Displaying publications 1 - 20 of 220 in total

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  1. Lie-Injo LE
    Med J Malaya, 1961 Dec;16:94-106.
    PMID: 14465149
    Matched MeSH terms: Hemoglobins, Abnormal*
  2. VELLA F, FIELD TE
    Med J Malaya, 1958 Dec;13(2):153-8.
    PMID: 13632213
    Matched MeSH terms: Hemoglobins*; Hemoglobins, Abnormal*
  3. VELLA F
    Med J Malaya, 1958 Jun;12(4):602-4.
    PMID: 13577152
    Matched MeSH terms: Hemoglobinopathies*; Hemoglobins*; Hemoglobins, Abnormal*
  4. George E, Faridah K
    Family Practitioner, 1986;9:38-40.
    Matched MeSH terms: Hemoglobins
  5. VELLA F, TAVARIA D
    Nature, 1961 May 20;190:729-30.
    PMID: 13780662
    Matched MeSH terms: Hemoglobins*
  6. VELLA F, SINGH RB
    Trans. R. Soc. Trop. Med. Hyg., 1959 Nov;53:534-5.
    PMID: 13841618
    Matched MeSH terms: Hemoglobins*
  7. WADSWORTH GR, LEE TS
    Med J Malaya, 1955 Sep;10(1):87-91.
    PMID: 13287498
    Matched MeSH terms: Hemoglobins*; Oxyhemoglobins*
  8. Lie-Injo LE
    Med J Malaya, 1972 Dec;27(2):120-4.
    PMID: 4268037
    Matched MeSH terms: Hemoglobins/biosynthesis; Hemoglobins, Abnormal/analysis*
  9. George-Kodiseri E, Faridah K, George-Vadaketh R, Lau PS, Ong MS, Tan TY, et al.
    Family Physician, 1989;1:34-42.
    Matched MeSH terms: Hemoglobins
  10. George-Kodiseri E, Mokhtar AB, Farida K, Wong HB, Duraisamy G
    Family Physician, 1991;3:28-30.
    Matched MeSH terms: Hemoglobins
  11. Blackwell RQ, Lie-Injo LE, Weng MI
    Trop Geogr Med, 1971 Sep;23(3):294-5.
    PMID: 5099000
    Matched MeSH terms: Hemoglobins/analysis*
  12. VELLA F
    Med J Malaya, 1959 Sep;14:31-5.
    PMID: 13855207
    Matched MeSH terms: Hemoglobins/chemistry*
  13. LEHMAN H, SINGH RB
    Nature, 1956 Sep 29;178(4535):695-6.
    PMID: 13369502
    Matched MeSH terms: Hemoglobin E*; Hemoglobins*
  14. George E, Huisman TH, Yang KG, Kutlari F, Wilson JB, Kutlar A, et al.
    Med. J. Malaysia, 1989 Sep;44(3):259-62.
    PMID: 2626142
    A new haemoglobin, Haemoglobin Malay is described in a 22 year old Malay. Structural analysis showed a AAC----AGC mutation in codon 17, with the production of an abnormal beta chain (beta Malay) that has an Asn----Ser substitution at position beta 19. This haemoglobin variant could not be detected by conventional procedures.
    Matched MeSH terms: Hemoglobins, Abnormal*
  15. Goh TH, Hariharan M, Tan CH
    Contraception, 1980 Oct;22(4):389-95.
    PMID: 7449387
    The increase in menstrual blood loss associated with copper-bearing IUDs may cause or aggravate pre-existing anaemia. In order to evaluate this risk, 84 Malaysian women wearing copper-IUDs were studied longitudinally by means of serial measurements of blood haemoglobin concentration (Hb), serum iron (S/Fe) and transferrin saturation (T/S). The initial Hb was under 12 gm% in 33.7% of patients. The mean Hb showed no significant change up to 12 months while S/Fe fell significantly at the end of this time; the T/S was significantly reduced as early as 6 months post-insertion. There is a significant risk of anaemia following copper-IUD insertion, particularly with long-term usage. Progestogen-releasing IUDs may offer the most feasible solution to this problem in our local context since oral medication with iron or drugs to reduce menstrual blood loss is not practicable.
    Matched MeSH terms: Hemoglobins*
  16. Lim W
    Med J Malaya, 1966 Dec;21(2):169-76.
    PMID: 4227389
    Matched MeSH terms: Hemoglobins/analysis*
  17. Poi Tzse Chiat D
    Med J Malaya, 1965 Mar;19(3):184-7.
    PMID: 4220470
    Matched MeSH terms: Hemoglobins, Abnormal*
  18. Boon WH
    Med J Malaya, 1968 Sep;23(1):61-6.
    PMID: 4237561
    Matched MeSH terms: Hemoglobins, Abnormal*
  19. COLBOURNE MJ, IKIN EW, MOURANT AE, LEHMANN H, THEIN H
    Nature, 1958 Jan 11;181(4602):119-20.
    PMID: 13493616
    Matched MeSH terms: Hemoglobin E*; Hemoglobins*
  20. Lie-Injo LE
    Blood, 1962 Nov;20:581-90.
    PMID: 13930509
    Five cases of severe hydrops and erythroblastosis fetalis in association with a large amount of Hb “Bart’s,” all of Chinese origin, are described. The following characteristic clinical and hematologic symptoms were found. There were generalized hydrops, ascites and gross enlargement of the liver. The spleen, however, was not ahvays enlarged. The placenta was large and friable. Severe erythroblastosis of the blood was always found, with reticulocytosis, many target cells and thin cells. The MCV of the red cells was very high. The cells showed an interesting sickling phenomenon. No evidence of isoimmunization was found. In eight parents examined, no abnormal hemoglobin was detected, and alkali-resistant hemoglobin and hemoglobin A2 were not found to be increased. Their blood showed microcytosis of the red cells cxcept in one father and one mother. In this mother, however, the blood was examimied after a blood transfusion. It is thought probable that these were cases of homozygous alpha-chain thalassemia.
    Matched MeSH terms: Hemoglobins*; Hemoglobins, Abnormal*
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