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English
The clinical spectrum of hereditary nephritis
scientific article published on 01 January 1985
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
title
The clinical spectrum of hereditary nephritis
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
author name string
J P Grünfeld
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
language of work or name
English
0 references
publication date
1 January 1985
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
published in
Kidney International
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
volume
27
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
page(s)
83-92
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ki.1985.14
0 references
cites work
Familial thrombocytopenia, elevated serum IgA levels and renal disease. A report of a kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A hereditary renal disease with clinical and histological picture as in chronic glomerulonephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new form of familial glomerulonephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial and nonfamilial benign hematuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FAMILIAL ASPECTS OF DIFFUSE RENAL DISEASES.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alport's syndrome. A report of 58 cases and a review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary Nephritis: A Re-examination of its Clinical and Genetic Features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive and nonprogressive hereditary chronic nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A follow-up study of hereditary chronic nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Etiology of Deafness in Alport's Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cochlear Abnormalities in Alport's Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HEREDITARY PHOTOMYOCLONUS ASSOCIATED WITH DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary renal disease with neurosensory hearing loss, prolinuria and ichthyosis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperuricemia and neurologic deficits. A family study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial nephrosis, nerve deafness, and hypoparathyroidism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal tubular acidosis and sensorineural deafness: an autosomal recessive syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Anterior lenticonus and Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hereditary nephropathy (Alport's syndrome)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary macrothrombocytopathia, nephritis and deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary Nephritis Associated with May-Hegglin Anomaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Antithyroid antibodies in Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nephropathy with nerve deafness (Alport's syndrome). Electron microscopic studies on the renal glomerulus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GLOMERULONEPHRITIS IN TWO SETS OF IDENTICAL TWINS. ELECTRON MICROSCOPIC STUDIES OF RENAL BIOPSY SPECIMENS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diffuse familial nephropathy: A clinicopathological study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development of the characteristic ultrastructural lesion of hereditary nephritis during the course of the disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Split and extremely thin glomerular basement membranes in hereditary nephropathy (Alport's syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The glomerular basal lamina in hereditary nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolated hematuria in children: indications for a renal biopsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basement membrane nephropathy: a new classification for Alport's syndrome and asymptomatic hematuria based on ultrastructural findings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nephritis with a characteristic renal lesion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of Goodpasture's Antigen in Male Patients With Familial Nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnosis of hereditary nephritis by failure of glomeruli to bind anti-glomerular basement membrane antibodies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nephritis. Clinical spectrum and mode of inheritance in five new kindreds
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial nephritis associated with the nephrotic syndrome. In a family with severe involvement in females
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HEREDITARY NEPHRITIS. REPORT OF A KINDRED
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemodynamically mediated glomerular injury and the progressive nature of kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1985.14
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/KI.1985.14
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
PubMed ID
3981875
1 reference
stated in
Europe PubMed Central
PubMed ID
3981875
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3981875%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 October 2019
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