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Publications by Gregory Hinkle
The V122I Mutation in Hereditary Transthyretin-Mediated Amyloidosis Is Significantly Associated With Polyneuropathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Transthyretin-Stabilizing Mutation T119M Is Not Associated With Protection Against Vascular Disease or Death in the UK Biobank
Related publications
Identifying Mixed Phenotype: Evaluating the Presence of Polyneuropathy in Patients With Hereditary Transthyretin-Mediated Amyloidosis With Cardiomyopathy
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
Cardiomyopathy Related to Transthyretin Val30met Mutation in Hereditary Systemic Amyloidosis
ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR
Alnylam Act®: Heterogenous Disease Manifestations of Hereditary Transthyretin-Mediated Amyloidosis
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Pharmacokinetics of Patisiran, the First Approved RNA Interference Therapy in Patients With Hereditary Transthyretin‐Mediated Amyloidosis
Journal of Clinical Pharmacology
Pharmacology
Impact of Patisiran, an RNAi Therapeutic, on Orthostatic Intolerance in Patients With Hereditary Transthyretin-Mediated Amyloidosis
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Quantitative Sensation and Autonomic Test Abnormalities in Transthyretin Amyloidosis Polyneuropathy
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)
Internal Medicine
Internal Medicine
Medicine
Tafamidis for Autonomic Neuropathy in Hereditary Transthyretin (ATTR) Amyloidosis: A Review
Clinical Autonomic Research
Medicine
Endocrine
Neurology
Autonomic Systems