A second case of inosine phosphorylase deficiency with severe T-cell abnormalities. 1977

M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli

UI MeSH Term Description Entries
D007111 Immunity, Cellular Manifestations of the immune response which are mediated by antigen-sensitized T-lymphocytes via lymphokines or direct cytotoxicity. This takes place in the absence of circulating antibody or where antibody plays a subordinate role. Cell-Mediated Immunity,Cellular Immune Response,Cell Mediated Immunity,Cell-Mediated Immunities,Cellular Immune Responses,Cellular Immunities,Cellular Immunity,Immune Response, Cellular,Immune Responses, Cellular,Immunities, Cell-Mediated,Immunities, Cellular,Immunity, Cell-Mediated,Response, Cellular Immune
D007153 Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. Antibody Deficiency Syndrome,Deficiency Syndrome, Immunologic,Deficiency Syndromes, Antibody,Deficiency Syndromes, Immunologic,Immunologic Deficiency Syndrome,Immunological Deficiency Syndromes,Antibody Deficiency Syndromes,Deficiency Syndrome, Antibody,Deficiency Syndrome, Immunological,Deficiency Syndromes, Immunological,Immunological Deficiency Syndrome,Syndrome, Antibody Deficiency,Syndrome, Immunologic Deficiency,Syndrome, Immunological Deficiency,Syndromes, Antibody Deficiency,Syndromes, Immunologic Deficiency,Syndromes, Immunological Deficiency
D008214 Lymphocytes White blood cells formed in the body's lymphoid tissue. The nucleus is round or ovoid with coarse, irregularly clumped chromatin while the cytoplasm is typically pale blue with azurophilic (if any) granules. Most lymphocytes can be classified as either T or B (with subpopulations of each), or NATURAL KILLER CELLS. Lymphoid Cells,Cell, Lymphoid,Cells, Lymphoid,Lymphocyte,Lymphoid Cell
D008297 Male Males
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D010430 Pentosyltransferases Enzymes of the transferase class that catalyze the transfer of a pentose group from one compound to another.
D011683 Purine-Nucleoside Phosphorylase An enzyme that catalyzes the reaction between a purine nucleoside and orthophosphate to form a free purine plus ribose-5-phosphate. EC 2.4.2.1. Inosine Phosphorylase,Nicotinamide Riboside Phosphorylase,Purine Nucleoside Phosphorylases,Nucleoside Phosphorylases, Purine,Phosphorylase, Inosine,Phosphorylase, Nicotinamide Riboside,Phosphorylase, Purine-Nucleoside,Phosphorylases, Purine Nucleoside,Purine Nucleoside Phosphorylase,Riboside Phosphorylase, Nicotinamide
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D004912 Erythrocytes Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN. Blood Cells, Red,Blood Corpuscles, Red,Red Blood Cells,Red Blood Corpuscles,Blood Cell, Red,Blood Corpuscle, Red,Erythrocyte,Red Blood Cell,Red Blood Corpuscle
D005347 Fibroblasts Connective tissue cells which secrete an extracellular matrix rich in collagen and other macromolecules. Fibroblast

Related Publications

M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
December 1982, Clinical and experimental immunology,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
December 1978, The Journal of pediatrics,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
January 2013, Journal of clinical immunology,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
December 2010, Journal of inherited metabolic disease,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
October 1989, Scandinavian journal of immunology,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
July 1977, The British journal of dermatology,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
March 1978, The Journal of pediatrics,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
May 1975, Lancet (London, England),
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
March 1988, Rinsho shinkeigaku = Clinical neurology,
M Hamet, and C Griscelli, and P Cartier, and J Ballay, and C de Bruyn, and P Hösli
June 1979, Journal of immunology (Baltimore, Md. : 1950),
Copied contents to your clipboard!