(Q37747364)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

review article

1 reference

title

Ultrastructural aspects of enterocyte defects in infancy and childhood (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

author name string

Theodore C Iancu

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

language of work or name

1 reference

1 May 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

Ultrastructural Pathology

2 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

volume

34

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

page(s)

117-125

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation

2 February 2020

cites work

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

Navajo microvillous inclusion disease is due to a mutation in MYO5B.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

Congenital disorder of glycosylation (CDG)-Ih patient with a severe hepato-intestinal phenotype and evolving central nervous system pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

Cryptogenic liver disease in four children: a novel congenital disorder of glycosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

Morphometric analysis of small intestinal mucosa. I. Methodology, epithelial volume compartments and enumeration of inter-epithelial space lymphocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

Quantitation of intraepithelial lymphocytes in human duodenum: what is normal?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

The intestinal microvillus. Ultrastructural variability in coeliac disease and cow's milk intolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

Simple method for diagnosing protein-losing enteropathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

The role of the microsomal triglygeride transfer protein in abetalipoproteinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913121003648410

10.3109/01913121003648410

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20455660%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference