Yahav Y - Search Results

1

Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests.

Augarten A, Berman H, Aviram M, Diver-Habber A, Akons H, Ben Tur L, Blau H, Kerem E, Rivlin J, Katznelson D, Szeinberg A, Kerem BS, Theodor L, Paret G, Yahav Y. Augarten A, et al. Among authors: yahav y. Clin Exp Med. 2003 Sep;3(2):119-23. doi: 10.1007/s10238-003-0014-z. Clin Exp Med. 2003. PMID: 14598187

2

The critical first six months in cystic fibrosis: a syndrome of severe bronchiolitis.

Katznelson D, Szeinberg A, Augarten A, Yahav Y. Katznelson D, et al. Among authors: yahav y. Pediatr Pulmonol. 1997 Aug;24(2):134-6; discussion 159-61. doi: 10.1002/(sici)1099-0496(199708)24:2<134::aid-ppul12>3.0.co;2-3. Pediatr Pulmonol. 1997. PMID: 9292909

3

Serum lipase levels pre and post Lundh meal: evaluation of exocrine pancreatic status in cystic fibrosis.

Augarten A, Katznelson D, Dubenbaum L, Doolman R, Sela BA, Lusky A, Szeinberg A, Kerem BS, Paret G, Gazit E, Sack J, Yahav Y. Augarten A, et al. Among authors: yahav y. Int J Clin Lab Res. 1998;28(4):226-9. doi: 10.1007/s005990050049. Int J Clin Lab Res. 1998. PMID: 9879495

4

Lundh meal: a single non-invasive challenge test for evaluation of exocrine and endocrine pancreatic function in cystic fibrosis patients.

Augarten A, Dubenbaum L, Yahav Y, Katznelson D, Szeinberg A, Blank A, Sack J. Augarten A, et al. Among authors: yahav y. Int J Clin Lab Res. 1999;29(3):114-6. doi: 10.1007/s005990050074. Int J Clin Lab Res. 1999. PMID: 10592108

5

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. Among authors: yahav y. 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

6

Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patients.

Augarten A, Akons H, Aviram M, Bentur L, Blau H, Picard E, Rivlin J, Miller MS, Katznelson D, Szeinberg A, Shmilovich H, Paret G, Laufer J, Yahav Y. Augarten A, et al. Among authors: yahav y. Pediatr Transplant. 2001 Oct;5(5):339-42. doi: 10.1034/j.1399-3046.2001.00019.x. Pediatr Transplant. 2001. PMID: 11560752

7

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

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

9

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: yahav y. 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

10

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: yahav y. Pediatrics. 1997 Sep;100(3):E5. doi: 10.1542/peds.100.3.e5. Pediatrics. 1997. PMID: 9271620

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