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Alport syndrome
scientific article published on 01 November 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Alport syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
main subject
Alport syndrome
1 reference
based on heuristic
inferred from title
author name string
C E Kashtan
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
A F Michael
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
language of work or name
English
0 references
publication date
1 November 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
published in
Kidney International
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
volume
50
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
page(s)
1445-1463
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ki.1996.459
0 references
cites work
HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A network model for the organization of type IV collagen molecules in basement membranes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The role of the main noncollagenous domain (NC1) in type IV collagen self-assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Attachment of cells to basement membrane collagen type IV.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Binding of laminin to type IV collagen: a morphological study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Models for the self-assembly of basement membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Colocalization of the genes for the alpha 3(IV) and alpha 4(IV) chains of type IV collagen to chromosome 2 bands q35-q37
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a novel sequence element in the common promoter region of human collagen type IV genes, involved in the regulation of divergent transcription
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of human collagen type IV genes is regulated by transcriptional and post-transcriptional mechanisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of a novel transcriptional silencer in the human collagen type IV gene COL4A2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genes COL4A5 and COL4A6, coding for basement membrane collagen chains alpha 5(IV) and alpha 6(IV), are located head-to-head in close proximity on human chromosome Xq22 and COL4A6 is transcribed from two alternative promoters
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization and expression of multiple alternatively spliced transcripts of the Goodpasture antigen gene region. Goodpasture antibodies recognize recombinant proteins representing the autoantigen and one of its alternative forms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basement membrane collagen in the kidney: regional localization of novel chains related to collagen IV
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of novel basement membrane components in the developing human kidney and eye.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative distribution of the alpha 1(IV), alpha 5(IV), and alpha 6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential expression of two basement membrane collagen genes, COL4A6 and COL4A5, demonstrated by immunofluorescence staining using peptide-specific monoclonal antibodies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Goodpasture antigen of the glomerular basement membrane: localization to noncollagenous regions of type IV collagen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic heterogeneity of Alport syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of classic Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of the gene for X-linked Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene mapping in Alport families with different basement membrane antigenic phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage studies in X-linked Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the COL4A5 collagen gene in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Different mutations in the COL4A5 collagen gene in two patients with different features of Alport syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of the COL4A5 gene in patients with Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alport syndrome caused by a 5' deletion within the COL4A5 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Major rearrangements in the α5(IV) collagen gene in three patients with alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expression.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alport syndrome and diffuse leiomyomatosis: Deletions in the 5′ end of the COL4A5 collagen gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the alpha 2(IV) basement membrane collagen gene of Caenorhabditis elegans produce phenotypes of differing severities.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of four novel mutations in the COL4A5 gene of patients with Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
COL4A5 splice site mutation and alpha 5(IV) collagen mRNA in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A splicing mutation in the alpha 5(IV) collagen gene of a family with Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An 8 bp deletion in exon 51 of the COL4A5 gene of an Alport syndrome patient
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the COL4A5 gene in Alport syndrome: a possible mutation in primordial germ cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Goodpasture antigen in Alport's syndrome: studies with a monoclonal antibody
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distribution of the alpha 1 and alpha 2 chains of collagen IV and of collagens V and VI in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunohistochemical study of alpha 1-5 chains of type IV collagen in hereditary nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of variant Alport phenotypes using an Alport-specific antibody probe.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetics of hereditary nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coordinate gene expression of the alpha3, alpha4, and alpha5 chains of collagen type IV. Evidence from a canine model of X-linked nephritis with a COL4A5 gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Seminars in medicine of the Beth Israel Hospital, Boston. Mutations in collagen genes as a cause of connective-tissue diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ANTERIOR LENTICONUS IN FAMILIAL HEMORRHAGIC NEPHRITIS. DEMONSTRATION OF LENS PATHOLOGY
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lens capsule abnormalities in Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nephritis. Early clinical, functional, and morphological studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Healthy female carriers of a gene for the Alport syndrome: Importance for genetic counseling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical spectrum of hereditary nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Überlegungen Zur Pathogenese Des Cochleo-Renalen Syndroms: Considerations on the Pathogenesis of the Cochleo-renal Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Concomitant progressive deafness, chronic nephritis, and ocular lens disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ocular findings in Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ocular signs in Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Posterior polymorphous dystrophy and Alport syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diffuse leiomyomatosis in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscular hypertrophy of the oesophagus and "Alport-like" glomerular lesions in a boy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in females
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alport’s Syndrome Associated with Macrothrombopathic Thrombocytopenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nephritis, deafness and abnormal thrombopoiesis. Study of a new kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary Thrombocytopenia, Deafness, and Renal Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Successful renal transplantation for Epstein syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nonfamilial hematuria associated with glomerular basement membrane alterations characteristic of hereditary nephritis: comparison with hereditary nephritis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alport's syndrome: specificity and pathogenesis of glomerular basement membrane alterations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glomerular basement membrane attenuation in familial nephritis and "benign" hematuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chronic hereditary nephritis. A clinicopathologic study of 23 new kindreds and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
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.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The thin glomerular basement membrane in children with haematuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal biopsy and family studies in 65 children with isolated hematuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A monoclonal antibody marker for Alport syndrome identifies the Alport antigen as the alpha 5 chain of type IV collagen.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunochemical studies of the Alport antigen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Erroneous genetic risk assessment of Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Outcome of thirty patients with Alport's syndrome after renal transplantation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The development of anti-glomerular basement membrane nephritis in two children with Alport's syndrome after renal transplantation: characterization of the antibody target
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal allograft survival according to primary diagnosis: a report of the North American Pediatric Renal Transplant Cooperative Study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acute Crescentic Glomerulonephritis Associated with Antiglomerular Basement Membrane Antibody in Alport's Syndrome After Second Transplantation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The pathogenesis of Alport syndrome involves type IV collagen molecules containing the alpha 3(IV) chain: evidence from anti-GBM nephritis after renal transplantation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular approach to inherited kidney disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal transplantation from living donor parents in two brothers with Alport syndrome. Can asymptomatic female carriers of the Alport gene be accepted as kidney donors?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.459
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/KI.1996.459
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
PubMed publication ID
8914010
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8914010
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8914010%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
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