Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rahaf AlTahan"'
Autor:
Rahaf Altahan, Mohammed Lafi Alanazi, Mohammed Abdulaziz Alharbi, Salman Almalki, Aziza Alswayyed, Laila Alsuhaibani
Publikováno v:
Clinical Case Reports, Vol 11, Iss 12, Pp n/a-n/a (2023)
Key Clinical Message We present an interesting case that showed a non‐hematopoietic structure embedded in the bone marrow biopsy. Given the clinical and morphological difficulties, it was challenging to identify this artifact's nature. Publishing t
Externí odkaz:
https://doaj.org/article/c610171ff3ad49768ce9466c4f6d91df
Autor:
Mohammed A. Bafail, Rahaf AlTahan, Manar A. Samman, Suha A. Tashkandi, Ibraheem H. Motabi, Abdul Ali Peer‐Zada
Publikováno v:
Clinical Case Reports, Vol 11, Iss 7, Pp n/a-n/a (2023)
Key Clinical Message Complete molecular remission in a “variant APL” patient with short isoform of PML‐RARα and FLT3‐ITD mutation was achieved in response to ATRA and ATO plus IDA instead of standard treatment protocol. The use of FLT3 inhib
Externí odkaz:
https://doaj.org/article/3d850dd1ae6c43448c3ca23808964ac4
Publikováno v:
Clinical Case Reports, Vol 7, Iss 3, Pp 558-563 (2019)
Key Clinical Message t(11;17) is a rare but recognized finding usually found in Acute Promyelocytic Leukemia with variant RARA translocation (APLv). We present a case of Acute Myeloid Leukemia with t(11;17) that has different break points than those
Externí odkaz:
https://doaj.org/article/84d0456836de49658392e10b3b6fddfb
Autor:
Suleimman Al-Sweedan, Rahaf Altahan
Publikováno v:
Hematology Reports, Vol 11, Iss 2 (2019)
Intrachromosomal amplification (iAMP) of chromosome 21 entity is associated with a dismal outcome in B cell Acute Lymphoblastic Leukemia (B-ALL). This cytogenetic abnormality is caused by a novel mechanism; breakage-fusion-bridge cycles followed by c
Externí odkaz:
https://doaj.org/article/078823a7071442a984ef2dd0950a4f23
Autor:
Rahaf Altahan, Areej Al Mugairi
Publikováno v:
Clinical Case Reports, Vol 7, Iss 9, Pp 1809-1810 (2019)
Abstract We present images (Figure 1A‐D) of a preterm girl who had severe anemia due to HDFN caused by maternal anti‐C and anti‐D alloantibodies. These images show erythrophagocytosis, which is a very interesting and rarely encountered feature.
Externí odkaz:
https://doaj.org/article/9fa6ad536ea14cd49c9f6813316627ee
Publikováno v:
The American journal of case reports. 23
BACKGROUND Angioimmunoblastic T cell lymphoma (AITL) is an aggressive and rare entity that comprises about 1-2% of all non-Hodgkin lymphomas. This entity carries many challenges that start at the diagnosis, as most patients present with non-specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86afb94a04739b36261e3579c5ca7913
https://pubmed.ncbi.nlm.nih.gov/35957503
https://pubmed.ncbi.nlm.nih.gov/35957503
Autor:
Batoul Baz, Dorota Monies, Thamer A Alamoudi, Ahmed Tarawah, Nouf S Al-Numair, Mahasen Saleh, Nada Al Tassan, Hala AbaAlkhail, M. Abouelhoda, Randa AlNounou, Hazza Alzahrani, Abdulrahman Al-Musa, Rahaf Altahan, Amjad Jabaan, Basma Al Abdulaziz, Tarek Owaidah
Publikováno v:
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-7 (2019)
NPJ Genomic Medicine
NPJ Genomic Medicine
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder. Around 490 mutations in ITGA2B and ITGB3 genes were reported. We aimed to use targeted next-generation sequencing (NGS) to identify variants in patients with GT. We screen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0ca044888b0a091b31dba2f34499d67
http://link.springer.com/article/10.1038/s41525-019-0079-6
http://link.springer.com/article/10.1038/s41525-019-0079-6
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 7, Iss 3, Pp 558-563 (2019)
Clinical Case Reports, Vol 7, Iss 3, Pp 558-563 (2019)
Key Clinical Message t(11;17) is a rare but recognized finding usually found in Acute Promyelocytic Leukemia with variant RARA translocation (APLv). We present a case of Acute Myeloid Leukemia with t(11;17) that has different break points than those
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69ee070023581c7d8a4d4303047cd0f6
http://europepmc.org/articles/PMC6406162
http://europepmc.org/articles/PMC6406162
Autor:
Eve Simoneau, Eman Alrijraji, Nouran Molla, Zahir T Fadel, Peter Metrakos, Rahaf Altahan, Louis-Martin Boucher, Ahmad Madkhali, Mazen Hassanain
Publikováno v:
Journal of the American College of Surgeons. 219:e105-e106
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2667e93a4e7147ff4b0ea1818d08e0e2
https://doi.org/10.1016/j.jamcollsurg.2014.07.666
https://doi.org/10.1016/j.jamcollsurg.2014.07.666