Results 171 to 180 of about 79,367 (221)

Thrombocytopenia, renal failure and hearing loss in a young patient: <i>MYH9</i>-related disorder. [PDF]

BMJ Case Rep
Nukala S, Aparna F, Feliciano M, Withey JL.   +3 more
europepmc   +1 more source

X-Linked Thrombocytopenia in a 6-Year-Old Boy. [PDF]

Turk Arch Pediatr
Miri-Aliabad G, Khajeh A, Nasri-Nasrabadi Z.   +2 more
europepmc   +1 more source

Refractory Immune Thrombocytopenic Purpura With Low Immature Platelet Fraction. [PDF]

Cureus
Ali K, Scotto T, Williams JM, Reddy P.
europepmc   +1 more source

A Case of Acute Kidney Injury During Eltrombopag Use Successfully Treated With Plasma Exchange in Addition to Antithrombotic Therapy. [PDF]

Kidney Med
Ueno N, Kusunoki Y, Kida T, Oda S, Yamano A, Nakayama F, Fukuda S, Ikeda N, Namba-Hamano T, Homma M, Takeji M.   +10 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Diagnostic accuracy of the PLASMIC score in patients with suspected thrombotic thrombocytopenic purpura: A systematic review and meta‐analysis

Transfusion, 2020
The PLASMIC score was developed to identify patients with thrombotic microangiopathy who are most likely to have immune thrombotic thrombocytopenic purpura (TTP) and benefit from therapeutic plasma exchange (TPE).
Koosha Paydary, Emma Banwell, Jiayi Tong, Yong Chen, A. Cuker   +4 more
semanticscholar   +1 more source

First‐in‐patient study of hetrombopag in patients with chronic idiopathic thrombocytopenic purpura

Journal of Thrombosis and Haemostasis, 2020
Idiopathic thrombocytopenic purpura (ITP) especially refractory and (or) relapsed ITP, is a serious and global health burden and its clinical treatment is far from being satisfied.
Zhenlei Wang, Li Chen, Fengkui Zhang, Hua Lu, Xiequn Chen, Aidong Wen, Jianmin Luo, Yu Hu, Yongsheng Wang, T. Niu, Li Zheng   +10 more
semanticscholar   +1 more source

Thrombotic Thrombocytopenic Purpura [PDF]

Thrombosis and Haemostasis, 1995
Recent studies indicate that CRTTP patients have excessive shear stress-induced platelet aggregation that is associated with the presence of ULvWF multimers in their plasma and increased vWF-binding to their platelets by flow cytometry. In these CRTTP patients, relapses, excessive shear-aggregation and the presence in their plasma of ULvWF forms are ...
openaire   +3 more sources

Thrombotic Thrombocytopenic Purpura

Pediatric Emergency Care, 2011
In 1924, Dr Eli Moschcowitz described a 16-year-old adolescent girl with abrupt onset of petechiae, hemolytic anemia, followed by paralysis, coma, and death. Autopsy showed widespread hyaline thrombi in the terminal arterioles and capillaries of various organs. The syndrome described by Moschowitz is now known as thrombotic thrombocytopenic purpura.
Alex Koyfman, Vincent W. Chiang, Elizabeth Brém   +2 more
openaire   +3 more sources

Immune Thrombocytopenic Purpura

New England Journal of Medicine, 2002
Immune thrombocytopenic purpura, which may lead to bleeding, is typically caused by antibodies directed against the platelet glycoprotein IIb/IIIa complex. Since the management of the disorder is different for children and adults, the authors of this up-to-date review provide separate sections on the two age groups.
Douglas B. Cines, Victor S. Blanchette
openaire   +5 more sources