(Q51203911)

English

Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys.

scientific article published in November 1967

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys. (English)

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

liver cirrhosis

0 references

author name string

Passarge E

1

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

McAdams AJ

2

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

language of work or name

0 references

publication date

1 November 1967

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

The Journal of Pediatrics

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

71

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

691-702

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

5

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980205-1

7 January 2021

Retinal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980205-1

7 January 2021

STUDIES OF A FAMILY WITH THE ORAL-FACIAL-DIGITAL SYNDROME.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980205-1

7 January 2021

PELIZAEUS-MERZBACHER DISEASE. A STUDY IN NOSOLOGY

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980205-1

7 January 2021

MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980205-1

7 January 2021

Metachromatic leukodystrophy (sulfatide lipidoses) cultured in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980205-1

7 January 2021

Oral-facial-digital syndrome, with polycystic kidneys and liver: pathological and cytogenetic studies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980205-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0022-3476(67)80205-1

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

1 reference

Europe PubMed Central

1 April 2018

http://europepmc.org/abstract/MED/4383264

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q51203911&oldid=1390719018"