240 related articles for article (PubMed ID: 14129142)
1. [ON A CASE OF DOUBLE DREPANOCYTOSIS-MICROCYTHEMIA HETEROZYGOSITY WITH DIMINUTION OF FRACTION A2].
CUTILLO S; MIRAGLIADELGIUDICE M; DEBELLIS U
Rass Int Clin Ter; 1963 Dec; 43():1251-64. PubMed ID: 14129142
[No Abstract] [Full Text] [Related]
2. INTERACTION OF HEMOGLOBIN LEPORE WITH SICKLE CELL TRAIT AND MICROCYTHEMIA (THALASSEMIA) IN A SOUTHERN ITALIAN FAMILY.
SILVESTRONI E; BIANCO I; BAGLIONI C
Blood; 1965 Apr; 25():457-69. PubMed ID: 14284335
[No Abstract] [Full Text] [Related]
3. [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; 20():509-13. PubMed ID: 14235120
[No Abstract] [Full Text] [Related]
4. [On the behavior of different types of hemoglobin (Hb A, A2, F, S and "Bart's") in thalassemia, drepanocytosis and microdrepanocythemia].
VENTRUTO V; DE ROSA L; CIMINO R; QUATTRIN N
Schweiz Med Wochenschr; 1962 Oct; 92():1322-4. PubMed ID: 13996677
[No Abstract] [Full Text] [Related]
5. [1ST CASE IN GUADELOUPE OF GENOTYPIC HEMOLYTIC ANEMIA WITH DREPANOCYTOSIS AND HEMOGLOBINOSIS D. HISTORY OF A DIAGNOSIS].
PINEAU A
Bull Soc Pathol Exot Filiales; 1963; 56():485-506. PubMed ID: 14081707
[No Abstract] [Full Text] [Related]
6. Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait.
NEEL JV; WELLS IC; ITANO HA
J Clin Invest; 1951 Oct; 30(10):1120-4. PubMed ID: 14888690
[No Abstract] [Full Text] [Related]
7. Variation in the amount of hemoglobin S in a patient with sickle cell trait and megaloblastic anemia.
HELLER P; YAKULIS VJ; EPSTEIN RB; FRIEDLAND S
Blood; 1963 Apr; 21():479-83. PubMed ID: 13953594
[No Abstract] [Full Text] [Related]
8. THREE INHERITED INTRA-ERYTHROCYTIC DEFECTS: HEREDITARY SPHEROCYTOSIS, HB S AND HB C.
THOMPSON RB; ROBERTSON MG
Acta Haematol; 1964 Oct; 32():233-8. PubMed ID: 14252557
[No Abstract] [Full Text] [Related]
9. [On a case of thalasso-drepanocytosis (Silvestroni-Bianco disease). Study of the hemoglobins and of the genetics. Splenectomy].
MARCHAL G; BILSKI-PASQUIER G; de GROUCHY ; COMBRISSON A; DEPLANTE R
Rev Hematol; 1960; 15():291-306. PubMed ID: 13766452
[No Abstract] [Full Text] [Related]
10. 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
Blood; 1953 Mar; 8(3):270-5. PubMed ID: 13032196
[No Abstract] [Full Text] [Related]
11. SIMULTANEOUS RADIOACTIVE TRACER STUDIES OF ERYTHROPOIESIS AND RED-CELL DESTRUCTION IN SICKLE-CELL DISEASE AND SICKLE-CELL HAEMOGLOBIN/THALASSAEMIA.
MALAMOS B; BELCHER EH; GYFTAKI E; BINOPOULOS D
Br J Haematol; 1963 Oct; 9():487-98. PubMed ID: 14076131
[No Abstract] [Full Text] [Related]
12. [ANEMIAS CAUSED BY ABNORMAL HEMOGLOBINS].
DREYFUS JC
Sem Hop; 1964 Apr; 40():1161-9. PubMed ID: 14146499
[No Abstract] [Full Text] [Related]
13. EFFECT OF IRON-DEFICIENCY ANAEMIA ON THE METABOLISM OF THE HETEROGENIC HAEMOGLOBINS IN SICKLE CELL TRAIT.
LEVERE RD; LICHTMAN HC; LEVINE J
Nature; 1964 May; 202():499-501. PubMed ID: 14167840
[No Abstract] [Full Text] [Related]
14. [A NEW KIND OF DREPANOCYTIC ANEMIA: HEMOGLOBIN A-HEMOGLOBIN LEPORE DISEASE].
SILVESTRONI E; BIANCO I
Prog Med (Napoli); 1963 Sep; 19():545-8. PubMed ID: 14122941
[No Abstract] [Full Text] [Related]
15. Abnormal hemoglobins; clinical disorders resulting from various combinations.
LAWRENCE JS; VALENTINE WN
Calif Med; 1955 Jan; 82(1):1-5. PubMed ID: 13230906
[TBL] [Abstract][Full Text] [Related]
16. [RELATIONS BETWEEN ANOMALIES OF HEMOGLOBIN SYNTHESIS AND HUMAN DISEASE].
PAULUZZI S
Recenti Prog Med; 1964 Dec; 37():533-76. PubMed ID: 14262942
[No Abstract] [Full Text] [Related]
17. QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROES.
WEINSTEIN ED; RUCKNAGEL DL; SHAW MW
Am J Hum Genet; 1965 Sep; 17(5):443-56. PubMed ID: 14334744
[No Abstract] [Full Text] [Related]
18. Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori.
Witkowska HE; Lubin BH; Beuzard Y; Baruchel S; Esseltine DW; Vichinsky EP; Kleman KM; Bardakdjian-Michau J; Pinkoski L; Cahn S
N Engl J Med; 1991 Oct; 325(16):1150-4. PubMed ID: 1891024
[No Abstract] [Full Text] [Related]
19. Mutation rates of the abnormal hemoglobin genes.
FROTA-PESSOA O; WAJNTAL A
Am J Hum Genet; 1963 Jun; 15(2):123-5. PubMed ID: 13945846
[No Abstract] [Full Text] [Related]
20. SPLENECTOMY FOR HYPERSPLENISM IN SICKLE CELL ANEMIA.
EGDAHL RH; MARTIN WW; HILKOVITZ G
JAMA; 1963 Nov; 186():745-8. PubMed ID: 14078086
[No Abstract] [Full Text] [Related]
[Next] [New Search]