Neuromuscular Medicine - ABPN - Article-Based Continuing Certification (ABCC) Pathway - Regional at North Carolina Area Health Education Centers

Neuromuscular Medicine Articles & Topics Lists

ABPN Expiration Date is 12/31/2024 for all Neuromuscular Medicine Topic Articles

Complete Neuromuscular Medicine ABCC Article List
Some or all of these articles may be protected by copyright. Please refer to the publisher’s copyright notice and policies.
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Neuromuscular Medicine Topics List
Topic 1 - Motor Neuron Disorders
Topic 2 - Neuromuscular Junction Disorders
Topic 3 - Spine/Root (Radiculopathies/Polyradiculopathies, Disc Herniation)
Topic 4 - Acquired Myopathies
Topic 5 - Hereditary Myopathies
Topic 6 - Mononeuropathies / Plexopathies
Topic 7 - Polyneuropathies / Autonomic Disorders - Acquired
Topic 8 - Polyneuropathies / Autonomic Disorders - Hereditary
Topic 9 - Polyneuropathies / Autonomic Disorders - Autoimmune
Topic 10 - Professionalism, Ethics, System Based Practices, Counseling

Topic 1 - Motor Neuron Disorders

(PubMed Abstract Only) Acute Flaccid Myelitis Associated With Enterovirus D68: A Review
Christy, A., & Messacar, K. (2019). Acute Flaccid Myelitis Associated With Enterovirus D68: A Review. Journal of child neurology, 34(9), 511–516. https://doi.org/10.1177/0883073819838376
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Amyotrophic Lateral Sclerosis: A Clinical Review
Masrori, P., & Van Damme, P. (2020). Amyotrophic lateral sclerosis: a clinical review. European journal of neurology, 27(10), 1918–1929. https://doi.org/10.1111/ene.14393
Advances in Treatment of Spinal Muscular Atrophy - New Phenotypes, New Challenges, New Implications for Care
Schorling, D. C., Pechmann, A., & Kirschner, J. (2020). Advances in Treatment of Spinal Muscular Atrophy - New Phenotypes, New Challenges, New Implications for Care. Journal of neuromuscular diseases, 7(1), 1–13. https://doi.org/10.3233/JND-190424
Prospective Natural History Study of C9orf72 ALS Clinical Characteristics and Biomarkers
Cammack, A. J., Atassi, N., Hyman, T., van den Berg, L. H., Harms, M., Baloh, R. H., Brown, R. H., van Es, M. A., Veldink, J. H., de Vries, B. S., Rothstein, J. D., Drain, C., Jockel-Balsarotti, J., Malcolm, A., Boodram, S., Salter, A., Wightman, N., Yu, H., Sherman, A. V., Esparza, T. J., … Miller, T. M. (2019). Prospective natural history study of C9orf72 ALS clinical characteristics and biomarkers. Neurology, 93(17), e1605–e1617. https://doi.org/10.1212/WNL.0000000000008359
Amyotrophic Lateral Sclerosis and Other Motor Neuron Diseases
Quinn, C., & Elman, L. (2020). Amyotrophic Lateral Sclerosis and Other Motor Neuron Diseases. Continuum (Minneapolis, Minn.), 26(5), 1323–1347. https://doi.org/10.1212/CON.0000000000000911
Promise of Nucleic Acid Therapeutics for Amyotrophic Lateral Sclerosis
Ito D. (2022). Promise of Nucleic Acid Therapeutics for Amyotrophic Lateral Sclerosis. Annals of neurology, 91(1), 13–20. https://doi.org/10.1002/ana.26259

