• A case of familial amyloid polyneuropathy due to Phe33Val TTR with vitreous involvement as the initial manifestation
• A patient with familial Mediterranean fever mimicking diarrhea-dominant irritable bowel syndrome who successfully responded to treatment with colchicine: a case report
• A severe form of amyloidotic polyneuropathy in a Costa Rican family with a rare transthyretin mutation (Glu54Lys)
• Amyloid protein of vessels in leptomeninges, cortices, choroid plexuses, and pituitary glands from patients with systemic amyloidosis
• Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I
• Amyloidosis cutis; a case of an intermediate form with almost general eruption and without evidence of visceral amyloid disorder
• Beta-2 microglobulin amyloidosis presenting as bilateral ovarian masses: a case report and review of the literature
• Biophysical Evidence for the Amyloid Formation of a Recombinant Rab2 Isoform of <em>Leishmania donovani</em>
• Biophysical Evidence for the Amyloid Formation of a Recombinant Rab2 Isoform of Leishmania donovani
• Clinical and pathological findings of non-Val30Met TTR type familial amyloid polyneuropathy in Japan
• Clinical characteristics and SAP scintigraphic findings in 10 patients with AGel amyloidosis
• Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis
• Clinical resolution of generalized lichen amyloidosis with dupilumab: a new alternative therapy
• Computer-assisted image analysis of amyloid deposits in abdominal fat pad aspiration biopsies
• Demonstration of plasma proteinase inhibitors in beta 2-microglobulin amyloid deposits
• Do you really know what you get: the benefits and doubts of domino liver transplantation
• Effects of sporadic transthyretin amyloidosis frequently on the gallbladder and the correlation between amyloid deposition in the gallbladder and heart: A forensic autopsy-based histopathological evaluation
• Familial amyloidotic polyneuropathy type 1 in Brazil is associated with the transthyretin Val30Met variant
• Familial cutaneous amyloidosis
• Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 1: peripheral neuropathies
• Hereditary fibrinogen A alpha-chain amyloidosis: phenotypic characterization of a systemic disease and the role of liver transplantation
• Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I
• Hereditary renal amyloidosis associated with variant lysozyme in a large English family
• Indications for liver transplantation in patients with amyloidosis: a single-center experience with 11 cases
• Lichen amyloidosus: a study of clinical, histopathologic and immunofluorescence findings in 30 cases
• Liver transplantation in transthyretin-related familial amyloid polyneuropathy
• Management of transthyretin amyloidosis
• MR of leptomeningeal spinal and posterior fossa amyloid
• Neuromuscular disease of the gastrointestinal tract
• Oleuropein aglycone: A polyphenol with different targets against amyloid toxicity
• Organ transplantation in hereditary apolipoprotein AI amyloidosis
• Outcome of liver transplantation for transthyretin amyloidosis: follow-up of Japanese familial amyloidotic polyneuropathy patients
• Peripheral nerve amyloidosis in sural nerve biopsies: a clinicopathologic analysis of 13 cases
• Peripheral nerve involvement in primary systemic AL amyloidosis: a clinical and electrophysiological study
• Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene
• Progressive wild-type transthyretin deposition after liver transplantation preferentially occurs onto myocardium in FAP patients
• Renal tubular and glomerular estrogen receptor ss levels are lower in lupus nephritis than in familial Mediterranean fever-associated renal amyloidosis
• Serum amyloid P component scintigraphy in familial amyloid polyneuropathy: regression of visceral amyloid following liver transplantation
• Shear wave elastography evaluation of liver, pancreas, spleen and kidneys in patients with familial mediterranean fever and amyloidosis
• Systemic Light Chain Amyloidosis, Version 2.2023, NCCN Clinical Practice Guidelines in Oncology
• The assessment of the nutritional status of patients with familial amyloid neuropathy type I (Corino Andrade's disease) who are candidates for orthotopic liver transplantation
• THE AUTOIMMUNE CONSTELLATION IN LICHEN AMYLOIDOSIS
• The Early Phase of β2-Microglobulin Aggregation: Perspectives From Molecular Simulations
• The first pure form of Ostertag-type amyloidosis in Japan: a sporadic case of hereditary fibrinogen Aalpha-chain amyloidosis associated with a novel frameshift variant
• The first pure form of Ostertag-type amyloidosis in Japan: a sporadic case of hereditary fibrinogen Aα-chain amyloidosis associated with a novel frameshift variant
• The value of screening biopsies in light-chain (AL) and transthyretin (ATTR) amyloidosis
• Transthyretin amyloidosis: a new mutation associated with dementia
• Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis
• Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation: A case report
• Treatment of amyloidosis
• Value of renal biopsy in the prognosis of liver transplantation in familial amyloid polyneuropathy ATTR Val30Met patients