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Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

http://www.wikidata.org/entity/Q58853184

about

Amyloid diseases of the heart: current and future therapies Endoplasmic reticulum quality control and systemic amyloid disease: Impacting protein stability from the inside out Systemic amyloidosis in England: an epidemiological study Pathophysiology and treatment of systemic amyloidosis.How to diagnose amyloidosis.Clinical and pathologic characteristics of hereditary apolipoprotein A-I amyloidosis in Ireland.Pathology and diagnosis of renal non-AL amyloidosis.Solid organ transplantation for non-TTR hereditary amyloidosis: report from the 1st International Workshop on the Hereditary Renal Amyloidoses Abstracts AApoAIL75P amyloidosis causes cirrhosis-like appearance of the liver in the absence of laboratory or clinical signs of hepatic dysfunction Double autologous bone marrow transplantation and orthotopic liver transplantation in a patient with primary light chain (AL) amyloidosis Renal Transplantation in Systemic Amyloidosis-Importance of Amyloid Fibril Type and Precursor Protein Abundance Hereditary lysozyme amyloidosis - phenotypic heterogeneity and the role of solid organ transplantation

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Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

http://www.wikidata.org/entity/Q58853184

description

im August 2006 veröffentlichter wissenschaftlicher Artikel

@de

scientific article published on 21 August 2006

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в жовтні 2006

@uk

name

Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

@en

Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

@nl

type

label

Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

@en

Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

@nl

prefLabel

Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

@en

Organ Transplantation in Hereditary Apolipoprotein AI Amyloidosis

@nl

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J.1600-6143.2006.01507.X

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American Journal of Transplantation

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Organ transplantation in hereditary apolipoprotein AI amyloidosis

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A Bybee

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A D Wechalekar

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A J Stangou

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D Rowczenio

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G A Tennent

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H J Goodman

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J Acheson

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J D Gillmore

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J Gilbertson

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J O'Grady

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P2860

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis

Variant apolipoprotein AI as a major constituent of a human hereditary amyloid

Human lysozyme gene mutations cause hereditary systemic amyloidosis.

Apolipoprotein AI and transthyretin as components of amyloid fibrils in a kindred with apoAI Leu178His amyloidosis.

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.

A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene.

The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide

Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.

Dialysis support of patients with primary systemic amyloidosis. A study of 211 patients.

Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene.

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2342-2347

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scholarly article

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10.1111/J.1600-6143.2006.01507.X

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10

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Helen J Lachmann

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2006-08-21T00:00:00Z

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16925563

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organ transplantation