Search Results - "DRACHMAN, BRIAN"
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Expert Consensus Recommendations for the Suspicion and Diagnosis of Transthyretin Cardiac Amyloidosis
Published in Circulation. Heart failure (01-09-2019)“…Cardiomyopathy is a manifestation of transthyretin amyloidosis (ATTR), which is an underrecognized systemic disease whereby the transthyretin protein misfolds…”
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Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs
Published in Heart failure reviews (01-03-2015)“…Transthyretin-cardiac amyloidoses (ATTR-CA) are an underdiagnosed but increasingly recognized cause of heart failure. Extracellular deposition of fibrillary…”
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Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy
Published in The New England journal of medicine (13-09-2018)“…In this randomized, controlled, phase 3 trial of tafamidis for transthyretin amyloid cardiomyopathy, tafamidis was associated with lower all-cause mortality…”
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Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis
Published in The New England journal of medicine (05-07-2018)“…This phase 3 trial tested inotersen, a modified oligonucleotide that targets TTR messenger RNA, in the treatment of hereditary transthyretin amyloidosis, a…”
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Long-Term Survival With Tafamidis in Patients With Transthyretin Amyloid Cardiomyopathy
Published in Circulation. Heart failure (01-01-2022)“…Tafamidis is approved in many countries for the treatment of transthyretin amyloid cardiomyopathy. This study reports data on the long-term efficacy of…”
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Treatment characteristics of patients with hereditary transthyretin amyloidosis: a cohort study
Published in Orphanet journal of rare diseases (08-05-2024)“…There are novel medications approved for the treatment of hereditary transthyretin amyloidosis (ATTRv), classified as transthyretin (TTR) stabilizers or gene…”
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Assessing mNIS+7Ionis and international neurologists' proficiency in a familial amyloidotic polyneuropathy trial
Published in Muscle & nerve (01-11-2017)“…ABSTRACT Introduction Polyneuropathy signs (Neuropathy Impairment Score, NIS), neurophysiologic tests (m+7Ionis), disability, and health scores were assessed…”
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ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable
Published in Orphanet journal of rare diseases (06-05-2021)“…The global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causing the ongoing coronavirus disease 2019 (COVID-19) pandemic…”
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The Cardiac Amyloidosis Registry Study (CARS): Rationale, Design and Methodology
Published in Journal of cardiac failure (01-05-2024)“…CARS (Cardiac Amyloidosis Registry Study) is a multicenter registry established in 2019 that includes patients with transthyretin (ATTR, wild-type and variant)…”
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Age- and Sex-Related Differences in Patients With Wild-Type Transthyretin Amyloidosis: Insights From THAOS
Published in JACC. Advances (Online) (01-08-2024)“…Wild-type transthyretin amyloidosis (ATTRwt amyloidosis) is primarily diagnosed in elderly men but diagnoses in younger patients and women have recently…”
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Rationale and design of a randomized trial of automated hovering for post-myocardial infarction patients: The HeartStrong program
Published in The American heart journal (01-09-2016)“…Background Coronary artery disease is the single leading cause of death in the United States, and medications can significantly reduce the rate of repeat…”
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Long-term survival in people with transthyretin amyloid cardiomyopathy who took tafamidis: A Plain Language Summary
Published in Future cardiology (01-01-2023)“…This summary presents the results from an ongoing, long-term extension study that followed an earlier study called ATTR-ACT. People who took part in this…”
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Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner
Published in BMC family practice (23-09-2020)“…Transthyretin amyloidosis (also known as ATTR amyloidosis) is a systemic, life-threatening disease characterized by transthyretin (TTR) fibril deposition in…”
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Assessing mNIS+7 Ionis and international neurologists' proficiency in a familial amyloidotic polyneuropathy trial
Published in Muscle & nerve (01-11-2017)“…Polyneuropathy signs (Neuropathy Impairment Score, NIS), neurophysiologic tests (m+7 ), disability, and health scores were assessed in baseline evaluations of…”
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A prospective study of continuous intravenous milrinone therapy for status IB patients awaiting heart transplant at home
Published in The Journal of heart and lung transplantation (01-09-2004)“…We performed a prospective study to determine the feasibility and safety of continuous intravenous milrinone therapy administered at home in patients listed as…”
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Genotype and Phenotype of Transthyretin Cardiac Amyloidosis
Published in Journal of the American College of Cardiology (12-07-2016)“…Abstract Background Transthyretin amyloidosis (ATTR) is a heterogeneous disorder with multiorgan involvement and a genetic or nongenetic basis. Objectives The…”
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A new transthyretin variant (Glu61Gly) associated with cardiomyopathy
Published in Amyloid (01-03-2007)“…We report the identification of a new transthyretin (TTR) gene mutation and variant protein, Glu61Gly, in a 55-year-old man with progressive cardiomyopathy,…”
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Treatment characteristics in a cohort of patients with hereditary transthyretin amyloidosis (S7.010)
Published in Neurology (25-04-2023)“…Abstract only…”
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Characteristics of a single-center cohort of patients with hereditary transthyretin amyloidosis (P13-8.015)
Published in Neurology (25-04-2023)“…Abstract only…”
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Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey)
Published in Journal of the American College of Cardiology (12-07-2016)“…Transthyretin amyloidosis (ATTR) is a heterogeneous disorder with multiorgan involvement and a genetic or nongenetic basis. The goal of this study was to…”
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