Neurology Rare Disease Resources
Chosen by Advanced
Practice Providers
  • Clinical guidelines
  • Patient support and education resources
  • Research updates
Hereditary ATTR amyloidosis is a genetic disorder caused by mutations in the transthyretin (TTR) gene, leading to the production of unstable TTR proteins that misfold and form amyloid...
CURATED BY: Tanya Geist,
RPA-C

New Guidelines for ATTRv Amyloidosis Stress Early Diagnosis and Treatment

Hereditary transthyretin (ATTRv) amyloidosis is a rare, fatal disease caused by mutations in the transthyretin (TTR) gene. The disease presents...
CURATED BY:
Jerrica Farias,
MN, ARNP, PMHNP-BC

Vutrisiran Shows Promising Results in Treating ATTRv Amyloidosis

Hereditary transthyretin (ATTRv) amyloidosis is a rare, inherited disease marked by rapid progression and severe, often fatal symptoms due to...
CURATED BY:
Jerrica Farias,
MN, ARNP, PMHNP-BC

New Staging System for Managing Primary Progressive Aphasias

Primary progressive aphasias (PPA) are neurodegenerative dementias marked by language impairments and are a significant cause of dementia in younger...
CURATED BY:
Kelly Papesh,
DNP, APRN, FNP-C

Physician Associate and Nurse Practitioner Contributors to the Neurology Rare Disease Center of Excellence

POCN’s Neurology Rare Disease Center of Excellence is curated by practicing clinical physician associates and nurse practitioners who review and select resources that are the most useful to their peers. They provide their expertise by hand-picking the latest content for advanced practice providers.

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