98 results on '"Tan, T.-T."'
Search Results
52. EFFECTS OF LUGOL'S SOLUTION ON THYROID FUNCTION IN NORMALS AND PATIENTS WITH UNTREATED THYROTOXICOSIS.
- Author
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TAN, T. T., MORAT, P., NG, M. L., and KHALID, B. A. K.
- Published
- 1989
- Full Text
- View/download PDF
53. Integration of porous silicon chips in an electronic artificial nose
- Author
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Letant, S. E., Content, S., Tan, T. T., Zenhausern, F., and Sailor, M. J.
- Published
- 2000
- Full Text
- View/download PDF
54. Correlation of oxygen vacancy concentration and thermoelectric properties in Na0.73CoO2-δ.
- Author
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Tsai, P. H., Norby, T., Tan, T. T., Donelson, R., Chen, Z. D., and Li, S.
- Subjects
SODIUM compounds ,OXYGEN ,POLYCRYSTALLINE semiconductors ,THERMOELECTRICITY ,ELECTRONS - Abstract
In this work, oxygen vacancies were precisely controlled by manipulating oxygen partial pressure and the oxygen partial pressure dependence of thermoelectric properties of polycrystalline Na
0.73 CoO2-δ was investigated. The results suggest that resistivity and thermopower augment simultaneously with increasing concentration of oxygen vacancies δ due to the recombination of electrons and holes and average Co valence state. The total thermal conductivity can be reduced by minimizing δ. The dimensionless figure of merit was strongly affected by δ at lower operating temperature. The experimental results provide guideline for the variation in performance of this material system under different processing and operating environments. [ABSTRACT FROM AUTHOR]- Published
- 2010
- Full Text
- View/download PDF
55. Sudden Fatty Liver Death: A Case Report and Overview
- Author
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Tan, T. T. Clarence
- Published
- 1983
- Full Text
- View/download PDF
56. Surgical treatment of endocrine hypertension: Experience in Malaysia
- Author
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Meah, F. A., Taha, A., Tay, K. S., Noor Hisham, A., Khalid, A. K., and Tan, T. T.
57. Management of novel influenza epidemics in Singapore: Consensus recommendations from the Hospital Influenza Workgroup (Singapore)
- Author
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Ang, B., Archuleta, S., Chiew, Y. F., Chlebicki, M. P., Chua, A., Fisher, D. A., Hsu, L. Y., Kang, M. L., Koh, Y. L., Kurup, A., Lee, C. C., Leo, Y. S., Leong, H. N., Lim, P. L., Ling, L. M., Ling, M. L., Lye, D. C. B., Tambyah, P., Tan, T. T., and Annelies Wilder-Smith
58. Properties of metal/poly(N-methylpyrrole) Schottky barriers
- Author
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Gardner, J W, primary and Tan, T T, additional
- Published
- 1989
- Full Text
- View/download PDF
59. Characteristics of micro-texture and meso-texture in (Bi, Pb)2Sr2Ca2Cu3O10 superconducting tapes.
- Author
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Tan, T. T., Li, S., Cooper, H., Gao, W., Liu, H. K., and Dou, S. X.
- Published
- 2001
- Full Text
- View/download PDF
60. Crystallographic orientation mapping with an electron backscattered diffraction technique in (Bi, Pb)2Sr2Ca2Cu3O10 superconductor tapes.
- Author
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Tan, T. T., Li, S., Oh, J. T., Gao, W., Liu, H. K., and Dou, S. X.
- Published
- 2001
- Full Text
- View/download PDF
61. Renocystograms and Intravenous Pyelograms.
- Author
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TAPLIN, G. V., DORE, E. K., JOHNSON, D. E., TAN, T. T., and HADDAD, G. N.
- Published
- 1962
62. Correlation of oxygen vacancy concentration and thermoelectric properties in Na0.73CoO2-δ.
- Author
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Tsai, P. H., Norby, T., Tan, T. T., Donelson, R., Chen, Z. D., and Li, S.
- Subjects
- *
SODIUM compounds , *OXYGEN , *POLYCRYSTALLINE semiconductors , *THERMOELECTRICITY , *ELECTRONS - Abstract
In this work, oxygen vacancies were precisely controlled by manipulating oxygen partial pressure and the oxygen partial pressure dependence of thermoelectric properties of polycrystalline Na0.73CoO2-δ was investigated. The results suggest that resistivity and thermopower augment simultaneously with increasing concentration of oxygen vacancies δ due to the recombination of electrons and holes and average Co valence state. The total thermal conductivity can be reduced by minimizing δ. The dimensionless figure of merit was strongly affected by δ at lower operating temperature. The experimental results provide guideline for the variation in performance of this material system under different processing and operating environments. [ABSTRACT FROM AUTHOR]
- Published
- 2010
- Full Text
- View/download PDF
63. Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
- Author
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Ali Al Asmari, Emmanuelle Szenker-Ravi, Carine Bonnard, Bruno Reversade, Laura Schultz-Rogers, I. Kraegeloh-Mann, Maha Abdulrahim, Hesham Aldhalaan, Byrappa Venkatesh, Célia Bosso-Lefèvre, Aida Telegrafi, Hiyam M. Marzouqa, Gunaseelan Narayanan, Sha Tang, Sonal Mahida, Melanie A. Simpson, Fowzan S. Alkuraya, Michelle Eio, Eissa Faqeih, Renske Oegema, Sarah Weckhuysen, George Grady, Joseph J. Barycki, Mohammed Al-Owain, Lamyaa A. Jad, David A. Koolen, Marjon van Slegtenhorst, Tyler Mark Pierson, Marisa V. Andrews, Rebecca Schüle, Reinhard Keimer, Amber Begtrup, Sateesh Maddirevula, Michael Muriello, Sakkubai Naidu, Damien Haye, Adel A H Mahmoud, Brian Ciruna, Abdullah Tamim, Thong Teck Tan, Rolph Pfundt, Peter Bauer, Jiin Ying Lim, Ali Awaji, Marco Tartaglia, Meral Gunay-Aygun, Eric W. Klee, Marcia C. Willing, Monica Yau, Angelika Riess, Diego Martinelli, Sabina Barresi, Sumanty Tohari, Werner Deigendesch, Dirk Lefeber, Saumya Shekhar Jamuar, Ludger Schöls, Ralitza H. Gavrilova, Alvin Yu Jin Ng, Hannah Stamberger, Suleyman Gulsuner, Adam Claridge-Chang, Élise Lebigot, Moeenaldeen Al-Sayed, Ee Shien Tan, Kagistia Hana Utami, Sarah B. Pierce, Helene Verhelst, Hankun Li, James C. Stewart, Ingo Helbig, Tal Gilboa, Mahmoud A. Pouladi, Hagar Mor-Shaked, Boris Keren, Ajay S. Mathuru, Holger Hengel, Michèl A.A.P. Willemsen, Nader Handal, Tahsin Stefan Barakat, Sulwan M. Algain, Terrence Thomas, Lance H. Rodan, Mais Hashem, Wendy G. Mitchell, Center for Reproductive Medicine, ARD - Amsterdam Reproduction and Development, ACS - Diabetes & metabolism, Clinical Genetics, Reversade, Bruno, Hengel, H., Bosso-Lefèvre, C., Grady, G., Szenker-Ravi, E., Li, H., Pierce, S., Lebigot, É., Tan, T.-T., Eio, M.Y., Narayanan, G., Utami, K.H., Yau, M., Handal, N., Deigendesch, W., Keimer, R., Marzouqa, H.M., Gunay-Aygun, M., Muriello, M.J., Verhelst, H., Weckhuysen, S., Mahida, S., Naidu, S., Thomas, T.G., Lim, J.Y., Tan, E.S., Haye, D., Willemsen, M.A.A.P., Oegema, R., Mitchell, W.G., Pierson, T.M., Andrews, M.V., Willing, M.C., Rodan, L.H., Barakat, T.S., van Slegtenhorst, M., Gavrilova, R.H., Martinelli, D., Gilboa, T., Tamim, A.M., Hashem, M.O., AlSayed, M.D., Abdulrahim, M.M., Al-Owain, M., Awaji, A., Mahmoud, A.A.H., Faqeih, E.A., Asmari, A.A., Algain, S.M., Jad, L.A., Aldhalaan, H.M., Helbig, I., Koolen, D.A., Riess, A., Kraegeloh-Mann, I., Bauer, P., Gulsuner, S., Stamberger, H., Ng, A.Y.J., Tang, S., Tohari, S., Keren, B., Schultz-Rogers, L.E., Klee, E.W., Barresi, S., Tartaglia, M., Mor-Shaked, H., Maddirevula, S., Begtrup, A., Telegrafi, A., Pfundt, R., Schüle, R., Ciruna, B., Bonnard, C., Pouladi, M.A., Stewart, J.C., Claridge-Chang, A., Lefeber, D.J., Alkuraya, F.S., Mathuru, A.S., Venkatesh, B., Barycki, J.J., Simpson, M.A., Jamuar, S.S., Schöls, L, and School of Medicine
- Subjects
0301 basic medicine ,Male ,Glycobiology ,General Physics and Astronomy ,VARIANTS ,Encephalopathy ,Neurodegenerative ,Germline ,0302 clinical medicine ,UDP-GLUCOSE DEHYDROGENASE ,Loss of Function Mutation ,Medicine and Health Sciences ,EMBRYOGENESIS ,2.1 Biological and endogenous factors ,UGDH protein, human ,Aetiology ,Child ,lcsh:Science ,Zebrafish ,UTILITY ,Genetics ,pathology [Organoids] ,Multidisciplinary ,Uridine diphosphate glucose dehydrogenase ,Uridine diphosphate ,DP-glucuronic acid ,Syndrome ,Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3] ,Hypotonia ,3. Good health ,Pedigree ,DEFICIENCY ,genetics [Loss of Function Mutation] ,Organoids ,genetics [Uridine Diphosphate Glucose Dehydrogenase] ,Child, Preschool ,Neurological ,Medicine ,Female ,ddc:500 ,medicine.symptom ,Oxidoreductases ,Engineering sciences. Technology ,Rare cancers Radboud Institute for Health Sciences [Radboudumc 9] ,ENZYME ,Adolescent ,CONGENITAL DISORDER ,Science ,Intellectual and Developmental Disabilities (IDD) ,genetics [Epilepsy] ,chemistry [Oxidoreductases] ,Genetics and Molecular Biology ,Genes, Recessive ,Biology ,Uridine Diphosphate Glucose Dehydrogenase ,Article ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,Protein Domains ,medicine ,Animals ,Humans ,Recessive ,Clinical genetics ,Allele ,Preschool ,Gene ,Loss function ,Alleles ,HEPARAN-SULFATE ,Phenocopy ,genetics [Oxidoreductases] ,Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7] ,Epilepsy ,GLYCOSYLATION ,Neurosciences ,Infant ,General Chemistry ,biology.organism_classification ,medicine.disease ,Brain Disorders ,carbohydrates (lipids) ,Kinetics ,030104 developmental biology ,Genes ,General Biochemistry ,Neuronal development ,lcsh:Q ,Human medicine ,030217 neurology & neurosurgery ,Congenital disorder - Abstract
Developmental epileptic encephalopathies are devastating disorders characterized by intractable epileptic seizures and developmental delay. Here, we report an allelic series of germline recessive mutations in UGDH in 36 cases from 25 families presenting with epileptic encephalopathy with developmental delay and hypotonia. UGDH encodes an oxidoreductase that converts UDP-glucose to UDP-glucuronic acid, a key component of specific proteoglycans and glycolipids. Consistent with being loss-of-function alleles, we show using patients’ primary fibroblasts and biochemical assays, that these mutations either impair UGDH stability, oligomerization, or enzymatic activity. In vitro, patient-derived cerebral organoids are smaller with a reduced number of proliferating neuronal progenitors while mutant ugdh zebrafish do not phenocopy the human disease. Our study defines UGDH as a key player for the production of extracellular matrix components that are essential for human brain development. Based on the incidence of variants observed, UGDH mutations are likely to be a frequent cause of recessive epileptic encephalopathy., German Research Foundation (DFG); European Union (European Union); NEUROMICS Network; International Coordination Action (ICA); Fund for Scientific Research Flanders (FWO); Netherlands Organization for Scientific Research (ZONMW VIDI); National Medical Research Council, Singapore; A Strategic Positioning Fund on Genetic Orphan Diseases (GODAFIT); Industry Alignment Fund on Singapore Childhood Undiagnosed Diseases Program (SUREKids); Biomedical Research Council, A*STAR; Diana and Steve Marienhoff Fashion Industries Guild Endowed Fellowship in Pediatric Neuromuscular Diseases; Fondazione Bambino Gesù (Vite Coraggiose); Canadian Institutes of Health Research; Natural Sciences and Engineering Research Council of Canada; Eurocores Program EuroEPINOMICS; University of Antwerp Research Fund; FRAXA Foundation; Brain & Behavior Research Foundation, NARSAD Young Investigator Grant
- Published
- 2020
64. Donor-Derived Candida dubliniensis Resulting in Perigraft Abscesses in a Liver Transplant Recipient Proven by Whole Genome Sequencing: A Case Report.
- Author
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Teh YE, Ang MLT, La MV, Gunalan V, Tan CK, Tan AL, Lin RTP, Tan TT, Jeyaraj PR, Cumaraswamy S, and Tan BH
- Subjects
- Candida, Female, Humans, Liver Abscess microbiology, Liver Transplantation methods, Middle Aged, Vena Cava, Inferior microbiology, Whole Genome Sequencing, Candidiasis etiology, Liver Transplantation adverse effects, Tissue Donors, Tissue and Organ Procurement methods, Transplants microbiology
- Abstract
Background: The transmission of fungi via transplant, although well-known, has not often been molecularly proven. We describe a case of donor-derived candidiasis verified by whole genome sequencing., Case Description: The multiorgan donor was a 42-year-old woman with subdural hemorrhage. Procurement of the thoracic organs was performed followed by the abdominal organs. Tissue from the left bronchus grew Candida dubliniensis. The liver recipient was a 63-year-old woman with cryptogenic liver cirrhosis. She was noted to have worsening leukocytosis on postoperative day (POD) 9. Computed tomography of the abdomen and pelvis showed multiple rim-enhancing collections around the graft. Percutaneous drainage was performed. Fluid cultures grew C dubliniensis. C dubliniensis isolated from the donor's left bronchus and the liver recipient's abscesses were verified to be related by whole genome sequencing. We postulate that C dubliniensis colonizing the donor's transected trachea could have contaminated the inferior vena cava when the former was left open after explant of the donor's lungs. A portion of the donor's contaminated inferior vena cava was transplanted along with the liver graft, resulting in the infected collections in the recipient., Conclusions: Our case report highlights the importance of maintaining a sterile field during organ procurement, especially in a multiorgan donor whose organs are explanted in succession., (Copyright © 2018 Elsevier Inc. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
65. A Case Report: Organs From a Donor With Highly Virulent Zoonotic Outbreak Strain of Streptococcus agalactiae Serotype III, Multilocus Sequence Type 283 Infective Endocarditis Did Not Result in Transmission With Adequate Prophylactic Antibiotic Cover.
- Author
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Sim J, Tan TT, Wijaya L, Sran HK, Thangaraju S, and Kee T
- Subjects
- Aged, Anti-Bacterial Agents therapeutic use, Disease Outbreaks, Endocarditis, Bacterial microbiology, Endocarditis, Bacterial transmission, Female, Humans, Kidney Transplantation methods, Male, Middle Aged, Multilocus Sequence Typing, Postoperative Complications microbiology, Serogroup, Streptococcal Infections microbiology, Streptococcal Infections transmission, Tissue Donors, Treatment Outcome, Antibiotic Prophylaxis methods, Endocarditis, Bacterial prevention & control, Kidney Transplantation adverse effects, Postoperative Complications prevention & control, Streptococcal Infections prevention & control, Streptococcus agalactiae genetics
- Abstract
In 2015, an outbreak involving a highly virulent zoonotic outbreak strain of Streptococcus agalactiae serotype III, multilocus sequence type 283 occurred in Singapore with increased neurologic complications, septic arthritis, and spinal infections in healthier patients. We report a case of a successful dual kidney transplant from a deceased donor with infective endocarditis and disseminated infection with the same strain of S agalactiae and we review the current literature., (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Published
- 2017
- Full Text
- View/download PDF
66. Recurrent trichosporonosis with central nervous system involvement in an allogeneic hematopoietic stem cell transplant recipient.
- Author
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Thien SY, Chung SJ, Tan AL, Hwang WY, Tan BH, and Tan TT
- Subjects
- Antifungal Agents administration & dosage, Caspofungin, Central Nervous System diagnostic imaging, Echinocandins administration & dosage, Echinocandins therapeutic use, Female, Humans, Hydrocephalus etiology, Hydrocephalus surgery, Immunocompromised Host, Immunosuppression Therapy adverse effects, Laminectomy, Lipopeptides administration & dosage, Lipopeptides therapeutic use, Magnetic Resonance Imaging, Opportunistic Infections cerebrospinal fluid, Opportunistic Infections complications, Opportunistic Infections microbiology, Recurrence, Transplantation, Autologous, Treatment Outcome, Triazoles administration & dosage, Triazoles therapeutic use, Trichosporonosis cerebrospinal fluid, Trichosporonosis complications, Trichosporonosis microbiology, Ventriculoperitoneal Shunt, Voriconazole administration & dosage, Voriconazole therapeutic use, Anemia, Aplastic therapy, Antibiotic Prophylaxis methods, Antifungal Agents therapeutic use, Central Nervous System microbiology, Hematopoietic Stem Cell Transplantation adverse effects, Opportunistic Infections drug therapy, Trichosporon isolation & purification, Trichosporonosis drug therapy
- Abstract
Trichosporon is an ubiquitous yeast that has emerged as an opportunistic pathogen in the immunocompromised host. We describe a case of invasive trichosporonosis in an allogeneic hematopoietic stem cell transplant (allo-HSCT) recipient while on caspofungin antifungal prophylaxis. She developed disseminated trichosporonosis in the pre-engraftment period and was successfully treated with voriconazole. She later developed 2 further episodes of invasive trichosporonosis involving the central nervous system. This case highlights the challenges of managing trichosporonosis in allo-HSCT recipients and suggests the need for lifelong therapy in some patients., (© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Published
- 2016
- Full Text
- View/download PDF
67. 5 year analysis of bacteriology culture in a tropical burns ICU.
- Author
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Chong SJ, Ahmed S, Tay JM, Song C, and Tan TT
- Subjects
- Adolescent, Adult, Aged, Burns surgery, Female, Humans, Intensive Care Units, Male, Middle Aged, Retrospective Studies, Singapore epidemiology, Surgical Wound Infection epidemiology, Surgical Wound Infection microbiology, Young Adult, Bacteremia epidemiology, Bacteremia microbiology, Burns microbiology
- Abstract
Introduction: Infection is a major cause of morbidity and mortality in burns patients., Methodology: A retrospective review of all 94 patients admitted to a regional burns ICU from 2004 to 2009 was performed. All the patients' data and records of all culture isolates from a computerized hospital wide database were studied. Epidemiology of the patients, bacteriology information including yield and correlation of bacteremia with positive cultures from other sites were examined. In addition, the relationship between burns excision surgeries to bacteremia was analyzed., Results: 402 tissue cultures, 238 wound swab cultures, 269 endotracheal cultures, 125 urine cultures, 236 tip of monitoring line cultures and 474 blood cultures were studied. Acinetobacter baumannii was the most prevalent bacteria for all culture methods. Within 24 h of bacteremia, the tissue, line tips, endotracheal and wound swab cultures had yielded very similar pathogens (>70% of the time) to those from the blood stream. Furthermore 60% of all bacteremic episodes occur within 48 h of the surgery., Conclusion: In ICUs where multidrug resistant pathogens are endemic, the choice of appropriate antimicrobial empiric cover should be guided by the intensity of colonization with these organisms as indicated by the cultures from various sites., (Copyright © 2011 Elsevier Ltd and ISBI. All rights reserved.)
- Published
- 2011
- Full Text
- View/download PDF
68. Primary cutaneous cryptococcosis due to Cryptococcus gattii in Singapore.
- Author
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Lingegowda BP, Koh TH, Ong HS, and Tan TT
- Subjects
- Adult, Cryptococcosis etiology, Cryptococcosis pathology, Humans, Immunocompetence, Male, Occupational Injuries complications, Scalp Dermatoses etiology, Scalp Dermatoses pathology, Singapore, Cryptococcosis microbiology, Cryptococcus gattii, Lacerations complications, Scalp injuries, Scalp Dermatoses microbiology
- Abstract
Cryptococcosis is an invasive fungal infection that occurs worldwide. Infections caused by Cryptococcus (C.) neoformans are commonly associated with immunocompromised patients, while those caused by C. gattii predominantly affect immunocompetent hosts. However, the latter has also been increasingly reported in immunocompromised patients such as those with HIV. Cutaneous involvement by C. gattii in immunocompetent patients is a rare manifestation, with only a few cases reported worldwide. C. gattii infection has rarely been reported in Singapore, with all three reported cases presenting as meningitis in immunocompetent individuals. Its natural habitat is the Eucalyptus tree, which is common in Singapore. We report the case of a 37-year-old migrant worker who had primary cutaneous infection due to C. gattii after sustaining traumatic inoculation.
