כניסה

د.راجح شرقية

פרסומים שפיטים

  1. Sharkia, R., Zalan, A., Jabareen-Masria, A., Zahalka, H., & Mahajnah, M. (2018). A new case confirming and expanding the phenotype spectrum of ADAT3related intellectual disability syndrome. European Journal of Medical Genetics. https://doi.org/10.1016/j.ejmg.2018.10.001
  2. Sharkia, R., Mahajnah, M.,  Sheikh-Muhammad A.,, Khatib, M., & Zalan, A. (2018). Trends in the prevalence of type 2 diabetes mellitus among Arabs in Israel: A community health survey. Global Advanced Research Journal of Medicine and Medical Sciences, 7(4), 98-104.
  3. Minnerop, M., Kurzwelly, D., Wagner, H., Soehn, A. S., Reichbauer, J., Tao, F., ... Sharkia, R., & Pyle, A. (2017). Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. Brain140(6), 1561-1578.
  4. Mahajnah, M., Sharkia, R., Shorbaji, N., & Zelnik, N. (2017). The Clinical Characteristics of ADHD Diagnosed in Adolescents in Comparison With Younger Children. Journal of Attention Disorders, 1087054717696768.
  5. Sharkia, R., Shalev, S. A., Zalan, A., Marom‐David, M., Watemberg, N., Urquhart, J. E., ... & Mahanjah, M. (2017). Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy. American Journal of Medical Genetics Part A173(4), 1051-1055.
  6. Hengel, H., Magee, A., Mahanjah, M., Vallat, J. M., Ouvrier, R., Abu-Rashid, M., ...... Bauer, P. & Sharkia, R., et al. (2017). CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis. Neurology Genetics3(2), e144.
  7. Rajech Sharkia, Holger Hengel, Ludger Schöls, Muhammad Athamna, Peter Bauer and Muhammad Mahajnah (2016) Parental mosaicism in another case of Dravet syndrome caused by a novel SCN1A deletion: a case report. Journal of Medical Case Reports, 10 (1):67. 
  8. Muhammad Mahajnah, Rajech Sharkia, Nadeem Shurbaji  and  Nathanel Zelnik. (2016) The Clinical Profile of ADHD – Impact of Ethnic and Social Diversities in Israel.  The Israel Medical Association journal: IMAJ18(6), 322.
  9. Rajech Sharkia, Muhammad Mahajnah, Muhammad Athamna, Ahmad Sheikh-Muhammad, Abdelnaser Zalan. (2016) Variations in Types of First-Cousin Marriages over a Two-Generation Period among Arabs in Israel. Advances in Anthropology, 5, 171-176.
  10. Rajech Sharkia, Jalal Tarabeia, Esmael Atamany, Muhammad Athamna, Stavit Allon-Shalev. (2015) Factors affecting the utilization of genetic counseling services among Israeli Arab women. Prenatal Diagnosis, 35:1-6.
  11. Muhammad Mahajnah, Rajech Sharkia, Haitham Shalabe, Ruth Terkel-Dawer, Ashraf Akawi and Nathanel Zelnik. (2015) Clinical Characteristics of Autism Spectrum Disorder in Israel - Impact of Ethnic and Social Diversities.  BioMed Research International, 2015:962093.
  12. Mayer AK, Mahajnah M, Zobor D, Bonin M, Sharkia R, Wissinger B. (2015) Novel homozygous large deletion including the 5' part of the SPATA7 gene in a consanguineous Israeli Muslim Arab family. Mol Vis. 15;21:306-15.
  13. Rajech Sharkia, Muhammad Mahajnah, Esmael Athamny, Mohammad Khatib, Ahmad Sheikh-Muhammad and Abdelnaser Zalan. (2015) CHANGES IN MARRIAGE PATTERNS AMONG THE ARAB COMMUNITY IN ISRAEL OVER A 60-YEAR PERIOD. Journal of Biosocial Science; 22: 1-5.
  14. Sharkia R., Mahajnah M, Zalan A, Sourlis C., Bauer P.  Schöls L. (2014) Sanfilippo type A: New Clinical Manifestations and Neuro-imaging findings in patients from the same family in Israel. Journal of Medical Case Reports, 8:78.
