Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis.
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Molecular Tweezers Targeting Transthyretin AmyloidosisBiochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis.Cerebral amyloid angiopathy: an overview.Familial amyloidotic polyneuropathy with muscle, vitreous, leptomeningeal, and cardiac involvement: phenotypic, pathological, and MRI description.Transthyretin mutations in hyperthyroxinemia and amyloid diseases.Glial cells in familial amyloidotic polyneuropathyOculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient.Neuropathologic analysis of Tyr69His TTR variant meningovascular amyloidosis with dementia.A novel amyloidogenic transthyretin variant, Gly53Ala, associated with intermittent headaches and ataxia.Amyloid neuropathies.Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF.Current and future treatment of amyloid diseases.beta2-Microglobulin is potentially neurotoxic, but the blood brain barrier is likely to protect the brain from its toxicity.Atypical familial motor neuropathy in patients with mutant TTR Ile68Leu.Amyloid fibril formation in the context of full-length protein: effects of proline mutations on the amyloid fibril formation of beta2-microglobulin.Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families.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.MRI analysis on a patient with the V30M mutation is characteristic of leptomeningeal amyloid.Cutaneous lymphatic amyloid deposits in "Hungarian-type" familial transthyretin amyloidosis: a case report.CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings.An aggressive form of familial amyloid polyneuropathy caused by a Glu54Gly mutation in the transthyretin gene.Suppression of choroid plexus transthyretin levels by antisense oligonucleotide treatment.A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation.Familial and Senile Amyloidosis Caused by Transthyretin
P2860
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P2860
Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Transthyretin Leu12Pro is asso ...... nd leptomeningeal amyloidosis.
@en
Transthyretin Leu12Pro is asso ...... nd leptomeningeal amyloidosis.
@nl
type
label
Transthyretin Leu12Pro is asso ...... nd leptomeningeal amyloidosis.
@en
Transthyretin Leu12Pro is asso ...... nd leptomeningeal amyloidosis.
@nl
prefLabel
Transthyretin Leu12Pro is asso ...... nd leptomeningeal amyloidosis.
@en
Transthyretin Leu12Pro is asso ...... nd leptomeningeal amyloidosis.
@nl
P2093
P356
P1433
P1476
Transthyretin Leu12Pro is asso ...... nd leptomeningeal amyloidosis.
@en
P2093
Hawkins PN
Morgan-Hughes JA
P304
P356
10.1093/BRAIN/122.2.183
P407
P478
122 ( Pt 2)
P50
P577
1999-02-01T00:00:00Z