Transthyretin amyloidosis: a new mutation associated with dementia.
about
A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindredMechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin AmyloidosisAutonomic dysfunction in familial amyloidotic polyneuropathy (FAP)Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis.Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathiesDetection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy.Mechanisms of cerebrovascular amyloid deposition. Lessons from mouse models.Cerebral amyloid angiopathy: an overview.Transthyretin mutations in hyperthyroxinemia and amyloid diseases.Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient.Chronic overproduction of transforming growth factor-beta1 by astrocytes promotes Alzheimer's disease-like microvascular degeneration in transgenic miceNeuropathologic analysis of Tyr69His TTR variant meningovascular amyloidosis with dementia.Cerebral amyloidosis: amyloid subunits, mutants and phenotypes.A novel amyloidogenic transthyretin variant, Gly53Ala, associated with intermittent headaches and ataxia.Genetic animal models of cerebral vasculopathies.Current and future treatment of amyloid diseases.A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementia.Liver transplantation as treatment for neurological disorders.A new transthyretin variant Leu55Gln in a patient with systemic amyloidosis.Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene.Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family--a follow-up autopsy report.Cutaneous lymphatic amyloid deposits in "Hungarian-type" familial transthyretin amyloidosis: a case report.CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings.Suppression of choroid plexus transthyretin levels by antisense oligonucleotide treatment.Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation.Postmortem findings in two familial amyloidosis patients with transthyretin variant Asp38Ala.Extended phenotype in the transthyretin Tyr77 familial amyloid polyneuropathy.Familial and Senile Amyloidosis Caused by TransthyretinJapanese monozygotic twins with familial amyloidotic polyneuropathy (FAP) (ATTR VaBOMet)
P2860
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P2860
Transthyretin amyloidosis: a new mutation associated with dementia.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Transthyretin amyloidosis: a new mutation associated with dementia.
@en
type
label
Transthyretin amyloidosis: a new mutation associated with dementia.
@en
prefLabel
Transthyretin amyloidosis: a new mutation associated with dementia.
@en
P2093
P2860
P356
P1433
P1476
Transthyretin amyloidosis: a new mutation associated with dementia.
@en
P2093
Gambetti P
Petersen RB
Richardson SL
P2860
P304
P356
10.1002/ANA.410410305
P577
1997-03-01T00:00:00Z