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The single nucleotide polymorphism rs2305957 G/A is not associated with recurrent pregnancy loss

Sharif, Fadel A.; Ashour, Mohammed J. (2017)
Background: This study was conducted in order to investigate the association between the single nucleotide polymorphism (SNP) rs2305957 G/A and recurrent pregnancy loss (RPL) in a group of Palestinian women residing in ...
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Polymorphism in Regulatory T-cell (Treg)-Related Genes Is Associated with Unexplained Recurrent Pregnancy Loss

Al-Ashi, Shadi F; Sharif, Fadel A.; Ashour, Mohammed J.; Badawi, Naim T. (Science Publishing Group, 2016)
In the absence of confirmed causes for around 50% of recurrent pregnancy loss (RPL) cases this study was conducted in order to investigate the association between single nucleotide polymorphism (SNP) in regulatory T-cell ...
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The relationship between gene polymorphisms of coagulation factors II, V and XI and risk of recurrent pregnancy loss in Palestine

Ashour, Mohammed J.; Sharif, Fadel A. (2015)
This retrospective case-control study was carried out in order to investigate the association between Factor II (G20210A), Factor V (G1691A, H1299R, Y1702C) and Factor XI (rs3756008 A> T) gene polymorphisms and recurrent ...
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Common MEFV Mutations in Palestinian Patients with Familial Mediterranean Fever

Ashour, Mohammed J.; Sharif, Fadel A. (2015)
Familial Mediterranean fever (FMF) is an autosomal recessive inflammatory disorder caused by mutations in the MEFV gene that encodes the pyrin protein. The disease is relatively common among people originating from the ...
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A Novel Transglutaminase-1 Missense Mutation in a Palestinian Family with Autosomal Recessive Congenital Ichthyosis: A Case Report

Ashour, Mohammed J.; Al-Ashi, Shadi F; Sharif, Fadel A. (SCIENCEDOMAIN International, 2015)
This work presents the molecular genetics investigation of a male neonate referred to our genetics laboratory with the diagnosis of classical lamellar ichthyosis (one form of autosomal recessive congenital ichthyosis). The ...
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Non-Syndromic autosomal recessive deafness in Gaza strip: A study of five GJB2 Gene mutations

Essammak, Badria F; Ashour, Mohammed J.; Sharif, Fadel A. (2014)
Hearing loss is a common, pan-ethnic and highly heterogeneous sensory disorder with an incidence of around 1 in 1000 infants. Genetic causes are thought to be responsible for more than 60% of the cases with the majority ...
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التشوهات الكروموسومية في الذكور المعرضين مهنيا للملوثات الكيميائية في قطاع غزة - فلسطين

Sharif, Fadel A.; Ashour, Mohammed J.; Laqqan, Mohammed M; Silmi, Ahmad S. (الجامعة الإسلامية - غزة, 2011)
Objective: This study was conducted to evaluate the frequency of chromosomal aberrations in peripheral blood lymphocytes from Palestinian males exposed to various chemical pollutants during their daily work. Subjects and ...
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Chromosomal aberrations in males occupationally exposed to chemical pollutants in the gaza strip-palestine

Laqqan, Mohammed M; Ashour, Mohammed J.; Silmi, Ahmad S.; Sharif, Fadel A. (2011)
Objective: This study was conducted to evaluate the frequency of chromosomal aberrations in peripheral blood lymphocytes from Palestinian males exposed to various chemical pollutants during their daily work. Subjects and ...
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Screening for Y-chromosome microdeletions in a population of infertile males in the Gaza Strip

Shaqalaih, Ashraf J; Abu Halima, Masood SH; Ashour, Mohammed J.; Sharif, Fadel A. (Sims Institute Press Ltd., 2009)
Infertility is an extraordinary public health problem in the Arab world, as it affects about 15% of couples seeking children. The male partner is responsible for infertility in approximately half of these cases. Classic ...

The institutional repository of the Islamic University of Gaza was established as part of the ROMOR project that has been co-funded with support from the European Commission under the ERASMUS + European programme. This publication reflects the views only of the author, and the Commission cannot be held responsible for any use which may be made of the information contained therein.

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Author
Ashour, Mohammed J. (9)
Sharif, Fadel A. (9)Al-Ashi, Shadi F (2)Laqqan, Mohammed M (2)Abu Halima, Masood SH (1)Badawi, Naim T. (1)Essammak, Badria F (1)Shaqalaih, Ashraf J (1)Silmi, Ahmad S. (1)Silmi, Ahmad S. (1)Subjectchromosomal aberrations (2)genotoxic (2)mutation (2)occupational exposure (2)pollutants (2)a/oligozoospermia (1)arnshl (1)as-pcr (1)autosomal recessive congenital ichthyosis (1)azfc partial deletion (1)... View MoreDate Issued2015 (3)2011 (2)2009 (1)2014 (1)2016 (1)2017 (1)

The institutional repository of the Islamic University of Gaza was established as part of the ROMOR project that has been co-funded with support from the European Commission under the ERASMUS + European programme. This publication reflects the views only of the author, and the Commission cannot be held responsible for any use which may be made of the information contained therein.

Contact Us | Send Feedback