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Publications by B LeChevalier
A Transthyretin Variant (Alanine 71) Associated With Familial Amyloidotic Polyneuropathy in a French Family.
Journal of Medical Genetics
Genetics
Related publications
A Transthyretin Variant (Alanine 49) Associated With Familial Amyloidotic Polyneuropathy in a French Family.
Journal of Medical Genetics
Genetics
Transthyretin Glu18, a New Variant Associated With Familial Amyloid Polyneuropathy
Journal of the University of Malaya Medical Centre
Medicine
Familial Amyloidotic Polyneuropathy Without Familial Occurrence: Carrier Detection by the Radioimmunoassay of Variant Transthyretin.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Familial Amyloidotic Polyneuropathy Associated With the Transthyretin CYS 114 Gene in a Russian Pair of Monozygotic Twins.
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Familial Amyloidotic Polyneuropathy in Hokkaido: A Case Report.
Japanese Journal of Medicine
Rapid Progression of Familial Amyloidotic Polyneuropathy
Neurology
Neurology
Bilateral Corneal Perforation in Familial Amyloidotic Polyneuropathy
Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Transthyretin-Associated Familial Amyloid Polyneuropathy - Current and Emerging Therapies
European Neurological Review
Neurology
Corneal Confocal Microscopy and Familial Amyloidotic Polyneuropathy
Journal Francais d'Ophtalmologie
Ophthalmology