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JACC: Cardiovascular Imaging, ISSN 1936-878X, 06/2011, Volume 4, Issue 6, pp. 659 - 670
In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aimed to assess the role of Tc-3,3-diphosphono-1,2-propanodicarboxylic... 
cardiac amyloidosis | hereditary transthyretin-related amyloidosis | diagnosis | 99mTc-DPD scintigraphy | prognosis | Tc-DPD scintigraphy
Journal Article
Journal Article
Circulation, ISSN 0009-7322, 05/2014, Volume 129, Issue 18, pp. 1840 - 1849
Journal Article
Medicine (United States), ISSN 0025-7974, 03/2017, Volume 96, Issue 10
Rationale: Hereditary amyloidosis is diagnosed worldwidely with an increasing incidence. As the most common form, transthyretin-related hereditary amyloidosis... 
case report | p.Leu75Pro | transthyretin-related hereditary amyloidosis | rs121918079 | renal insufficiency | TTR mutation | MEDICINE, GENERAL & INTERNAL | POLYNEUROPATHY | LIVER-TRANSPLANTATION | INVOLVEMENT | DISEASE | KIDNEY
Journal Article
Medicine, ISSN 0025-7974, 03/2017, Volume 96, Issue 10, p. e5737
Hereditary amyloidosis is diagnosed worldwidely with an increasing incidence. As the most common form, transthyretin-related hereditary amyloidosis (ATTR... 
Prealbumin - genetics | Amyloid Neuropathies, Familial - genetics | Humans | Amyloid Neuropathies, Familial - complications | Vomiting - etiology | Adult | Male | Mutation, Missense | Renal Insufficiency - etiology | Amyloid Neuropathies, Familial - diagnosis | Care and treatment | Amyloidosis | Kidney failure | Risk factors
Journal Article
Journal of the Peripheral Nervous System, ISSN 1085-9489, 12/2012, Volume 17, Issue 4, pp. 385 - 390
Journal Article
Neurology Asia, ISSN 1823-6138, 2008, Volume 13, Issue 2, pp. 121 - 124
Familial amyloid polyneuropathy is commonly the result of deposition of variant transthyretin in nerves and other organs. Apart from the Val30Met variant... 
HONG-KONG CHINESE | SERIES | HEREDITARY | IDENTIFICATION | CLINICAL NEUROLOGY
Journal Article