Topic 2 - Neuromuscular Junction Disorders

(PubMed Abstract Only) Immunosuppressive and Immunomodulatory Therapies for Neuromuscular Diseases. Part II: New and Novel Agents
Farmakidis, C., Dimachkie, M. M., Pasnoor, M., & Barohn, R. J. (2020). Immunosuppressive and immunomodulatory therapies for neuromuscular diseases. Part II: New and novel agents. Muscle & nerve, 61(1), 17–25. https://doi.org/10.1002/mus.26711
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Long-Term Effect of Thymectomy Plus Prednisone Versus Prednisone Alone in Patients With Non-Thymomatous Myasthenia Gravis: 2-Year Extension of the MGTX Randomised Trial
Wolfe, G. I., Kaminski, H. J., Aban, I. B., Minisman, G., Kuo, H. C., Marx, A., Ströbel, P., Mazia, C., Oger, J., Cea, J. G., Heckmann, J. M., Evoli, A., Nix, W., Ciafaloni, E., Antonini, G., Witoonpanich, R., King, J. O., Beydoun, S. R., Chalk, C. H., Barboi, A. C., … MGTX Study Group (2019). Long-term effect of thymectomy plus prednisone versus prednisone alone in patients with non-thymomatous myasthenia gravis: 2-year extension of the MGTX randomised trial. The Lancet. Neurology, 18(3), 259–268. https://doi.org/10.1016/S1474-4422(18)30392-2
Long-Term Follow-Up, Quality of Life, and Survival of Patients With Lambert-Eaton Myasthenic Syndrome
Lipka, A. F., Boldingh, M. I., van Zwet, E. W., Schreurs, M. W. J., Kuks, J. B. M., Tallaksen, C. M., Titulaer, M. J., & Verschuuren, J. J. G. M. (2020). Long-term follow-up, quality of life, and survival of patients with Lambert-Eaton myasthenic syndrome. Neurology, 94(5), e511–e520. https://doi.org/10.1212/WNL.0000000000008747
Congenital Myasthenic Syndromes in Adult Neurology Clinic: A Long Road to Diagnosis and Therapy
Kao, J. C., Milone, M., Selcen, D., Shen, X. M., Engel, A. G., & Liewluck, T. (2018). Congenital myasthenic syndromes in adult neurology clinic: A long road to diagnosis and therapy. Neurology, 91(19), e1770–e1777. https://doi.org/10.1212/WNL.0000000000006478
Drugs That Induce or Cause Deterioration of Myasthenia Gravis: An Update
Sheikh, S., Alvi, U., Soliven, B., & Rezania, K. (2021). Drugs That Induce or Cause Deterioration of Myasthenia Gravis: An Update. Journal of clinical medicine, 10(7), 1537. https://doi.org/10.3390/jcm10071537
(PubMed Abstract Only) Safety, Efficacy, and Tolerability of Efgartigimod in Patients With Generalised Myasthenia Gravis (ADAPT): A Multicentre, Randomised, Placebo-Controlled, Phase 3 Trial
Howard, J. F., Jr, Bril, V., Vu, T., Karam, C., Peric, S., Margania, T., Murai, H., Bilinska, M., Shakarishvili, R., Smilowski, M., Guglietta, A., Ulrichts, P., Vangeneugden, T., Utsugisawa, K., Verschuuren, J., Mantegazza, R., & ADAPT Investigator Study Group (2021). Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial. The Lancet. Neurology, 20(7), 526–536. https://doi.org/10.1016/S1474-4422(21)00159-9
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Topic 3 - Spine/Root (Radiculopathies/Polyradiculopathies, Disc Herniation)

