Similar articles for PMID: 14311973

Year	Number of Results
1946	1
1947	3
1948	2
1949	3
1950	3
1951	3
1952	2
1953	6
1954	2
1955	5
1956	6
1957	11
1958	8
1959	8
1960	4
1961	7
1962	9
1963	22
1964	29
1965	21
1966	7
1967	2
1968	3
1969	1
1971	1
1972	3
1973	7
1974	4
1975	4
1976	5
1978	2
1979	2
1980	2
1983	1
1985	1
1988	1
1989	1
1993	1
1994	1
1998	1
2001	1
2005	1
2008	1
2009	1
2012	2
2013	1
2014	1
2015	1
2016	2
2018	1
2019	1
2020	1
2021	1
2024	0

1

A NEW HAEMOGLOBIN, D IBADAN (BETA-87 THREONINE -- LYSINE), PRODUCING NO SICKLE-CELL HAEMOGLOBIN D DISEASE WITH HAEMOGLOBIN S.

WATSON-WILLIAMS EJ, BEALE D, IRVINE D, LEHMANN H. WATSON-WILLIAMS EJ, et al. Nature. 1965 Mar 27;205:1273-6. doi: 10.1038/2051273a0. Nature. 1965. PMID: 14311973 No abstract available.

2

Sickle cell haemoglobin and two types of thalassaemia in the same family.

RUSSO G, MOLLICA F. RUSSO G, et al. Acta Haematol. 1962;28:329-40. doi: 10.1159/000207298. Acta Haematol. 1962. PMID: 13975667 No abstract available.

3

[A NEW KIND OF DREPANOCYTIC ANEMIA: HEMOGLOBIN A-HEMOGLOBIN LEPORE DISEASE].

SILVESTRONI E, BIANCO I. SILVESTRONI E, et al. Prog Med (Napoli). 1963 Sep 30;19:545-8. Prog Med (Napoli). 1963. PMID: 14122941 Italian. No abstract available.

4

SICKLE-CELL HAEMOGLOBIN K DISEASE.

O GORMAN P, ALLSOPP KM, LEHMANN H, SUKUMARAN PK. O GORMAN P, et al. Br Med J. 1963 Nov 30;2(5369):1381-2. doi: 10.1136/bmj.2.5369.1381. Br Med J. 1963. PMID: 14063031 Free PMC article. No abstract available.

5

SIMULTANEOUS PRESENCE OF HAEMOGLOBIN I AND HAEMOGLOBIN BART'S IN A DEER.

SWARUP S, RAY HN, GHOSH SK, CHATTERJEA JB. SWARUP S, et al. Bull Calcutta Sch Trop Med. 1964 Jul;12:97-8. Bull Calcutta Sch Trop Med. 1964. PMID: 14238717 No abstract available.

6

THE RELATION OF ALKALI-RESISTANT HAEMOGLOBIN IN THALASSAEMIA AND ABNORMAL HAEMOGLOBIN SYNDROMES TO FOETAL HAEMOGLOBIN.

STURGEON P, SCHROEDER WA, JONES RT, BERGREN WR. STURGEON P, et al. Br J Haematol. 1963 Oct;9:438-45. doi: 10.1111/j.1365-2141.1963.tb05467.x. Br J Haematol. 1963. PMID: 14076125 No abstract available.

7

HOMOZYGOUS SICKLE-CELL ANAEMIA ARISING FROM TWO DIFFERENT HAEMOGLOBINS S. INTERACTION OF HAEMOGLOBINS S AND STANLEYVILLE-II.

HALL-CRAGGS M, MARSDEN PD, RAPER AB, LEHMANN H, BEALE D. HALL-CRAGGS M, et al. Br Med J. 1964 Jul 11;2(5401):87-9. doi: 10.1136/bmj.2.5401.84. Br Med J. 1964. PMID: 14147795 Free PMC article. No abstract available.

8

Studies on abnormal hemoglobins. VI. Electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon.

SINGER K, FISHER B. SINGER K, et al. Blood. 1953 Mar;8(3):270-5. Blood. 1953. PMID: 13032196 Free article. No abstract available.

9

[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. SILVESTRONI E, et al. Prog Med (Napoli). 1964 Aug 15;20:509-13. Prog Med (Napoli). 1964. PMID: 14235120 Italian. No abstract available.

10

Haemoglobin DIbadan in a haemoglobin S endemic population.

Falusi AG, Ogunmola GB, Esan GJ. Falusi AG, et al. Afr J Med Med Sci. 1979 Sep-Dec;8(3-4):95-101. Afr J Med Med Sci. 1979. PMID: 122322

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