  15. Martial Mallaret, Matthis Synofzik3 Jaeho Lee, Cari A. Sagum, Muhammad Mahajnah, Rajech Sharkia, Nathalie Drouot, Mathilde Renaud, Fabrice A.C. Klein, Mathieu Anheim, Christine Tranchant, Cyril Mignot, Jean-Louis Mandel, Mark Bedford, Mustafa A. Salih, , Peter Bauer, Rebecca Schüle, Ludger Schöls, Marcelo Aldaz, Michel Koenig. (2014) The tumor suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation. Brain, 137; 411–419.
  16. Sharkia, R., Mahajnah, M., Zalan, A., Athamna, M., Azem, A., Badarneh, K., and Faris, F. (2013) Comparative screening of FMF mutations in various communities of the Israeli society. European journal of medical genetics. ‏ 56(7):351-5
  17. Sharkia, R. Athamny, E. Khatib, M.  Sheikh-Muhammad, A. Azem, A. and  Mahajnah, M. (2011). Consanguinity and Its Effect on Morbidity and Congenital disorders among Arabs in Israel. In: Human Genetic diseases, Dijana Plaseska-Karanfilska (Ed.), ISBN: 978-953-307-936-3, InTech, Available from: http://www.intechopen.com/articles/show/title/consanguinity-and-its-effect-on-morbidity-and-congenital-disorders-among-arabs-in-israel
  18. Sharkia, R., Azem, A., Kaiyal, Q., Zelnik, N. and Mahajnah, M. (2010) Mental Retardation and Consanguinity in a Selected Region of the Israeli Arab Community. Cent. Eur. J. Med. 5(1): 91-96.
  19. Bonshitien, A. Parnas A., Sharkia, R., Niv, A., Mizrahi, I., Azem, A.,     Weiss, C. (2009) Differential effects of co-chaperonin homologs on cpn60 oligomers. Cell Stress and Chaperones 14:5.509-519.
  20. Sharkia R,  Zaid M, Athamna A, Cohen D, Azem A, Zalan A. (2008). The changing pattern of consanguinity in a selected region of the Israeli Arab community.  American Journal of Human Biology 20: 72-77.
  21. Sharkia R, Medlej B, Zalan A, (2006) Determination of class-X  students' knowledge level and attitudes towards genetic disorders and consanguinity. Alresala 13:186-209.
  22. Sharkia, R., Athamna, A., Zaid, M., Gnaim, L., Zalan, A. (2005)  Knowledge Level and Attitudes of Arab Students in Beit Berl College regarding Genetic Disorders, Consanguinity and Genetic Counseling. ATEE Proceedings.
  23. Sharkia, R., Viitanen, P., Levy-Rimler, G., Weiss, C., Niv, A., Azem, A (2003) On the oligomeric state of chloroplast chaperonin 10 and chaperonin 20. Biochem.et  Biophysica. Acta. 1651(1-2), 76-84.
  24. Sharkia, R., Viitanen, P., Levy-Rimler, G., Weiss, C., Niv, A., Azem, A. (2003) "The higher plant chaperonins". In: Annual Plant Reviews, Protein – protein interactions in plant biology (eds M. McManus, W. Laing and Allan, A.), Sheffield Academic Press, England. 7,181-203.
  25. Levy-Rimler, G., Viitanen, P., Weiss, C., Sharkia, R., Greenberg, A., Niv, A., Lustig, A., Azem, A. (2001) "The effect of nucleotides and mitochondrial chaperonin 10 on the structure and chaperone activity of mitochondrial chaperonin 60". Eur. J. Biochem., 268, 3465-3472.
  26. Drechsler, Z., Sharkia, R., Cabantchik, I., Beer, S., (1994) "The relationship of arginine groups to photosynthetic HCO3- uptake in Ulva sp. mediated by a putative anion exchanger". Planta, 194, 250-255.
  27. Sharkia, R., Beer, S., Cabantchik, I., (1994) "A membrane-located polypeptide of Ulva sp. which may be involved in HCO3- uptake is recognized by antibodies raised against the human red blood cell anion exchange protein". Planta, 194, 247-249.
  28. Sharkia, R., Drechsler, Z., Cabantchik, I., Beer, S., (1993) "Bicarbonate uptake in the marine macroalgae Ulva sp. Is inhibited by classical probes of anion exchange by red blood cells". Planta, 191, 34-40.

Sharkia, R. (1993) Auxin Binding Protein in the gap junction as a receptor for Auxin hormone. Biology teacher Journal, 51, 44-56.

 
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