(Q34003555)

30 July 2017

1 reference

title

Small-intestinal abnormalities in cystic fibrosis patients (English)

1 reference

30 July 2017

0 references

E. Eggermont

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1743211

14 November 2022

K. De Boeck

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1743211

14 November 2022

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=1743211

14 November 2022

publication date

1 October 1991

1 reference

full work available at URL

30 July 2017

http://link.springer.com/content/pdf/10.1007/BF01954999.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF01954999/fulltext.html

14 November 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF01954999

14 November 2022

1 reference

European Journal of Pediatrics

14 November 2022

published in

1 reference

30 July 2017

150

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30 July 2017

12

1 reference

30 July 2017

824-828

1 reference

https://scigraph.springernature.com/pub.10.1007/bf01954999

30 July 2017

0 references

cites work

Meconium in health and in disease

1 reference

12 December 2020

Enhanced intestinal glucose and alanine transport in cystic fibrosis

1 reference

12 December 2020

LIGHT AND ELECTRON MICROSCOPIC EXAMINATION OF THE SMALL BOWEL OF CHILDREN WITH CYSTIC FIBROSIS

1 reference

12 December 2020

Prenatal diagnosis of cystic fibrosis by assay of amniotic fluid microvillar enzymes

1 reference

12 December 2020

Coprologic anomaly in mucoviscidosis. Presence of albumin in low concentration in the feces

1 reference

12 December 2020

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

12 December 2020

Small intestinal permeability and orocaecal transit time in cystic fibrosis

1 reference

12 December 2020

Fetal abnormalities in cystic fibrosis suggest a deficiency in proteolysis of cholecystokinin

1 reference

12 December 2020

Ileal pH in cystic fibrosis

1 reference

12 December 2020

Evidence for a prostaglandin-independent defect in chloride reabsorption in the loop of henle as a proximal cause of Bartter's syndrome

1 reference

12 December 2020

Pancreatic function testing in meconium disease in cystic fibrosis

1 reference

12 December 2020

Gastrointestinal manifestations of cystic fibrosis: a review

1 reference

12 December 2020

Comparison of gastrointestinal pH in cystic fibrosis and healthy subjects

1 reference

12 December 2020

The role of the small intestine in cystic fibrosis patients.

1 reference

12 December 2020

Enzymic activities in meconium from human foetuses and newborns

1 reference

12 December 2020

Prenatal diagnosis of cystic fibrosis. II. Meconium ileus in affected fetuses

1 reference

12 December 2020

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

1 reference

12 December 2020

Meconium ileus equivalent complicating cystic fibrosis in postneonatal children and young adults. Report of 12 cases

1 reference

12 December 2020

Prenatal detection of cystic fibrosis; comparative study of maltase and alkaline phosphatase activities in amniotic fluid

1 reference

12 December 2020

Enhanced glucose absorption in the jejunum of patients with cystic fibrosis

1 reference

12 December 2020

Pancreozymin secretin test of exocrine pancreatic funtion in cystic fribrosis and the significance of the result for the pathogenesis of the disease

1 reference

12 December 2020

Human intestinal mucin in cystic fibrosis

1 reference

12 December 2020

The molecular basis of chloride channel dysregulation in cystic fibrosis

1 reference

12 December 2020

Hormonal abnormalities of the pancreas and gut in cystic fibrosis

1 reference

12 December 2020

Excessive faecal losses of vitamin A (retinol) in cystic fibrosis.

1 reference

12 December 2020

Lactulose-rhamnose intestinal permeability in children with cystic fibrosis

1 reference

12 December 2020

A right lower quadrant mass in cystic fibrosis: a diagnostic challenge

1 reference

12 December 2020

1 reference

12 December 2020

Intestinal permeability to [51Cr]EDTA in children with cystic fibrosis

1 reference

12 December 2020

Intestinal mucins from normal subjects and patients with cystic fibrosis. Variable contents of the disulphide-bound 118 kDa glycoprotein and different reactivities with an anti-(118 kDa glycoprotein) antibody

1 reference

12 December 2020

Disaccharidases in amniotic fluid as possible prenatal marker for cystic fibrosis

1 reference

12 December 2020

Modern problems in paediatrics

32

11

137

K Launiala

1968

1 reference

Archives francaises de pediatrie

14 November 2022

43

32

733

Y Pecau

1975

1 reference

14 November 2022

Identifiers

DOI

10.1007/BF01954999

1 reference

Dimensions Publication ID

30 July 2017

0 references

1 reference