Multidisciplinary approach in the management of hATTR
- PMID: 32474919
- DOI: 10.1111/eci.13296
Multidisciplinary approach in the management of hATTR
Similar articles
-
Hereditary Transthyretin Amyloid Cardiomyopathy.JAMA Cardiol. 2022 Feb 1;7(2):236. doi: 10.1001/jamacardio.2021.5006. JAMA Cardiol. 2022. PMID: 34935856 No abstract available.
-
Autonomic involvement in hereditary transthyretin amyloidosis (hATTR amyloidosis).Clin Auton Res. 2019 Apr;29(2):245-251. doi: 10.1007/s10286-018-0514-2. Epub 2018 Mar 6. Clin Auton Res. 2019. PMID: 29511897 Review.
-
Correlation between Sudoscan and COMPASS 31: assessment of autonomic dysfunction on hATTR V30M patients.Amyloid. 2019;26(sup1):23. doi: 10.1080/13506129.2019.1582494. Amyloid. 2019. PMID: 31343356 No abstract available.
-
Mutant Thr95Ile Transthyretin-Related Cardiac Amyloidosis With Polyneuropathy.Circ J. 2019 Oct 25;83(11):2328. doi: 10.1253/circj.CJ-19-0281. Epub 2019 Jun 26. Circ J. 2019. PMID: 31243187 No abstract available.
-
Diabetic gastrointestinal autonomic neuropathy.Curr Ther Endocrinol Metab. 1997;6:462-5. Curr Ther Endocrinol Metab. 1997. PMID: 9174790 Review. No abstract available.
Cited by
-
Integrated specialty care for amyloidosis: a scoping review using the Consolidated Framework for Implementation Research.BMC Health Serv Res. 2025 Mar 21;25(1):415. doi: 10.1186/s12913-025-12520-3. BMC Health Serv Res. 2025. PMID: 40114122 Free PMC article.
-
Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden.Orphanet J Rare Dis. 2021 Jun 10;16(1):266. doi: 10.1186/s13023-021-01910-5. Orphanet J Rare Dis. 2021. PMID: 34112225 Free PMC article.
-
Management of Hereditary Transthyretin Amyloidosis (ATTRv) Patients and Asymptomatic Carriers in Spain: The EMPATIa Study.J Clin Med. 2024 Dec 13;13(24):7587. doi: 10.3390/jcm13247587. J Clin Med. 2024. PMID: 39768509 Free PMC article.
-
Multidisciplinary amyloidosis care in the era of personalized medicine.Front Neurol. 2022 Oct 13;13:935936. doi: 10.3389/fneur.2022.935936. eCollection 2022. Front Neurol. 2022. PMID: 36341129 Free PMC article. Review.
-
Clinical and Genotype Characteristics and Symptom Migration in Patients With Mixed Phenotype Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey.Cardiol Ther. 2024 Mar;13(1):117-135. doi: 10.1007/s40119-023-00344-3. Epub 2023 Dec 20. Cardiol Ther. 2024. PMID: 38117424 Free PMC article.
References
REFERENCES
-
- Shin SC, Robinson-Papp J. Amyloid neuropathies. Mt Sinai J Med. 2012;79(6):733-748.
-
- Blancas-Mejía LM, Ramirez-Alvarado M. Systemic amyloidoses. Annu Rev Biochem. 2013;82:745-774.
-
- Ripoll-Vera T, Buades J, Cisneros E, et al. Cardiac involvement in a patient cohort with Val30Met mutation Transthyretin amyloidosis. Rev Esp Cardiol. 2019;72(1):92-94.
-
- Sekijima Y. Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments. J Neurol Neurosurg Psychiatry. 2015;86(9):1036-1043.
-
- Coelho T, Maurer MS, Suhr OB. THAOS - the Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis. Curr Med Res Opin. 2013;29(1):63-76.
MeSH terms
Supplementary concepts
LinkOut - more resources
Full Text Sources