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Cystic fibrosis with meconium ileus
Known as:
Meconium obstruction of intestine in mucoviscidosis
, meconium ileus cystic fibrosis
A congenital metabolic detected in the neonatal period that is characterized by the presence of a meconium ileus. The disease affects the exocrine…
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National Institutes of Health
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Related topics
Related topics
7 relations
Congenital fecaliths
Cystic Fibrosis
Delayed passage of meconium
Exocrine pancreas
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Broader (1)
Neonatal disorder
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Intestinal complications of cystic fibrosis
D. Borowitz
,
D. Gelfond
Current opinion in pulmonary medicine
2013
Corpus ID: 22318561
Purpose of review The article reviews advances in gastrointestinal aspects of cystic fibrosis (CF) published in the literature…
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Review
2011
Review
2011
Guidelines for the diagnosis and management of distal intestinal obstruction syndrome in cystic fibrosis patients.
C. Colombo
,
H. Ellemunter
,
R. Houwen
,
A. Munck
,
Chris Taylor
,
M. Wilschanski
Journal of Cystic Fibrosis
2011
Corpus ID: 24347445
Highly Cited
2010
Highly Cited
2010
Defining DIOS and Constipation in Cystic Fibrosis With a Multicentre Study on the Incidence, Characteristics, and Treatment of DIOS
R. Houwen
,
H. V. D. van der Doef
,
+7 authors
M. Wilschanski
Journal of Pediatric Gastroenterology and…
2010
Corpus ID: 32861812
Objectives: Various definitions for distal intestinal obstruction syndrome (DIOS), meconium ileus equivalent, and constipation in…
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2003
2003
Treatment of gastrointestinal problems in cystic fibrosis
M. Mascarenhas
Current treatment options in gastroenterology
2003
Corpus ID: 39412366
Opinion statementThe gastrointestinal (GI) manifestations of cystic fibrosis (CF) are varied and include pancreatic insufficiency…
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Highly Cited
1998
Highly Cited
1998
Gastro-oesophageal reflux in infants under 6 months with cystic fibrosis
R. Heine
,
B. Button
,
A. Olinsky
,
P. Phelan
,
A. Catto-Smith
Archives of Disease in Childhood
1998
Corpus ID: 516160
AIM To establish the incidence of pathological gastro-oesophageal reflux (GOR) in newly diagnosed infants with cystic fibrosis…
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Highly Cited
1996
Highly Cited
1996
Deficiency of vitamins E and A in cystic fibrosis is independent of pancreatic function and current enzyme and vitamin supplementation
L. Lancellotti
,
C. D'Orazio
,
G. Mastella
,
G. Mazzi
,
U. Lippi
European Journal of Pediatrics
1996
Corpus ID: 23027317
AbstractThe aim of this study was to evaluate to what extent serum vitamins A and E in cystic fibrosis are affected by the…
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Review
1994
Review
1994
Agenesis of pancreas
P. Voldsgaard
,
N. Kryger‐Baggesen
,
I. Lisse
Acta paediatrica
1994
Corpus ID: 31320055
Complete agenesis of pancreas is a rare and lethal condition. Four cases have previously been reported in combination with other…
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Highly Cited
1993
Highly Cited
1993
Correlation between genotype and phenotype in patients with cystic fibrosis
C. Boeck
1993
Corpus ID: 19864760
Review
1992
Review
1992
Cystic fibrosis: gastrointestinal complications.
J. Littlewood
British Medical Bulletin
1992
Corpus ID: 24138035
An individual who has cystic fibrosis (CF) may suffer from gastrointestinal problems related to inadequately controlled…
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Review
1983
Review
1983
Incidence of Distal Intestinal Obstruction Syndrome in Cystic Fibrosis
B. Rosenstein
,
T. Langbaum
Journal of Pediatric Gastroenterology and…
1983
Corpus ID: 43204426
A variety of intestinal complications, including constipation, abdominal pain, palpable cecal masses, intestinal obstruction…
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