Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Mohammad S, Abdelgawwad"'
Autor:
Jingrui Sui, Wenjing Cao, Konstantine Halkidis, Mohammad S. Abdelgawwad, Nicole K. Kocher, Bryan Guillory, Lance A. Williams, Radhika Gangaraju, Marisa B. Marques, X. Long Zheng
Publikováno v:
Blood Advances, Vol 3, Iss 24, Pp 4177-4186 (2019)
Abstract: Immune thrombotic thrombocytopenic purpura (iTTP) is primarily caused by immunoglobulin G (IgG)–type autoantibodies that bind and inhibit plasma ADAMTS13 activity and/or accelerate its clearance from circulation. Approximately 50% of pati
Externí odkaz:
https://doaj.org/article/3075a9848ea04a87aa80ea5d219f1fe4
Autor:
Isaac N, Naazie, Isibor, Arhuidese, Mohammad S, Abdelgawwad, Jonathan, Unkart, Michael S, Conte, Mahmoud B, Malas
Publikováno v:
Annals of Vascular Surgery. 88:79-89
Different renin-angiotensin-aldosterone system inhibitor (RAASI) usage patterns exist among patients undergoing lower extremity bypass (LEB) for peripheral arterial disease. We studied the association of RAASI usage patterns with LEB outcomes to dete
Autor:
Liang Zheng, Mohammad S. Abdelgawwad, Di Zhang, Leimeng Xu, Shi Wei, Wenjing Cao, X. Long Zheng
Publikováno v:
Haematologica, Vol 105, Iss 4 (2020)
Thrombotic thrombocytopenic purpura (TTP) is caused by severe deficiency of ADAMTS13 (A13), a plasma metalloprotease that cleaves endothelium-derived von Willebrand factor (VWF). However, severe A13 deficiency alone is often not sufficient to cause a
Externí odkaz:
https://doaj.org/article/c99fbb0d3c3342cdac7355f8667a3e73
Autor:
Liang Zheng, Yingying Mao, Mohammad S. Abdelgawwad, Nicole K. Kocher, Mandy Li, Xiangrong Dai, Benjamin Li, X. Long Zheng
Publikováno v:
Blood Advances, Vol 1, Iss 1, Pp 75-83 (2016)
Abstract: Thrombotic thrombocytopenic purpura (TTP), a potentially fatal blood clot disorder, is primarily caused by severe deficiency of plasma ADAMTS13 activity resulting from acquired autoantibodies. Plasma exchange is the only effective initial t
Externí odkaz:
https://doaj.org/article/34c526799c7b469d8a77d8247241821c
Autor:
Liang Zheng, Wenjing Cao, X. Long Zheng, Di Zhang, Mohammad S. Abdelgawwad, Shi Wei, Leimeng Xu
Publikováno v:
Haematologica. 105:1107-1119
Thrombotic thrombocytopenic purpura (TTP) is caused by severe deficiency of ADAMTS13 (A13), a plasma metalloprotease that cleaves endothelium-derived von Willebrand factor (VWF). However, severe A13 deficiency alone is often not sufficient to cause a
Autor:
Mohammad S. Abdelgawwad, Jenny K. McDaniel, Douglas B. Cines, Khalil Bdeir, Matthew B. Renfrow, Audra A. Hargett, Wenjing Cao, X. Long Zheng
Publikováno v:
Journal of Thrombosis and Haemostasis. 17:596-606
Essentials Biological activity of human neutrophil peptide (HNP)-1 in hemostasis under physiological conditions is not fully understood. HNP-1 inhibits the adhesion/aggregation of murine platelets on a fibrillar collagen surface or an activated endot
Autor:
X. Long Zheng, Nicole K. Kocher, Mohammad S. Abdelgawwad, Wenjing Cao, Liang Zheng, Lance A. Williams
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 38:2731-2743
Objective— ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type 1 repeats-13) cleaves VWF (von Willebrand factor). This process is essential for hemostasis. Severe deficiency of plasma ADAMTS13 activity, most commonly resulting from
Autor:
Marisa B. Marques, Konstantine Halkidis, Wenjing Cao, Lance A. Williams, Nicole K. Kocher, Bryan Guillory, Jingrui Sui, Radhika Gangaraju, X. Long Zheng, Mohammad S. Abdelgawwad
Immune thrombotic thrombocytopenic purpura (iTTP) is primarily caused by immunoglobulin G (IgG)–type autoantibodies that bind and inhibit plasma ADAMTS13 activity and/or accelerate its clearance from circulation. Approximately 50% of patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c9f0561b02a93a9ec962ed2df421b02
https://europepmc.org/articles/PMC6929391/
https://europepmc.org/articles/PMC6929391/
Publikováno v:
Thromb Haemost
Background Proteolytic cleavage of von Willebrand factor (VWF) by a plasma a disintegrin and metalloproteinase with a thrombospondin type 1 motifs, member 13 (ADAMTS13) is regulated by shear stress and binding of coagulation factor VIII, platelets or
Autor:
Camli Al-Sadek, Henry W. Lim, Nabiha Yusuf, Prescilia Isedeh, Casey D. Morrow, Sejong Bae, William Van Der Pol, Hana N. Ahmed, Craig A. Elmets, Abdullah Shaheen, Erin M. Burns, Mohammad S. Abdelgawwad, Thompson M Foy, Sumeira Huda, Iltefat H. Hamzavi, Anum F. Muzaffar, Indermeet Kohli
Publikováno v:
Exp Dermatol
IMPORTANCE: Studies have begun to investigate the complex relationship between host and microorganism in non-infectious pathologies such as acne, atopic dermatitis, and psoriasis. Though the skin is continuously exposed to environmental stressors suc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e36d341241585b675e125f8ab5f0c5a
https://europepmc.org/articles/PMC7394481/
https://europepmc.org/articles/PMC7394481/