BIOMAT Database Logo BIOMAT Database Logo

[Pyruvate kinase deficiency in hereditary, non-spherocytic hemolytic anemia]. 1966

C Gasser, and H R Marti

UI MeSH Term Description Entries
D008297 Male Males
D008659 Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) Thesaurismosis,Diseases, Metabolic,Disease, Metabolic,Metabolic Disease,Thesaurismoses
D011770 Pyruvate Kinase ATP:pyruvate 2-O-phosphotransferase. A phosphotransferase that catalyzes reversibly the phosphorylation of pyruvate to phosphoenolpyruvate in the presence of ATP. It has four isozymes (L, R, M1, and M2). Deficiency of the enzyme results in hemolytic anemia. EC 2.7.1.40. L-Type Pyruvate Kinase,M-Type Pyruvate Kinase,M1-Type Pyruvate Kinase,M2-Type Pyruvate Kinase,Pyruvate Kinase L,R-Type Pyruvate Kinase,L Type Pyruvate Kinase,M Type Pyruvate Kinase,M1 Type Pyruvate Kinase,M2 Type Pyruvate Kinase,Pyruvate Kinase, L-Type,Pyruvate Kinase, M-Type,Pyruvate Kinase, M1-Type,Pyruvate Kinase, M2-Type,Pyruvate Kinase, R-Type,R Type Pyruvate Kinase
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
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
D000745 Anemia, Hemolytic, Congenital Hemolytic anemia due to various intrinsic defects of the erythrocyte. Anemia, Hemolytic, Hereditary,Congenital Hemolytic Anemia,Hemolytic Anemia, Congenital,Hemolytic Anemia, Hereditary,Hereditary Hemolytic Anemia,Anemia, Congenital Hemolytic,Anemia, Hereditary Hemolytic,Anemias, Congenital Hemolytic,Anemias, Hereditary Hemolytic,Congenital Hemolytic Anemias,Hemolytic Anemias, Congenital,Hemolytic Anemias, Hereditary,Hereditary Hemolytic Anemias

Related Publications

C Gasser, and H R Marti
[Non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency].
June 1967, L'union medicale du Canada,
C Gasser, and H R Marti
[NON-SPHEROCYTIC CONGENITAL HEMOLYTIC ANEMIA CAUSED BY PYRUVATE-KINASE DEFICIENCY].
January 1964, Bulletins et memoires de la Societe medicale des hopitaux de Paris,
C Gasser, and H R Marti
[From gene to disease; hereditary non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency].
September 2002, Nederlands tijdschrift voor geneeskunde,
C Gasser, and H R Marti
Hereditary non-spherocytic hemolytic anemia of the pyruvate-kinase deficient type.
April 1963, Annals of internal medicine,
C Gasser, and H R Marti
[Hereditary non-spherocytic hemolytic anemia].
November 1960, Revista medica de Chile,
C Gasser, and H R Marti
[Hereditary non-spherocytic hemolytic anemia].
January 1965, Revista espanola de pediatria,
C Gasser, and H R Marti
[HEREDITARY HEMOLYTIC ANEMIA WITH PYRUVATE-KINASE DEFICIENCY].
June 1964, Minerva medica,
C Gasser, and H R Marti
[Congenital non spherocytic hemolytic anemia caused by pyruvate kinase abnormalities].
January 1966, Haematologica,
C Gasser, and H R Marti
Pyruvate kinase activity of erythrocytes in hereditary non-spherocytic hemolytic anemias.
January 1969, Polish medical journal,
C Gasser, and H R Marti
[Pyruvate kinase activity of erythrocytes in hereditary non-spherocytic hemolytic anemias].
January 1968, Polskie Archiwum Medycyny Wewnetrznej,
Copied contents to your clipboard!