Displaying publications 1 - 20 of 39 in total

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  1. Arora S, Kanneppady SK, Banavar SR, Jnanendrappa N
    QJM, 2019 Aug 01;112(8):615-616.
    PMID: 31120127 DOI: 10.1093/qjmed/hcz117
  2. Balasingam S, Azman RR, Nazri M
    QJM, 2016 Feb;109(2):121-2.
    PMID: 26101228 DOI: 10.1093/qjmed/hcv121
  3. Chang CY
    QJM, 2022 Jan 09;114(12):900.
    PMID: 34672355 DOI: 10.1093/qjmed/hcab269
  4. Chaubal T, Bapat R, Wadkar P
    QJM, 2017 Aug 01;110(8):527.
    PMID: 28453856 DOI: 10.1093/qjmed/hcx090
  5. Chaubal T, Bapat R, Wadkar P
    QJM, 2017 Dec 01;110(12):841-842.
    PMID: 29025105 DOI: 10.1093/qjmed/hcx164
  6. Cheo SW, Ong SAM, Low QJ, Tan YA, Chia YK
    QJM, 2020 Oct 01;113(10):743-746.
    PMID: 32240316 DOI: 10.1093/qjmed/hcaa107
  7. Cheo SW, Ahmad Akbar RZ, Abd Rahman F, Abdul Rashid WNF', Tan YA, Low QJ
    QJM, 2020 Nov 01;113(11):809-812.
    PMID: 32275748 DOI: 10.1093/qjmed/hcaa122
  8. Cheo SW, Low QJ
    QJM, 2019 Mar 01;112(3):221-222.
    PMID: 30247725 DOI: 10.1093/qjmed/hcy210
  9. Cheo SW, Low QJ, Mow WC, Chia YK
    QJM, 2019 May 01;112(5):381-382.
    PMID: 30517761 DOI: 10.1093/qjmed/hcy284
  10. Cheo SW, Low QJ, Tan YA, Chia YK
    QJM, 2020 Feb 01;113(2):131-132.
    PMID: 31168610 DOI: 10.1093/qjmed/hcz137
  11. Cheo SW, Low QJ
    QJM, 2021 05 19;114(3):219-220.
    PMID: 32539138 DOI: 10.1093/qjmed/hcaa196
  12. Ghauth S, Toong LY, Sakina G, Liew YT
    QJM, 2022 Jan 09;114(12):889-890.
    PMID: 34597409 DOI: 10.1093/qjmed/hcab256
  13. Kanneppady SK, Kanneppady SS, Chaubal T, Bapat R
    QJM, 2018 Oct 01;111(10):753-754.
    PMID: 29788120 DOI: 10.1093/qjmed/hcy100
  14. Khositseth S, Bruce LJ, Walsh SB, Bawazir WM, Ogle GD, Unwin RJ, et al.
    QJM, 2012 Sep;105(9):861-77.
    PMID: 22919024 DOI: 10.1093/qjmed/hcs139
    Distal renal tubular acidosis (dRTA) caused by mutations of the SLC4A1 gene encoding the erythroid and kidney isoforms of anion exchanger 1 (AE1 or band 3) has a high prevalence in some tropical countries, particularly Thailand, Malaysia, the Philippines and Papua New Guinea (PNG). Here the disease is almost invariably recessive and can result from either homozygous or compound heterozygous SLC4A1 mutations.
  15. Low QJ, Hon SA, Garry Siow PW, Lim TH, Lee RA, Tan YA, et al.
    QJM, 2020 Oct 01;113(10):753-754.
    PMID: 31995198 DOI: 10.1093/qjmed/hcaa014
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