Alport's syndrome (Q33678707)

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scientific article

Language	Label	Description	Also known as
English	Alport's syndrome	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

Europe PubMed Central

Alport's syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Alport syndrome

1 reference

based on heuristic

inferred from title

author name string

Flinter F

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 April 1997

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

326-330

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Abnormal Segregation in Hereditary Renal Disease with Deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

A heredo-familial syndrome characterized by renal disease, inner ear deafness, and ocular changes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Smooth-muscle tumours of the oesophagus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Hereditary disorders of the glomerular basement membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

A mutation causing Alport syndrome with tardive hearing loss is common in the western United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Hereditary nephropathy (Alport syndrome): correlation of clinical data with glomerular basement membrane alterations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Alport's syndrome. A report of 58 cases and a review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

X-linked inheritance of Alport syndrome: family P revisited

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Hereditary macrothrombocytopathia, nephritis and deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Isolation of a collagen from basement membranes containing three identical - chains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Hereditary nephropathy with hearing loss. "Alport's syndrome"

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Localization of the gene for X-linked Alport's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Variants of Alport's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Genetics of classic Alport's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Localization of the gene for classic Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Reversal of deafness after renal transplantation in Alport's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Lenticonus anterior and Alport's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Effect of renal transplantation on uremic deafness: A Long-Term study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Antithyroid antibodies in Alport's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

21 June 2018

Alport's syndrome of hereditary nephritis with deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

30 October 2018

3rd International Workshop on Alport Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050922

30 October 2018

Hereditary nephropathy with nerve deafness (Alport's syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial interstitial nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Concomitant progressive deafness, chronic nephritis, and ocular lens disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital hereditary hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The glomerular basement membrane in benign familial hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID 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

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary Nephritis Associated with May-Hegglin Anomaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport's syndrome or hereditary nephritis?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial glomerulonephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hematuria; clinico-pathological correlations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical spectrum of hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9138159

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.34.4.326

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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