A Search Service for Abbreviation / Long Form

■ Abbreviation / Long Form : PS / pancreatic sufficiency

[Related PubMed/MEDLINE]
Total Number of Papers: 43
[Entries Per Page]
 per page
Page Control
Page: of
Abbreviation:   PS  (>> Co-occurring Abbreviation)
Long Form:   pancreatic sufficiency
 Abbreviation Variation
 Long Form Variation
 Pair(Abbreviation/Long Form) Variation
No. Year Title Co-occurring Abbreviation
2017 Pancreatic insufficiency in Cystic Fibrosis. PI
2017 Serum zinc concentration in cystic fibrosis patients with CFTR I1234V mutation associated with pancreatic sufficiency. BMI, CF, PI, Zn
2016 (13)C mixed triglyceride breath testing using infrared spectrometry: comparison of two devices in early infancy. CF, MTG, NDIRS, PI
2016 CFTR and/or pancreatitis susceptibility genes mutations as risk factors of pancreatitis in cystic fibrosis patients? AP, CF, RAP
2016 Secretin-enhanced Magnetic Resonance Cholangio-pancreatography in Pancreatic Insufficient and Pancreatic Sufficient Cystic Fibrosis Patients. CF, PI, SE-MRCP
2014 Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case-control study. CF, ICM, NPD, PI
2014 Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis. CF, PIP
2013 Differences in the pattern of structural abnormalities on CT scan in patients with cystic fibrosis and pancreatic sufficiency or insufficiency. CF, PI
2012 Vitamin D in children with cystic fibrosis. PI
10  2011 CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR. CF, CFTR
11  2010 Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data. CF, CFTR, ICM, PI
12  2010 Non-classic cystic fibrosis associated with D1152H CFTR mutation. CF, CFTR, PI
13  2010 Self-reported use of vitamins and other nutritional supplements in adult patients with cystic fibrosis. Is daily practice in concordance with recommendations? CF, PI
14  2010 Transient elastography in patients with cystic fibrosis. CF, CFLD, kPa, PI, TE
15  2009 ERGs in children with pancreatic enzyme insufficient and pancreatic enzyme sufficient cystic fibrosis. ERGs, PI, RBP
16  2009 Exocrine pancreatic function testing in patients with cystic fibrosis and pancreatic sufficiency: a correlation study. CF, CFA, IRT
17  2009 Symptomatic pancreatitis in patients with cystic fibrosis. CF, PI
18  2008 Decreased total serum coenzyme-Q10 concentrations: a longitudinal study in children with cystic fibrosis. CF, PI
19  2008 The changing face of the exocrine pancreas in cystic fibrosis: pancreatic sufficiency, pancreatitis and genotype. CF, CFTR
20  2008 The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype. CF
21  2007 Airway nitric oxide in patients with cystic fibrosis is associated with pancreatic function, Pseudomonas infection, and polyunsaturated fatty acids. AA, CF, eNO, FA, nNO, NO, PI
22  2007 Pancreatic phenotype in infants with cystic fibrosis identified by mutation screening. CF, PI
23  2007 Vitamins A and E and pulmonary exacerbations in patients with cystic fibrosis. CF, PI
24  2006 Helicobacter pylori and Clostridium difficile in cystic fibrosis patients. CD, CF
25  2005 Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype. CF, CI, PI
26  2004 CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis. cAMP, CF, CFTR
27  2004 Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood. CF, PD
28  2004 Dietary intakes in adult patients with cystic fibrosis--do they achieve guidelines? BMI, CF, CFRD, EAR, RNI
29  2004 Genotype/phenotype correlation of the G85E mutation in a large cohort of cystic fibrosis patients. CF, PI
30  2004 Pancreatitis in hispanic patients with cystic fibrosis carrying the R334W mutation. CF
31  2004 [Cystic fibrosis from the exocrine pancreatic point of view]. CF, CFTR, PI
32  2003 Longitudinal follow-up of exocrine pancreatic function in pancreatic sufficient cystic fibrosis patients using the fecal elastase-1 test. CF, EPF, PI
33  2002 The pancreas in cystic fibrosis. CF
34  2002 Urogenital abnormalities in male children with cystic fibrosis. CBAVD, CF, PI
35  2002 Variability of fecal pancreatic elastase measurements in cystic fibrosis patients. CF, EL-1, PD, PI
36  2001 Neonatal screening for cystic fibrosis: long-term clinical balance. CF, PI, PI
37  2000 Evaluation of fecal pancreatic elastase-1 as a measure of pancreatic exocrine function in children with cystic fibrosis. CF, EL-1, PI
38  1995 Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosis. PI
39  1993 Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis. CF, CFTR, PI
40  1992 Genetic determination of exocrine pancreatic function in cystic fibrosis. CF, CFTR, PI
41  1992 Pathophysiology of the pancreas in cystic fibrosis. CF, PI
42  1991 Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease. Application in the identification of a cystic fibrosis patient with atypical clinical course. CF, CFTR, PCR, PI
43  1989 DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis. CF, PI