Kerem BS - Search Results

1

The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype.

Augarten A, Ben Tov A, Madgar I, Barak A, Akons H, Laufer J, Efrati O, Aviram M, Bentur L, Blau H, Paret G, Wilschanski M, Kerem BS, Yahav Y. Augarten A, et al. Among authors: kerem bs. Eur J Gastroenterol Hepatol. 2008 Mar;20(3):164-8. doi: 10.1097/MEG.0b013e3282f36d04. Eur J Gastroenterol Hepatol. 2008. PMID: 18301294

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

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.

4

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.

5

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.

6

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

7

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

8

Correlation between genotype and phenotype in patients with cystic fibrosis.

Augarten A, Kerem BS, Kerem E, Gazit E, Yahav Y. Augarten A, et al. Among authors: kerem bs. N Engl J Med. 1994 Mar 24;330(12):866. N Engl J Med. 1994. PMID: 8114851 No abstract available.

9

Cost-benefit analysis of a national screening programme for cystic fibrosis in an Israeli population.

Ginsberg G, Blau H, Kerem E, Springer C, Kerem BS, Akstein E, Greenberg A, Kolumbos A, Abeliovich D, Gazit E, et al. Ginsberg G, et al. Among authors: kerem bs. Health Econ. 1994 Jan-Feb;3(1):5-23. doi: 10.1002/hec.4730030104. Health Econ. 1994. PMID: 8167800

10

[Screening for carriers of cystic fibrosis mutations in Ashkenazi volunteers].

Zamostiano R, Nolman S, Yahav J, Schonberg A, Kerem BS, Gazit E. Zamostiano R, et al. Among authors: kerem bs. Harefuah. 1993 Feb 15;124(4):202-5, 247. Harefuah. 1993. PMID: 8495900 Hebrew.

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