[Thrombotic thrombocytopenic purpura: report of a case recovering after splenectomy and plasma exchange]. 1985

H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori

UI MeSH Term Description Entries
D008297 Male Males
D010951 Plasma Exchange Removal of plasma and replacement with various fluids, e.g., fresh frozen plasma, plasma protein fractions (PPF), albumin preparations, dextran solutions, saline. Used in treatment of autoimmune diseases, immune complex diseases, diseases of excess plasma factors, and other conditions. Exchange, Plasma,Exchanges, Plasma,Plasma Exchanges
D011697 Purpura, Thrombotic Thrombocytopenic An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases. Moschkowitz Disease,Purpura, Thrombotic Thrombopenic,Thrombotic Thrombocytopenic Purpura, Congenital,Thrombotic Thrombocytopenic Purpura, Familial,Congenital Thrombotic Thrombocytopenic Purpura,Familial Thrombotic Thrombocytopenia Purpura,Familial Thrombotic Thrombocytopenic Purpura,Microangiopathic Hemolytic Anemia, Congenital,Moschcowitz Disease,Schulman-Upshaw Syndrome,Thrombotic Microangiopathy, Familial,Thrombotic Thrombocytopenic Purpura,Upshaw Factor, Deficiency of,Upshaw-Schulman Syndrome,Familial Thrombotic Microangiopathy,Microangiopathy, Familial Thrombotic,Schulman Upshaw Syndrome,Thrombocytopenic Purpura, Thrombotic,Thrombopenic Purpura, Thrombotic,Thrombotic Thrombopenic Purpura,Upshaw Schulman Syndrome
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D013156 Splenectomy Surgical procedure involving either partial or entire removal of the spleen. Splenectomies

Related Publications

H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
November 1983, Archives of internal medicine,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
November 1957, The New England journal of medicine,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
February 1966, Archives of internal medicine,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
December 1984, Canadian Medical Association journal,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
May 1979, Lancet (London, England),
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
January 1990, Current studies in hematology and blood transfusion,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
February 2001, Therapeutic apheresis : official journal of the International Society for Apheresis and the Japanese Society for Apheresis,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
October 1986, Scandinavian journal of haematology,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
January 1969, Acta haematologica,
H Nozaki, and M Shimizu, and K Noguchi, and K Watanabe, and T Nagao, and S Arimori
January 1992, Nihon rinsho. Japanese journal of clinical medicine,
Copied contents to your clipboard!