Browse publications by year: 2004

  1. Spacey SD, Szczygielski BI, Young SP, Hukin J, Selby K, Snutch TP
    Can J Neurol Sci, 2004 Aug;31(3):383-6.
    PMID: 15376485
    BACKGROUND: Friedrich ataxia (FRDA1) is most often the result of a homozygous GAA repeat expansion in the first intron of the frataxin gene (FRDA gene). This condition is seen in individuals of European, North African, Middle Eastern and Indian descent and has not been reported in Southeast Asian populations. Approximately 4% of FRDA1 patients are compound heterozygotes. These patients have a GAA expansion on one allele and a point mutation on the other and have been reported to have an atypical phenotype.

    OBJECTIVE: To describe a novel dinucleotide deletion in the FRDA gene in two Malaysian siblings with FRDA1.

    SETTING: Tertiary referral university hospital setting.

    PATIENTS AND METHODS: A previously healthy 10-year-old Malaysian boy, presented with fever, lethargy, headaches, dysarthria, dysphagia, vertigo and ataxia which developed over a one week period. His neurological exam revealed evidence of dysarthria and ataxia, mild generalized weakness and choreoform movements of the tongue and hands. His reflexes were absent and Babinski sign was present bilaterally. A nine-year-old sister was found to have mild ataxia but was otherwise neurologically intact.

    RESULTS: Molecular genetic studies demonstrated that both siblings were compound heterozygotes with a GAA expansion on one allele and a novel dinucleotide deletion on the other allele.

    CONCLUSIONS: We describe a novel dinucleotide deletion in the first exon of the FRDA gene in two siblings with FRDA1. Additionally this is the first report of FRDA1 occurring in a family of southeast Asian descent, it demonstrates intrafamilial phenotypic variability, and confirms that atypical phenotypes are associated with compound heterozygosity.

    MeSH terms: Child; Chorea/genetics*; Female; Friedreich Ataxia/genetics*; Humans; Malaysia; Male; Pedigree; Gene Deletion*; Iron-Binding Proteins/genetics*; Siblings
  2. Choi C
    Sci. Am., 2004 Sep;291(3):21A, 22.
    PMID: 15376742
    MeSH terms: Animals; Bangladesh/epidemiology; Chiroptera/virology*; Disease Outbreaks; Humans; Malaysia/epidemiology; Zoonoses; Nipah Virus*; Henipavirus Infections/epidemiology; Henipavirus Infections/transmission*
  3. Kumar S, Miranda-Massari JR, Gonzalez MJ, Riordan HD
    P R Health Sci J, 2004 Jun;23(2):125-6.
    PMID: 15377062
    We report a case of jellyfish envenomation in a 39 year old male. He was stung extensively on both lower limbs by an unidentified jellyfish. This occurred in shallow waters of a beach in the vicinity of Labuan Island, Malaysia. The patient received ambulatory treatment with parenteral and oral ascorbate with remarkable recovery.
    MeSH terms: Adult; Animals; Antioxidants/administration & dosage*; Ascorbic Acid/administration & dosage; Ascorbic Acid/therapeutic use*; Bites and Stings/drug therapy*; Bites and Stings/etiology; Cnidarian Venoms/adverse effects*; Humans; Infusions, Intravenous; Male; Treatment Outcome; Scyphozoa*
  4. Kashiwazaki Y, Na YN, Tanimura N, Imada T
    J Virol Methods, 2004 Nov;121(2):259-61.
    PMID: 15381364
    A monoclonal antibody (MAb) based solid-phase blocking ELISA was developed for detection of antibodies to Nipah virus. The ELISA was designed to detect remaining antigens on the plate with anti-Nipah MAb conjugate after the reaction with sample serum, and enabled simple procedure, detection of neutralizing antibody to Nipah virus, and application of samples from different animal species. Forty of 200 swine reference sera examined were positive by the ELISA, of which thirty seven were found positive by serum neutralization test. Sera from a total of 131 fruit bats captured in Malaysia were also tested and all found negative by the both tests. It is considered that the solid-phase blocking ELISA can be used as a screening test for Nipah virus infection followed by the serum neutralization test as confirmatory test.
    MeSH terms: Animals; Antibodies, Monoclonal; Antibodies, Viral/blood*; Antigens, Viral; Cattle; Chiroptera/blood*; Enzyme-Linked Immunosorbent Assay/methods*; Enzyme-Linked Immunosorbent Assay/standards; Humans; Malaysia/epidemiology; Mass Screening/methods; Neutralization Tests/standards; Swine/blood*; Nipah Virus/immunology; Nipah Virus/isolation & purification*; Henipavirus Infections/blood; Henipavirus Infections/epidemiology; Henipavirus Infections/veterinary
  5. Ali MF, Heng LY, Ratnam W, Nais J, Ripin R
    Bull Environ Contam Toxicol, 2004 Sep;73(3):535-42.
    PMID: 15386176
    MeSH terms: Copper*; Environmental Monitoring; Malaysia; Mining*; Waste Disposal, Fluid; Water Pollutants/analysis*; Metals, Heavy/analysis*; Rivers
  6. Lee K, Ng SF, Ng EL, Lim ZY
    J Exp Child Psychol, 2004 Oct;89(2):140-58.
    PMID: 15388303 DOI: 10.1016/j.jecp.2004.07.001
    Previous studies on individual differences in mathematical abilities have shown that working memory contributes to early arithmetic performance. In this study, we extended the investigation to algebraic word problem solving. A total of 151 10-year-olds were administered algebraic word problems and measures of working memory, intelligence quotient (IQ), and reading ability. Regression results were consistent with findings from the arithmetic literature showing that a literacy composite measure provided greater contribution than did executive function capacity. However, a series of path analyses showed that the overall contribution of executive function was comparable to that of literacy; the effect of executive function was mediated by that of literacy. Both the phonological loop and the visual spatial sketchpad failed to contribute directly; they contributed only indirectly by way of literacy and performance IQ, respectively.
    MeSH terms: Child; Educational Status*; Female; Humans; Malaysia; Male; Mathematics*; Memory, Short-Term*; Models, Psychological; Problem Solving*; Reading*; Regression Analysis
  7. Enjeti AK, Tien SL, Sivaswaren CR
    Hematol. J., 2004;5(5):419-25.
    PMID: 15448668
    Cytogenetic analysis performed at diagnosis is considered to be the most valuable prognostic factor in acute myeloid leukemia (AML). Large systematic studies of cytogenetic abnormalities in AML patients from Southeast Asia are not available. The karyotypic patterns in AML patients from a single center in Singapore were studied and compared with reports from other regions of the world to identify possible geographic heterogeneity.
    MeSH terms: Acute Disease; Adolescent; Adult; Aged; Aged, 80 and over; Aneuploidy; China/ethnology; Chromosome Aberrations*; Chromosomes, Human/ultrastructure*; Ethnic Groups/genetics; Female; Humans; India/ethnology; Indonesia/ethnology; Karyotyping; Leukemia, Myeloid/classification; Leukemia, Myeloid/genetics*; Leukemia, Myeloid/epidemiology; Leukemia, Myeloid/pathology; Malaysia/ethnology; Male; Middle Aged; Singapore/epidemiology
  8. Sreetharan SS, Prepageran N, Satwant S
    Singapore Med J, 2004 Oct;45(10):487-8.
    PMID: 15455170
    Reports of ingested foreign bodies penetrating the pharynx and migrating through the neck are rare, and mostly involved fish bones. We describe a 44-year-old man who was involved in a motor vehicle accident and accidentally swallowed his tooth. The swallowed tooth penetrated the pharynx and became lodged adjacent to his right thyroid gland. It was successfully removed via neck exploration and the patient recovered well.
    MeSH terms: Accidents, Traffic; Adult; Foreign-Body Migration/diagnosis; Humans; Male; Neck*; Tooth; Tooth Fractures/complications
  9. Pritchard LI, Daniels PW, Melville LF, Kirkland PD, Johnson SJ, Lunt R, et al.
    Vet. Ital., 2004 Oct-Dec;40(4):438-45.
