Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases. - Wikidata - wikimedia - TriplyDB

Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

http://www.wikidata.org/entity/Q31118069

about

Proteomics and mass spectrometry in the diagnosis of renal amyloidosis Rare and unusual clinicopathologic presentation of renal AL amyloidosis.Leukocyte chemotactic factor 2 amyloidosis (ALECT2) is a common form of renal amyloidosis among Egyptians.Value of antibodies to free light chains in immunoperoxidase studies of renal biopsies Immunoglobulin light chain amyloidosis: 2014 update on diagnosis, prognosis, and treatment.The spectrum of kidney pathology in B-cell chronic lymphocytic leukemia / small lymphocytic lymphoma: a 25-year multicenter experience.Amyloid nephropathy A comparison of immunohistochemistry and mass spectrometry for determining the amyloid fibril protein from formalin-fixed biopsy tissue.Leukocyte Cell-Derived Chemotaxin 2-Associated Amyloidosis: A Recently Recognized Disease with Distinct Clinicopathologic Characteristics A Patient with Abnormal Kidney Function and a Monoclonal Light Chain in the Urine.Prevalence and organ distribution of leukocyte chemotactic factor 2 amyloidosis (ALECT2) among decedents in New Mexico.Recent advances in the understanding of immune-mediated nephrotic syndrome: diagnostic and prognostic implications.Paraprotein-Related Kidney Disease: Glomerular Diseases Associated with Paraproteinemias.Immunoglobulin light chain amyloidosis: 2016 update on diagnosis, prognosis, and treatment.Monoclonal gammopathy of renal significance: Diagnostic workup.Long-term prognosis of AL and AA renal amyloidosis: a Japanese single-center experience.Clinical Presentation of Tubulointerstitial Nephritis Caused by Amyloid Light-chain Amyloidosis in a Patient with Sjögren's Syndrome.Heavy and Light chain amyloidosois presenting as complete heart block: A rare presentation of a rare disease Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII.Pathology and diagnosis of renal non-AL amyloidosis.Hereditary Renal Amyloidosis Associated With a Novel Apolipoprotein A-II Variant.Dysproteinemias and Glomerular Disease.Misdiagnosing renal amyloidosis as minimal change disease.The Complexity and Heterogeneity of Monoclonal Immunoglobulin-Associated Renal Diseases.Kidney biopsy in AA amyloidosis: impact of histopathology on prognosis.Revisiting renal amyloidosis with clinicopathological characteristics, grading, and scoring: A single-institutional experience.Systemic amyloidoses and proteomics: The state of the art.

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P2860

Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

http://www.wikidata.org/entity/Q31118069

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2013 nî lūn-bûn

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2013 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2013年の論文

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Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

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Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

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Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

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Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

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Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

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Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.

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Clinical Journal of the American Society of Nephrology

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Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases

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Ahmet Dogan

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Anthony M Valeri

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Jason D Theis

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Julie A Vrana

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Loren Herrera Hernandez

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P2860

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis

Purification and primary amino acid sequence of a novel neutrophil chemotactic factor LECT2

A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves

Immunoglobulin heavy-chain-associated amyloidosis

Renal involvement in systemic amyloidosis--an Italian retrospective study on epidemiological and clinical data at diagnosis.

Glomeruli of Dense Deposit Disease contain components of the alternative and terminal complement pathway.

Classification of amyloidosis by laser microdissection and mass spectrometry-based proteomic analysis in clinical biopsy specimens.

Mass spectrometry-based proteomic diagnosis of renal immunoglobulin heavy chain amyloidosis.

Medullary amyloidosis associated with apolipoprotein A-IV deposition.

Prevalence and morphology of leukocyte chemotactic factor 2-associated amyloid in renal biopsies.

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