(Q36958957)

English

Familial hematuria

scientific article published on 02 October 2007

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Statements

scholarly article

1 reference

Europe PubMed Central

17 August 2017

2 references

Europe PubMed Central

3 July 2020

Familial hematuria (English)

1 reference

Europe PubMed Central

17 August 2017

urination disorder

1 reference

3 July 2020

author name string

Clifford E Kashtan

1

1 reference

Europe PubMed Central

17 August 2017

publication date

2 October 2007

1 reference

Europe PubMed Central

17 August 2017

1 October 2009

1 reference

3 July 2020

Pediatric Nephrology

2 references

Europe PubMed Central

17 August 2017

3 July 2020

24

1 reference

Europe PubMed Central

17 August 2017

1951-1958

1 reference

Europe PubMed Central

17 August 2017

10

1 reference

Europe PubMed Central

17 August 2017

copyright license

Creative Commons Attribution

1 reference

3 July 2020

copyright status

0 references

https://scigraph.springernature.com/pub.10.1007/s00467-007-0622-z

0 references

Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Renal transplantation in patients with Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Distribution of type IV collagen in the cochlea in Alport syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Retransplantation in Alport post-transplant anti-GBM disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Epidermal basement membrane alpha 5(IV) expression in females with Alport syndrome and severity of renal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Targets of alloantibodies in Alport anti-glomerular basement membrane disease after renal transplantation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Treatment of X-linked hereditary nephritis in Samoyed dogs with angiotensin converting enzyme (ACE) inhibitor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

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=2731159

29 September 2017

Ophthalmologic assessment of young patients with Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

27 June 2018

The effect of aldosterone blockade in patients with Alport syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

4 September 2018

Cyclosporin therapy in patients with Alport syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

4 September 2018

Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

4 September 2018

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

4 September 2018

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

4 September 2018

High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

4 September 2018

MYH9-Related Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

20 October 2018

Alport syndrome and the X chromosome: implications of a diagnosis of Alport syndrome in females

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolated hematuria in children: indications for a renal biopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin basement membrane nephropathy as a cause of recurrent haematuria in childhood

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal biopsy and family studies in 65 children with isolated hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID 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

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistologic studies of type IV collagen in anterior lens capsules of patients with Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemical study of alpha 1-5 chains of type IV collagen in hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal allograft survival according to primary diagnosis: a report of the North American Pediatric Renal Transplant Cooperative Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent corneal erosion associated with Alport's syndrome. Rapid communication

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular manifestations of autosomal recessive Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked Alport syndrome in females

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal biopsy diagnosis in children presenting with haematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term effects of cyclosporine A in Alport's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hematurias: what we know and what we don't

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephroprotection by antifibrotic and anti-inflammatory effects of the vasopeptidase inhibitor AVE7688

1 reference

https://pubmed.ncbi.nlm.nih.gov/17912554

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-007-0622-Z

1 reference

Europe PubMed Central

17 August 2017

1 reference

Europe PubMed Central

17 August 2017

1 reference

Europe PubMed Central

17 August 2017

ResearchGate publication ID

0 references

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