BIOMAT Database Logo BIOMAT Database Logo

Primary immunodeficiency disease presenting in midlife. 1996

S J Kornfeld, and R N Haire, and G W Litman

UI MeSH Term Description Entries
D008040 Genetic Linkage The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME. Genetic Linkage Analysis,Linkage, Genetic,Analyses, Genetic Linkage,Analysis, Genetic Linkage,Genetic Linkage Analyses,Linkage Analyses, Genetic,Linkage Analysis, Genetic
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D011505 Protein-Tyrosine Kinases Protein kinases that catalyze the PHOSPHORYLATION of TYROSINE residues in proteins with ATP or other nucleotides as phosphate donors. Tyrosine Protein Kinase,Tyrosine-Specific Protein Kinase,Protein-Tyrosine Kinase,Tyrosine Kinase,Tyrosine Protein Kinases,Tyrosine-Specific Protein Kinases,Tyrosylprotein Kinase,Kinase, Protein-Tyrosine,Kinase, Tyrosine,Kinase, Tyrosine Protein,Kinase, Tyrosine-Specific Protein,Kinase, Tyrosylprotein,Kinases, Protein-Tyrosine,Kinases, Tyrosine Protein,Kinases, Tyrosine-Specific Protein,Protein Kinase, Tyrosine-Specific,Protein Kinases, Tyrosine,Protein Kinases, Tyrosine-Specific,Protein Tyrosine Kinase,Protein Tyrosine Kinases,Tyrosine Specific Protein Kinase,Tyrosine Specific Protein Kinases
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000361 Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. Hypogammaglobulinemia,Agammaglobulinemias,Hypogammaglobulinemias
D014960 X Chromosome The female sex chromosome, being the differential sex chromosome carried by half the male gametes and all female gametes in human and other male-heterogametic species. Chromosome, X,Chromosomes, X,X Chromosomes

Related Publications

S J Kornfeld, and R N Haire, and G W Litman
Immunodeficiency Presenting as an Undiagnosed Disease.
February 2017, Pediatric clinics of North America,
S J Kornfeld, and R N Haire, and G W Litman
Child abuse presenting as immunodeficiency disease.
September 1978, The Journal of pediatrics,
S J Kornfeld, and R N Haire, and G W Litman
Primary human immunodeficiency virus infection presenting as elevated aminotransferases.
June 2010, Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi,
S J Kornfeld, and R N Haire, and G W Litman
Primary human immunodeficiency virus infection presenting as acute pancreatitis.
April 2004, Southern medical journal,
S J Kornfeld, and R N Haire, and G W Litman
Ischaemic heart disease in primary immunodeficiency.
November 1998, Lancet (London, England),
S J Kornfeld, and R N Haire, and G W Litman
Progressive encephalopathy in primary immunodeficiency disease.
January 2002, Clinical immunology (Orlando, Fla.),
S J Kornfeld, and R N Haire, and G W Litman
Primary Neuritic Hansen's Disease presenting as Ulnar Nerve Abscess in a Human Immunodeficiency Virus Positive Patient.
January 2015, Indian journal of leprosy,
S J Kornfeld, and R N Haire, and G W Litman
Primary immunodeficiency disease and hematology.
January 2016, [Rinsho ketsueki] The Japanese journal of clinical hematology,
S J Kornfeld, and R N Haire, and G W Litman
Primary Immunodeficiency Disease Mimicking Pediatric Bechet's Disease.
January 2021, Children (Basel, Switzerland),
S J Kornfeld, and R N Haire, and G W Litman
Primary Immunodeficiency Diseases Presenting with Chalazia as the First Manifestation.
February 2021, Ocular immunology and inflammation,
Copied contents to your clipboard!