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Journal Abstract Search
501 related items for PubMed ID: 14235120
1. [A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)]. SILVESTRONI E, BIANCO I. Prog Med (Napoli); 1964 Aug 15; 20():509-13. PubMed ID: 14235120 [No Abstract] [Full Text] [Related]
2. [PRESENCE OF MICROCYTHEMIA WITH NORMAL AMOUNT OF HEMOGLOBIN A2 AND ELEVATED AMOUNT OF HEMOGLOBIN F IN A CALABRIAN FAMILY (THIRD VARIETY OF MICROCYTHEMIA)]. SILVESTRONI E, BIANCO I, BRANCATI C. Policlinico Prat; 1964 Oct 19; 71():1543-5. PubMed ID: 14213722 [No Abstract] [Full Text] [Related]
4. [HOMOZYGOUS HEMOGLOBIN S AND ALPHA THALASSEMIC DISEASE]. AKSOY M. Turk Tip Cemiy Mecm; 1963 Jun 19; 29():299-305. PubMed ID: 14047036 [No Abstract] [Full Text] [Related]
5. Sickle cell haemoglobin and two types of thalassaemia in the same family. RUSSO G, MOLLICA F. Acta Haematol; 1962 Jun 19; 28():329-40. PubMed ID: 13975667 [No Abstract] [Full Text] [Related]
15. Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D. STURGEON P, ITANO HA, BERGREN WR. Blood; 1955 May 11; 10(5):389-404. PubMed ID: 14363320 [No Abstract] [Full Text] [Related]
20. [The hemoglobin picture in microdrepanocytic disease and in drepanocytic anemia]. SILVESTRONI E, BIANCO I, MUZZOLINI M, ROBERTI L. Prog Med (Napoli); 1960 Jan 31; 16():37-44. PubMed ID: 14446800 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]