Epidural Steroid Injection Versus Conservative Treatment for Patients With Lumbosacral Radicular Pain: A Meta-Analysis of Randomized Controlled Trials
Yang, S., Kim, W., Kong, H. H., Do, K. H., & Choi, K. H. (2020). Epidural steroid injection versus conservative treatment for patients with lumbosacral radicular pain: A meta-analysis of randomized controlled trials. Medicine, 99(30), e21283. https://doi.org/10.1097/MD.0000000000021283
Perioperative Neurologic Complications in Adult Spinal Deformity Surgery: Incidence and Risk Factors in 564 Patients
Kim, H. J., Iyer, S., Zebala, L. P., Kelly, M. P., Sciubba, D., Protopsaltis, T. S., Gupta, M., Neuman, B. J., Mundis, G. M., Ames, C. P., Smith, J. S., Hart, R., Burton, D., Klineberg, E. O., & International Spine Study Group (ISSG) (2017). Perioperative Neurologic Complications in Adult Spinal Deformity Surgery: Incidence and Risk Factors in 564 Patients. Spine, 42(6), 420–427. https://doi.org/10.1097/BRS.0000000000001774
(PubMed Abstract Only) Cervical Epidural Steroid Injection: Techniques and Evidence
House, L. M., Barrette, K., Mattie, R., & McCormick, Z. L. (2018). Cervical Epidural Steroid Injection: Techniques and Evidence. Physical medicine and rehabilitation clinics of North America, 29(1), 1–17. https://doi.org/10.1016/j.pmr.2017.08.001
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Disorders of the Cauda Equina
Goodman B. P. (2018). Disorders of the Cauda Equina. Continuum (Minneapolis, Minn.), 24(2, Spinal Cord Disorders), 584–602. https://doi.org/10.1212/CON.0000000000000584
Far Lateral Lumbar Disc Herniation Part 1: Imaging, Neurophysiology and Clinical Features
Berra, L. V., Di Rita, A., Longhitano, F., Mailland, E., Reganati, P., Frati, A., & Santoro, A. (2021). Far lateral lumbar disc herniation part 1: Imaging, neurophysiology and clinical features. World journal of orthopedics, 12(12), 961–969. https://doi.org/10.5312/wjo.v12.i12.961
(PubMed Abstract Only) A Narrative Review and Future Considerations of Spinal Cord Stimulation, Dorsal Root Ganglion Stimulation and Peripheral Nerve Stimulation
Malinowski, M. N., Chopra, P. R., Tieppo Francio, V., Budwany, R., & Deer, T. R. (2021). A narrative review and future considerations of spinal cord stimulation, dorsal root ganglion stimulation and peripheral nerve stimulation. Current opinion in anaesthesiology, 34(6), 774–780. https://doi.org/10.1097/ACO.0000000000001072
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Can purchase article via Current Opinion in Anesthesiology: https://journals.lww.com/co-anesthesiology/Abstract/2021/12000/A_narrative_review_and_future_considerations_of.19.aspx

Topic 4 - Acquired Myopathies

Toxic Myopathies
Doughty, C. T., & Amato, A. A. (2019). Toxic Myopathies. Continuum (Minneapolis, Minn.), 25(6), 1712–1731. https://doi.org/10.1212/CON.0000000000000806
(PubMed Abstract Only) Classification and Management of Adult Inflammatory Myopathies
Selva-O'Callaghan, A., Pinal-Fernandez, I., Trallero-Araguás, E., Milisenda, J. C., Grau-Junyent, J. M., & Mammen, A. L. (2018). Classification and management of adult inflammatory myopathies. The Lancet. Neurology, 17(9), 816–828. https://doi.org/10.1016/S1474-4422(18)30254-0
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Can purchase article via The Lancet Neurology: https://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30254-0/fulltext
Anti-HMGCR Myopathy
Mohassel, P., & Mammen, A. L. (2018). Anti-HMGCR Myopathy. Journal of neuromuscular diseases, 5(1), 11–20. https://doi.org/10.3233/JND-170282
Secondary Myopathy Due to Systemic Diseases
Finsterer, J., Löscher, W. N., Wanschitz, J., Quasthoff, S., & Grisold, W. (2016). Secondary myopathy due to systemic diseases. Acta neurologica Scandinavica, 134(6), 388–402. https://doi.org/10.1111/ane.12576
(PubMed Abstract Only) Immune-Mediated Neuromuscular Complications of Graft-Versus-Host Disease
Saw, J. L., Sidiqi, M. H., Mauermann, M. L., Alkhateeb, H., & Naddaf, E. (2021). Immune-mediated neuromuscular complications of graft-versus-host disease. Muscle & nerve, 63(6), 852–860. https://doi.org/10.1002/mus.27214
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Epidemiology and Natural History of Inclusion Body Myositis: A 40-Year Population-Based Study
Shelly, S., Mielke, M. M., Mandrekar, J., Milone, M., Ernste, F. C., Naddaf, E., & Liewluck, T. (2021). Epidemiology and Natural History of Inclusion Body Myositis: A 40-Year Population-Based Study. Neurology, 96(21), e2653–e2661. https://doi.org/10.1212/WNL.0000000000012004

Topic 5 - Hereditary Myopathies

Skeletal Muscle Channelopathies
Phillips, L., & Trivedi, J. R. (2018). Skeletal Muscle Channelopathies. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 15(4), 954–965. https://doi.org/10.1007/s13311-018-00678-0
Diagnosis and Treatment of Mitochondrial Myopathies
Ahmed, S. T., Craven, L., Russell, O. M., Turnbull, D. M., & Vincent, A. E. (2018). Diagnosis and Treatment of Mitochondrial Myopathies. Neurotherapeutics: the journal of the American Society for Experimental NeuroTherapeutics, 15(4), 943–953. https://doi.org/10.1007/s13311-018-00674-4
Pompe Disease: From Basic Science to Therapy
Kohler, L., Puertollano, R., & Raben, N. (2018). Pompe Disease: From Basic Science to Therapy. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 15(4), 928–942. https://doi.org/10.1007/s13311-018-0655-y
Diagnosis and Management of Duchenne Muscular Dystrophy, Part 1: Diagnosis, and Neuromuscular, Rehabilitation, Endocrine, and Gastrointestinal and Nutritional Management
Birnkrant, D. J., Bushby, K., Bann, C. M., Apkon, S. D., Blackwell, A., Brumbaugh, D., Case, L. E., Clemens, P. R., Hadjiyannakis, S., Pandya, S., Street, N., Tomezsko, J., Wagner, K. R., Ward, L. M., Weber, D. R., & DMD Care Considerations Working Group (2018). Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. The Lancet. Neurology, 17(3), 251–267. https://doi.org/10.1016/S1474-4422(18)30024-3
(PubMed Abstract Only) Metabolic Myopathies: A Practical Approach
Lilleker, J. B., Keh, Y. S., Roncaroli, F., Sharma, R., & Roberts, M. (2018). Metabolic myopathies: a practical approach. Practical neurology, 18(1), 14–26. https://doi.org/10.1136/practneurol-2017-001708
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Panorama of the Distal Myopathies
Savarese, M., Sarparanta, J., Vihola, A., Jonson, P. H., Johari, M., Rusanen, S., Hackman, P., & Udd, B. (2020). Panorama of the distal myopathies. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 39(4), 245–265. https://doi.org/10.36185/2532-1900-028

Topic 6 - Mononeuropathies / Plexopathies

Recent Advances in Ultrasound Diagnosis of Carpal Tunnel Syndrome
Yoshii, Y., Zhao, C., & Amadio, P. C. (2020). Recent Advances in Ultrasound Diagnosis of Carpal Tunnel Syndrome. Diagnostics (Basel, Switzerland), 10(8), 596. https://doi.org/10.3390/diagnostics10080596
Modern Treatment of Perineuriomas: A Case-Series and Systematic Review
Uerschels, A. K., Krogias, C., Junker, A., Sure, U., Wrede, K. H., & Gembruch, O. (2020). Modern treatment of perineuriomas: a case-series and systematic review. BMC neurology, 20(1), 55. https://doi.org/10.1186/s12883-020-01637-z
Cubital Tunnel Syndrome: Current Concepts
Nakashian, M. N., Ireland, D., & Kane, P. M. (2020). Cubital Tunnel Syndrome: Current Concepts. Current reviews in musculoskeletal medicine, 13(4), 520–524. https://doi.org/10.1007/s12178-020-09650-y
Long-Term Outcome of Brachial Plexus Reimplantation After Complete Brachial Plexus Avulsion Injury
Kachramanoglou, C., Carlstedt, T., Koltzenburg, M., & Choi, D. (2017). Long-Term Outcome of Brachial Plexus Reimplantation After Complete Brachial Plexus Avulsion Injury. World neurosurgery, 103, 28–36. https://doi.org/10.1016/j.wneu.2017.03.052
(PubMed Abstract Only) Role of Electrodiagnosis in Nerve Transfers for Focal Neuropathies and Brachial Plexopathies
Robinson, L. R., & Binhammer, P. (2022). Role of electrodiagnosis in nerve transfers for focal neuropathies and brachial plexopathies. Muscle & nerve, 65(2), 137–146. https://doi.org/10.1002/mus.27376
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Variability in Electrodiagnostic Findings Associated With Neurogenic Thoracic Outlet Syndrome
Mul, K., Pesser, N., Vervaart, K., Teijink, J., van Nuenen, B., & van Alfen, N. (2022). Variability in electrodiagnostic findings associated with neurogenic thoracic outlet syndrome. Muscle & nerve, 65(1), 34–42. https://doi.org/10.1002/mus.27395

