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Journal Abstract Search
168 related items for PubMed ID: 7343525
1. Primary hyperoxaluria and adenosine deaminase deficiency without immunodeficiency. Perignon JL, Hamet M, Broyer M, Griscelli C, Lenoir G, Cartier P. Int J Pediatr Nephrol; 1980 Mar; 1(1):26-9. PubMed ID: 7343525 [No Abstract] [Full Text] [Related]
2. Complete adenosine deaminase (ADA) deficiency without immunodeficiency, and primary hyperoxaluria, in a 12-year-old boy. Perignon JL, Hamet M, Cartier P, Griscelli C. Adv Exp Med Biol; 1980 Mar; 122A():403-8. PubMed ID: 6968500 [No Abstract] [Full Text] [Related]
3. A family of adenosine deaminase deficiency with severe combined immunodeficiency. Tsuchiya S, Narisawa K, Konno T, Tada K. Jinrui Idengaku Zasshi; 1979 Jun; 24(2):95-8. PubMed ID: 529554 [No Abstract] [Full Text] [Related]
4. [Adenosine deaminase deficit in severe combined immunodeficiency (author's transl)]. Español Borén T, Jacques Castro G, Torán Fuentes N, Vives-Corrons JL. Sangre (Barc); 1981 Jun; 26(6):1129-38. PubMed ID: 6805082 [No Abstract] [Full Text] [Related]
5. Genetic deficiencies of adenosine deaminase and purine nucleoside phosphorylase and their implications for therapy of leukemias. Hirschhorn R, Ratech H. Curr Top Hematol; 1983 Jun; 4():1-35. PubMed ID: 6413135 [No Abstract] [Full Text] [Related]
9. [Adenosine deaminase deficiency and severe combined immunodeficiency]. Ueland PM. Tidsskr Nor Laegeforen; 1980 Feb 20; 100(5):274-6. PubMed ID: 7385150 [No Abstract] [Full Text] [Related]
10. Genetic deficiencies of adenosine deaminase and purine nucleoside phosphorylase: overview, genetic heterogeneity and therapy. Hirschhorn R. Birth Defects Orig Artic Ser; 1983 Feb 20; 19(3):73-81. PubMed ID: 6418227 [No Abstract] [Full Text] [Related]
11. Adenosine and deoxyadenosine metabolism in the erythrocytes of a patient with adenosine deaminase deficiency. Sahota A, Simmonds HA, Potter CF, Watson JG, Hugh-Jones K, Perrett D. Adv Exp Med Biol; 1980 Feb 20; 122A():397-401. PubMed ID: 6999851 [No Abstract] [Full Text] [Related]