Kerem B - Search Results

1

Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations.

Wilschanski M, Yahav Y, Yaacov Y, Blau H, Bentur L, Rivlin J, Aviram M, Bdolah-Abram T, Bebok Z, Shushi L, Kerem B, Kerem E. Wilschanski M, et al. Among authors: kerem b, kerem e. N Engl J Med. 2003 Oct 9;349(15):1433-41. doi: 10.1056/NEJMoa022170. N Engl J Med. 2003. PMID: 14534336 Free article. Clinical Trial.

2

Cystic fibrosis manifested as undescended testis and absence of vas deferens.

Goshen R, Kerem E, Shoshani T, Kerem BS, Feigin E, Zamir O, Yahav Y. Goshen R, et al. Among authors: kerem bs, kerem e. Pediatrics. 1992 Dec;90(6):982-3. Pediatrics. 1992. PMID: 1359500 No abstract available.

3

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

Kerem E, Corey M, Kerem BS, Rommens J, Markiewicz D, Levison H, Tsui LC, Durie P. Kerem E, et al. Among authors: kerem bs. N Engl J Med. 1990 Nov 29;323(22):1517-22. doi: 10.1056/NEJM199011293232203. N Engl J Med. 1990. PMID: 2233932 Free article.

4

Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus.

Kerem E, Corey M, Kerem B, Durie P, Tsui LC, Levison H. Kerem E, et al. Among authors: kerem b. J Pediatr. 1989 May;114(5):767-73. doi: 10.1016/s0022-3476(89)80134-9. J Pediatr. 1989. PMID: 2715890

5

Shoshani T, Kerem E, Szeinberg A, Augarten A, Yahav Y, Cohen D, Rivlin J, Tal A, Kerem B. Shoshani T, et al. Among authors: kerem b, kerem e. J Clin Invest. 1994 Apr;93(4):1502-7. doi: 10.1172/JCI117128. J Clin Invest. 1994. PMID: 7512981 Free PMC article.

6

Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the W1282X and delta F508 mutations.

Avner R, Laufer N, Safran A, Kerem BS, Friedmann A, Mitrani-Rosenbaum S. Avner R, et al. Among authors: kerem bs. Hum Reprod. 1994 Sep;9(9):1676-80. doi: 10.1093/oxfordjournals.humrep.a138772. Hum Reprod. 1994. PMID: 7530726

7

A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian Jews.

Shoshani T, Berkun Y, Yahav Y, Augarten A, Bashan N, Rivlin Y, Gazit E, Sereth H, Kerem E, Kerem BS. Shoshani T, et al. Among authors: kerem bs, kerem e. Genomics. 1993 Jan;15(1):236-7. doi: 10.1006/geno.1993.1046. Genomics. 1993. PMID: 7679367 No abstract available.

8

Congenital bilateral absence of vas deferens in the absence of cystic fibrosis.

Augarten A, Yahav Y, Kerem BS, Halle D, Laufer J, Szeinberg A, Dor J, Mashiach S, Gazit E, Madgar I. Augarten A, et al. Among authors: kerem bs. Lancet. 1994 Nov 26;344(8935):1473-4. doi: 10.1016/s0140-6736(94)90292-5. Lancet. 1994. PMID: 7968122

9

Difference in frequencies of the cystic fibrosis alleles, delta F508 and W1282X, between carriers and patients.

Kalman YM, Kerem E, Darvasi A, DeMarchi J, Kerem B. Kalman YM, et al. Among authors: kerem b, kerem e. Eur J Hum Genet. 1994;2(2):77-82. doi: 10.1159/000472347. Eur J Hum Genet. 1994. PMID: 8044659

10

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. Among authors: kerem bs, kerem e. Lancet. 1993 Jul 3;342(8862):25-6. doi: 10.1016/0140-6736(93)91885-p. Lancet. 1993. PMID: 8100293

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