(Q30501666)

11 August 2017

0 references

Hereditary nephropathy with hematuria (Alport's syndrome) (English)

1 reference

11 August 2017

1 reference

A. Chiricosta

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

17 March 2023

S. L. Jindal

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

17 March 2023

J. Metuzals

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

17 March 2023

B. Koch

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

17 March 2023

language of work or name

English

0 references

publication date

1 February 1970

1 reference

PMCID

1946490

11 August 2017

28 February 1970

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4905862

full work available at URL

17 March 2023

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4905862/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4905862/pdf/?tool=EBI

17 March 2023

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

https://europepmc.org/articles/PMC1946490

17 March 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

https://europepmc.org/articles/PMC1946490?pdf=render

17 March 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4905862

Canadian Medical Association Journal

17 March 2023

published in

1 reference

11 August 2017

102

1 reference

11 August 2017

396-401

1 reference

11 August 2017

4

1 reference

Abnormal Segregation in Hereditary Renal Disease with Deafness

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

A genetic study of hereditary renal dysfunction with associated nerve deafness

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Apparent free amino acids in deproteinized plasma of normal and uremic persons

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Hereditary hematuria, nephropathy and deafness; preliminary report.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Charcot-Marie-Tooth disease and nephritis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Pathological findings in patients with tyrosinemia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Renal pathology in hereditary nephritis with nerve deafness.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Pathology of end-stage kidney disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Immunosuppressive therapy of chronic renal disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Familial Hyperprolinemia, Cerebral Dysfunction and Renal Anomalies Occurring in a Family with Hereditary Nephropathy and Deafness

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Alport's syndrome of hereditary nephritis with deafness.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Hereditary nephropathy, deafness and renal foam cells.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Clinical experiences with kanamycin.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Hereditary renal disease associated with nerve deafness and ocular lesions.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

The pathogenesis of glomerulonephritis

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1946490

26 November 2018

1 reference

12 December 2020

[The periodic disease]

1 reference

12 December 2020

1 reference

12 December 2020

Histopathologic changes in methionine excess

1 reference

12 December 2020

A follow-up study of hereditary chronic nephritis

1 reference

12 December 2020

A clinical study of hereditary interstitial pyelonephritis

1 reference

12 December 2020

Kanamycin nephrotoxicity

1 reference

12 December 2020

Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland

1 reference

12 December 2020

HEREDITARY NEPHRITIS. REPORT OF A KINDRED

1 reference

12 December 2020

Congenital hereditary hematuria

1 reference

12 December 2020

[A hereditary kidney disease with hematuria as the principle symptom.]

1 reference

12 December 2020

Familial glomerulonephritis and aminoaciduria

1 reference

12 December 2020

Alport's syndrome (hereditary nephritis with deafness

1 reference

12 December 2020

Hereditary interstitial nephritis associated with polyneuropathy

1 reference

12 December 2020

Hereditary factors in chronic Bright's disease; a study of two affected kindreds

1 reference

12 December 2020

Familial hematuric nephritis

1 reference

12 December 2020

Angiokeratoma corporis diffusum universale (Fabry); first American report of a rare disorder

1 reference

12 December 2020

HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS

1 reference

12 December 2020

CONGENITAL HEREDITARY NEPHRITIS WITH NERVE DEAFNESS

1 reference

12 December 2020

The spectrum of hereditary renal diseases

1 reference

12 December 2020

ANTERIOR LENTICONUS IN FAMILIAL HEMORRHAGIC NEPHRITIS. DEMONSTRATION OF LENS PATHOLOGY

1 reference

12 December 2020

Renal dysplasia in a family with multiple hereditary abnormalities including iliac horns

1 reference

12 December 2020

Identifiers

PMCID

1946490

1 reference

11 August 2017

1 reference

PMCID

1946490