Bentur L - Search Results

1

Vitamins A and E and pulmonary exacerbations in patients with cystic fibrosis.

Hakim F, Kerem E, Rivlin J, Bentur L, Stankiewicz H, Bdolach-Abram T, Wilschanski M. Hakim F, et al. Among authors: bentur l. J Pediatr Gastroenterol Nutr. 2007 Sep;45(3):347-53. doi: 10.1097/MPG.0b013e31804069e5. J Pediatr Gastroenterol Nutr. 2007. PMID: 17873748

2

Wheezing in infants with cystic fibrosis: clinical course, pulmonary function, and survival analysis.

Kerem E, Reisman J, Corey M, Bentur L, Canny G, Levison H. Kerem E, et al. Among authors: bentur l. Pediatrics. 1992 Nov;90(5):703-6. Pediatrics. 1992. PMID: 1408543

3

Renal calcium handling in cystic fibrosis: lack of evidence for a primary renal defect.

Bentur L, Kerem E, Couper R, Baumal R, Canny G, Durie P, Levison H. Bentur L, et al. J Pediatr. 1990 Apr;116(4):556-60. doi: 10.1016/s0022-3476(05)81602-6. J Pediatr. 1990. PMID: 1690795

4

Clinical-physiologic correlations in acute asthma of childhood.

Kerem E, Canny G, Tibshirani R, Reisman J, Bentur L, Schuh S, Levison H. Kerem E, et al. Among authors: bentur l. Pediatrics. 1991 Apr;87(4):481-6. Pediatrics. 1991. PMID: 2011424

5

Predicting the need for hospitalization in children with acute asthma.

Kerem E, Tibshirani R, Canny G, Bentur L, Reisman J, Schuh S, Stein R, Levison H. Kerem E, et al. Among authors: bentur l. Chest. 1990 Dec;98(6):1355-61. doi: 10.1378/chest.98.6.1355. Chest. 1990. PMID: 2245674

6

Sequential pulmonary function measurements during treatment of infantile chronic interstitial pneumonitis.

Kerem E, Bentur L, England S, Reisman J, O'Brodovich H, Bryan AC, Levison H. Kerem E, et al. Among authors: bentur l. J Pediatr. 1990 Jan;116(1):61-7. doi: 10.1016/s0022-3476(05)81646-4. J Pediatr. 1990. PMID: 2295964

7

Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel.

Kerem E, Kalman YM, Yahav Y, Shoshani T, Abeliovich D, Szeinberg A, Rivlin J, Blau H, Tal A, Ben-Tur L, et al. Kerem E, et al. Hum Genet. 1995 Aug;96(2):193-7. doi: 10.1007/BF00207378. Hum Genet. 1995. PMID: 7635469

8

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation.

Augarten A, Kerem BS, Yahav Y, Noiman S, Rivlin Y, Tal A, Blau H, Ben-Tur L, Szeinberg A, Kerem E, et al. Augarten A, et al. Lancet. 1993 Jul 3;342(8862):25-6. doi: 10.1016/0140-6736(93)91885-p. Lancet. 1993. PMID: 8100293

9

The significance of sweat Cl/Na ratio in patients with borderline sweat test.

Augarten A, Hacham S, Kerem E, Sheva Kerem B, Szeinberg A, Laufer J, Doolman R, Altshuler R, Blau H, Bentur L, et al. Augarten A, et al. Among authors: bentur l. Pediatr Pulmonol. 1995 Dec;20(6):369-71. doi: 10.1002/ppul.1950200606. Pediatr Pulmonol. 1995. PMID: 8649916

10

Dietary intakes of young children with cystic fibrosis: is there a difference?

Bentur L, Kalnins D, Levison H, Corey M, Durie PR. Bentur L, et al. J Pediatr Gastroenterol Nutr. 1996 Apr;22(3):254-8. doi: 10.1097/00005176-199604000-00006. J Pediatr Gastroenterol Nutr. 1996. PMID: 8708878

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