Hereditary transthyretin amyloidosis from a Scandinavian perspective.
about
Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin AmyloidosisIncidence and survival in non-hereditary amyloidosis in SwedenVariation in amount of wild-type transthyretin in different fibril and tissue types in ATTR amyloidosisNoncerebral Amyloidoses: Aspects on Seeding, Cross-Seeding, and Transmission.A competition assay to identify amyloidogenesis inhibitors by monitoring the fluorescence emitted by the covalent attachment of a stilbene derivative to transthyretin.Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases.Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis.Amyloid in the cardiovascular system: a reviewInvolvement of Macrophages in the Pathogenesis of Familial Amyloid Polyneuropathy and Efficacy of Human iPS Cell-Derived Macrophages in Its TreatmentImpact of genotype and phenotype on cardiac biomarkers in patients with transthyretin amyloidosis - Report from the Transthyretin Amyloidosis Outcome Survey (THAOS).Familial Transthyretin Amyloidosis with Variant Asp38Ala Presenting with Orthostatic Hypotension and Chronic Diarrhea.Gastric emptying in hereditary transthyretin amyloidosis: the impact of autonomic neuropathyLoss of gastric interstitial cells of Cajal in patients with hereditary transthyretin amyloidosis.THAOS: gastrointestinal manifestations of transthyretin amyloidosis - common complications of a rare disease.Amyloid structure--one but not the same: the many levels of fibrillar polymorphism.Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis.Transthyretin proteins regulate angiogenesis by conferring different molecular identities to endothelial cellsDisease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective.Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.A Swedish family with the rare Phe33Leu transthyretin mutation.The "Wagshurst study": p.Val40Ile transthyretin gene variant causes late-onset cardiomyopathy.Heart transplantation in a 68-year-old patient with senile systemic amyloidosis.Prevalence of isolated atrial amyloidosis in young patients affected by congestive heart failure.Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathyPhenotypic and genotypic heterogeneity in transthyretin-related cardiac amyloidosis: towards tailoring of therapeutic strategies?Selection of hereditary transthyretin amyloid patients for liver transplantation: the Swedish experienceMyocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathyUnderstanding and Ameliorating the TTR Amyloidoses
P2860
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P2860
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
description
2003 nî lūn-bûn
@nan
2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
@ast
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
@en
type
label
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
@ast
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
@en
prefLabel
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
@ast
Hereditary transthyretin amyloidosis from a Scandinavian perspective.
@en
P2093
P2860
P1476
Hereditary transthyretin amyloidosis from a Scandinavian perspective
@en
P2093
A Danielsson
G Holmgren
I Hastrup Svendsen
P J Ranløv
R Andersson
P2860
P304
P356
10.1046/J.1365-2796.2003.01173.X
P407
P50
P577
2003-09-01T00:00:00Z