Kerem BS - Search Results

1

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

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. 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. J Clin Invest. 1994 Apr;93(4):1502-7. doi: 10.1172/JCI117128. J Clin Invest. 1994. PMID: 7512981 Free PMC article.

6

Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21.

Shoshani T, Augarten A, Yahav J, Gazit E, Kerem B. Shoshani T, et al. Hum Mol Genet. 1994 Apr;3(4):657-8. doi: 10.1093/hmg/3.4.657. Hum Mol Genet. 1994. PMID: 7520798 No abstract available.

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

Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis.

Sereth H, Shoshani T, Bashan N, Kerem BS. Sereth H, et al. Among authors: kerem bs. Hum Genet. 1993 Oct 1;92(3):289-95. doi: 10.1007/BF00244474. Hum Genet. 1993. PMID: 7691712

9

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

10

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. Eur J Hum Genet. 1994;2(2):77-82. doi: 10.1159/000472347. Eur J Hum Genet. 1994. PMID: 8044659

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