Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Achandira M. Udayakumar"'
Autor:
Achandira M. Udayakumar, Nagla Fawaz, Anil Pathare, Shakila Asraf, Mohammed Al-Huneini, Khalil Al-Farsi, Salam Al-Kindi, Murtadha Al-Khabouri
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 17, Iss 3, Pp 286-292 (2017)
Clonal cytogenetic abnormalities have been reported among 30–80% of patients with myelodysplastic syndromes (MDS); however, 20–70% of patients with MDS show a normal karyotype that may nevertheless harbour a cryptic genetic alteration. Earlier re
Externí odkaz:
https://doaj.org/article/9a7036c9ee1a4aa581d320984a7f7066
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 15, Iss 3, Pp 411-414 (2015)
Follicular dendritic cell sarcoma (FDCS) is a rare neoplasm with a non-specific and insidious presentation further complicated by the difficult diagnostic and therapeutic assessment. It has a low to intermediate risk of recurrence and metastasis. Unl
Externí odkaz:
https://doaj.org/article/1187d475a10642638087a76aa6bca743
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 15, Iss 3, Pp 415-419 (2015)
The duplication of the short arm of chromosome 7 as de novo is extremely rare. The phenotype spectrum varies depending on the region of duplication. We report a case of de novo duplication of chromosomal region 7p21.1p22.2 in a three-year-old male ch
Externí odkaz:
https://doaj.org/article/4049e17e908d479f92540eebe3300e05
Autor:
Nagla Fawaz, Salam Alkindi, Khalil Al-Farsi, Murtadha Al-Khabouri, Shakila Asraf, Achandira M. Udayakumar, Mohammed Al-Huneini, Anil Pathare
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 17, Iss 3, Pp 286-292 (2017)
Clonal cytogenetic abnormalities have been reported among 30–80% of patients with myelodysplastic syndromes (MDS); however, 20–70% of patients with MDS show a normal karyotype that may nevertheless harbour a cryptic genetic alteration. Earlier re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90b91ed90e06b057e685aadffa6b494
https://journals.squ.edu.om/index.php/squmj/article/view/2225
https://journals.squ.edu.om/index.php/squmj/article/view/2225
Publikováno v:
Acta Haematologica Polonica. 46:368-371
Fanconi anemia (FA) is a genetic disorder of chromosomal instability. One of the routine methods of confirmation for FA includes chromosome breakage analysis, using crosslink-inducing agents. Bone marrow karyotyping at diagnosis and further follow-up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7154c2c28a73b8a95251948ebb2de1f
https://doi.org/10.1016/j.achaem.2015.10.003
https://doi.org/10.1016/j.achaem.2015.10.003
Autor:
Achandira M, Udayakumar, Nagla, Fawaz, Anil, Pathare, Shakila, Asraf, Mohammed, Al-Huneini, Khalil, Al-Farsi, Salam, Al-Kindi, Murtadha, Al-Khabouri
Publikováno v:
Sultan Qaboos University medical journal. 17(3)
Clonal cytogenetic abnormalities have been reported among 30–80% of patients with myelodysplastic syndromes (MDS); however, 20–70% of patients with MDS show a normal karyotype that may nevertheless harbour a cryptic genetic alteration. Earlier re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b61e1d0ddb4304d2eda9d5cc020832f0
https://pubmed.ncbi.nlm.nih.gov/29062550
https://pubmed.ncbi.nlm.nih.gov/29062550
Publikováno v:
Leukemia & Lymphoma. 55:2672-2674
Leukemia in twins was first reported in 1928, and subsequent studies have demonstrated an increased risk in monozygotic twins [1]. Identical but non-constitutive genetic changes in leukemia cells f...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::059d7cdeb132c3b958140ec37f9ea358
https://doi.org/10.3109/10428194.2014.900764
https://doi.org/10.3109/10428194.2014.900764
Publikováno v:
Journal of Applied Genetics. 50:73-76
Pericentric inversion of chromosome 9 involving the qh region is relatively common as a constitutional genetic aberration without any apparent phenotypic consequences. However, it has not been established as an acquired abnormality in cancer. Among t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305548dd5f77115f6c61c42e19292e9c
https://doi.org/10.1007/bf03195656
https://doi.org/10.1007/bf03195656
Autor:
Salam Alkindi, John Alexander Raeburn, Asem A. Alghzaly, Shanmugakonar Muralitharan, Achandira M. Udayakumar, Anil Pathare
Publikováno v:
Archives of Medical Research. 38:797-802
We describe a case of acute myeloid leukemia (AML) in which trisomy 21 was the sole acquired cytogenetic abnormality. The immunophenotype showed positivity for CD7 and CD9 along with CD13, CD33, and CD34. The chromosomal analysis of bone marrow showe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c185be3aa13e7263582f237a592c331c
https://doi.org/10.1016/j.arcmed.2007.04.007
https://doi.org/10.1016/j.arcmed.2007.04.007
Autor:
Yasser Wali, Ashfaq Ahmed Khan, Achandira M. Udayakumar, Anil Pathare, Heba Soliman, John Alexander Raeburn, Wafa Bashir, Zakia Al-Lamki, Mathew Zacharia
Publikováno v:
Archives of Medical Research. 38:305-312
Background Chromosomal abnormalities have important diagnostic and prognostic significance in acute lymphoblastic leukemia (ALL). The purpose of this study was to define and classify the frequency and type of chromosomal abnormalities among newly dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::500340b1f843a0a5e4f7ab0478e8a0f4
https://doi.org/10.1016/j.arcmed.2006.10.006
https://doi.org/10.1016/j.arcmed.2006.10.006