Zalan A - Search Results

1

Comparative screening of FMF mutations in various communities of the Israeli society.

Sharkia R, Mahajnah M, Zalan A, Athamna M, Azem A, Badarneh K, Faris F. Sharkia R, et al. Among authors: zalan a. Eur J Med Genet. 2013 Jul;56(7):351-5. doi: 10.1016/j.ejmg.2013.04.002. Epub 2013 Apr 18. Eur J Med Genet. 2013. PMID: 23602951

2

The changing pattern of consanguinity in a selected region of the Israeli Arab community.

Sharkia R, Zaid M, Athamna A, Cohen D, Azem A, Zalan A. Sharkia R, et al. Among authors: zalan a. Am J Hum Biol. 2008 Jan-Feb;20(1):72-7. doi: 10.1002/ajhb.20678. Am J Hum Biol. 2008. PMID: 17941037

3

Sanfilippo type A: new clinical manifestations and neuro-imaging findings in patients from the same family in Israel: a case report.

Sharkia R, Mahajnah M, Zalan A, Sourlis C, Bauer P, Schöls L. Sharkia R, et al. Among authors: zalan a. J Med Case Rep. 2014 Feb 28;8:78. doi: 10.1186/1752-1947-8-78. J Med Case Rep. 2014. PMID: 24576347 Free PMC article.

4

Factors affecting the utilization of genetic counseling services among Israeli Arab women.

Sharkia R, Tarabeia J, Zalan A, Atamany E, Athamna M, Allon-Shalev S. Sharkia R, et al. Among authors: zalan a. Prenat Diagn. 2015 Apr;35(4):370-5. doi: 10.1002/pd.4550. Epub 2015 Feb 12. Prenat Diagn. 2015. PMID: 25512120

5

CHANGES IN MARRIAGE PATTERNS AMONG THE ARAB COMMUNITY IN ISRAEL OVER A 60-YEAR PERIOD.

Sharkia R, Mahajnah M, Athamny E, Khatib M, Sheikh-Muhammad A, Zalan A. Sharkia R, et al. Among authors: zalan a. J Biosoc Sci. 2016 Mar;48(2):283-7. doi: 10.1017/S0021932015000103. Epub 2015 May 22. J Biosoc Sci. 2016. PMID: 25997496

6

Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy.

Sharkia R, Shalev SA, Zalan A, Marom-David M, Watemberg N, Urquhart JE, Daly SB, Bhaskar SS, Williams SG, Newman WG, Spiegel R, Azem A, Elpeleg O, Mahajnah M. Sharkia R, et al. Among authors: zalan a. Am J Med Genet A. 2017 Apr;173(4):1051-1055. doi: 10.1002/ajmg.a.38140. Am J Med Genet A. 2017. PMID: 28328138

7

A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome.

Sharkia R, Zalan A, Jabareen-Masri A, Zahalka H, Mahajnah M. Sharkia R, et al. Among authors: zalan a. Eur J Med Genet. 2019 Nov;62(11):103549. doi: 10.1016/j.ejmg.2018.10.001. Epub 2018 Oct 6. Eur J Med Genet. 2019. PMID: 30296593

8

Exploration of Risk Factors for Type 2 Diabetes among Arabs in Israel.

Sharkia R, Sheikh-Muhammad A, Mahajnah M, Khatib M, Zalan A. Sharkia R, et al. Among authors: zalan a. Ann Glob Health. 2019 May 10;85(1):67. doi: 10.5334/aogh.2350. Ann Glob Health. 2019. PMID: 31074599 Free PMC article.

9

A novel biallelic loss-of-function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro-facio-thoracic dysplasia.

Sharkia R, Zalan A, Jabareen-Masri A, Hengel H, Schöls L, Kessel A, Azem A, Mahajnah M. Sharkia R, et al. Among authors: zalan a. Am J Med Genet A. 2019 Jul;179(7):1338-1345. doi: 10.1002/ajmg.a.61168. Epub 2019 May 18. Am J Med Genet A. 2019. PMID: 31102500

10

The Current and Forecasted Status of Type 2 Diabetes in the Arab Society of Israel.

Zalan A, Sheikh-Muhammad A, Khatib M, Sharkia R. Zalan A, et al. Curr Diabetes Rev. 2021;17(8):e050421192659. doi: 10.2174/1573399817666210405100108. Curr Diabetes Rev. 2021. PMID: 33820521

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