Zobrazeno 1 - 10 of 106 pro vyhledávání: '"Mohammad, AJ"'
1
A persistent cough as atypical clinical presentation of intrathoracic extramedullary hematopoiesis (EMH) in a female with thalassemia intermedia
Autor: Abdulla, Mohammad AJ, Yassin, Mohamed A, Abdelrazek, Mohamed, Mudawi, Deena, Ibrahim, Firyal, Soliman, Dina S., ElOmri, Halima, Nashwan, Abdulqadir J, Fernihough, Liam, de Sanctis, Vincenzo, Soliman, Ashraf T
Publikováno v: Acta bio-medica : Atenei Parmensis
Extramedullary hematopoiesis (EMH) is a rare disorder, defined as the appearance of hematopoietic elements outside the bone marrow or peripheral blood. The most common sites of EMH are liver and spleen, but it has been documented in other organs such
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::83118b27f843dddf781e6ac7deeccd4c
http://europepmc.org/articles/PMC6179037
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2
Akademický článek
Large vessel involvement in biopsy-proven giant cell arteritis: incidence, distribution, and predictors.
Autor: Naderi, N1 (AUTHOR) carl.turesson@med.lu.se, Mohammad, AJ2,3,4 (AUTHOR), Turesson, C4,5 (AUTHOR)
Publikováno v: Scandinavian Journal of Rheumatology. May2017, Vol. 46 Issue 3, p215-221. 7p. 2 Charts, 2 Graphs.
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4
Final Height and Endocrine Complications in Patients with β-Thalassemia Intermedia: Our Experience in Non-Transfused Versus Infrequently Transfused Patients and Correlations with Liver Iron Content
Autor: Yassin, Mohamed A., Soliman, Ashraf T., De Sanctis, Vincenzo, Yassin, Khadra S., Abdulla, Mohammad AJ.
Publikováno v: Mediterranean Journal of Hematology and Infectious Diseases
Background β-thalassemia intermedia (TI) spans a wide spectrum of severity and carries higher morbidity than previously recognized, including extramedullary hematopoiesis, leg ulcers, gallstones, thrombosis, secondary heart failure, pulmonary hypert
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::26a74b263bf05f97239f5a845c30b21a
http://europepmc.org/articles/PMC6548215
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5
T Prolymphocytic Leukemia, a rare disease, case presentation with typical pathological findings and review of management
Autor: Mohamed A. Yassin, Liam J. Fernyhough, Dina Sameh Soliman, Mohammad Aj. Abdulla, Firyal Ibrahim, Sonia Allouch, Ahmad Al-Sabbagh, Mahmoud Aldapt, Halima El-Omri
Publikováno v: International Journal of Case Reports.
Background: Prolymphocytic leukemia (PLL) is a rare disease, accounting for < 2% of lymphoid leukemias [1].There are 2 quite different entities with distinct pathologic features and different therapeutic strategies, T-cell and B-cell [2]. T-PLL is mo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::000a917c63ef619546ce7bdea6ee7a61
https://doi.org/10.28933/ijcr-2018-11-0907
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6
Akademický článek
Association of cigarette smoking with organ damage in primary systemic vasculitis.
Autor: Mohammad, AJ1,2 (AUTHOR) aladdin.mohammad@med.lu.se, Segelmark, M1 (AUTHOR)
Publikováno v: Scandinavian Journal of Rheumatology. Jan2011, Vol. 40 Issue 1, p51-56. 6p. 3 Charts, 1 Graph.
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7
Akademický článek
Swedish Society of Rheumatology 2018 guidelines for investigation, treatment, and follow-up of giant cell arteritis.
Autor: Turesson, C, Börjesson, O, Larsson, K, Mohammad, AJ, Knight, A, Mohammad, A J
Publikováno v: Scandinavian Journal of Rheumatology; Jul2019, Vol. 48 Issue 4, p259-265, 7p, 4 Charts
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8
Akademický článek
Epidemiology of primary systemic vasculitis in children: a population-based study from southern Sweden.
Autor: Mossberg, M, Segelmark, M, Kahn, R, Englund, M, Mohammad, AJ, Mohammad, A J
Publikováno v: Scandinavian Journal of Rheumatology; Jul2018, Vol. 47 Issue 4, p295-302, 8p, 1 Diagram, 2 Charts, 2 Graphs, 1 Map
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9
Akademický článek
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10
Akademický článek
The extent and pattern of organ damage in small vessel vasculitis measured by the Vasculitis Damage Index (VDI)
Autor: Mohammad AJ, Bakoush O, Sturfelt G, Segelmark M
Publikováno v: Scandinavian Journal of Rheumatology; Aug2009, Vol. 38 Issue 4, p268-275, 8p
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