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Kumar, Neeraj

https://orcid.org/0000-0003-4222-2851

Mayo Clinic

Mayo Clinic

Citations 7

The Origin of Woltman's Sign of Myxedema (P05.256)
Klaas, James P. , Kumar, Neeraj , Burkholder, David B. , Boes, Christopher J.

Neurology | December 7, 2023 | Volume: 80 | Issue: 7_supplement | Pages: No page available

10.1212/wnl.80.7_supplement.p05.256 Get It

Longitudinal clinical, neuropsychological, and neuroimaging characterization of a kindred with a 12-octapeptide repeat insertion in PRNP: the next generation
Townley, Ryan , Polsinelli, Angelina J. , Fields, Julie A. , Graff‐Radford, Jonathan , Kantarci, Kejal , Lowe, Val J. , Rademakers, Rosa , Baker, Matt , Kumar, Neeraj , Townley, Ryan A , Kantarci, Kejal M, Rademakers, Rosa V, Baker, Matt C, Kantarci, Kejal , Machulda, Mary M. , Jones, David T. , Boeve, Bradley F.

Neurocase | June 30, 2020 | Volume: 26 | Issue: 4 | Pages: 211-219

10.1080/13554794.2020.1787458 Get It

Neuroimaging and clinical features in type II (late-onset) Alexander disease
Graff‐Radford, Jonathan , Schwartz, Kara M., Gavrilova, Ralitza H. , Kumar, Neeraj , Lachance, Daniel Honore

Neurology | December 5, 2013 | Volume: 82 | Issue: 1 | Pages: 49-56

10.1212/01.wnl.0000438230.33223.bc Get It

P3–093: FDG‐PET and PiB‐PET imaging in asymptomatic at‐risk carriers of a novel octapeptide repeat insertion in PRNP
Lowe, Val J. , Przybelski, Scott A. , Weigand, Stephen D. , Spychalla, Anthony J., Jones, David, Kumar, Neeraj , Rademakers, Rosa , Petersen, Ronald, Parisi, Joseph, Boeve, Bradley F. , Kantarci, Kejal , Vemuri, Prashanthi , Jones, David, McDade, Eric , Baker, Matthew , Knopman, David S. , Petersen, Ronald, Dickson, Dennis W. , Jack, Clifford R.

Alzheimer's & Dementia | October 9, 2013 | Volume: 9 | Issue: 4S_Part_14 | Pages: No page available

10.1016/j.jalz.2013.05.1163 Get It

Adult-onset autosomal dominant leukodystrophy presenting with REM sleep behavior disorder
Flanagan, Eoin P. , Gavrilova, Ralitza H. , Kumar, Neeraj , Jelsing, Elena J., Silber, Michael H. , Boeve, Bradley F. , Flanagan, E P

Neurology | December 14, 2012 | Volume: 80 | Issue: 1 | Pages: 118-120

10.1212/wnl.0b013e31827b1b2a Get It

Neurotoxicology
Tormoehlen, Laura M. , Kumar, Neeraj

Neurology Clinical Practice | December 10, 2012 | Volume: 2 | Issue: 4 | Pages: 301-310

10.1212/cpj.0b013e318278be1e Get It

Ventral “Spinal Epidural Meningeal Cysts”—Not Epidural and Not Cysts? Case Series and Review of the Literature
Ball, Bret Gene, Mokri, Bahram, Kumar, Neeraj , Piepgras, David G., Luetmer, Patrick H. , Giannini, Caterina

Neurosurgery | August 5, 2011 | Volume: 70 | Issue: 2 | Pages: 320-328

10.1227/neu.0b013e318230968c Get It

Abstract BACKGROUND: Ventral spinal epidural meningeal cysts are rare entities for which the pathogenesis is poorly understood. OBJECTIVE: We present the clinical, radiographic, surgical, and pathologic findings of 4 patients with extensive ventral spinal epidural meningeal cysts and review the relevant literature. In addition, we discuss a suspected mechanism for pathogenesis. METHODS: Four patients with anterior spinal epidural meningeal cysts are retrospectively reviewed. RESULTS: Ventral spinal epidural meningeal cysts are often large, extending on average from C2 to L1 in our series. Patients typically present with a prolonged course of symptoms and signs, including segmental muscle weakness and atrophy, subtle myelopathy, mild to moderate spinal pain, and headache. Histopathologic analysis of the cyst wall demonstrates collagenous tissue consistent with dura but without arachnoid features. Dynamic computed tomographic myelography is the study of choice for localization of the primary dural defect. Patient symptoms and neurological deficits routinely improve after appropriate surgical intervention. CONCLUSION: Diverse signs and symptoms herald the presentation of ventral spinal meningoceles. Intraoperative, radiographic, and pathological findings are all suggestive of an intradural dissection as the etiology. Hence, they may be more appropriately named “ventral spinal intradural dissecting meningoceles.” Definitive treatment involves identification and obliteration of the dural defect.