Displaying publications 941 - 960 of 1801 in total

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  1. Chen PC, Noordin RA, Ngor LY
    Med J Malaysia, 1979 Dec;34(2):100-7.
    PMID: 548710
    Matched MeSH terms: Infant, Newborn
  2. Lim MA, Wong WP, Sinnathuray TA
    Br J Obstet Gynaecol, 1977 Aug;84(8):600-4.
    PMID: 889748
    The characteristics of normal labour in 977 Malay, Chinese and Indian parturients were established from a retrospective study. Indian babies were found to be significantly smaller than Malay babies which were significantly smaller than Chinese babies (P less than 0-05, P less than 0-05). The mean duration of the first stage of labour taken from the time of admission to the labour ward was 3-4 hours in primiparae and 2-7 hours in multiparae. The mean durations of the second stage of labour were 23-7 minutes and 13-1 minutes respectively. Curves of mean dilatation of cervix and probit analysis at 80% revealed significant differences in the progress of normal labour in primiparae among the three racial groups. The Indian primiparae not only had a slower rate of cervical dilatation but seemed to reach the accelerated phase of dilatation later. No significant differences were noticed in the labours of multiparae.
    Matched MeSH terms: Infant, Newborn
  3. Lal M, Said MY
    Med J Malaysia, 1974 Jun;28(4):283-6.
    PMID: 4278623
    Matched MeSH terms: Infant, Newborn
  4. Liew SH
    Med J Malaysia, 1974 Jun;28(4):293-5.
    PMID: 4278975
    Matched MeSH terms: Infant, Newborn
  5. Damodaran A, Nair S, Somasundram R
    Med J Malaysia, 1973 Dec;28(2):99-102.
    PMID: 4276265
    Matched MeSH terms: Infant, Newborn
  6. Meade MS
    Soc Sci Med, 1978 Jun;12(2D):95-102.
    PMID: 705375
    Matched MeSH terms: Infant, Newborn
  7. Tan KL
    J Singapore Paediatr Soc, 1977 Dec;19(4):238-40.
    PMID: 616476
    Matched MeSH terms: Infant, Newborn
  8. George R, Hoi Sen Y, Lim G, Boo LJ
    Med J Malaysia, 1975 Dec;30(2):83-7.
    PMID: 1228386
    Matched MeSH terms: Infant, Newborn
  9. Singh N, Menon V
    Med J Malaysia, 1975 Dec;30(2):93-7.
    PMID: 1228388
    Matched MeSH terms: Infant, Newborn
  10. Iqbal QM
    Med J Malaysia, 1974 Sep;29(1):60-3.
    PMID: 4282633
    Matched MeSH terms: Infant, Newborn
  11. Chen PC
    Trop Geogr Med, 1973 Jun;25(2):197-204.
    PMID: 4717277
    Matched MeSH terms: Infant, Newborn
  12. Dondero TJ, Sivanandam S
    Med J Malaysia, 1973 Jun;27(4):306-9.
    PMID: 4270791
    Matched MeSH terms: Infant, Newborn
  13. Menon R
    Med J Malaya, 1972 Dec;27(2):115-9.
    PMID: 4268036
    Matched MeSH terms: Infant, Newborn
  14. Sinniah D, Tay LK, Dugdale AE
    Arch Dis Child, 1971 Oct;46(249):712-5.
    PMID: 5118063
    Matched MeSH terms: Infant, Newborn
  15. Barclay R
    Ann Trop Med Parasitol, 1969 Dec;63(4):473-88.
    PMID: 4393668
    Matched MeSH terms: Infant, Newborn
  16. Eng LI, Kamuzora H, Lehmann H
    J Med Genet, 1974 Mar;11(1):25-30.
    PMID: 4837284
    Matched MeSH terms: Infant, Newborn
  17. Alina MF, Azma RZ, Norunaluwar J, Azlin I, Darnina AJ, Cheah FC, et al.
    J Hum Genet, 2020 Mar;65(3):263-270.
    PMID: 31863082 DOI: 10.1038/s10038-019-0700-7
    G6PD deficiency is the commonest enzyme deficiency found in humans. Current diagnostic methods lack sensitivity to detect all cases of G6PD deficiency. We evaluated the reverse dot blot flow-through hybridisation assay designed to detect simultaneously multiple known G6PD mutations in a group of Malaysian neonates. Archival DNA samples from 141 G6PD-deficient neonates were subjected to reverse dot blot flow-through hybridisation assay using the GenoArray Diagnostic Kit (Hybribio Limited, Hong Kong) and DNA sequencing. The method involved PCR amplification of 5 G6PD exons using biotinylated primers, hybridisation of amplicons to a membrane containing oligoprobes designed for G6PD mutations known to occur in the Malaysian population and colour detection by enzyme immunoassay. The assay detected 13 of the 14 G6PD mutations and genotyped 133 (94.3%) out of 141 (102 males, 39 females) cases. Among the 39 female G6PD-deficient neonates, there were 7 homozygous and 6 compound heterozygous cases. The commonest alleles were G6PD Viangchan 871G > A (21%) and G6PD Mahidol 487G > A(20%) followed by G6PD Mediterranean 563C > T, (14%), G6PD Vanua Lava 383T > C (12%), G6PD Canton 1376G > T (10%), G6PD Orissa 131C > G (6.3%) G6PD Coimbra 592C > T (5.6%) plus 6 other mutations. DNA sequencing of remaining cases revealed 6 cases of intron 11 nt 93C > T not previously reported in Malaysia and two novel mutations, one case each of nt 1361G > T and nt 1030G > A. We found the reverse dot blot assay easy to perform, rapid, accurate and reproducible, potentially becoming an improved diagnostic test for G6PD deficiency.
    Matched MeSH terms: Infant, Newborn
  18. Chin KY, Pang KL
    Front Pediatr, 2020;8:563.
    PMID: 33072660 DOI: 10.3389/fped.2020.00563
    Isoflavones are dietary phytoestrogens commonly found in soy-based products. The widespread presence of isoflavones in soy infant formula and breast milk may have long-lasting effects on the development of sex hormone-sensitive organs like the skeleton. Animal early-life programming models are suitable for testing the skeletal effects of pre- and neonatal exposure of soy isoflavones. This review aims to collate the impacts of early-life exposure of soy isoflavones as evidenced in animal models. The isoflavones previously studied include daidzein, genistein, or a combination of both. They were administered to rodent pups during the first few days postnatal, but prolonged exposure had also been studied. The skeletal effects were observed when the animals reached sexual maturity or after castration to induce bone loss. In general, neonatal exposure to soy isoflavones exerted beneficial effects on the skeletal system of female rodents, but the effects on male rodents seem to depend on the time of exposure and require further examinations. It might also protect the animals against bone loss due to ovariectomy at adulthood but not upon orchidectomy. The potential benefits of isoflavones on the skeletal system should be interpreted together with its non-skeletal effects in the assessment of its safety and impacts.
    Matched MeSH terms: Infant, Newborn
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