(Q43547193)

24 November 2017

title

Ocular histopathologic changes in a case of a-beta-lipoproteinemia (Bassen-Kornzweig syndrome) (English)

1 reference

7 May 2023

1 reference

7 May 2023

author name string

L. Von Sallmann

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5359538

7 May 2023

A. H. Gelderman

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5359538

7 May 2023

L. Laster

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5359538

7 May 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5359538

7 May 2023

publication date

1 January 1969

1 reference

full work available at URL

24 November 2017

http://link.springer.com/content/pdf/10.1007/BF00944003.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00944003/fulltext.html

7 May 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00944003

7 May 2023

1 reference

Documenta Ophthalmologica

7 May 2023

published in

1 reference

24 November 2017

volume

26

1 reference

24 November 2017

page(s)

451-460

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00944003

24 November 2017

exact match

0 references

cites work

Retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5359538

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

CONGENITAL BETA-LIPOPROTEIN DEFICIENCY: AN HEREDITARY DISORDER INVOLVING A DEFECT IN THE ABSORPTION AND TRANSPORT OF LIPIDS

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5359538

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

DEMYELINATING CENTRAL NERVOUS SYSTEM DISEASE, MACULAR ATROPHY AND ACANTHOCYTOSIS (BASSEN-KORNZWEIG SYNDROME)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5359538

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/BF00944003

1 reference

24 November 2017

1 reference