(Q51122241)

30 March 2018

title

Neurologic Disorders and Liver Disease (English)

1 reference

https://api.crossref.org/works/10.1080/00325481.1971.11697596

26 March 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4999165

26 March 2023

author name string

S. O'Reilly

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4999165

26 March 2023

language of work or name

English

0 references

publication date

1 September 1971

1 reference

30 March 2018

full work available at URL

http://www.tandfonline.com/doi/pdf/10.1080/00325481.1971.11697596

1 reference

https://api.crossref.org/works/10.1080/00325481.1971.11697596

26 March 2023

published in

Postgraduate Medicine

1 reference

30 March 2018

volume

50

1 reference

30 March 2018

issue

3

1 reference

30 March 2018

page(s)

126-133

1 reference

30 March 2018

PORTAL-SYSTEMIC ENCEPHALOPATHY NEUROLOGICAL COMPLICATIONS OF LIVER DISEASE

cites work

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

Spastic paraparesis following portacaval shunts

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

Persistent choreo-athetotic movements in liver disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

Neonatal hyperbilirubinemia and kernicterus. Experimental support for treatment by exposure to visible light

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

Beta-galactosidase deficiency in the hurler syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

Gargoylism: hydrolysis of beta-galactosides and tissure accumulation of galactose- and mannose-containing compounds

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00325481.1971.11697596

The Quarterly Journal of Medicine

21 January 2018

2

20

421

Walshe JM

1951

1 reference

https://api.crossref.org/works/10.1080/00325481.1971.11697596

Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea

26 March 2023

series ordinal

11

1 reference

https://api.crossref.org/works/10.1080/00325481.1971.11697596

26 March 2023

Phenylalaninemia

series ordinal

18

1 reference

https://api.crossref.org/works/10.1080/00325481.1971.11697596

26 March 2023

Identifiers

1 reference

30 March 2018

release_qvly3rj57vdldcxax356rm6uzq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/qvly3rj57vdldcxax356rm6uzq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

30 March 2018