Zobrazeno 1 - 10
of 44
pro vyhledávání: '"AZMA RZ"'
Publikováno v:
Medicine & Health. 16:39-49
Haematopoietic progenitor stem cells acquired from the peripheral blood have been increasingly used to treat patient with haematological malignancy. The success of the allogeneic peripheral blood stem cell transplantation (PBSCT) is significantly dep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::265955c64a56f76357405fa91878de4d
https://doi.org/10.17576/mh.2021.1601.05
https://doi.org/10.17576/mh.2021.1601.05
Autor:
Khairina Kamarudin, Hafiza Alauddin, Azma Rz, Noor-Farisah Razak, Loh C-Khai, Norunaluwar Jalil, Danny Koh-Xuan-Rong, Azlin Ithnin, Tang Yee Loong, Endom Ismail, Ainoon Othman, Hamidah Alias, Zarina Abdul Latiff
Publikováno v:
Hemoglobin. 42:247-251
Nondeletional α-globin mutations are known to cause more serious clinical effects than deletional ones. A rare IVS-I-1 (G>A) (HBA2: c.95+1G>A) donor splice site mutation interferes with normal splicing of pre mRNA and results in activation of a cryp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bab6116bfa34d51e11c299f03fd8c6bb
https://doi.org/10.1080/03630269.2018.1528985
https://doi.org/10.1080/03630269.2018.1528985
Autor:
Kean-Chang Phang, Azma Rz, Faridah Abd Rahman, Meer-Taher Shabani-Rad, Ariz Akhter, Adnan Mansoor, Nur Maya Sabrina Tizen, Ghaleb Elyamany, Noraidah Masir
Publikováno v:
Journal of Clinical Pathology. 71:215-220
AimsThe cell of origin (COO) based molecular characterisation into germinal centre B-cell-like (GCB) and activated B-cell-like (ABC) subtypes are central to the pathogenesis and clinical course in diffuse large B-cell lymphoma (DLBCL). Globally, clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0313720db93273be5cdf79f9568ba7d7
https://doi.org/10.1136/jclinpath-2017-204548
https://doi.org/10.1136/jclinpath-2017-204548
Autor:
Suria Abdul Aziz, Omayma Saad Eldeen Bakheet, S.F. Chandramaya, Azma Rz, Nurasyikin Y, Noraidah Masir
Publikováno v:
Medicine & Health. 12:66-82
Acute myeloid leukaemia (AML) is the most common subtype of acute leukaemias with a poor outcome. Msi2 protein is a newly discovered prognostic marker and it has been considered as a new target for therapy in AML. The study of Msi2 protein expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2b5e520c01088fc8f6620fdb466a732
https://doi.org/10.17576/mh.2017.1201.08
https://doi.org/10.17576/mh.2017.1201.08
Autor:
C-Khai Loh, Ho Wai Koo, Hamidah Alias, Farah Azima Abdul Muttlib, Woon Lee Yong, Hafiza Alauddin, Azma Rz, Sie Chong Doris Lau
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-8 (2018)
Background Acquired thrombotic thrombocytopenia purpura is very rarely encountered in children. It is often misdiagnosed initially when the condition is not inherited. Case presentation We describe a 3-year-old Malay boy who presented with simple feb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b62b90c7dcf5580e778cc7c9d91aa73
https://pubmed.ncbi.nlm.nih.gov/30223886
https://pubmed.ncbi.nlm.nih.gov/30223886
Publikováno v:
Medicine & Health (Universiti Kebangsaan Malaysia); Jun2021, Vol. 16 Issue 1, p39-49, 11p
Autor:
Ainoon Othman, Hafiza Alauddin, Azma Rz, Noor-Farisah Razak, Noor-Adilah Jaapar, Zarina Abdul-Latiff, Azlin Ithnin, Hamidah Alias, C-Khai Loh
Publikováno v:
Hemoglobin. 38:277-281
Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] is a rare hemoglobin (Hb) variant due to a mutation at codon 59 of the α2- or α1-globin gene resulting in a glycine to aspartic acid substitution. Two siblings with a unique coinheritance of Hb Adana a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1098d29d3d51d26562d1b7b77897bbdc
https://doi.org/10.3109/03630269.2014.916720
https://doi.org/10.3109/03630269.2014.916720
Autor:
Hamidah Alias, Ainoon Othman, Syahzuwan Hassan, Azlin Ithnin, Jalil Norunaluwar, Hafiza Alauddin, Malisa Mohd Yusoff, Zarina Abdul Latiff, Azma Rz, Nor Rafeah Tumian
Publikováno v:
Hemoglobin. 43:351-351
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8433ca477130fab6f6e50ca004c4616
https://doi.org/10.1080/03630269.2020.1718904
https://doi.org/10.1080/03630269.2020.1718904
Autor:
Loh C-Khai, Hafiza Alauddin, Norunaluwar Jalil, Azma Rz, Nur Zainura Mohamad, Zarina Abdul Latiff
Publikováno v:
Hemoglobin. 43:357-357
IVS-I-2 (T>C) (HBB: c.92 ± 2T>C) is a point mutation that affect the splice junction between the exon and intron of the HBB gene. The aberrant splicing site generates an abnormal mRNA. It is a rare...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d07413505e3eafdf9c63b7119c42f335
https://doi.org/10.1080/03630269.2020.1717737
https://doi.org/10.1080/03630269.2020.1717737
Autor:
Ghaleb Elyamany, Meer-Taher Shabani-Rad, Douglas A. Stewart, Salwati Shuib, Noraidah Masir, Adnan Mansoor, Azma Rz, Fariborz Rashid-Kolvear, Gary D. Sinclair, Ariz Akhter, Muhammad Kashif Mughal
Publikováno v:
Diagnostic Pathology
Background The World Health Organization (WHO) classification system defines recurrent chromosomal translocations as the sole diagnostic and prognostic criteria for acute leukemia (AL). These fusion transcripts are pivotal in the pathogenesis of AL.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be63b313abef56ba041b6507701aecaa
https://doi.org/10.1186/s13000-016-0541-z
https://doi.org/10.1186/s13000-016-0541-z