Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Mohammad Abu-Tineh"'
Autor:
Mostafa Najim, Mohammad Abu-Tineh, Awni Alshurafa, Mohamed Izham Mohamed Ibrahim, Soubiya Ansari, Hazem Faraj, Saif Alateeg, Susanna Jane Akiki, Mohamed A. Yassin
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
ABSTRACTBackground Myeloproliferative neoplasms (MPNs) are hematological disorders characterized by abnormal production of myeloid cells due to genetic mutations. Since 2013, researchers have identified somatic mutations in the Calreticulin (CALR) ge
Externí odkaz:
https://doaj.org/article/8fad399548d140829ec749fe345f77c6
Autor:
Mohammad S. Afana, Mohammad Abu-Tineh, Awni Alshurafa, Khalid Ahmed, Mohammed Abdulgayoom, Mohamed A. Yassin
Publikováno v:
Case Reports in Oncology, Vol 17, Iss 1, Pp 91-95 (2024)
Introduction: Polycythemia vera (PV) is one of the myeloproliferative neoplasms (MPN) diagnosed by World Health Organization (WHO) criteria 2016, which requires the presence of 3 major criteria: high hemoglobin/hematocrit, bone marrow findings, and J
Externí odkaz:
https://doaj.org/article/ce0de06cb3634723811c73a281c827b6
Autor:
Mohammad Abu-Tineh, Mohammed A. Alamin, Esra’a Aljaloudi, Awni Alshurafa, Beatriz Garcia-Cañibano, Ruba Y. Taha, Sarah A. Elkourashy
Publikováno v:
Case Reports in Oncology, Vol 16, Iss 1, Pp 1300-1305 (2023)
Introduction: Lambert-Eaton myasthenia syndrome (LEMS) is a rare autoimmune disorder characterized by autoantibodies targeting presynaptic neuromuscular junctions. It results in muscle weakness and autonomic dysfunction. LEMS can be idiopathic or ass
Externí odkaz:
https://doaj.org/article/09271d1cbcf740aaa34110cd632aa4cf
Autor:
Mohammad S. Afana, Mohammad Abu-Tineh, Awni Alshurafa, Ahmed K. Yasin, Khalid Ahmed, Mohammed Abdulgayoom, Mohamed A. Yassin
Publikováno v:
Hematology, Vol 28, Iss 1 (2023)
ABSTRACTSickle cell disease (SCD) is one of the most common hematological diseases, which results in variable complications. The treatment of SCD is evolving but limited options are available for now. Acute chest syndrome (ACS) is one of the serious
Externí odkaz:
https://doaj.org/article/04148f6046f54c1aa1b3c9dfccac19ad
Publikováno v:
Case Reports in Oncology, Vol 16, Iss 1, Pp 56-62 (2023)
Mastocytosis is a heterogeneous group of disorders in which mast cells exhibit clonal proliferation that infiltrates one or more organs. In cutaneous mastocytosis, the mast cells infiltrate the skin only, whereas systemic mastocytosis is diagnosed wh
Externí odkaz:
https://doaj.org/article/9ac002fdae7d4422a17a4924378bd615
Autor:
Elrazi A. Ali, Mohammad Abu-Tineh, Mohamed Abdelrazek, Mahir Petkar, Mzaki Karzoun, Eihab A. Subahi, Lajos Szabados, Mohamed A. Yassin
Publikováno v:
Case Reports in Oncology, Vol 15, Iss 2, Pp 755-761 (2022)
Chronic myeloid leukemia (CML) is a hematologic malignancy that has significant improvement in its prognosis after the introduction of tyrosine kinase inhibitors. Transformation to accelerated phase or blast phase can happen. Myeloid sarcoma or chlor
Externí odkaz:
https://doaj.org/article/3ec57762d78e48ee874937757264adfe
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Sickle cell leg ulcers (SCLUs) are usually chronic, painful, and devastating complications of sickle cell disease. Skin vaso-occlusion with compromised blood flow, chronic inflammation, and endothelial dysfunction is thought to be the underlying mech
Externí odkaz:
https://doaj.org/article/1f185503c0474a658b5f4d2c8eb125d3
Autor:
Abdulrahman Al‐Abdulmalek, Reem Al‐Suliman, Mohammad Abu‐Tineh, Mostafa Ali, Mohamed A. Yassin
Publikováno v:
Clinical Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract The relationship between chronic myelogenous leukemia (CML) and tuberous sclerosis (TS) is unusual and uncommon. Here, we report a 24‐year‐old woman diagnosed with TS and later identified with CML, as the second case reported with such c
Externí odkaz:
https://doaj.org/article/91e468329b24477c9775e1cf0bffb327
Publikováno v:
Case Reports in Oncology, Vol 14, Iss 3, Pp 1435-1440 (2021)
The coexistence of dual hematological neoplasms is an unusual and challenging presentation due to the different combination of etiopathology. The presentation of synchronous dual hematological malignancies can be one of the 3 types: myeloid + lymphoi
Externí odkaz:
https://doaj.org/article/7c1ee90c32314028ba3c064f278f563e
Autor:
Basel Elsayed, Amgad M. Elshoeibi, Mohamed Elhadary, Khaled Ferih, Ahmed Adel Elsabagh, Alaa Rahhal, Mohammad Abu-Tineh, Mohammad S. Afana, Mohammed Abdulgayoom, Mohamed Yassin
Publikováno v:
Diagnostics, Vol 13, Iss 6, p 1123 (2023)
Philadelphia-negative (Ph-) myeloproliferative neoplasms (MPNs) are a group of hematopoietic malignancies identified by clonal proliferation of blood cell lineages and encompasses polycythemia vera (PV), essential thrombocythemia (ET), and primary my
Externí odkaz:
https://doaj.org/article/fd04a3194489487a89d605e38f525079