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Publications by Anastasia McManus
Identifying Mixed Phenotype: Evaluating the Presence of Polyneuropathy in Patients With Hereditary Transthyretin-Mediated Amyloidosis With Cardiomyopathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Related publications
The V122I Mutation in Hereditary Transthyretin-Mediated Amyloidosis Is Significantly Associated With Polyneuropathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Diagnostic Challenges in Hereditary Transthyretin Amyloidosis With Polyneuropathy: Avoiding Misdiagnosis of a Treatable Hereditary Neuropathy
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)
Internal Medicine
Internal Medicine
Medicine
Pharmacokinetics of Patisiran, the First Approved RNA Interference Therapy in Patients With Hereditary Transthyretin‐Mediated Amyloidosis
Journal of Clinical Pharmacology
Pharmacology
Cardiomyopathy Related to Transthyretin Val30met Mutation in Hereditary Systemic Amyloidosis
ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR
Impact of Patisiran, an RNAi Therapeutic, on Orthostatic Intolerance in Patients With Hereditary Transthyretin-Mediated Amyloidosis
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Assessment of Patients With Hereditary Transthyretin Amyloidosis – Understanding the Impact of Management and Disease Progression
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Internal Medicine
Medicine
Alnylam Act®: Heterogenous Disease Manifestations of Hereditary Transthyretin-Mediated Amyloidosis
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Risk Factors for Mortality in Patients With Hereditary Transthyretin-Mediated Amyloidosis: An Analysis of APOLLO and Global Open Label Extension Studies
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology