(Q35899321)

11 August 2017

Charcot-Marie-Tooth disease and nephritis (English)

1 reference

11 August 2017

G. Lemieux

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6054293

28 July 2023

J. A. Neemeh

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6054293

28 July 2023

language of work or name

English

0 references

publication date

1 November 1967

1 reference

PMCID

1923627

full work available at URL

11 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/6054293/pdf/?tool=EBI

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%3A6054293

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/6054293/?tool=EBI

28 July 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6054293

https://europepmc.org/articles/PMC1923627

28 July 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6054293

https://europepmc.org/articles/PMC1923627?pdf=render

28 July 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%3A6054293

Canadian Medical Association Journal

28 July 2023

published in

1 reference

11 August 2017

97

1 reference

11 August 2017

20

1 reference

11 August 2017

1193-1198

1 reference

A genetic study of hereditary renal dysfunction with associated nerve 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=1923627

CONGENITAL RENAL DISEASE, DEAFNESS AND MYOPIA IN ONE FAMILY.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1923627

Alport's syndrome of hereditary nephritis with deafness.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1923627

Hereditary nephropathy, deafness and renal foam cells.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1923627

Hereditary renal disease associated with nerve deafness and ocular lesions.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1923627

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

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1923627

Hereditary Renal Disease Associated with Deafness-Alport's Syndrome

24 September 2018

1 reference

12 December 2020

POLYNEUROPATHY IN CHRONIC RENAL INSUFFICIENCY

1 reference

12 December 2020

Charcot-Marie-Tooth disease with associated myopathy. A report of a family

1 reference

12 December 2020

A clinical study of hereditary interstitial pyelonephritis

1 reference

12 December 2020

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

1 reference

12 December 2020

Uremic polyneuropathy

1 reference

12 December 2020

Familial glomerulonephritis and aminoaciduria

1 reference

12 December 2020

Hereditary interstitial nephritis associated with polyneuropathy

1 reference

12 December 2020

[CHARCOT-MARIE AMYOTROPHY ASSOCIATED WITH A BILATERAL OPTIC ATROPHY.]

1 reference

12 December 2020

CHARCOT-MARIE-TOOTH DISEASE

1 reference

12 December 2020

The hereditary renal diseases

1 reference

12 December 2020

[Case of Friedreich disease with Charcot-Marie amyotrophy clinical study.]

1 reference

12 December 2020

Vertebral deformities and other anomalies in Charcot-Marie-Tooth disease

1 reference

12 December 2020

Identifiers

PMCID

1923627

1 reference

11 August 2017

1 reference

PMCID

1923627