(Q41845146)

13 October 2017

Juvenile nephronophthisis associated with retinal pigmentary dystrophy, cerebellar ataxia, and skeletal abnormalities (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1008585

Juvenile nephronophthisis

14 August 2022

main subject

1 reference

1 reference

Popović-Rolović M

1

1 reference

13 October 2017

Calić-Perisíc N

2

1 reference

13 October 2017

Negovanović D

4

1 reference

13 October 2017

M. Popović-Rolović

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1008585

14 August 2022

N. Calić-Perisíc

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1008585

14 August 2022

G. Bunjevacki

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1008585

14 August 2022

D. Negovanović

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1008585

14 August 2022

language of work or name

English

0 references

publication date

1 October 1976

1 reference

full work available at URL

13 October 2017

https://europepmc.org/articles/PMC1546134

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1008585

https://europepmc.org/articles/PMC1546134?pdf=render

14 August 2022

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%3A1008585

Archives of Disease in Childhood

14 August 2022

published in

1 reference

13 October 2017

51

1 reference

13 October 2017

10

1 reference

13 October 2017

801-803

1 reference

Juvenile familial nephropathy with tapetoretinal degeneration. A new oculorenal dystrophy

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1546134

Hereditary nephritis, retinitis pigmentosa and chromosomal abnormalities

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1546134

Familial nephropathy associatdd with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1546134

Familial Renal-Retinal Dystrophy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1546134

FAMILIAL NEPHROPATHY WITH RETINITIS PIGMENTOSA; A NEW OCULORENAL SYNDROME IN ADULTS

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1008585

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Juvenile nephronophthisis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1008585

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Tubulo-interstitial nephropathy in children with tapeto-retinal degeneration (Senior's syndrome. (1 case)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1008585

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.51.10.801

1 reference

13 October 2017

1 reference

13 October 2017

1 reference