Bentur L - Search Results

1

A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations.

Kerem E, Rave-Harel N, Augarten A, Madgar I, Nissim-Rafinia M, Yahav Y, Goshen R, Bentur L, Rivlin J, Aviram M, Genem A, Chiba-Falek O, Kraemer MR, Simon A, Branski D, Kerem B. Kerem E, et al. Among authors: bentur l. Am J Respir Crit Care Med. 1997 Jun;155(6):1914-20. doi: 10.1164/ajrccm.155.6.9196095. Am J Respir Crit Care Med. 1997. PMID: 9196095

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

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

5

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

6

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

7

A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype.

Kerem E, Nissim-Rafinia M, Argaman Z, Augarten A, Bentur L, Klar A, Yahav Y, Szeinberg A, Hiba O, Branski D, Corey M, Kerem B. Kerem E, et al. Among authors: bentur l. Pediatrics. 1997 Sep;100(3):E5. doi: 10.1542/peds.100.3.e5. Pediatrics. 1997. PMID: 9271620

8

The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutation.

Chiba-Falek O, Kerem E, Shoshani T, Aviram M, Augarten A, Bentur L, Tal A, Tullis E, Rahat A, Kerem B. Chiba-Falek O, et al. Among authors: bentur l. Genomics. 1998 Nov 1;53(3):276-83. doi: 10.1006/geno.1998.5517. Genomics. 1998. PMID: 9799593

9

Clinical and genetic risk factors for cystic fibrosis-related liver disease.

Wilschanski M, Rivlin J, Cohen S, Augarten A, Blau H, Aviram M, Bentur L, Springer C, Vila Y, Branski D, Kerem B, Kerem E. Wilschanski M, et al. Among authors: bentur l. Pediatrics. 1999 Jan;103(1):52-7. doi: 10.1542/peds.103.1.52. Pediatrics. 1999. PMID: 9917439

10

Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat tests.

Augarten A, Shmilovich H, Doolman R, Aviram M, Akons H, Ben Tur L, Blau H, Kerem E, Rivlin J, Sela BA, Szeinberg A, Yahav Y. Augarten A, et al. Pediatr Pulmonol. 2000 Oct;30(4):320-3. doi: 10.1002/1099-0496(200010)30:4<320::aid-ppul8>3.0.co;2-e. Pediatr Pulmonol. 2000. PMID: 11015133

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