Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Rebecca Truty

Alnylam Act®: Heterogenous Disease Manifestations of Hereditary Transthyretin-Mediated Amyloidosis

Journal of Cardiac Failure
Cardiovascular MedicineCardiology
2019English

Possible Precision Medicine Implications From Genetic Testing Using Combined Detection of Sequence and Intragenic Copy Number Variants in a Large Cohort With Childhood Epilepsy

Epilepsia Open
Neurology
2019English

Related publications

THAOS: Gastrointestinal Manifestations of Transthyretin Amyloidosis - Common Complications of a Rare Disease

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2014English

The V122I Mutation in Hereditary Transthyretin-Mediated Amyloidosis Is Significantly Associated With Polyneuropathy

Journal of Cardiac Failure
Cardiovascular MedicineCardiology
2019English

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 MedicineMedicine
2019English

Impact of Patisiran, an RNAi Therapeutic, on Orthostatic Intolerance in Patients With Hereditary Transthyretin-Mediated Amyloidosis

Journal of Cardiac Failure
Cardiovascular MedicineCardiology
2019English

Pharmacokinetics of Patisiran, the First Approved RNA Interference Therapy in Patients With Hereditary Transthyretin‐Mediated Amyloidosis

Journal of Clinical Pharmacology
Pharmacology
2019English

Cardiomyopathy Related to Transthyretin Val30met Mutation in Hereditary Systemic Amyloidosis

ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR
2015English

Identifying Mixed Phenotype: Evaluating the Presence of Polyneuropathy in Patients With Hereditary Transthyretin-Mediated Amyloidosis With Cardiomyopathy

Journal of Cardiac Failure
Cardiovascular MedicineCardiology
2019English

Diagnostic Challenges in Hereditary Transthyretin Amyloidosis With Polyneuropathy: Avoiding Misdiagnosis of a Treatable Hereditary Neuropathy

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
2017English

Tafamidis for Autonomic Neuropathy in Hereditary Transthyretin (ATTR) Amyloidosis: A Review

Clinical Autonomic Research
MedicineEndocrineNeurologyAutonomic Systems
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy