An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation

Genotypic and phenotypic correlation in an Italian population of hereditary amyloidosis TTR-related (HA-TTR): clinical and neurophysiological aids to diagnosis and some reflections on misdiagnosis

(2012) Fabrizio Salvi et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Regional difference and similarity of familial amyloidosis with polyneuropathy in France

(2012) David Adams et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Amyloid neuropathies

(2012) David Adams et al.   CURRENT OPINION IN NEUROLOGY

Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease

(2012) S. Lattante et al.   NEUROLOGY

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

(2012) T. Coelho et al.   NEUROLOGY

Long-term survival after liver transplantation in patients with familial amyloid polyneuropathy

(2012) T. Yamashita et al.   NEUROLOGY

Diagnosis of sporadic transthyretin Val30Met familial amyloid polyneuropathy: a practical analysis

(2011) Haruki Koike et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients

(2011) Manuel Cappellari et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

Progressive muscular atrophy and other lower motor neuron syndromes of adults

(2010) Lewis P. Rowland   MUSCLE & NERVE

Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin

(2008)   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM