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Items: 50

1.

Clinical evidence that V456A is a Cystic Fibrosis causing mutation in South Asians.

Uppaluri L, England SJ, Scanlin TF.

J Cyst Fibros. 2012 Jul;11(4):312-5. doi: 10.1016/j.jcf.2012.02.001. Epub 2012 Mar 5.

2.

Adolescent development and energy expenditure in females with cystic fibrosis.

Stallings VA, Tomezsko JL, Schall JI, Mascarenhas MR, Stettler N, Scanlin TF, Zemel BS.

Clin Nutr. 2005 Oct;24(5):737-45. Epub 2005 Apr 8.

PMID:
16182037
3.

Altered terminal glycosylation and the pathophysiology of CF lung disease.

Rhim AD, Stoykova LI, Trindade AJ, Glick MC, Scanlin TF.

J Cyst Fibros. 2004 Aug;3 Suppl 2:95-6.

4.

A girl with cystic fibrosis and failure to thrive.

Kamath BM, Bhargava S, Markowitz JE, Ruchelli E, Scanlin TF, Mascarenhas M.

J Pediatr. 2003 Jul;143(1):115-9. No abstract available.

PMID:
12915836
5.

Alpha1,3fucosyltransferases in cystic fibrosis airway epithelial cells.

Stoykova LI, Liu A, Scanlin TF, Glick MC.

Biochimie. 2003 Mar-Apr;85(3-4):363-7.

PMID:
12770774
6.

Gene therapy of cystic fibrosis (CF) airways: a review emphasizing targeting with lactose.

Klink DT, Glick MC, Scanlin TF.

Glycoconj J. 2001 Sep;18(9):731-40. Review.

PMID:
12386459
7.

Terminal glycosylation in cystic fibrosis (CF): a review emphasizing the airway epithelial cell.

Rhim AD, Stoykova L, Glick MC, Scanlin TF.

Glycoconj J. 2001 Sep;18(9):649-59. Review.

PMID:
12386452
8.

A six-month study of growth and energy expenditure in children with cystic fibrosis taking a pulmonary inhalation medication (rhDNase).

Fung EB, Barden EM, Wasserman D, Zemel BS, Heinrich BT, Scanlin TF, Stallings VA.

J Am Coll Nutr. 1999 Aug;18(4):330-8.

PMID:
12038476
9.

Glycosylation and the cystic fibrosis transmembrane conductance regulator.

Scanlin TF, Glick MC.

Respir Res. 2001;2(5):276-9. Epub 2001 Aug 7. Review.

10.

Activity of fucosyltransferases and altered glycosylation in cystic fibrosis airway epithelial cells.

Glick MC, Kothari VA, Liu A, Stoykova LI, Scanlin TF.

Biochimie. 2001 Aug;83(8):743-7.

PMID:
11530206
11.

Terminal glycosylation and disease: influence on cancer and cystic fibrosis.

Scanlin TF, Glick MC.

Glycoconj J. 2000 Jul-Sep;17(7-9):617-26. Review.

PMID:
11421353
12.
13.

Terminal glycosylation of cystic fibrosis airway epithelial cells.

Rhim AD, Kothari VA, Park PJ, Mulberg AE, Glick MC, Scanlin TF.

Glycoconj J. 2000 Jun;17(6):385-91.

PMID:
11294504
14.

Prospective evaluation of growth, nutritional status, and body composition in children with cystic fibrosis.

Stettler N, Kawchak DA, Boyle LL, Propert KJ, Scanlin TF, Stallings VA, Zemel BS.

Am J Clin Nutr. 2000 Aug;72(2):407-13.

PMID:
10919935
15.

A prospective study of body composition changes in children with cystic fibrosis.

Stettler N, Kawachak DA, Boyle LL, Propert KJ, Scanlin TF, Stallings VA, Zemel BS.

Ann N Y Acad Sci. 2000 May;904:406-9.

PMID:
10865779
16.

Longitudinal analysis shows serum carotenoid concentrations are low in children with cystic fibrosis.

Kawchak DA, Sowell AL, Hofley PM, Zemel BS, Scanlin TF, Stallings VA.

J Am Diet Assoc. 1999 Dec;99(12):1569-72. No abstract available.

PMID:
10608954
17.

Terminal glycosylation in cystic fibrosis.

Scanlin TF, Glick MC.

Biochim Biophys Acta. 1999 Oct 8;1455(2-3):241-53. Review.

18.

Enhanced efficiency of lactosylated poly-L-lysine-mediated gene transfer into cystic fibrosis airway epithelial cells.

Kollen WJ, Schembri FM, Gerwig GJ, Vliegenthart JF, Glick MC, Scanlin TF.

Am J Respir Cell Mol Biol. 1999 May;20(5):1081-6.

PMID:
10226080
19.

High-efficiency transfer of cystic fibrosis transmembrane conductance regulator cDNA into cystic fibrosis airway cells in culture using lactosylated polylysine as a vector.

Kollen WJ, Mulberg AE, Wei X, Sugita M, Raghuram V, Wang J, Foskett JK, Glick MC, Scanlin TF.

Hum Gene Ther. 1999 Mar 1;10(4):615-22.

PMID:
10094204
20.

Acute pulmonary exacerbation is not associated with increased energy expenditure in children with cystic fibrosis.

Stallings VA, Fung EB, Hofley PM, Scanlin TF.

J Pediatr. 1998 Mar;132(3 Pt 1):493-9.

PMID:
9544907
21.

Glycosylated polylysines. Nonviral vectors for gene transfer into cystic fibrosis airway epithelial cells.

Kollen W, Erbacher P, Midoux P, Roche AC, Monsigny M, Glick MC, Scanlin TF.

Chest. 1997 Jun;111(6 Suppl):95S-96S. No abstract available.

PMID:
9184547
22.

Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis.

Zemel BS, Kawchak DA, Cnaan A, Zhao H, Scanlin TF, Stallings VA.

Pediatr Res. 1996 Oct;40(4):578-86.

PMID:
8888286
23.

Gluconoylated and glycosylated polylysines as vectors for gene transfer into cystic fibrosis airway epithelial cells.

Kollen WJ, Midoux P, Erbacher P, Yip A, Roche AC, Monsigny M, Glick MC, Scanlin TF.

Hum Gene Ther. 1996 Aug 20;7(13):1577-86.

PMID:
8864758
24.
25.

Longitudinal, prospective analysis of dietary intake in children with cystic fibrosis.

Kawchak DA, Zhao H, Scanlin TF, Tomezsko JL, Cnaan A, Stallings VA.

J Pediatr. 1996 Jul;129(1):119-29.

PMID:
8757571
27.

Energy expenditure and genotype of children with cystic fibrosis.

Tomezsko JL, Stallings VA, Kawchak DA, Goin JE, Diamond G, Scanlin TF.

Pediatr Res. 1994 Apr;35(4 Pt 1):451-60. Review.

PMID:
7519343
28.

Body composition of children with cystic fibrosis with mild clinical manifestations compared with normal children.

Tomezsko JL, Scanlin TF, Stallings VA.

Am J Clin Nutr. 1994 Jan;59(1):123-8.

PMID:
8279392
29.

Dietary intake of healthy children with cystic fibrosis compared with normal control children.

Tomezsko JL, Stallings VA, Scanlin TF.

Pediatrics. 1992 Oct;90(4):547-53.

PMID:
1408508
30.

Preparation of isolated surface membranes from cystic fibrosis airway epithelial cells.

Harsch AD, Xu J, Bevins CL, Glick MC, Scanlin TF.

Chest. 1992 Mar;101(3 Suppl):58S-60S. No abstract available.

PMID:
1371735
31.

Management and survival of meconium ileus. A 30-year review.

Del Pin CA, Czyrko C, Ziegler MM, Scanlin TF, Bishop HC.

Ann Surg. 1992 Feb;215(2):179-85.

32.
34.

Additional fucosyl residues on membrane glycoproteins but not a secreted glycoprotein from cystic fibrosis fibroblasts.

Wang YM, Hare TR, Won B, Stowell CP, Scanlin TF, Glick MC, Hård K, van Kuik JA, Vliegenthart JF.

Clin Chim Acta. 1990 May;188(3):193-210.

PMID:
2387072
35.

Lack of proteolytic processing of alpha-L-fucosidase in human skin fibroblasts.

Leibold DM, Robinson CB, Scanlin TF, Glick MC.

J Cell Physiol. 1988 Dec;137(3):411-20.

PMID:
3192622
36.
37.
38.

Characterization of human fibronectin glycopeptides from cystic fibrosis and control skin fibroblasts.

Stowell CP, Scanlin TF, Glick MC.

Carbohydr Res. 1986 Aug 15;151:279-92.

PMID:
3768895
39.

Hemoptysis and anemia in a 3-year-old boy.

Levy J, Kolski GB, Scanlin TF.

Ann Allergy. 1985 Sep;55(3):439-40, 486-9. No abstract available.

PMID:
3839987
40.

Altered fucosylation of membrane glycoproteins from cystic fibrosis fibroblasts.

Scanlin TF, Wang YM, Glick MC.

Pediatr Res. 1985 Apr;19(4):368-74.

PMID:
4000763
41.

Cardiac involvement in cystic fibrosis: early noninvasive detection and vasodilator therapy.

Moskowitz WB, Gewitz MH, Heyman S, Ruddy RM, Scanlin TF.

Pediatr Pharmacol (New York). 1985;5(2):139-48.

PMID:
3900900
42.

Pregnancy in patients with cystic fibrosis.

Palmer J, Dillon-Baker C, Tecklin JS, Wolfson B, Rosenberg B, Burroughs B, Holsclaw DS Jr, Scanlin TF, Huang NN, Sewell EM.

Ann Intern Med. 1983 Nov;99(5):596-600.

PMID:
6638717
43.

Hypoelectrolytemia as a presentation and complication of cystic fibrosis.

Ruddy R, Anolik R, Scanlin TF.

Clin Pediatr (Phila). 1982 Jun;21(6):367-9.

PMID:
7075099
44.

Glycoproteins in culture medium: a comparison from cystic fibrosis and control skin fibroblasts.

Scanlin TF, Voynow JA, Thomas EJ, Glick MC.

Biochemistry. 1982 Feb 2;21(3):491-7. No abstract available.

PMID:
7066301
45.

alpha-L-Fucosidase in cystic fibrosis.

Scanlin TF, Glick MC.

Clin Chim Acta. 1981 Aug 10;114(2-3):269-74. No abstract available.

PMID:
7285350
46.

Cystic fibrosis: current trends in research.

Scanlin TF.

Clin Chest Med. 1980 Sep;1(3):423-7. Review. No abstract available.

PMID:
7028382
47.

Abnormal distribution of alpha-L-fucosidase in cystic fibrosis: decreased activity in serum.

Scanlin TF, Matacic SS, Glick MC.

Clin Chim Acta. 1979 Jan 15;91(2):197-202.

PMID:
759048
48.

Abnormal distribution of alpha-L-fucosidase in cystic fibrosis: increased activity in skin fibroblasts.

Scanlin TF, Matacic SS, Pace M, Santer UV, Glick MC.

Biochem Biophys Res Commun. 1977 Dec 7;79(3):869-76. No abstract available.

PMID:
597312
49.

Letter: C3 in cystic fibrosis.

Scanlin TF Jr, Norman ME, Rosenlund ML.

Lancet. 1975 Jun 21;1(7921):1382. No abstract available.

PMID:
48969
50.

Letter: Vocal cord paralysis in cystic fibrosis.

Scanlin TF, Shapiro RS, Rosenlund ML.

J Pediatr. 1975 Jun;86(6):984-5. No abstract available.

PMID:
1127540

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