Israel S - Search Results

1

Non-confined long-standing blood chimerism in a spontaneous monochorionic dizygotic twin pregnancy.

Daum H, Frumkin A, Meiner V, Werner M, Macarov M, Gillis D, Israel S, Abed El Latif M, Meir K, Gielchinsky Y. Daum H, et al. Among authors: israel s. Int J Gynaecol Obstet. 2020 Mar;148(3):399-400. doi: 10.1002/ijgo.13022. Epub 2019 Nov 26. Int J Gynaecol Obstet. 2020. PMID: 31671208 No abstract available.

2

The Many Faces of Non-Classic Congenital Adrenal Hyperplasia.

Ayalon-Dangur I, Segev-Becker A, Ayalon I, Eyal O, Israel S, Weintrob N. Ayalon-Dangur I, et al. Among authors: israel s. Isr Med Assoc J. 2017 May;19(5):317-322. Isr Med Assoc J. 2017. PMID: 28513122 Free article. Review. No abstract available.

3

Pregnancy in women with nonclassic congenital adrenal hyperplasia: Time to conceive and outcome.

Eyal O, Ayalon-Dangur I, Segev-Becker A, Schachter-Davidov A, Israel S, Weintrob N. Eyal O, et al. Among authors: israel s. Clin Endocrinol (Oxf). 2017 Nov;87(5):552-556. doi: 10.1111/cen.13429. Epub 2017 Aug 16. Clin Endocrinol (Oxf). 2017. PMID: 28731586

4

Identification of 33 novel HLA alleles in Arab potential bone marrow donors.

Bishara A, Brautbar C, Cereb N, Israel S. Bishara A, et al. Among authors: israel s. HLA. 2020 Feb;95(2):128-130. doi: 10.1111/tan.13764. Epub 2019 Nov 27. HLA. 2020. PMID: 31738479

5

Distribution of the V281L mutation of the CYP21 gene in Israeli congenital adrenal hyperplasia patients and its association with HLA- B14.

Israel S, Weinrib L, Weintrob N, Miller K, Brautbar C. Israel S, et al. Pediatr Endocrinol Rev. 2006 Aug;3 Suppl 3:447-50. Pediatr Endocrinol Rev. 2006. PMID: 17551464

6

Adult height of subjects with nonclassical 21-hydroxylase deficiency.

Eyal O, Tenenbaum-Rakover Y, Shalitin S, Israel S, Weintrob N. Eyal O, et al. Among authors: israel s. Acta Paediatr. 2013 Apr;102(4):419-23. doi: 10.1111/apa.12147. Epub 2013 Jan 28. Acta Paediatr. 2013. PMID: 23298233

7

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.

Weintrob N, Brautbar C, Pertzelan A, Josefsberg Z, Dickerman Z, Kauschansky A, Lilos P, Peled D, Phillip M, Israel S. Weintrob N, et al. Among authors: israel s. Eur J Endocrinol. 2000 Sep;143(3):397-403. doi: 10.1530/eje.0.1430397. Eur J Endocrinol. 2000. PMID: 11022183

8

Decreased cortisol secretion in nonclassical 21-hydroxylase deficiency before and during glucocorticoid therapy.

Weintrob N, Israel S, Lazar L, Lilos P, Brautbar C, Phillip M, Pertzelan A. Weintrob N, et al. Among authors: israel s. J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):985-91. doi: 10.1515/jpem.2002.15.7.985. J Pediatr Endocrinol Metab. 2002. PMID: 12199343

9

HLA class II immunogenetics of IDDM in Yemenite Jews.

Israel S, Kwon OJ, Weintrob N, Sprecher E, Bloch K, Assa S, Brautbar C, Vardi P. Israel S, et al. Hum Immunol. 1998 Nov;59(11):728-33. doi: 10.1016/s0198-8859(98)00074-3. Hum Immunol. 1998. PMID: 9796741

10

Effect of polymorphism in insulin locus and HLA on type 1 diabetes in four ethnic groups in Israel.

Benedek G, Brautbar C, Vardi P, Sharon N, Weintrob N, Zung A, Israel S. Benedek G, et al. Among authors: israel s. Tissue Antigens. 2009 Jan;73(1):33-8. doi: 10.1111/j.1399-0039.2008.01153.x. Epub 2008 Oct 24. Tissue Antigens. 2009. PMID: 19000139

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