BIOMAT Database Logo BIOMAT Database Logo

[Mu-chain disease and hypergammaglobulinemia--an unusual immunoglobulin disorder with general lymphadenopathy]. 1973

O Wetter

UI MeSH Term Description Entries
D007075 Immunoglobulin M A class of immunoglobulin bearing mu chains (IMMUNOGLOBULIN MU-CHAINS). IgM can fix COMPLEMENT. The name comes from its high molecular weight and originally was called a macroglobulin. Gamma Globulin, 19S,IgM,IgM Antibody,IgM1,IgM2,19S Gamma Globulin,Antibody, IgM
D008206 Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. Lymphatism,Status Lymphaticus,Disease, Lymphatic,Diseases, Lymphatic,Lymphatic Disease
D001796 Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. Blood Protein Disorder,Disorder, Blood Protein,Disorders, Blood Protein,Protein Disorder, Blood,Protein Disorders, Blood
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006942 Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. Hyperimmunoglobulinemia,Hypergammaglobulinemias,Hyperimmunoglobulinemias
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

Related Publications

O Wetter
Proteinaceous lymphadenopathy with hypergammaglobulinemia.
April 1979, The American journal of surgical pathology,
O Wetter
Light chain disease with hypergammaglobulinemia.
May 1984, Journal of the Medical Association of Thailand = Chotmaihet thangphaet,
O Wetter
Unusual sequences in the murine immunoglobulin mu-delta heavy-chain region.
January 1983, Nature,
O Wetter
[Lymphadenopathy associated with hypergammaglobulinemia (author's transl)].
January 1974, [Rinsho ketsueki] The Japanese journal of clinical hematology,
O Wetter
Mu heavy chain disease with MYD88 L265P mutation: an unusual manifestation of lymphoplasmacytic lymphoma.
August 2022, Diagnostic pathology,
O Wetter
Anderson-Fabry disease: an unusual presentation with lymphadenopathy.
September 1989, Journal of the Royal Society of Medicine,
O Wetter
Somatic hypermutation of an immunoglobulin mu heavy chain transgene.
February 1993, The Journal of experimental medicine,
O Wetter
Immunoglobulin M heavy chain disease: intracellular origin of the mu chain fragment.
August 1970, Science (New York, N.Y.),
O Wetter
Kappa-chain deficiency. An immunoglobulin disorder.
May 1976, The New England journal of medicine,
O Wetter
Correction: Mu heavy chain disease with MYD88 L265P mutation: An unusual manifestation of lymphoplasmacytic lymphoma.
October 2022, Diagnostic pathology,
Copied contents to your clipboard!