- ►diabetesjournals.org A Moran, C Milla, R Ducret, KS Nair - Diabetes, 2001 - Am Diabetes Assoc Cystic fibrosis (CF) patients are reported to experience chronic protein catabolism. Since diabetes
or impaired glucose tolerance (IGT) is common in CF, we hypothesized that their protein catabolic
state is related to reduced insulin secretion or reduced insulin action. A total of 12 ... Cited by 27 - Related articles - BL Direct - All 5 versions
DS Hardin, A LeBlanc, S Lukenbaugh, L Para, DK … - Pediatrics, 1998 - Am Acad Pediatrics Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Facebook Add to Reddit
Add to Technorati Add to Twitter What's this? ... From the * Department of Pediatrics, University
of Texas Health Science Center, Houston, Texas; the Department of Medicine, Baylor ... Cited by 48 - Related articles - BL Direct - All 5 versions
- ►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 with CFRD. The oral agent repaglinide ... Cited by 34 - Related articles - BL Direct - All 8 versions
- ►diabetesjournals.org [PDF] DS Hardin, A LeBlanc, L Para, DK Seilheimer - Diabetes, 1999 - Am Diabetes Assoc Patients with cystic fibrosis (CF)-related diabetes (CFRD) have clinical features of both type 1
and type 2 diabetes. Past studies have documented peripheral insulin resistance in CF, and
some studies have noted high hepatic glucose production (HGP) in CF patients. We ... Cited by 41 - Related articles - BL Direct - All 4 versions
A Moran, P Diem, DJ Klein, MD Levitt, RP Robertson - 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 insufficiency (EXO), including 9 receiving insulin ... Cited by 76 - Related articles - All 7 versions
M Löhr, P Goertchen, H Nizze, NS Gould, VE Gould, M … - 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 severely altered pancreatic tissues showed end ... Cited by 38 - Related articles - All 2 versions
[CITATION] Abnormal lipid levels in cystic fibrosis
V Figueroa, C Milla, EJ Parks, SJ Schwarzenberg, A … - Am J Clin Nutr, 2002 Cited by 6 - Related articles
- ►cnfindpark.cn V Figueroa, C Milla, EJ Parks, SJ … - American Journal of …, 2002 - ajcn.cnfindpark.cn 1 From the Divisions of Endocrinology (VF and AM), Pulmonology (CM), and Gastroenterology
and Nutrition (SJS), Department of Pediatrics, and the Department of Food Science and Nutrition
(EJP), University of Minnesota, Minneapolis and St Paul. ... 2 Supported by a grant from ... Cited by 14 - Related articles - BL Direct - All 8 versions
S Lanng, B Thorsteinsson, ME Roder, J … - CLINICAL …, 1994 - interscience.wiley.com It is also possible that your web browser is not configured or not able to display style sheets.
In this case, although the visual presentation will be degraded, the site should continue to be
functional. We recommend using the latest version of Microsoft or Mozilla web browser to ... Cited by 49 - Related articles - BL Direct - All 3 versions
