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Laughlin, Ruple S

0000-0002-1884-5824

Mayo Clinic

Mayo Clinic

Citations 5

Severe Parsonage-Turner Syndrome and Surgically Managed Traumatic Brachial Plexopathy

Neurology | August 28, 2026 | Volume: 107 | Issue: 6 | Pages: No page available

10.1212/wnl.0000000000218501 | PMID 42664489

Prospective Evaluation of Machine‐Assisted Electrophysiologic and Online Clinical Diagnostic Support Tools in Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Journal of the Peripheral Nervous System | December 19, 2025 | Volume: 30 | Issue: 4 | Pages: No page available

10.1111/jns.70084 | PMID 41414759

ABSTRACT Background and Aims Chronic inflammatory demyelinating polyradiculoneuropathy ( CIDP ) is a common, treatable, autoimmune, neuropathy frequently misdiagnosed. The complex electrodiagnostic ( EDX ) criteria required for diagnosis are challenging to apply in routine practice. This study evaluates the effectiveness of a machine‐assisted EDX tool in real‐time identification of demyelinating nerve conduction studies ( NCS ) stipulated by 2021‐ EAN / PNS CIDP criteria in conjunction with an online CIDP clinical probability calculator. Methods We prospectively evaluated 100 consecutive patients with referral or EDX diagnosis of polyradiculoneuropathy beginning January 1, 2024. Fifty patients were included, each from Jacksonville and Rochester Mayo Clinics. Routine electromyography ( EMG ) reports were compared to a machine‐assisted support tool applying 2021‐ EAN / PNS CIDP EDX criteria to NCS assessing demyelination. The EDX ‐assistant performance was compared to the final clinical diagnosis and our previously reported online CIDP clinical prediction tool ( https://news.mayocliniclabs.com/cidp‐calculator/ ). Results Among 100 patients (60% male; median age 64), 30 had a final clinical CIDP diagnosis with 29 having intravenous immunoglobulin follow‐up; 27 (93%) improved and 2 (7%) stabilized. Routine EMGs reported demyelination in 14 of 30 (47%), with 46% sensitivity and 79% specificity. The EDX ‐assistant identified CIDP demyelination in 28 of 30 (93%), with 93% sensitivity and 57% specificity. The clinical calculator detected CIDP in 30 of 30 (100%) with 86% specificity, increasing to 94% after excluding false positives lacking demyelinating features on the EDX tool. Interpretation A real‐time machine‐assisted EDX support tool, used with a clinical web‐based calculator, streamlines CIDP assessment by improving standardized identification of 2021‐EAN/PNS CIDP demyelinating NCS criteria and aiding clinical decisions.
Electrodiagnostic Characteristics Suggestive of Muscle-Specific Kinase Myasthenia Gravis

Neurology Clinical Practice | March 16, 2022 | Volume: 12 | Issue: 3 | Pages: 211-217

10.1212/cpj.0000000000001166 | PMID 35747537

Neurofascin-155 Immunoglobulin Subtypes

Neurology | October 11, 2021 | Volume: 97 | Issue: 24 | Pages: No page available

10.1212/wnl.0000000000012932 | PMID 34635556

Improving accuracy of myasthenia gravis autoantibody testing by reflex algorithm

Neurology | September 17, 2020 | Volume: 95 | Issue: 22 | Pages: No page available

10.1212/wnl.0000000000010910 | PMID 32938782