Results 221 to 230 of about 27,505 (253)

Erratum for Nivolumab-induced Thrombotic Thrombocytopenic Purpura in Patients with Gastric Tube Cancer. [PDF]

Intern Med
Yoshida Y, Toriyabe S, Imai H, Sasaki K, Kasahara Y, Ouchi K, Saijo K, Onodera K, Ishioka C.   +8 more
europepmc   +1 more source

Adult patients with immune thrombocytopenic purpura. New expectations [PDF]

, 2014
Gómez Almaguer, David
core  

From Common Symptom to Critical Diagnosis: Vertigo as a Clue to Thrombotic Thrombocytopenic Purpura. [PDF]

Cureus
Stern AJ, Munoz NR, Khan R, Agwuegbo CC, Yasin S, Pearson M, Gauhar F.   +6 more
europepmc   +1 more source

A Rare But Fatal Toxicity: Immune Checkpoint Inhibitor-Related Acquired Thrombotic Thrombocytopenic Purpura. [PDF]

J Immunother Precis Oncol
Yikilmaz AS, Hernandez CMR.
europepmc   +1 more source

Raising Suspicion of Thrombotic Thrombocytopenic Purpura in a Patient With a Pre-existing Autoimmune Disease. [PDF]

Cureus
Murugan NL, Mensah R, Singh A.
europepmc   +1 more source

Thrombotic Thrombocytopenic Purpura [PDF]

Annual Review of Medicine, 1988
Platelet thrombus formation in small vessels is triggered by certain stimuli, including vascular injury, primary platelet agglutination, or both. The formation and dissolution of platelet thrombi is modulated by proteolysis, plasma factors, PGI2 synthesis and stability, and immune mechanisms.
openaire   +4 more sources

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

Some of the next articles are maybe not open access.

Related searches:

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

Thrombotic thrombocytopenic purpura

Blood Coagulation & Fibrinolysis, 1992
Thrombotic thrombocytopenic purpura is an uncommon disorder, but it continues to be of considerable interest. The disease mechanisms are unclear and the aetiology is unknown. Perhaps most enigmatic of all, the mode of action of plasma therapy, which successfully induces remission in about two-thirds of cases, is wholly inexplicable. There are currently
Theodore E. Warkentin, William G. Murphy, Jane C. Moore, Catherine P.M. Hayward, John G. Kelton   +4 more
openaire   +3 more sources