Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Hatem Elghezal"'
Autor:
Hatem Elghezal
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 5, Iss 2, Pp 35-36 (2022)
NA [JBCGenetics 2022; 5(2.000): 35-36]
Externí odkaz:
https://doaj.org/article/8d11910611224596a5a053634d91014c
Autor:
Nawaf Alkhayat, Ghaleb Elyamany, Yasser Elborai, Qanita Sedick, Mohammad Alshahrani, Omar Al Sharif, Abdulmalik Alenezy, Amjad Hammdan, Hatem Elghezal, Omar Alsuhaibani, Mansour S. Aljabry, May AlMoshary, Eman Al Mussaed
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-11 (2019)
Abstract Background Childhood Acute Leukemia (AL) is characterized by recurrent genetic aberrations in 60% of AML cases and 90% of ALL cases. Insufficient data exists of rare cytogenetic abnormalities in AL. Therefore, we tested rare cytogenetic abno
Externí odkaz:
https://doaj.org/article/b55d7fca52f44ddebb9ef81726568a3e
Autor:
Nawaf Alkhayat, Yasser Elborai, Omer Al Sharif, Mohammad Al Shahrani, Omar Alsuhaibani, Mohammed Awad, Hatem Elghezal, Inesse ben-abdallah Bouhajar, Mona Alfaraj, Eman Al Mussaed, Fahad Alabbas, Ghaleb Elyamany
Publikováno v:
Clinical Medicine Insights: Oncology, Vol 11 (2017)
Background: Childhood acute lymphoblastic leukemia (ALL) is characterized by recurrent genetic aberrations. The identification of those abnormalities is clinically important because they are considered significant risk-stratifying markers. Aims: Ther
Externí odkaz:
https://doaj.org/article/211e9ee9ac7e4d9b9d263231b26114c2
Autor:
Ghaleb Elyamany, Kamal Fadalla, Hatem Elghezal, Omar Alsuhaibani, Hani Osman, Abdulaziz Al-Abulaaly
Publikováno v:
Clinical Medicine Insights: Pathology, Vol 2014, Iss 7, Pp 21-27 (2014)
Externí odkaz:
https://doaj.org/article/6c798222ab00434aa847ddb370cceccb
Autor:
Sana Bouraoui, Soumaya Mougou, Afef Drira, Faten Tabka, Nouha Bouali, Najib Mrizek, Hatem Elghezal, Ali Saad
Publikováno v:
International Journal of Occupational Medicine and Environmental Health, Vol 26, Iss 1, Pp 144-154 (2013)
Objectives: The aim of this study is to assess chromosomal damage in Tunisian hospital workers occupationally exposed to low levels of ionizing radiation (IR). Materials and Methods: The cytokinesis-block micronucleus (CBMN) assay in the peripheral l
Externí odkaz:
https://doaj.org/article/721573aa5dbd4533a1733b644e913ca4
Autor:
Ghaleb Elyamany, Ali Matar Alzahrani, Eman Al Mussaed, Hassan Aljasem, Sultan Alotaibi, Hatem Elghezal
Publikováno v:
Case Reports in Hematology, Vol 2015 (2015)
The recent World Health Organization (WHO) classification defines mantle cell lymphoma (MCL) as a distinct entity characterized by a unique immunophenotype and a molecular hallmark of chromosomal translocation t(11;14)(q13;q32). We report an unusual
Externí odkaz:
https://doaj.org/article/49634086d3bf45a0ba091ed5ea0e105b
Autor:
Abir Gmidène, Hatem Elghezal, Hlima Sennana, Yosra Ben Youssef, Balkiss Meddeb, Moez Elloumi, Abderrahim Khlif, Ali Saad
Publikováno v:
Advances in Hematology, Vol 2009 (2009)
In this study, Forty-one out of fifty-seven Tunisian children with B-lineage acute lymphoblastic leukemia (B-ALL), and without cytogenetically detectable recurrent abnormalities at the time of the diagnosis, were evaluated by fluorescence in situ hyb
Externí odkaz:
https://doaj.org/article/05646d84e6c84e1fb51ae403e123b25b
Publikováno v:
J Pediatr Genet
Ring chromosome 15 is a rare chromosomal disorder, which usually occurs during early embryonic development via spontaneous errors and has variable presentation. To date, 89 cases of this condition have been reported. This case report describes a 5-ye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::090e67ca72da3721234ff9df4acc7d67
https://doi.org/10.1055/s-0040-1721135
https://doi.org/10.1055/s-0040-1721135
Autor:
Ayesh Almazyad, Abdullah Al Jasser, Amal Alhashem, Omar Alsuhaibani, Ahmed Alfares, Khowla Alfayez, Inesse Ben Abdallah, Hatem Elghezal, Nasser Almobadel
Publikováno v:
European journal of medical genetics. 64(7)
Ring X is a chromosomal anomaly mainly seen in females with turner syndrome and usually present in mosaic form with 45,X cells (45,X/46,X,r(X)) because of their mitotic instability. In males it is an extremely rare finding because large nullisomy for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d0fb9f4ec64e7eb7e09dd986905147b
https://pubmed.ncbi.nlm.nih.gov/33872775
https://pubmed.ncbi.nlm.nih.gov/33872775
Autor:
Ghaleb Elyamany, Qanita Sedick, Omar Alsuhaibani, Nawaf Alkhayat, Eman Al Mussaed, Abdulmalik Alenezy, Hatem Elghezal, Mohammad Alshahrani, Mansour S. Aljabry, Amjad Hammdan, May AlMoshary, Omar Al Sharif, Yasser Elborai
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-11 (2019)
Molecular Cytogenetics
Molecular Cytogenetics
Background Childhood Acute Leukemia (AL) is characterized by recurrent genetic aberrations in 60% of AML cases and 90% of ALL cases. Insufficient data exists of rare cytogenetic abnormalities in AL. Therefore, we tested rare cytogenetic abnormalities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc91cf26026efaf8e90498965ee6114d
https://doi.org/10.1186/s13039-019-0454-0
https://doi.org/10.1186/s13039-019-0454-0