    PMID: 20422566
    The authors have characterised the genetic diversity of the bluetongue virus (BTV) RNA segments 3 and 10 from Indonesia, Malaysia and Australia. Analysis of RNA segment 3, which codes for the core protein VP3, showed conserved sequences in the previously defined Australasian topotype, but which further divided into four distinct clades or genotypes. Certain genotypes appeared to be geographically restricted while others were distributed widely throughout South-East Asia. Ongoing surveillance programmes in Australia have identified the movement of Indonesian genotypes into northern Australia and possible reassortment among them. Similarly, analysis of RNA segment 10, which codes for the non-structural protein NS3/3A, showed they were also conserved and grouped into five clades or genotypes, three Asian and two North American/South African.
    MeSH terms: Animals; Asia, Southeastern; Australia; Bluetongue virus; Genotype; Indonesia; Malaysia; RNA; United States; Genetic Variation; Conserved Sequence
  10. Ling TC, Loong CK, Tan WS, Tey BT, Abdullah WM, Ariff A
    J Microbiol, 2004 Sep;42(3):228-32.
    PMID: 15459653
    In this paper, we investigated the development of a simplified and rapid primary capture step for the recovery of M13 bacteriophage from particulate-containing feedstock. M13 bacteriophage, carrying an insert, was propagated and subsequently purified by the application of both conventional multiple steps and expanded bed anion exchange chromatography. In the conventional method, precipitation was conducted with PEG/NaCl, and centrifugation was also performed. In the single step expanded bed anion exchange adsorption, UpFront FastLine 20 (20 mm i.d.) from UpFront Chromatography was used as the contactor, while 54 ml (Ho = 15 cm) of STREAMLINE DEAE (rho = 1.2 g/cm3) from Amersham Pharmacia Biotechnology was used as the anion exchanger. The performance of the two methods were evaluated, analysed, and compared. It was demonstrated that the purification of the M13 bacteriophage, using expanded bed anion exchange adsorption, yielded the higher recovery percentage, at 82.86%. The conventional multiple step method yielded the lower recovery percentage, 36.07%. The generic application of this integrated technique has also been assessed.
    MeSH terms: Adsorption; Biotechnology/methods; Centrifugation; Chromatography, Ion Exchange/methods*; Viral Plaque Assay; Chemical Precipitation; Time Factors; Bacteriophage M13/isolation & purification*
  11. Khan N, Craig DQ
    J Pharm Sci, 2004 Dec;93(12):2962-71.
    PMID: 15459945
    Gelucire 50/13 alone and solid dispersions in this material containing two model drugs (10% w/w caffeine and paracetamol) have been studied with a view to establishing the mechanism underpinning changes in drug-release characteristics as a function of storage time and temperature. The lipid systems were fabricated into tablets and stored for up to 180 days at temperatures of 20 and 37 degrees C. The dispersions were studied using differential scanning calorimetry (DSC), scanning electron microscopy, and dissolution testing. DSC studies indicated that the Gelucire 50/13 exists in two principal melting forms (melting points 38 and 43 degrees C) that undergo transformation to the higher melting form on storage at 37 degrees C. Scanning electron microscopy studies indicated that the systems exhibit "blooming," with crystal formation on the surface being apparent on storage at both temperatures. The dissolution rate increased on storage, with the effect being particularly marked at higher storage temperatures and for the paracetamol systems. However, whereas these changes corresponded well to those seen for the morphology, the correlation between the changes in dissolution and those of the DSC profiles was poor. The study has suggested a novel explanation for the storage instability of Gelucire 50/13 whereby the change in dissolution is associated not with molecular rearrangement as such but with the gross distribution of the constituent components, this in turn altering the physical integrity of the lipid bases.
    MeSH terms: Dosage Forms; Drug Stability; Drug Storage/methods; Drug Storage/standards*; Lipids/analysis; Lipids/chemistry*; Solubility; Temperature
  12. Panneerchelvam S, Kumara KT, KokFai L, Saravanakumar M, Sumathy V, Yuvaneswari KC, et al.
    J Forensic Sci, 2004 Sep;49(5):1132-3.
