[Waldenström's benign hyperglobulinemic purpura]. 1986

M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli

UI MeSH Term Description Entries
D011694 Purpura, Hyperglobulinemic Purplish or brownish red discoloration of the skin associated with increase in circulating polyclonal globulins, usually GAMMA-GLOBULINS. This syndrome often occurs on the legs of women aged 20 to 40 years. Benign Hyperglobulinemic Purpura of Waldenström,Hypergammaglobulinemic Purpura of Waldenstrom,Hyperglobulinemic Purpura,Hyperglobulinemic Purpura of Waldenström,Waldenstrom Hyperglobulinemic Purpura,Hyperglobulinemic Purpura, Waldenstrom,Hyperglobulinemic Purpuras,Purpura, Waldenstrom Hyperglobulinemic,Purpuras, Hyperglobulinemic,Waldenstrom Hypergammaglobulinemic Purpura,Waldenström Hyperglobulinemic Purpura
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000974 Antibodies, Antinuclear Autoantibodies directed against various nuclear antigens including DNA, RNA, histones, acidic nuclear proteins, or complexes of these molecular elements. Antinuclear antibodies are found in systemic autoimmune diseases including systemic lupus erythematosus, Sjogren's syndrome, scleroderma, polymyositis, and mixed connective tissue disease. Anti-DNA Antibodies,Antibodies, Anti-DNA,Antinuclear Antibodies,Antinuclear Autoantibodies,Antinuclear Autoantibody,Antinuclear Factors,Antinuclear Antibody,Antinuclear Factor,Anti DNA Antibodies,Antibody, Antinuclear,Autoantibody, Antinuclear,Factor, Antinuclear
D012859 Sjogren's Syndrome Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. Sicca Syndrome,Sjogren Syndrome,Sjogrens Syndrome,Syndrome, Sicca,Syndrome, Sjogren's

Related Publications

M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
April 1958, Nordisk medicin,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
January 1968, Thrombosis et diathesis haemorrhagica. Supplementum,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
April 1966, Wiadomosci lekarskie (Warsaw, Poland : 1960),
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
February 1957, L'union medicale du Canada,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
January 1984, Haematologica,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
January 1967, Lille medical : journal de la Faculte de medecine et de pharmacie de l'Universite de Lille,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
January 1983, Annales de dermatologie et de venereologie,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
January 1956, Acta haematologica,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
October 1990, Annales de pediatrie,
M B Santiago, and E C de Mendonça, and N B de Melo, and A Gabriel Júnior, and W Cossermelli
November 1970, Schweizerische medizinische Wochenschrift,
Copied contents to your clipboard!