Citations 39

Neurologic Clinical, Electrophysiologic, and Pathologic Characteristics of Primary vs Secondary Neurolymphomatosis

Neurology | September 3, 2024 | Volume: 103 | Issue: 6 | Pages: No page available

10.1212/wnl.0000000000209777 | PMID 39226481

Machine-learning Techniques Applied to F-wave Waveforms Can Predict the Likelihood and Survival of ALS Patients (P6-11.003)

Neurology | April 9, 2024 | Volume: 102 | Issue: 7_supplement_1 | Pages: No page available

10.1212/wnl.0000000000206208

Correlation of Electromyography Findings to Muscle Biopsy Findings in Patients with Suspected Myopathy (P3.445)

Neurology | December 7, 2023 | Volume: 90 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.90.15_supplement.p3.445

Educational Intervention Reduces Utilization of Low-Value Testing in Cerebrovascular Inpatients: An Example of Rapidly Implementable Quality Improvement (P2.309)

Neurology | December 7, 2023 | Volume: 86 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.86.16_supplement.p2.309

Neurolymphomatosis: Clinical, Radiographic, and Pathologic Characteristics (S45.005)

Neurology | December 7, 2023 | Volume: 88 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.88.16_supplement.s45.005

Ganglioside composite testing identifies immune responsive motor-onset MADSAM and MMN (P5.111)

Neurology | December 7, 2023 | Volume: 88 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.88.16_supplement.p5.111

An Atypical Presentation of Bortezomib-Induced Peripheral Neuropathy (1625)

Neurology | December 7, 2023 | Volume: 96 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.96.15_supplement.1625

Clinical and Electrophysiological Findings in C9orf72 ALS (P2-13.006)

Neurology | December 6, 2023 | Volume: 98 | Issue: 18_supplement | Pages: No page available

10.1212/wnl.98.18_supplement.3374

Femoral neuropathy: A clinical and electrodiagnostic review

Muscle & Nerve | November 9, 2023 | Volume: 69 | Issue: 1 | Pages: 64-71

10.1002/mus.27994 | PMID 37941415

AbstractIntroduction/AimsFemoral neuropathies can cause severe, prolonged debility, yet there have been few clinical and electrodiagnostic (EDx) studies addressing this condition. The aim of this study was to better understand the etiologies, EDx features, and clinical course of femoral neuropathy.MethodsWe identified patients evaluated at Mayo Clinic Rochester between January 1, 1999 and July 31, 2019, with possible new femoral neuropathy ascertained via International Classification of Diseases‐versions 9 and 10 diagnosis codes presenting within 6 months of symptom onset.ResultsA retrospective review of 1084 records was performed and we ultimately identified 159 patients with isolated femoral neuropathy for inclusion. The most common femoral neuropathy etiologies were compressive (40%), perioperative stretch (35%), and inflammatory (6%). Presenting symptoms included weakness (96%), sensory loss (73%), and pain (53%). Presenting motor physical exam findings demonstrated moderate weakness (34%) or no activation (25%) of knee extension and mild (32%) or moderate (35%) weakness of hip flexion. Seventy‐two percent of patients underwent EDx testing, including 22 with femoral motor nerve conduction studies. Treatment often involved physical therapy (89%) and was otherwise etiology‐specific. In patients with follow‐up data available (n = 154), 83% had subjective clinical improvement at follow‐up with a mean time to initial improvement of 3.3 months and mean time to recovery at final follow‐up of 14.8 months. Only 48% of patients had nearly complete or complete recovery.DiscussionIn our cohort, the most common etiologies of femoral neuropathy were compression or perioperative stretch with high initial morbidity. Although motor recovery is common, improvement is often prolonged and incomplete.
Education Research: Virtual Residency Interviews and the Second Look

Neurology Education | October 17, 2023 | Volume: 2 | Issue: 4 | Pages: No page available

10.1212/ne9.0000000000200095 | PMID 39359318