- ►diabetesjournals.org A Moran, J Phillips, C Milla - Diabetes Care, 2001 - Am Diabetes Assoc CONCLUSIONS—In response to subcutaneous insulin lispro, postprandial glucose
excursion was significantly diminished and insulin secretion was enhanced
compared with a control meal in which no medication was given to patients ... Cited by 34 - Related articles - BL Direct - All 8 versions
J Rosenecker, I Eichler, H Barmeier, H von … - Pediatric pulmonology, 2001 - interscience.wiley.com The prevalence of cystic fibrosis-related diabetes melltitus (CFRD) is
increasing as patients with cystic fibrosis (CF) live longer. Because patients
with CFRD are insulin-deficient, the standard medical treatment is ... Cited by 31 - Related articles - BL Direct - All 3 versions
H Kentrup, H Bongers, M Spengler, G … - European journal of pediatrics, 1999 - Springer Abstract Impaired glucose tolerance (IGT) is an increasingly frequent
complication of cystic ®brosis (CF). In CF patients, a fast postprandial rise
in plasma glucose is typically followed by a delayed but prolonged insulin ... Cited by 23 - Related articles - BL Direct - All 4 versions
- ►fetalneonatal.com L Dobson, AT Hattersley, S Tiley, S Elworthy … - Archives of disease in childhood, 2002 - fetalneonatal.com We noticed that in CF patients with diabetes the initiation of insulin treatment
was associated with a notable clinical improvement that could not be explained
by the treatment of their relatively mild hyperglycaemia. In addition ... Cited by 38 - Related articles - BL Direct - All 10 versions
M Löhr, P Goertchen, H Nizze, NS Gould, VE … - Virchows Archiv, 1989 - Springer Summary. The pancreases of 23 patients (mean age 10.5 years, range 5-22) years
dying of cystic fibro- sis (CF) were evaluated at autopsy by routine his- tology
and immunostaining for changes in their endocrine cell compartment. The ... Cited by 38 - Related articles - All 2 versions
A Moran, P Diem, DJ Klein, MD Levitt, RP … - The Journal of pediatrics, 1991 - Elsevier To characterize pancreatic endocrine secretion and to examine interrelationships
among alterations in alpha, beta, and pancreatic polypeptide cell function in
patients with cystic fibrosis (CF), we studied 19 patients with exocrine ... Cited by 76 - Related articles - All 7 versions
M Couce, TD O'Brien, A Moran, PC Roche, PC … - Journal of Clinical Endocrinology & Metabolism, 1996 - Endocrine Soc Page 1. 0021-972x196/$03.00/0 Journal of Clinical Endocrinology and Metabolism
Copyright 0 1996 by The Endocrine Society Vol. 81, No. 3 Printed in USA ... Cited by 55 - Related articles - BL Direct - All 4 versions
- ►nih.gov [PDF] L Dobson, CD Sheldon, AT Hattersley - Journal of the Royal Society of Medicine, 2004 - pubmedcentral.nih.gov Cystic-fibrosis-related diabetes (CFRD) is an increasingly prevalent and
important complication of cystic fibrosis (CF). CFRD presents many new
diagnostic and manage- ment challenges to the multidisciplinary CF team. In ... Cited by 19 - Related articles - BL Direct - All 5 versions
DS Hardin, A Moran - Endocrinology and metabolism clinics of North America, 1999 - Elsevier Cystic fibrosis is the most commonly inherited life-threatening disease of
Caucasians, with an incidence of 1 case per 3000 live births in the United
States. 16 The primary gene defect located on chromosome 7 was discovered ... Cited by 54 - Related articles - BL Direct - All 10 versions
