Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mohamed A.M El-Menoufy"'
Publikováno v:
Egyptian Rheumatologist, Vol 41, Iss 2, Pp 105-109 (2019)
Background: Rheumatoid arthritis (RA) is associated with accelerated atherosclerosis which is not fully explained by traditional risk factors. Such excess risk appears to be driven by systemic inflammation. Aim of the work: Aim of the work was to com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f362cf9a33dcf1db663d7c107e39efe
https://doi.org/10.1016/j.ejr.2018.06.003
https://doi.org/10.1016/j.ejr.2018.06.003
Publikováno v:
Journal of the Egyptian National Cancer Institute, Vol 30, Iss 4, Pp 133-138 (2018)
Background: Monosomy 7 (−7) or deletion in its long arm [del(7q)] is among the most common chromosomal abnormalities in myeloid malignancies. There are prognostic variations between −7 and del(7q) in acute myeloid leukemia (AML) and myelodysplast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c379a7712db7cca7dda46d2915791b0
https://pubmed.ncbi.nlm.nih.gov/30472199
https://pubmed.ncbi.nlm.nih.gov/30472199
Publikováno v:
The Egyptian Journal of Haematology. 44:28
Background Cholelithiasis (gallstone disease) is found in more than one-half of the patients with sickle cell disease (SCD) by the age of 30 years. Complications of symptomatic cholelithiasis may precipitate to recurrent sickle cell crises, which add
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83116e26fcfe822548688df747dcefbd
https://doi.org/10.4103/ejh.ejh_34_18
https://doi.org/10.4103/ejh.ejh_34_18
Publikováno v:
The Egyptian Journal of Haematology. 43:138
Background T315I is the most difficult type of point mutation that appears during treatment of chronic myeloid leukemia (CML). It represents kind of a ‘gatekeeper’ that controls access of small molecule inhibitors and confers resistance to the mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6aef1e23c0d68c10b36f33b4ca5fc5af
https://doi.org/10.4103/ejh.ejh_18_18
https://doi.org/10.4103/ejh.ejh_18_18
Publikováno v:
The Egyptian Journal of Haematology. 43:38
Background The Philadelphia chromosome is the hallmark of chronic myeloid leukemia (CML). As the disease progresses to accelerated phase and blast crisis (BC), clonal evolution may occur with the emergence of additional chromosomal abnormalities. Wil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8de1be7c3576f22311df82760698e89
https://doi.org/10.4103/ejh.ejh_5_18
https://doi.org/10.4103/ejh.ejh_5_18
Publikováno v:
The Egyptian Journal of Surgery. 36:181
Splenomegaly and massive splenomegaly are common clinical findings in hematological diseases especially in inherited hemoglobin disorders (sickle cell disease and thalassemia) and hematologic malignancies. Laparoscopic splenectomy (LS) is the gold st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c0fe9404a15e7d14cb9d8d5a5659e7d
https://doi.org/10.4103/1110-1121.204534
https://doi.org/10.4103/1110-1121.204534