(Q21203045)

Dimensions

1050159098

18 August 2022

Jacques Schmitz

series ordinal

2

author given names

Jacques

author last names

Schmitz

1 reference

Dimensions

1050159098

18 August 2022

Olivier Goulet

series ordinal

3

author given names

Olivier

author last names

Goulet

1 reference

Dimensions

1050159098

Orphanet Journal of Rare Diseases

18 August 2022

language of work or name

English

0 references

publication date

26 June 2006

5 references

23 March 2019

21 March 2019

30 June 2019

12 October 2019

1 September 2020

5 references

23 March 2019

21 March 2019

30 June 2019

12 October 2019

1 September 2020

1

0 references

issue

1

0 references

page(s)

22

0 references

copyright license

Creative Commons Attribution 2.0 Generic

5 references

23 March 2019

21 March 2019

30 June 2019

12 October 2019

on focus list of Wikimedia project

1 September 2020

copyright status

copyrighted

0 references

ScienceSource

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/1750-1172-1-22

0 references

cites work

Acetylated sialic acid residues and blood group antigens localise within the epithelium in microvillous atrophy indicating internal accumulation of the glycocalyx

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Autophagocytosis of the apical membrane in microvillus inclusion disease

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Microvillous inclusion disease: an evolving condition.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Siblings with microvillous inclusion disease

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Congenital microvillous atrophy: specific diagnostic features

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Familial microvillous atrophy: a clinicopathological survey of 23 cases

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Familial enteropathy: A syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Microvillus inclusion disease: specific diagnostic features shown by alkaline phosphatase histochemistry

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Microvillous inclusion disease. The importance of electron microscopy for diagnosis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

Disorders of the cytoskeleton of the enterocyte.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1523325

New perspectives for children with microvillous inclusion disease: early small bowel transplantation

30 May 2018

1 reference

12 December 2020

CD10: a valuable tool for the light microscopic diagnosis of microvillous inclusion disease (familial microvillous atrophy)

1 reference

12 December 2020

Recurrent episodes of necrotizing enterocolitis complicating congenital microvillous atrophy

1 reference

12 December 2020

Enterocyte apoptosis and proliferation are increased in microvillous inclusion disease (familial microvillous atrophy)

1 reference

12 December 2020

Treatment of microvillus inclusion disease by intestinal transplantation

1 reference

12 December 2020

Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies

1 reference

12 December 2020

[CD10 expression in a case of microvillous inclusion disease]

1 reference

12 December 2020

Abnormal expression of brush-border membrane transporters in the duodenal mucosa of two patients with microvillus inclusion disease

1 reference

12 December 2020

Successful intestinal transplantation for microvillus inclusion disease

1 reference

12 December 2020

The constitutive exocytotic pathway in microvillous atrophy

1 reference

12 December 2020

The value of polyclonal carcinoembryonic antigen immunostaining in the diagnosis of microvillous inclusion disease

1 reference

12 December 2020

Combined bowel-liver transplantation in an infant with microvillous inclusion disease

1 reference

12 December 2020

Pancreatic Function in the Reserpinized Rabbit—a Model for Cystic Fibrosis. I. Effect of Secretin

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1750-1172-1-22

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1186/1750-1172-1-22

0 references