Topic 7 - Polyneuropathies / Autonomic Disorders - Acquired

Diabetic Neuropathy
Feldman, E. L., Callaghan, B. C., Pop-Busui, R., Zochodne, D. W., Wright, D. E., Bennett, D. L., Bril, V., Russell, J. W., & Viswanathan, V. (2019). Diabetic neuropathy. Nature reviews. Disease primers, 5(1), 41. https://doi.org/10.1038/s41572-019-0092-1
Chemotherapy-Induced Peripheral Neuropathy: A Current Review
Staff, N. P., Grisold, A., Grisold, W., & Windebank, A. J. (2017). Chemotherapy-induced peripheral neuropathy: A current review. Annals of neurology, 81(6), 772–781. https://doi.org/10.1002/ana.24951
Longitudinal Assessment of Small Fiber Neuropathy: Evidence of a Non-Length-Dependent Distal Axonopathy
Khoshnoodi, M. A., Truelove, S., Burakgazi, A., Hoke, A., Mammen, A. L., & Polydefkis, M. (2016). Longitudinal Assessment of Small Fiber Neuropathy: Evidence of a Non-Length-Dependent Distal Axonopathy. JAMA neurology, 73(6), 684–690. https://doi.org/10.1001/jamaneurol.2016.0057
Autoimmune Autonomic Neuropathies and Ganglionopathies: Epidemiology, Pathophysiology, and Therapeutic Advances
Golden, E. P., & Vernino, S. (2019). Autoimmune autonomic neuropathies and ganglionopathies: epidemiology, pathophysiology, and therapeutic advances. Clinical autonomic research : official journal of the Clinical Autonomic Research Society, 29(3), 277–288. https://doi.org/10.1007/s10286-019-00611-1
Management of Neuropathic Pain in Polyneuropathy
Peltier, A. C., & Wood, D. (2020). Management of Neuropathic Pain in Polyneuropathy. Continuum (Minneapolis, Minn.), 26(5), 1299–1322. https://doi.org/10.1212/CON.0000000000000928
(ADL Article) Diagnosis and Management of Sensory Polyneuropathy
Gwathmey, K. G., & Pearson, K. T. (2019). Diagnosis and management of sensory polyneuropathy. BMJ (Clinical research ed.), 365, l1108. https://doi.org/10.1136/bmj.l1108

