Results 151 to 160 of about 68,977 (202)

A 35-year-old man with immune thrombotic thrombocytopenic purpura presenting with dark urine. [PDF]

CMAJ
Bhangu G, Arreglo R, Merkeley H.
europepmc   +1 more source

Systematic Literature Review of the Economic and Quality of Life Burden of Congenital and Immune-Mediated Thrombotic Thrombocytopenic Purpura. [PDF]

J Blood Med
Kaur H, Ghoshal D, Khurana IS.
europepmc   +1 more source

Unmet health care needs in immune thrombotic thrombocytopenic purpura survivors. [PDF]

Res Pract Thromb Haemost
Story CM, Brown J, Martin C, Chaturvedi S.   +3 more
europepmc   +1 more source

Pathological Allostery in ADAMTS13: Autoantibody-Induced Modulation and Its Role in Immune Thrombotic Thrombocytopenic Purpura (iTTP). [PDF]

Pharmaceuticals (Basel)
Gil M, Halkidis K.
europepmc   +1 more source

Idiopathic thrombotic thrombocytopenic purpura

Acta Médica del Centro, 2009
Carmen Garrido Arce, Claudia Roche Albernas, Yanet González Riera, Elvys Pérez Bada, Nadia Patricia Rodríguez Villalta   +4 more
doaj  

Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies [PDF]

Journal of Thrombosis and Haemostasis, 2017
Essentials An international collaboration provides a consensus for clinical definitions. This concerns thrombotic microangiopathies and thrombotic thrombocytopenic purpura (TTP).
Flora Peyvandi, Marie Scully, Bernhard Lämmle   +2 more
exaly   +4 more sources

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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, Elizabeth, Brém, Vincent W, Chiang   +2 more
openaire   +2 more sources

Thrombotic Thrombocytopenic Purpura

Acta Medica Scandinavica, 1952
Abstract 1.1. The clinical and pathologic observations of two cases of thrombotic thrombocytopenic purpura are presented. 2.2. This condition is characterized by the clinical triad of (1) hemolytic anemia; (2) thrombocytopenic purpura and (3) mental and neurologic abnormalities which may be bizarre or transient.
F, RACKOW, L, STEINGOLD, J H F, WOOD
openaire   +4 more sources

THROMBOTIC THROMBOCYTOPENIC PURPURA

Medical Journal of Australia, 1957
A 40-year-old obese black woman has had weakness and epigastric pain for several weeks and diarrhea and vomiting for four days. She does not appear acutely ill; the physical examination is normal except for abdominal tenderness. Her hematocrit is 25 percent. The platelet count is 10,000 per cubic millimeter.
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
W G, Murphy, J C, Moore, T E, Warkentin, C P, Hayward, J G, Kelton   +4 more
openaire   +2 more sources