Recommendations for the diagnosis and management of transthyretin amyloidosis with gastrointestinal manifestations
Transthyretin amyloid (ATTR) amyloidosis is an adult-onset, rare systemic disorder
characterized by the accumulation of misfolded fibrils in the body, including the peripheral …
characterized by the accumulation of misfolded fibrils in the body, including the peripheral …
Management of gastrointestinal complications in hereditary transthyretin amyloidosis: a single-center experience over 40 years
J Wixner, OB Suhr, I Anan - Expert Review of Gastroenterology & …, 2018 - Taylor & Francis
ABSTRACT Introduction: Hereditary transthyretin amyloidosis (ATTRm amyloidosis) is a rare
disease caused by the deposition and accumulation of insoluble non-native transthyretin …
disease caused by the deposition and accumulation of insoluble non-native transthyretin …
[PDF][PDF] Gastrointestinal manifestations in hereditary transthyretin amyloidosis: a single-centre experience
M Luigetti, A Tortora, A Romano… - J. Gastrointest. Liver …, 2020 - academia.edu
ABSTRACT Background & Aims: Hereditary transthyretin (ATTRv) amyloidosis represents a
diagnostic challenge considering the great variability in clinical presentation and multiorgan …
diagnostic challenge considering the great variability in clinical presentation and multiorgan …
[PDF][PDF] Transthyretin Amyloidosis with Gastrointestinal Manifestation
R Nakov, S Sarafov, V Nakov… - J Gastrointestin …, 2019 - pdfs.semanticscholar.org
Transthyretin amyloidosis (ATTR) is a rare, progressive, life-threatening, hereditary disorder
caused by mutations in the transthyretin gene. Due to the phenotypic heterogeneity, ATTR is …
caused by mutations in the transthyretin gene. Due to the phenotypic heterogeneity, ATTR is …
[HTML][HTML] Identification and management of gastrointestinal manifestations of hereditary transthyretin amyloidosis: Recommendations from an Italian group of experts
M Cappello, G Barbara, M Bellini, D Consalvo… - Digestive and Liver …, 2024 - Elsevier
Gastrointestinal manifestations are common across all hereditary transthyretin amyloidosis
(ATTRv) genotypes. However, they are poorly specific, and their recognition as part of …
(ATTRv) genotypes. However, they are poorly specific, and their recognition as part of …
[HTML][HTML] Diagnosis and treatment of gastrointestinal dysfunction in hereditary TTR amyloidosis
L Obici, OB Suhr - Clinical Autonomic Research, 2019 - Springer
Purpose To review the management of gastrointestinal symptoms in patients with hereditary
transthyretin amyloidosis, discussing diagnostic evaluations, assessment of disease …
transthyretin amyloidosis, discussing diagnostic evaluations, assessment of disease …
Hereditary transthyretin amyloidosis: clinical presentation and management updates
C Schwartzlow, M Kazamel - Journal of clinical neuromuscular …, 2020 - journals.lww.com
Hereditary transthyretin amyloidosis, once a rare progressive neuropathy and/or
cardiomyopathy, is now recognized with increasing worldwide frequency, various …
cardiomyopathy, is now recognized with increasing worldwide frequency, various …
[HTML][HTML] Hereditary Transthyretin Amyloidosis with Polyneuropathy: Monitoring and Management
V Vélez-Santamaría, V Nedkova-Hristova… - … Journal of General …, 2022 - ncbi.nlm.nih.gov
Hereditary Transthyretin Amyloidosis with Polyneuropathy: Monitoring and Management - PMC
Back to Top Skip to main content NIH NLM Logo Access keys NCBI Homepage MyNCBI …
Back to Top Skip to main content NIH NLM Logo Access keys NCBI Homepage MyNCBI …
[HTML][HTML] Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathy
L Poli, B Labella, S Cotti Piccinelli, F Caria… - Frontiers in …, 2023 - frontiersin.org
Amyloidoses represent a group of diseases characterized by the pathological accumulation
in the extracellular area of insoluble misfolded protein material called “amyloid”. The …
in the extracellular area of insoluble misfolded protein material called “amyloid”. The …
[HTML][HTML] Hereditary transthyretin amyloidosis: a case report
A Lee, NM Fine, V Bril, D Delgado, C Hahn - Journal of Medical Case …, 2022 - Springer
Background Hereditary transthyretin amyloidosis is an uncommon multisystem disorder
caused by mutation of the transthyretin protein, leading to peripheral neuropathy often with …
caused by mutation of the transthyretin protein, leading to peripheral neuropathy often with …
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