(Q39850441)

15 September 2017

title

Chronic hereditary nephritis. A clinicopathologic study of 23 new kindreds and review of the literature (English)

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15 September 2017

Farboody GH

1

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15 September 2017

Valenzuela R

2

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15 September 2017

McCormack LJ

3

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15 September 2017

Kallen R

4

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15 September 2017

Osborne DG

5

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15 September 2017

language of work or name

English

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publication date

1 November 1979

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15 September 2017

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15 September 2017

volume

10

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15 September 2017

issue

6

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15 September 2017

page(s)

655-668

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HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

15 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Alport's syndrome of hereditary nephritis with deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Alport's syndrome. A report of three Swedish families

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary nephritis. Clinical spectrum and mode of inheritance in five new kindreds

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Renal Interstitial Foam Cells. A Light and Electron Microscopic Study

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary nephritis. Early clinical, functional, and morphological studies

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Progressive and nonprogressive hereditary chronic nephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Idiopathic hematuria of childhoodPathologic findings in the Kidney in six patients

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Development of the characteristic ultrastructural lesion of hereditary nephritis during the course of the disease

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary nephropathy with nerve deafness (Alport's syndrome). Electron microscopic studies on the renal glomerulus

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

A low-viscosity epoxy resin embedding medium for electron microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Familial benign essential hematuria

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

The nephropathy of the nail-patella syndrome. Clinicopathologic analysis of 11 kindred.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

The relationship between cochlea and kidney

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Diffuse familial nephropathy: A clinicopathological study

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

A follow-up study of hereditary chronic nephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary nephritis. A poorly known entity

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Glomerulonephritis (second of three parts).

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary macrothrombocytopathia, nephritis and deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary Thrombocytopenia, Deafness, and Renal Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary renal disease with neurosensory hearing loss, prolinuria and ichthyosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Familial nephropathy associatdd with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary Nephritis (Alportʼs Syndrome) in a New Kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Antithyroid antibodies in Alport's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

In-vivo activation of complement in hereditary nephropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Population genetics of Alport's syndrome. Hypothesis of abnormal segregation and the necessary existence of mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary Nephritis: A Re-examination of its Clinical and Genetic Features

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

The Etiology of Deafness in Alport's Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Hereditary nephritis with nerve deafness. Immunofluorescent studies on the kidney, with a consideration of discordant immunoglobulin-complement immunofluorescent reactions

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

Two families with Alport's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2879%2980110-0

7 January 2021

10.1016/S0046-8177(79)80110-0

Identifiers

DOI

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15 September 2017

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