    PMID: 15461127
    MeSH terms: China/ethnology; Ethnic Groups/genetics*; Gene Frequency*; Genetics, Population*; Humans; Malaysia; Polymorphism, Genetic*; DNA Fingerprinting/methods; Tandem Repeat Sequences*
  13. Kannan K, Corsolini S, Falandysz J, Fillmann G, Kumar KS, Loganathan BG, et al.
    Environ Sci Technol, 2004 Sep 1;38(17):4489-95.
    PMID: 15461154
    Perfluorooctanesulfonyl fluoride based compounds have been used in a wide variety of consumer products, such as carpets, upholstery, and textiles. These compounds degrade to perfluorooctanesulfonate (PFOS), a persistent metabolite that accumulates in tissues of humans and wildlife. Previous studies have reported the occurrence of PFOS, perfluorohexanesulfonate (PFHxS), perfluorooctanoate (PFOA), and perfluorooctanesulfonamide (PFOSA) in human sera collected from the United States. In this study, concentrations of PFOS, PFHxS, PFOA, and PFOSA were measured in 473 human blood/serum/plasma samples collected from the United States, Colombia, Brazil, Belgium, Italy, Poland, India, Malaysia, and Korea. Among the four perfluorochemicals measured, PFOS was the predominant compound found in blood. Concentrations of PFOS were the highest in the samples collected from the United States and Poland (>30 ng/mL); moderate in Korea, Belgium, Malaysia, Brazil, Italy, and Colombia (3 to 29 ng/mL); and lowest in India (<3 ng/mL). PFOA was the next most abundant perfluorochemical in blood samples, although the frequency of occurrence of this compound was relatively low. No age- or gender-related differences in the concentrations of PFOS and PFOA were found in serum samples. The degree of association between the concentrations of four perfluorochemicals varied, depending on the origin of the samples. These results suggested the existence of sources with varying levels and compositions of perfluorochemicals, and differences in exposure patterns to these chemicals, in various countries. In addition to the four target fluorochemicals measured, qualitative analysis of selected blood samples showed the presence of other perfluorochemicals such as perfluorodecanesulfonate (PFDS), perfluoroheptanoic acid (PFHpA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluorododecanoic acid (PFDoA), and perfluoroundecanoic acid (PFUnDA) in serum samples, at concentrations approximately 5- to 10-fold lower than the concentration of PFOS. Further studies should focus on identifying sources and pathways of human exposure to perfluorochemicals.
    MeSH terms: Belgium; Brazil; Caprylates/blood*; Demography; Environmental Exposure; Environmental Monitoring*; Environmental Pollutants/blood*; Female; Floors and Floorcoverings; Fluorocarbons/blood*; Humans; India; Italy; Korea; Malaysia; Male; Poland; Sulfonamides/blood*; Sulfonic Acids/blood*; Textiles; United States; Alkanesulfonic Acids/blood*
  14. Hasmah MS, Omar AR, Wan KF, Hair-Bejo M, Aini I
    Acta Virol., 2004;48(2):85-9.
    PMID: 15462283
    It has been shown that a chicken anemia virus (CAV) isolates which had undergone 60 passages in MSB-1 cells (SMSC-1/P60, 3-1/P60) acquired 33-66 nucleotide substitutions at the coding region resulting in 13-16 amino acid changes as compared to the CAV isolates passaged only 5 times in MSB-1 cells (SMSC-1 and 3-1) (Chowdhury et al., Arch. Virol. 148, 2437-2448, 2003). In this study we found that a low CAV (BL-5) and a high CAV passage (BL-5/P90) differed by only 15 nucleotide substitutions resulting in 11 amino acid changes. Phylogenetic analysis based on VP1 also revealed that both isolates were close to each other but not to other CAV isolates from Malaysia, namely SMSC-1 and 3-1.
    MeSH terms: Animals; Cell Line; DNA, Viral/isolation & purification; DNA, Viral/chemistry; Molecular Sequence Data; Phylogeny; Serial Passage; Genetic Variation*; Point Mutation/genetics; Sequence Homology; Sequence Analysis, DNA; Chicken anemia virus/genetics*; Chicken anemia virus/growth & development*; Amino Acid Substitution/genetics; Capsid Proteins/genetics
  15. Liew AG, Idris A, Wong CH, Samad AA, Noor MJ, Baki AM
    Waste Manag Res, 2004 Aug;22(4):226-33.
