Citations 107

Peripheral Neuropathy in AL Amyloidosis: Clinical Presentations and Outcomes of Current Therapies (S21.008)

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

10.1212/wnl.0000000000205041

Long-term Outcomes in Seropositive Autoimmune Autonomic Ganglionopathy (S9.004)

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

10.1212/wnl.0000000000205398

Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States : Recommendations from a panel of experts

Muscle & Nerve | January 4, 2024 | Volume: 69 | Issue: 3 | Pages: 273-287

10.1002/mus.28026 | PMID 38174864

Abstract Hereditary transthyretin (ATTRv; v for variant) amyloidosis is a rare, multisystem, progressive, and fatal disease in which polyneuropathy is a cardinal manifestation. Due to a lack of United States (US)‐specific guidance on ATTRv amyloidosis with polyneuropathy, a panel of US‐based expert clinicians convened to address identification, monitoring, and treatment of this disease. ATTRv amyloidosis with polyneuropathy should be suspected in unexplained progressive neuropathy, especially if associated with systemic symptoms or family history. The diagnosis is confirmed through genetic testing, biopsy, or cardiac technetium‐based scintigraphy. Treatment should be initiated as soon as possible after diagnosis, with gene‐silencing therapeutics recommended as a first‐line option. Consensus is lacking on what represents “disease progression” during treatment; however, the aggressive natural history of this disease should be considered when evaluating the effectiveness of any therapy.
Clinicopathologic Findings in Patients With Paraneoplastic Neuropathies and Antibodies Strongly Associated With Cancer

Neurology | December 18, 2023 | Volume: 102 | Issue: 2 | Pages: No page available

10.1212/wnl.0000000000207982 | PMID 38165318

Muscle Biopsy and Electromyography Correlation (P3.442)

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

10.1212/wnl.90.15_supplement.p3.442

Peripheral Nerve Amyloidosis: Phenotype, Natural History, And Autonomic Dysfunction In Inherited Versus Acquired Subtypes (S36.008)

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.s36.008

Neuropathy Improvement Following Peripheral Blood Stem Cell Transplantation For POEMS Syndrome. (S16.007)

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.s16.007

Neuropathy Improvement Following Peripheral Blood Stem Cell Transplantation For POEMS Syndrome. (I6-2.002)

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.i6-2.002

Peripheral Nerve Amyloidosis: Phenotype, Natural History, And Autonomic Dysfunction In Inherited Versus Acquired Subtypes (I6-1.006)

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.i6-1.006

Myopathy: An Underrecognized Presentation of Transthyretin Amyloidosis (S42.005)

Neurology | December 7, 2023 | Volume: 92 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.92.15_supplement.s42.005