Progressive liver failure in a patient with adult Niemann-Pick disease associated with generalized AL amyloidosis (Q72011839)

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22 October 2019

title

Progressive liver failure in a patient with adult Niemann-Pick disease associated with generalized AL amyloidosis (English)

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22 October 2019

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H. Zhou

1

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21 July 2024

R. P. Linke

2

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21 July 2024

H. E. Schaefer

3

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21 July 2024

W. Möbius

4

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21 July 2024

U. Pfeifer

5

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21 July 2024

language of work or name

English

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National Center for Biotechnology Information

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21 July 2024

publication date

1 January 1995

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full work available at URL

22 October 2019

http://link.springer.com/content/pdf/10.1007/BF00192120.pdf

file format

Portable Document Format

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http://link.springer.com/article/10.1007/BF00192120/fulltext.html

21 July 2024

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http://link.springer.com/content/pdf/10.1007/BF00192120

21 July 2024

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21 July 2024

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7655746%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

volume

426

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22 October 2019

issue

6

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22 October 2019

page(s)

635-639

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Cholestasis and liver failure with lambda-AL amyloidosis

22 October 2019

cites work

1 reference

12 December 2020

Linkage of Niemann-Pick disease type C to human chromosome 18

1 reference

12 December 2020

Amyloid production in human myeloma stem-cell culture, with morphologic evidence of amyloid secretion by associated macrophages

1 reference

12 December 2020

Case report: serendipitous Gaucher's disease presenting as elevated erythrocyte sedimentation rate due to monoclonal gammopathy

1 reference

12 December 2020

Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic forms

1 reference

12 December 2020

Immunoglobulin heavy-chain-associated amyloidosis

1 reference

12 December 2020

Gaucher's disease: a disease with chronic stimulation of the immune system

1 reference

12 December 2020

Amyloidosis: a final common pathway for protein deposition in tissues

1 reference

12 December 2020

Liver findings in Niemann-Pic disease type C

1 reference

12 December 2020

Mechanisms of disease: monoclonal immunoglobulin deposition. Amyloidosis, light chain deposition disease, and light and heavy chain deposition disease

1 reference

12 December 2020

Case records of the Massachusetts Genral Hospital. Weekly clinicopathological exercises. Case 23-1968

1 reference

12 December 2020

Light chain deposition disease of the liver associated with AL-type amyloidosis and severe cholestasis

1 reference

12 December 2020

Niemann-Pick disease type B: clinical signs and follow-up of a new case

1 reference

12 December 2020

Coexistence of IgA myeloma and Gaucher's disease

1 reference

12 December 2020

Cirrhosis and portal hypertension in a patient with adult Niemann-Pick disease

1 reference

12 December 2020

Fatal liver failure in two children with Niemann-Pick disease type B

1 reference

12 December 2020

The cerebral defect in Tay-Sachs disease and Niemann-Pick disease

1 reference

12 December 2020

Polyclonal B-cell lymphocytosis and hypergammaglobulinemia in patients with Gaucher disease

1 reference

12 December 2020

Liver failure and the sea-blue histiocyte/adult Niemann-Pick disease. Case report and review of the literature

1 reference

12 December 2020

Orthotopic liver transplantation in two adults with Niemann-Pick and Gaucher's diseases: implications for the treatment of inherited metabolic disease

1 reference

12 December 2020

Amyloidosis. An unusual complication of Gaucher's disease

1 reference

12 December 2020

Primary amyloidosis associated with Gaucher's disease

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12 December 2020

1 reference

12 December 2020

Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosis

1 reference

12 December 2020

Primary amyloidosis as a rare cause of acute liver insufficiency

1 reference

12 December 2020

Primary amyloidosis of the liver

1 reference

12 December 2020

Pathology of dysproteinemia: light chain amyloidosis, non-amyloid immunoglobulin deposition disease, cryoglobulinemia syndromes, and macroglobulinemia of Waldenström

1 reference

12 December 2020

Amyloid deposits and amyloidosis. The beta-fibrilloses (first of two parts).

1 reference

12 December 2020

Immunoglobulin abnormalities in Gaucher's disease. Report of 16 cases

1 reference

12 December 2020

Biochemical studies in Niemann-Pick disease. III. In vitro and in vivo assays of sphingomyelin degradation in cultured skin fibroblasts and amniotic fluid cells for the diagnosis of the various forms of the disease

1 reference

12 December 2020

Severe intrahepatic cholestasis in primary amyloidosis: a report of four cases and a review of the literature

1 reference

12 December 2020

Deletion of arginine (608) in acid sphingomyelinase is the prevalent mutation among Niemann-Pick disease type B patients from northern Africa

1 reference

12 December 2020

A case of prominent hepatic cholestasis developing to hepatic failure in lambda-AL amyloidosis

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00192120

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7655746%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

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