Topic 8 - Polyneuropathies / Autonomic Disorders - Hereditary

Underestimated Associated Features in CMT Neuropathies: Clinical Indicators for the Causative Gene?
Werheid, F., Azzedine, H., Zwerenz, E., Bozkurt, A., Moeller, M. J., Lin, L., Mull, M., Häusler, M., Schulz, J. B., Weis, J., & Claeys, K. G. (2016). Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?. Brain and behavior, 6(4), e00451. https://doi.org/10.1002/brb3.451
(PubMed Abstract Only) Next-Generation Sequencing in Charcot-Marie-Tooth Disease: Opportunities and Challenges
Pipis, M., Rossor, A. M., Laura, M., & Reilly, M. M. (2019). Next-generation sequencing in Charcot-Marie-Tooth disease: opportunities and challenges. Nature reviews. Neurology, 15(11), 644–656. https://doi.org/10.1038/s41582-019-0254-5
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Can purchase article via Nature Reviews Neurology: https://www.nature.com/articles/s41582-019-0254-5
Orthostatic Hypotension in Hereditary Transthyretin Amyloidosis: Epidemiology, Diagnosis and Management
Palma, J. A., Gonzalez-Duarte, A., & Kaufmann, H. (2019). Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management. Clinical autonomic research : official journal of the Clinical Autonomic Research Society, 29(Suppl 1), 33–44. https://doi.org/10.1007/s10286-019-00623-x
Expert Consensus Recommendations to Improve Diagnosis of ATTR Amyloidosis With Polyneuropathy
Adams, D., Ando, Y., Beirão, J. M., Coelho, T., Gertz, M. A., Gillmore, J. D., Hawkins, P. N., Lousada, I., Suhr, O. B., & Merlini, G. (2021). Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy. Journal of neurology, 268(6), 2109–2122. https://doi.org/10.1007/s00415-019-09688-0
(PubMed Abstract Only) A Consensus Statement on the Surgical Treatment of Charcot-Marie-Tooth Disease
Pfeffer, G. B., Gonzalez, T., Brodsky, J., Campbell, J., Coetzee, C., Conti, S., Guyton, G., Herrmann, D. N., Hunt, K., Johnson, J., McGarvey, W., Pinzur, M., Raikin, S., Sangeorzan, B., Younger, A., Michalski, M., An, T., & Noori, N. (2020). A Consensus Statement on the Surgical Treatment of Charcot-Marie-Tooth Disease. Foot & ankle international, 41(7), 870–880. https://doi.org/10.1177/1071100720922220
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(PubMed Abstract Only) Charcot-Marie-Tooth Disease Misdiagnosed as Chronic Inflammatory Demyelinating Polyradiculoneuropathy: An International Multicentric Retrospective Study
Hauw, F., Fargeot, G., Adams, D., Attarian, S., Cauquil, C., Chanson, J. B., Créange, A., Gendre, T., Deiva, K., Delmont, E., Francou, B., Genestet, S., Kuntzer, T., Latour, P., Le Masson, G., Magy, L., Nardin, C., Ochsner, F., Sole, G., Stojkovic, T., … Echaniz-Laguna, A. (2021). Charcot-Marie-Tooth disease misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: An international multicentric retrospective study. European journal of neurology, 28(9), 2846–2854. https://doi.org/10.1111/ene.14950
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Topic 9 - Polyneuropathies / Autonomic Disorders - Autoimmune

