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Recommendations for the diagnosis and management of transthyretin amyloidosis with gastrointestinal manifestations.
Nakov R, Suhr OB, Ianiro G, Kupcinskas J, Segal JP, Dumitrascu DL, Heinrich H, Mikolasevic I, Stojkovic-Lalosevic M, Barbov I, Sarafov S, Tournev I, Nakov V, Wixner J. Nakov R, et al. Eur J Gastroenterol Hepatol. 2021 May 1;33(5):613-622. doi: 10.1097/MEG.0000000000002030. Eur J Gastroenterol Hepatol. 2021. PMID: 33394808 Review.
Transthyretin amyloid (ATTR) amyloidosis is an adult-onset, rare systemic disorder characterized by the accumulation of misfolded fibrils in the body, including the peripheral nerves, the heart and the gastrointestinal tract. Gastrointestinal manifestations a …
Transthyretin amyloid (ATTR) amyloidosis is an adult-onset, rare systemic disorder characterized by the accumulation of misfolded fib …
Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis.
Puig-Carrion GD, Reyentovich A, Katz SD. Puig-Carrion GD, et al. Clin Auton Res. 2019 Sep;29(Suppl 1):45-53. doi: 10.1007/s10286-019-00629-5. Epub 2019 Aug 26. Clin Auton Res. 2019. PMID: 31452023 Free PMC article. Review.
Depending on the disease subtype, fibrillar deposits in a several organs including the heart, kidney, liver, and peripheral nerves cause organ dysfunction and associated morbidity and mortality. ...Cardiac amyloidosis is often under-recognized in its early st …
Depending on the disease subtype, fibrillar deposits in a several organs including the heart, kidney, liver, and peripheral nerves …
Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm.
Sekijima Y, Ueda M, Koike H, Misawa S, Ishii T, Ando Y. Sekijima Y, et al. Orphanet J Rare Dis. 2018 Jan 17;13(1):6. doi: 10.1186/s13023-017-0726-x. Orphanet J Rare Dis. 2018. PMID: 29343286 Free PMC article. Review.
Hereditary ATTR (ATTRm) amyloidosis (also called transthyretin-type familial amyloid polyneuropathy [ATTR-FAP]) is an autosomal-dominant, adult-onset, rare systemic disorder predominantly characterized by irreversible, progressive, and persistent peripheral nerve da …
Hereditary ATTR (ATTRm) amyloidosis (also called transthyretin-type familial amyloid polyneuropathy [ATTR-FAP]) is an autosomal-domin …
An evaluation of patisiran: a viable treatment option for transthyretin-related hereditary amyloidosis.
Milani P, Mussinelli R, Perlini S, Palladini G, Obici L. Milani P, et al. Expert Opin Pharmacother. 2019 Dec;20(18):2223-2228. doi: 10.1080/14656566.2019.1671352. Epub 2019 Sep 30. Expert Opin Pharmacother. 2019. PMID: 31566422 Review.
Introduction: Hereditary transthyretin-mediated amyloidosis (ATTRv; v for variant) is a rare, progressive, fatal multi-systemic disease, autosomal dominantly inherited with heterogeneous clinical phenotype caused by mutations in the TTR gene. Mutations promoting proteolyti …
Introduction: Hereditary transthyretin-mediated amyloidosis (ATTRv; v for variant) is a rare, progressive, fatal multi-systemic disea …
Primary systemic amyloidosis.
Comenzo RL. Comenzo RL. Curr Treat Options Oncol. 2000 Apr;1(1):83-9. doi: 10.1007/s11864-000-0018-9. Curr Treat Options Oncol. 2000. PMID: 12057064 Review.
Patients with unexplained heart failure, hepatomegaly, nephrotic syndrome, or peripheral neuropathy should be evaluated for primary systemic (amyloid light-chain, or AL) amyloidosis by first seeking evidence of a clonal plasma cell disorder with serum and urine immu …
Patients with unexplained heart failure, hepatomegaly, nephrotic syndrome, or peripheral neuropathy should be evaluated for primary s …
Significance of Oligomeric and Fibrillar Species in Amyloidosis: Insights into Pathophysiology and Treatment.
Koike H, Iguchi Y, Sahashi K, Katsuno M. Koike H, et al. Molecules. 2021 Aug 22;26(16):5091. doi: 10.3390/molecules26165091. Molecules. 2021. PMID: 34443678 Free PMC article. Review.
Amyloidosis is a term referring to a group of various protein-misfolding diseases wherein normally soluble proteins form aggregates as insoluble amyloid fibrils. ...Disease-modifying therapies based on the pathophysiology of amyloidosis have now become availa …
Amyloidosis is a term referring to a group of various protein-misfolding diseases wherein normally soluble proteins form aggregates a …
Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy.
Ackermann EJ, Guo S, Booten S, Alvarado L, Benson M, Hughes S, Monia BP. Ackermann EJ, et al. Amyloid. 2012 Jun;19 Suppl 1:43-4. doi: 10.3109/13506129.2012.673140. Epub 2012 Apr 12. Amyloid. 2012. PMID: 22494066
Transthyretin (TTR)-associated amyloidosis is a late-onset autosomal-dominant genetic disease. Over 100 amyloidogenic mutations have been identified in TTR which destabilize the TTR tetramer thereby inducing the formation of amyloid fibrils in tissues such as the heart and …
Transthyretin (TTR)-associated amyloidosis is a late-onset autosomal-dominant genetic disease. Over 100 amyloidogenic mutations have …
Carpal tunnel syndrome in hemodialysis patients as a dialysis-related amyloidosis manifestation--incidence, risk factors and results of surgical treatment.
Kopeć J, Gadek A, Drozdz M, Miśkowiec K, Dutka J, Sydor A, Chowaniec E, Sułowicz W. Kopeć J, et al. Med Sci Monit. 2011 Sep;17(9):CR505-9. doi: 10.12659/msm.881937. Med Sci Monit. 2011. PMID: 21873947 Free PMC article.
BACKGROUND: Carpal tunnel syndrome (CTS) is the most common complication of dialysis-related amyloidosis (DRA) developing in patients on long-term dialysis therapy. ...
BACKGROUND: Carpal tunnel syndrome (CTS) is the most common complication of dialysis-related amyloidosis (DRA) developing in patients …
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