Results 101 to 110 of about 1,268 (176)

Abstract

JPGN Reports, Volume 6, Issue S2, Page S1-S814, September 2025.
wiley   +1 more source

Treatment failure in celiac disease due to coexistent exocrine pancreatic insufficiency [PDF]

, 1987
A 17-year-old white adolescent had a history of chronic diarrhea, delayed puberty, and growth failure. Investigations excluded cystic fibrosis, Shwachman syndrome, and endocrine causes of growth failure.
Weizman, Z., Cleghorn, G.J., Kopelman, H.R., Durie, P.R., Hamilton, J.R.   +4 more
core  

UEG Week 2024 Moderated Posters

United European Gastroenterology Journal, Volume 12, Issue S8, Page 201-664, October 2024.
wiley   +1 more source

[Implementation of the neonatal cystic fibrosis screening program in Switzerland: beginning January 2011] [PDF]

, 2011
The diagnosis of cystic fibrosis (CF) is often delayed because of the nonspecificity of a wide variety of clinical symptoms at disease onset. Newborn screening for CF has been advocated to reduce delays in diagnosis, facilitating preventive care for ...
Mornand, Anne, Hafen, Gaudenz, Barben, Jürg   +2 more
core  

Dépistage néonatal systématique de la mucoviscidose en Suisse: dès janvier 2011 [PDF]

, 2011
The diagnosis of cystic fibrosis (CF) is often delayed because of the nonspecificity of a wide variety of clinical symptoms at disease onset. Newborn screening for CF has been advocated to reduce delays in diagnosis, facilitating preventive care for ...
Mornand, Anne, Hafen, Gaudenz, Barben, Jürg   +2 more
core  

Exocrine Pancreatic Dysfunction in Malnourished Australian Aboriginal Children [PDF]

, 1991
Pancreatic exocrine dysfunction has been frequently recorded in protein-energy malnutrition in underdeveloped countries. In addition, the pancreas requires optimal nutrition for enzyme synthesis and potentially correctable pancreatic enzyme insufficiency
Greer, R, Bowling, F. G., Shepherd, R. W., Forrest, Y., Erlich, J, Cleghorn, GJ, Holt, TL, Shepherd, RW, Cleghorn, G. J., Bowling, FG, Holt, T. L., Ehrlich, J., Forrest, Y, Greer, R.   +13 more
core  

Dépistage néonatal systématique de la mucoviscidose en Suisse: dès janvier 2011 [Implementation of the neonatal cystic fibrosis screening program in Switzerland: beginning January 2011]. [PDF]

, 2011
The diagnosis of cystic fibrosis (CF) is often delayed because of the nonspecificity of a wide variety of clinical symptoms at disease onset. Newborn screening for CF has been advocated to reduce delays in diagnosis, facilitating preventive care for ...
Barben, J., Mornand, A., Hafen, G.
core  

Commercially Bottled Purified Water as an Alternative Instrument Feed Water in Automated Time-Resolved Fluorescent Immunoassay for TSH, 17-OHP and IRT in Neonatal Screening

Philippine Journal of Pathology, 2018
Objective. The study was undertaken to determine if commercially bottled purified water can be used as substitute instrument feed water for three (3) newborn screening immunoassays. Methdology.
Emilio Villanueva III, Roel Martin Bumalay, John Michael Rivera   +2 more
doaj  

363 Monthly variation in newborn screening immunoreactive trypsinogen concentrations [IRT]

Journal of Cystic Fibrosis, 2007
Montgomery, M.D., Lim, V., Menon, S., Larsen, C.L., Wilde, H.M., Bridge, P.J., Lyon, M.E.   +6 more
openaire   +1 more source

476 How stable is immunoreactive trypsinogen (IRT) on newborn screening cards?

Journal of Cystic Fibrosis, 2006
Larsen, C.L., Menoe, S., Semple, L., Bridge, P.J., Montgomery, M.D., Lyon, M.D.   +5 more
openaire   +1 more source