Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases. (Q31118069)

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1 March 2020

title

Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases (English)

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4

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author name string

Samar M Said

1

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1 March 2020

Sanjeev Sethi

2

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Anthony M Valeri

3

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Lynn D Cornell

5

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1 March 2020

Mary E Fidler

6

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1 March 2020

Loren Herrera Hernandez

7

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Julie A Vrana

8

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Jason D Theis

9

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Patrick S Quint

10

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Ahmet Dogan

11

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Samih H Nasr

12

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publication date

23 May 2013

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Clinical Journal of the American Society of Nephrology

1 March 2020

published in

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volume

8

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issue

9

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page(s)

1515-1523

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The diagnosis and characteristics of renal heavy-chain and heavy/light-chain amyloidosis and their comparison with renal light-chain amyloidosis

1 March 2020

cites work

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

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

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Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosis

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Leukocyte chemotactic factor 2: A novel renal amyloid protein

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New insights into systemic amyloidosis: the importance of diagnosis of specific type

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

21 June 2018

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Immunoglobulin light and heavy chain amyloidosis AL/AH: renal pathology and differential diagnosis

21 June 2018

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Immunohistochemical classification of amyloid in surgical pathology revisited.

21 June 2018

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

21 June 2018

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Molecular mechanisms of amyloidosis

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

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21 June 2018

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Human lysozyme gene mutations cause hereditary systemic amyloidosis

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12 December 2020

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12 December 2020

Identifiers

DOI

10.2215/CJN.10491012

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1 March 2020

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