    PMID: 15462329
    This study reports the use of sewage sludge generated from sewage treatment plant (STP) as raw material in a clay brick-making process. The physico-chemical and mineralogical characterization of the sewage sludge and clay were carried out in order to identify the major technological constraints and to define the sludge pretreatment requirements if necessary. Moreover, the effects on processing conditions and/or on changes of typical final characteristics are also evaluated. Bricks were produced with sewage sludge additions ranging from 10 to 40% by dry weight. The texture and finishing of the surface of sludge-amended clay bricks were rather poor. As for the physical and chemical properties, bricks with a sludge content of up to 40 wt.% were capable of meeting the relevant technical standards. However, bricks with more than 30 wt.% sludge addition are not recommended for use since they are brittle and easily broken even when handled gently. A tendency for a general degradation of brick properties with sludge additions was observed due to its refractory nature. Therefore, sludge bricks of this nature are only suitable for use as common bricks, which are normally not exposed to view, because of poor surface finishing.
    MeSH terms: Aluminum Silicates; Conservation of Natural Resources; Construction Materials*; Materials Testing; Sewage*
  16. Abegunde AT
    Lancet, 2004;364(9441):1217.
    PMID: 15464180 DOI: 10.1016/S0140-6736(04)17132-8
    Comment on: Singh B, Kim Sung L, Matusop A, Radhakrishnan A, Shamsul SS, Cox-Singh J, Thomas A, Conway DJ. A large focus of naturally acquired Plasmodium knowlesi infections in human beings. Lancet. 2004 Mar 27;363(9414):1017-24. PubMed PMID: 15051281.
    MeSH terms: Adult; Animals; Diagnosis, Differential; Female; Humans; Malaria/diagnosis; Malaria/parasitology; Malaria/transmission*; Malaria/veterinary*; Malaysia; Male; Monkey Diseases/parasitology; Monkey Diseases/transmission*; Zoonoses/transmission; Plasmodium knowlesi*
  17. Bonfield W
    Med J Malaysia, 2004 May;59 Suppl B:1.
    PMID: 15468788
    MeSH terms: Bone and Bones/surgery*; Humans; Materials Testing*; Prosthesis Design; Durapatite*; Equipment Failure Analysis*
  18. Cao Y
    Med J Malaysia, 2004 May;59 Suppl B:2.
    PMID: 15468789
    MeSH terms: Animals; Bone and Bones/cytology; Cartilage, Articular/cytology; Humans; Immunocompetence/immunology*; Tendons/cytology; Tissue Engineering/methods*; Stem Cell Transplantation
  19. Aminuddin BS
    Med J Malaysia, 2004 May;59 Suppl B:3-4.
    PMID: 15468790
    Management of severe tracheal anomalies remains a clinical challenge. Tissue engineering offers new hope in trachea reconstruction surgery. However to date no optimal technique achieved in the formation of human or animal trachea. The main problem lies on the biomaterial used and the complex city of forming trachea in vivo. This study was aimed at creating tissue-engineered trachea cartilage from easily accessible human and animal nasal septum cartilage using internal scaffold and biodegradable human and animal fibrin.
    MeSH terms: Animals; Humans; Mice, Nude; Rabbits; Trachea/pathology; Trachea/surgery*; Chondrocytes/pathology; Chondrocytes/transplantation*; Absorbable Implants; Polyethylene; Tissue Engineering*; Mice
  20. Samsudin AR
    Med J Malaysia, 2004 May;59 Suppl B:6.
    PMID: 15468791
    MeSH terms: Adult; Aged; Aging/physiology*; Biocompatible Materials*; Bone Regeneration/physiology; Child; Facial Bones/physiopathology; Facial Bones/surgery*; Humans; Maxillofacial Development/physiology*; Bone Remodeling/physiology; Prostheses and Implants*
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