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Hereditary ATTR amyloidosis

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Search Period All yearsLast 12 monthsLast 5 years Topic All topicsGeneralNutrition and dietAlternative treatment methods Type of research Any type of researchHighest quality evidence only (79)Meta-analysis (11)Treatment guideline (1)Phase 3 study (29)Randomized trial (23)Systematic review (15)Clinical trial (345)Review article (146)Early study (phase 1 or 2) (7)Case report (135)Laboratory or animal study (8)Commentary or editorial (72) Studies currently recruiting participants only (34)

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Publications and studies (1285)

• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Amyloid Polyneuropathy and Myocardial Amyloidosis 10 Years after Domino Liver Transplantation from a Patient with a Transthyretin Ser50Arg Mutation. (2017/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A novel transthyretin variant V28S (p.V48S) with a double-nucleotide substitution in the same codon. (2017/12/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Prevalence of mutant ATTR cardiac amyloidosis in elderly African Americans with heart failure. (2017/12/01) ♡
• Prevalence of Monoclonal Gammopathy in Wild-Type Transthyretin Amyloidosis. (2017/12/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Cardiac amyloidosis: An update on diagnosis and treatment. (2017/12/01) ♡
• With Alnylam's amyloidosis success, RNAi approval hopes soar. (2017/11/09) ♡
• Serum Proteomic Variability Associated with Clinical Phenotype in Familial Transthyretin Amyloidosis (ATTRm). (2017/11/03) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. The Utility of (99m)Tc-DPD Scintigraphy in the Diagnosis of Cardiac Amyloidosis: An Australian Experience. (2017/11/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Diagnosis and Treatment of Transthyretin Cardiac Amyloidosis. Progress and Hope. (2017/11/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Ocular Manifestations of Familial Transthyretin Amyloidosis. (2017/11/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Clinical and pathological findings in familial amyloid polyneuropathy caused by a transthyretin E61K mutation. (2017/10/15) ♡
• Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with severe aortic stenosis undergoing transcatheter aortic valve replacement. (2017/10/07) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Carpal Tunnel Biopsy Identifying Transthyretin Amyloidosis. (2017/10/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Familial amyloid polyneuropathy. (2017/10/01) ♡
• Association Between Ruptured Distal Biceps Tendon and Wild-Type Transthyretin Cardiac Amyloidosis. (2017/09/12) ♡
• Phase 3 studyiResearch in a large group of patients, the final step before a treatment can be approved. What comes out here carries significant weight. Long-term safety and efficacy of tafamidis for the treatment of hereditary transthyretin amyloid polyneuropathy: results up to 6 years. (2017/09/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Ocular Amyloidosis. (2017/09/01) ♡
• Outcomes of Patients With Familial Transthyretin Amyloidosis After Liver Transplantation. (2017/09/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Acquired transthyretin amyloidosis after domino liver transplant: Phenotypic correlation, implication of liver retransplantation. (2017/08/15) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Vitreous amyloidosis with autonomic neuropathy of the digestive tract associated with a novel transthyretin p.Gly87Arg variant in a Bangladeshi patient: a case report. (2017/08/13) ♡
• Semi-quantitative models for identifying potent and selective transthyretin amyloidogenesis inhibitors. (2017/08/01) ♡
• Sural nerve injury in familial amyloid polyneuropathy: MR neurography vs clinicopathologic tools. (2017/08/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Cardiac amyloidosis: pathogenesis, clinical context, diagnosis and management options. (2017/08/01) ♡
• Magnetic Resonance in Transthyretin Cardiac Amyloidosis. (2017/07/25) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Lipid Nanoparticle Systems for Enabling Gene Therapies. (2017/07/05) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Vitreous Amyloidosis: Ocular, Systemic, and Genetic Insights. (2017/07/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Late onset cardiomyopathy as presenting sign of ATTR A45G amyloidosis caused by a novel TTR mutation (p.A65G). (2017/07/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Cardiac Amyloidosis: Diagnosis and Treatment Strategies. (2017/07/01) ♡
• Cutaneous nerve biomarkers in transthyretin familial amyloid polyneuropathy. (2017/07/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths. (2017/06/21) ♡
• Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis. (2017/06/21) ♡
• Differential expression of Cathepsin E in transthyretin amyloidosis: from neuropathology to the immune system. (2017/06/06) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Diagnosis of cardiac transthyretin amyloidosis based on multimodality imaging. (2017/06/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy. (2017/06/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Genetic testing improves identification of transthyretin amyloid (ATTR) subtype in cardiac amyloidosis. (2017/06/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Cervicomedullary compression as the main manifestation of wild-type transthyretin amyloidosis. (2017/06/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Cognitive impairment in liver transplanted patients with transthyretin-related hereditary amyloid polyneuropathy. (2017/06/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. How your ears can tell what is hidden in your heart: wild-type transthyretin amyloidosis as potential cause of sensorineural hearing loss in elderly—AmyloDEAFNESS pilot study. (2017/06/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Corino de Andrade disease: mechanisms and impact on reproduction. (2017/06/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Design and Rationale of the Phase 3 ATTR-ACT Clinical Trial (Tafamidis in Transthyretin Cardiomyopathy Clinical Trial). (2017/06/01) ♡
• Blood Proteomic Profiling in Inherited (ATTRm) and Acquired (ATTRwt) Forms of Transthyretin-Associated Cardiac Amyloidosis. (2017/04/07) ♡
• Impact of genotype and phenotype on cardiac biomarkers in patients with transthyretin amyloidosis - Report from the Transthyretin Amyloidosis Outcome Survey (THAOS). (2017/04/06) ♡
• Peripheral nerve ultrasonography in patients with transthyretin amyloidosis. (2017/04/01) ♡
• Novel screening for transthyretin amyloidosis by using fat ultrasonography. (2017/04/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Transthyretin amyloidosis: an under-recognized neuropathy and cardiomyopathy. (2017/03/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Worth the RISC? (2017/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation: A case report. (2017/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [A case of secondary glaucoma due to a familial amyloid polyneuropathy (transthyretin mutation)]. (2017/03/01) ♡
• Randomized researchiParticipants were divided into groups by lottery and compared with each other. This reduces the chance that a difference is due to something other than the treatment. Tafamidis delays disease progression in patients with early stage transthyretin familial amyloid polyneuropathy: additional supportive analyses from the pivotal trial. (2017/03/01) ♡
• The importance of pre-clinical studies in animal models of TTR amyloidosis for the discovery of novel patient disease biomarkers. (2017/03/01) ♡

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