MB, McGuone D, Jerath N.U., Musolino PL, Journal of clinical neuroscience, 1/1/2016
• Epidural Spinal Cord Stimulation: A Novel Therapy in the Treatment of Restless Legs Syndrome  
  Holland MT, Rettenmaier LA, Flouty OE, Thomsen TR, Jerath N.U., Reddy CG, World Neurosurgery, 1/1/2016
• Progressive lower extremity weakness and axonal sensorimotor polyneuropathy from a mutation in KIF5A (c611G>A;pArg204Gln)  
  Jerath N.U., Grider T, Shy ME, Case Reports in Genetics, 1/29/2015
• Rare Manifestation of a c290 C>T, pGly97Glu VCP Mutation  
  Jerath N.U., Crockett CD, Moore SA, et al, Case Reports in Genetics, 1/1/2015
• Prolongation of F-wave minimal latency: A Sensitive Predictor of Polyneuropathy  
  Jerath N.U., Aul E, Reddy CG, Azadeh H, Swenson A, Kimura J, International Journal of Neuroscience, 1/1/2015
• Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p112-p12) deletion  
  Jerath N.U., Kamholz J, Grider T, Harper A, Swenson A, Shy ME, Muscle & Nerve, 1/1/2015
• A case of neuromyotonia and axonal motor neuropathy: A report of a HINT 1 mutation in the United States  
  Jerath N.U., Shy ME, Grider T, Gutmann L., Muscle & Nerve, 1/1/2015
• Factors influencing aversion to specific electrodiagnostic studies  
  Jerath N.U., Strader SB, Reddy CG, Swenson A, Kimura J, Aul E, Brain and Behavior, 1/1/2014
• Hereditary motor and sensory neuropathies: Understanding molecular pathogenesis could lead to future treatment strategies  
  Jerath N.U., Shy ME, Biochimica Et Biophysica Acta, 1/1/2014
• Treating epilepsy in the setting of medical comorbidities  
  Jerath N.U., Lamichhane D, Jasti M, Yarlagadda V, Zilli E, Nazzal Y, et al, Current Treatment Options in Neurology, 1/1/2014
• Volumetric vs Lund-Mackay Computed Tomographic Staging for Assessment of Chronic Rhinosinusitis  
  Pallanch JF et al, International Forum of Allergy and Rhinology, 1/1/2013
• Neuroleukemiosis: an unusual cause of peripheral neuropathy  
  Reddy CG, Mauermann ML, Solomon BM, et al (Jerath NU), Leukemia & Lymphoma, 1/1/2012
• Gender differences in presenting signs and symptoms of acute ischemic stroke: a population-based study  
  Jerath N.U., Reddy CG, Freeman WD, Jerath AU, Brown RD, Gender Medicine, 1/1/2011
• The biography of Mary E O'Sullivan: an early American headache specialist  
  Jerath N.U., Newman JS, Boes CJ, Cephalalgia: an International Journal of Headache, 1/1/2009
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Books/Book Chapters

• Clinical Neurophysiology 
  Chapter: F wave, A wave, H reflex, and Blink reflex. 
  Jerath N.U. and Kimura J.Editors: Levin and Chauvel.Elsevier2019
• Video Vignettes for Atlas of Sleep Medicine. 
  Dyken M, Lin-Dyken D, Jerath N.ElsevierEdition 2nd,2014
• The Power of People-Skills. 
  Jerath N and Jerath A.Editors: Lulu.Edition 1st,2007
• Affirmations for Academic Success. 
  Jerath A and Jerath N.Editors: Lulu.Edition 1st,2006
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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
• A Unique Manifestation of a VCP mutation.
  Jerath N.U., Carrel-Krusen Neuromuscular Symposium; Unusual Neuromuscular Disease Conference, American Academy of Neurology, Philadelphia, PA, 2014; Dallas, TX, 2015, 1/1/2015
• An under recognized case of neuromyotonia and an axonal motor neuropathy in a 30 year old man: the first report of a HINT 1 mutation in the United States.
  Jerath N.U., Unusual Neuromuscular Disease Conference, American Academy of Neurology, Washington, DC, 1/1/2015
• Prolongation of F-wave minimal latency: A Sensitive Predictor of Polyneuropathy.
  Jerath N.U., American Academy of Neuromuscular and Electrodiagnostic Medicine, Savannah, GA, 1/1/2014
• A 6 year old girl with bilateral foot drop.
  Jerath N.U., Carrel-Krusen Neuromuscular Symposium, Dallas, TX, 1/1/2014
• Coexistence of a T118M PMP22 missense mutation and Hereditary Neuropathy with Liability to Pressure Palsy.
  Jerath N.U., Muscle Dystrophy Association, Chicago, IL, 1/1/2014
• Sudden Visual Spatial Memory Loss as presenting manifestations of CJD.
  Jerath N.U., American Neurological Association, Boston, MA, 1/1/2013
• Factors Influencing Aversion to Electromyography and Nerve Conduction Studies.
  Jerath N.U., American Academy of Neuromuscular and Electrodiagnostic Medicine, San Antonio, TX, 1/1/2013
• Inflammatory Cerebral Amyloid Angiopathy: As Unrecognized cause of reversible dementia.
  Jerath N.U., American Neurological Association, Boston, MA, 1/1/2013
• Subarachnoid Hemorrhage and Acute Hydrocephalus in a patient with familial TTR amyloidosis.
  Jerath N.U., American Neurological Association, Boston, MA, 1/1/2013
• Important Attributes of a Physician from a Patient�s Perspective.
  Jerath N.U., AAMC, Houston, TX, 1/1/2009
• The Effect of Statins on the Enlargement of Intracerebral Hemorrhage.
  Jerath N.U., International Stroke Conference, San Diego, CA, 1/1/2009
• Biography of Mary E. O�Sullivan.
  Jerath N.U., American Headache Society; American Academy of Neurology, Chicago, IL, 2008; Boston, MA, 2008, 1/1/2008
• Gender Differences in Presentation of Acute Ischemic Stroke.
  Jerath N.U., International Stroke Conference, New Orleans, LA, 1/1/2008
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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
• Diabetic Neuropathy. 
  University of Iowa - 1/1/2014
• Friedrich�s Ataxia. 
  University of Iowa - 1/1/2014
• Hereditary Spastic Paraparesis. 
  University of Iowa - 1/1/2014
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