(PubMed Abstract Only) Immunosuppressive and Immunomodulatory Therapies for Neuromuscular Diseases. Part I: Traditional Agents
Farmakidis, C., Dimachkie, M. M., Pasnoor, M., & Barohn, R. J. (2020). Immunosuppressive and immunomodulatory therapies for neuromuscular diseases. Part I: Traditional agents. Muscle & nerve, 61(1), 5–16. https://doi.org/10.1002/mus.26708
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Can purchase article via Muscle & Nerve: https://onlinelibrary.wiley.com/doi/abs/10.1002/mus.26708
(ADL Article) Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome: A Longitudinal Cohort Study
Keddie, S., Foldes, D., Caimari, F., Baldeweg, S. E., Bomsztyk, J., Ziff, O. J., Fehmi, J., Cerner, A., Jaunmuktane, Z., Brandner, S., Yong, K., Manji, H., Carr, A., Rinaldi, S., Reilly, M. M., D'Sa, S., & Lunn, M. P. (2020). Clinical characteristics, risk factors, and outcomes of POEMS syndrome: A longitudinal cohort study. Neurology, 95(3), e268–e279. https://doi.org/10.1212/WNL.0000000000009940
(PubMed Abstract Only) Clinical Spectrum of Neuromuscular Complications After Immune Checkpoint Inhibition
Puwanant, A., Isfort, M., Lacomis, D., & Živković, S. A. (2019). Clinical spectrum of neuromuscular complications after immune checkpoint inhibition. Neuromuscular disorders : NMD, 29(2), 127–133. https://doi.org/10.1016/j.nmd.2018.11.012
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Can purchase article via Neuromuscular Disorders: https://www.nmd-journal.com/article/S0960-8966(18)30487-5/fulltext
Placebo Effect in Chronic Inflammatory Demyelinating Polyneuropathy: The PATH Study and a Systematic Review
Lewis, R. A., Cornblath, D. R., Hartung, H. P., Sobue, G., Lawo, J. P., Mielke, O., Durn, B. L., Bril, V., Merkies, I. S. J., Bassett, P., Cleasby, A., van Schaik, I. N., & PATH study group (2020). Placebo effect in chronic inflammatory demyelinating polyneuropathy: The PATH study and a systematic review. Journal of the peripheral nervous system : JPNS, 25(3), 230–237. https://doi.org/10.1111/jns.12402
Antibodies to Neurofascin, Contactin-1, and Contactin-Associated Protein 1 in CIDP: Clinical Relevance of IgG Isotype
Cortese, A., Lombardi, R., Briani, C., Callegari, I., Benedetti, L., Manganelli, F., Luigetti, M., Ferrari, S., Clerici, A. M., Marfia, G. A., Rigamonti, A., Carpo, M., Fazio, R., Corbo, M., Mazzeo, A., Giannini, F., Cosentino, G., Zardini, E., Currò, R., Gastaldi, M., … Franciotta, D. (2019). Antibodies to neurofascin, contactin-1, and contactin-associated protein 1 in CIDP: Clinical relevance of IgG isotype. Neurology(R) neuroimmunology & neuroinflammation, 7(1), e639. https://doi.org/10.1212/NXI.0000000000000639
Peripheral Neuropathies Associated With Monoclonal Gammopathies
Naddaf, E., & Mauermann, M. L. (2020). Peripheral Neuropathies Associated With Monoclonal Gammopathies. Continuum (Minneapolis, Minn.), 26(5), 1369–1383. https://doi.org/10.1212/CON.0000000000000919

Topic 10 - Professionalism, Ethics, System Based Practices, Counseling

(ADL Article) Invited Article: Professionalism in Neurology: The Role of Law
Larriviere, D., & Beresford, H. R. (2008). Invited article: professionalism in neurology: the role of law. Neurology, 71(16), 1283–1288. https://doi.org/10.1212/01.wnl.0000327605.40374.49
Estimating and Communicating Prognosis in Advanced Neurologic Disease
Holloway, R. G., Gramling, R., & Kelly, A. G. (2013). Estimating and communicating prognosis in advanced neurologic disease. Neurology, 80(8), 764–772. https://doi.org/10.1212/WNL.0b013e318282509c
Continuous Quality Improvement in Neuromuscular and Electrodiagnostic Practice
American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM). Last reviewed 2019.
(PubMed Abstract Only) Delays in Diagnosis of Duchenne Muscular Dystrophy: An Evaluation of Genotypic and Sociodemographic Factors
Counterman, K. J., Furlong, P., Wang, R. T., & Martin, A. S. (2020). Delays in diagnosis of Duchenne muscular dystrophy: An evaluation of genotypic and sociodemographic factors. Muscle & nerve, 61(1), 36–43. https://doi.org/10.1002/mus.26720
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Can purchase article via Muscle & Nerve: https://onlinelibrary.wiley.com/doi/epdf/10.1002/mus.26720
(PubMed Abstract Only) Interprofessional Care for Neuromuscular Disease
Howard, I., & Potts, A. (2019). Interprofessional Care for Neuromuscular Disease. Current treatment options in neurology, 21(8), 35. https://doi.org/10.1007/s11940-019-0576-z
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Can purchase article via Current Treatment Options in Neurology: https://link.springer.com/article/10.1007/s11940-019-0576-z
Doctor-Should I Get the COVID-19 Vaccine? Infection and Immunization in Individuals With Neuromuscular Disorders
Živković, S. A., Gruener, G., Narayanaswami, P., & AANEM Quality and Patient Safety Committee (2021). Doctor-Should I get the COVID-19 vaccine? Infection and immunization in individuals with neuromuscular disorders. Muscle & nerve, 63(3), 294–303. https://doi.org/10.1002/mus.27179