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genetics & heredity (18) 18
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Amyloid, ISSN 1350-6129, 01/2019, Volume 26, Issue 1, pp. 3 - 9
Diagnosis in the early stages of hereditary transthyretin (ATTR) amyloidosis is imperative to support timely treatment to prevent or delay disease progression.... 
minimum criteria for diagnosis | carrier | amyloidosis | predicted age of disease onset | transthyretin | diagnosis | hereditary | ATTR | follow up | MEDICINE, RESEARCH & EXPERIMENTAL | MANAGEMENT | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEDICINE, GENERAL & INTERNAL | VAL30MET MUTATION
Journal Article
Amyloid, ISSN 1350-6129, 12/2011, Volume 18, Issue 4, pp. 200 - 205
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 08/2019, Volume 403, pp. 1 - 6
Despite growing numbers of patients diagnosed with late-onset hereditary ATTR V30M amyloidosis with polyneuropathy (ATTRv-PN), this condition remains poorly... 
Hereditary transthyretin amyloidosis | Early-onset ATTRv-PN | Polyneuropathy | Late-onset ATTRv-PN | Familial amyloid polyneuropathy | Polyneuropathies | Amyloidosis | Index Medicus
Journal Article
Journal Article
Journal Article
European Journal of Heart Failure, ISSN 1388-9842, 10/2018, Volume 20, Issue 10, pp. 1417 - 1425
Journal Article
Journal Article
神経治療学, ISSN 0916-8443, 2018, Volume 35, Issue 3, pp. 278 - 282
Transthyretin (TTR) is a representative amyloidogenic protein in humans. TTR protein destabilised by TTR gene mutation is prone to dissociate from its native... 
amyloid | disease modifying therapy | familial amyloid polyneuropathy | transthyretin |