Changes in nerve conduction studies predate clinical symptoms onset in early onset Val30Met hereditary ATTR amyloidosis

Plasma neurofilament light chain: an early biomarker for hereditary ATTR amyloid polyneuropathy

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Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care

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Early data on long‐term efficacy and safety of inotersen in patients with hereditary transthyretin amyloidosis: a 2‐year update from the open‐label extension of the NEURO‐TTR trial

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Diagnosis and Screening of Patients with Hereditary Transthyretin Amyloidosis (hATTR): Current Strategies and Guidelines

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Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

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Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee

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Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease

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Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis

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Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis

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Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm

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Early skin denervation in hereditary and iatrogenic transthyretin amyloid neuropathy

(2017) Teruaki Masuda et al.   NEUROLOGY

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In vivo detection of nerve injury in familial amyloid polyneuropathy by magnetic resonance neurography

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Update in the diagnosis and management of transthyretin familial amyloid polyneuropathy

(2014) Violaine Plante-Bordeneuve   JOURNAL OF NEUROLOGY

Neurophysiological markers of small fibre neuropathy in TTR-FAP mutation carriers

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Neurophysiological techniques to detect early small-fiber dysfunction in transthyretin amyloid polyneuropathy

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Guideline of transthyretin-related hereditary amyloidosis for clinicians

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Tafamidis for transthyretin familial amyloid polyneuropathy: A randomized, controlled trial

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Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant

(2011) P. T. Sattianayagam et al.   EUROPEAN HEART JOURNAL

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(2011) Violaine Planté-Bordeneuve et al.   LANCET NEUROLOGY

Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30)

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Motor Unit Number Estimation in the Assessment of Performance and Function in Motor Neuron Disease

(2008) Mark B. Bromberg et al.   Physical Medicine and Rehabilitation Clinics of North America