- Published
- 2011
69. Chiral capillary electrophoresis with cationic pyrrolidinium-beta-cyclodextrin derivatives as chiral selectors.
- Author
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Xiao Y, Wang Y, Ong TT, Ge L, Tan SN, Young DJ, Tan TT, and Ng SC
- Subjects
- Cations, Chromatography, Liquid, Hydrogen-Ion Concentration, Magnetic Resonance Spectroscopy, Mass Spectrometry, Stereoisomerism, Electrophoresis, Capillary methods, Pyrrolidines chemistry, beta-Cyclodextrins chemistry
- Abstract
New single-isomer, cationic beta-cyclodextrins, including mono-6-deoxy-6-pyrrolidine-beta-cyclodextrin chloride (pyCDCl), mono-6-deoxy-6-(N-methyl-pyrrolidine)-beta-cyclodextrin chloride (N-CH(3)-pyCDCl), mono-6-deoxy-6-(N-(2-hydroxyethyl)-pyrrolidine)-beta-cyclodextrin chloride (N-EtOH-pyCDCl), mono-6-deoxy-6-(2-hydroxymethyl-pyrrolidine)-beta-cyclodextrin chloride (2-MeOH-pyCDCl) were synthesized and used as chiral selectors in capillary electrophoresis for the enantioseparation of carboxylic and hydroxycarboxylic acids and dansyl amino acids. The unsubstituted pyCDCl exhibited the greatest resolving ability. Most analytes were resolved over a wide range of pH from 6.0 to 9.0 with this chiral selector. In general, increasing pH led to a decrease in resolution. The effective mobilities of all the analytes were found to decrease with increasing CD concentration. The optimal concentration for most carboxylic acids and dansyl amino acid was in the range 5-7.5 mM and >15 mM for hydroxycarboxylic acids. (1)H NMR experiments provided direct evidence of inclusion in the CD cavity.
- Published
- 2010
- Full Text
- View/download PDF
70. Autonomic dysfunction in recovered severe acute respiratory syndrome patients.
- Author
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Lo YL, Leong HN, Hsu LY, Tan TT, Kurup A, Fook-Chong S, and Tan BH
- Subjects
- Adolescent, Adult, Autonomic Nervous System physiopathology, Autonomic Nervous System Diseases psychology, Dizziness virology, Fatigue Syndrome, Chronic psychology, Humans, Male, Middle Aged, Neurologic Examination, Peripheral Nerves physiopathology, Peripheral Nervous System Diseases physiopathology, Peripheral Nervous System Diseases virology, Respiratory Insufficiency virology, Sleep Wake Disorders virology, Surveys and Questionnaires, Autonomic Nervous System Diseases physiopathology, Autonomic Nervous System Diseases virology, Fatigue Syndrome, Chronic physiopathology, Fatigue Syndrome, Chronic virology, Severe Acute Respiratory Syndrome complications
- Published
- 2005
71. Distribution of epstein-barr virus antigenic sites on the carboxyl terminal end of ribonucleotide reductase against nasopharyngeal carcinoma serum antibodies using an immunoabsorption method.
- Author
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Gan YY, Hu R, Chai D, Tan TT, Gan YH, Chan SH, Tsao SY, and Gan LH
- Subjects
- Amino Acid Sequence, Antibodies, Viral blood, Antibodies, Viral metabolism, Antigens, Viral immunology, Antigens, Viral metabolism, Base Sequence, Carcinoma virology, Epitope Mapping, Herpesvirus 4, Human enzymology, Herpesvirus 4, Human genetics, Humans, Immunosorbent Techniques, Molecular Sequence Data, Nasopharyngeal Neoplasms virology, Open Reading Frames, Recombinant Proteins biosynthesis, Recombinant Proteins immunology, Ribonucleotide Reductases chemistry, Ribonucleotide Reductases genetics, Carcinoma immunology, Herpesvirus 4, Human immunology, Nasopharyngeal Neoplasms immunology, Ribonucleotide Reductases immunology
- Abstract
In an attempt to clone and express proteins from the Epstein-Barr virus (EBV) cDNA library to be used as antigens in an enzyme-linked immunosorbent assay (ELISA) format to test against the antibodies found in the sera of nasopharyngeal carcinoma (NPC) patients, we have isolated and characterized three clones. All three clones expressed the same polypeptides of different lengths, which belong to the carboxyl terminal end of the large subunit of ribonucleotide reductase (RR) of the EBV genome. All three clones were found to be immunogenic and could be used in an IgA and IgG ELISA against the NPC sera with various degrees of sensitivity and specificity. Because the clones varied in length, this difference provides a simple system to determine where most of the antibody epitopes lies on the protein. We designed an immunoabsorption assay and a mathematical model to help map the segment of the polypeptide most immunogenic to 43 NPC patients. Results were unexpected: 77% of the patients were most immunogenic to region z, which was the smallest fragment among the three fragments studied. Fragment z was only 33 amino acids in length. Only 14% and 19% of patients showed the most immunogenic region in segment x and y, respectively. This variation could be due to major histocompatibility complex antigens. The patients could be divided into three groups based on the immunoabsorption assays, in which each group responded to a different immunodominant segment in the RR antigen. The largest group responded to an immunodominant segment, which was only 33 amino acids long. This domain was coded for by the gene fragment from nucleotide 78,129 to nucleotide 78,227 of the EBV genome. This segment of the protein would be suitable for further epitope mapping studies., (Copyright 1999 Wiley-Liss, Inc.)
- Published
- 1999
- Full Text
- View/download PDF
72. Steroid-induced osteoporosis--a cause for concern?
- Author
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Tan TT, Lau IS, Kong NC, and Zainal AG
- Subjects
- Adult, Bone Density drug effects, Bone Density physiology, Femur Neck drug effects, Femur Neck metabolism, Humans, Lumbar Vertebrae drug effects, Lumbar Vertebrae metabolism, Lupus Erythematosus, Systemic drug therapy, Lupus Erythematosus, Systemic metabolism, Middle Aged, Osteoporosis physiopathology, Osteoporosis therapy, Glucocorticoids adverse effects, Osteoporosis chemically induced
- Published
- 1997
73. Levels of thyroxine, TSH, thyroid volume and mental performance among Orang Asli in selected settlements in Malaysia.
- Author
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Osman A, Zaleha MI, Iskandar ZA, Tan TT, Ali MM, Roslan I, and Khalid BA
- Subjects
- Adolescent, Adult, Female, Goiter, Endemic physiopathology, Humans, Intelligence Tests, Malaysia epidemiology, Male, Nutrition Surveys, Prevalence, Socioeconomic Factors, Goiter, Endemic blood, Goiter, Endemic ethnology, Iodine deficiency, Mental Processes physiology, Thyrotropin blood, Thyroxine blood
- Abstract
A significant difference in the levels of thyroxine (T4), thyroid stimulating hormone (TSH) and thyroid volume among settlements at various selected Orang Asli locations is reported. The levels improved according to the level of socio-economic development. No significant difference was found in mental performance by location.
- Published
- 1996
74. The surgical treatment of adrenal diseases.
- Author
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Meah FA, Abdullah T, Jasmi AY, Hisham AN, Tan TT, Khalid BA, and Tahir A
- Subjects
- Adrenal Gland Diseases diagnosis, Adrenal Gland Diseases epidemiology, Adrenal Gland Diseases surgery, Adrenalectomy, Adult, Cushing Syndrome diagnosis, Cushing Syndrome epidemiology, Female, Humans, Hyperaldosteronism diagnosis, Hyperaldosteronism epidemiology, Incidence, Male, Pheochromocytoma diagnosis, Pheochromocytoma epidemiology, Sex Distribution, Singapore epidemiology, Treatment Outcome, Cushing Syndrome surgery, Hyperaldosteronism surgery, Pheochromocytoma surgery, Postoperative Complications physiopathology
- Abstract
Between January 1978 to December 1993, 130 cases of adrenal diseases were diagnosed and surgically treated at the National University of Malaysia. They were 58 cases (44.6%) of Conn's syndrome, 40 cases (30.7%) of Cushing's syndrome, 20 cases (15.3%) of phaeochromocytoma and 12 cases (9.2%) of adrenocortical carcinoma (ACC). The commonest cause of Conn's syndrome was an adenoma (96.5%) which affected the left gland four times more than the right gland. Cushing's syndrome was caused by adrenocortical adenoma (32.5%), diffuse bilateral adrenal hyperplasia (40.0%), pigmented macronodular hyperplasia (20.0%) and adrenal carcinoma (7.5%). Twenty-five percent of the phaeochromocytomas were extraadrenal in origin arising mainly from the abdominal sympathetic chain. More than 50% of ACCs were non-functioning tumours. Fifty percent of the patients with ACC had inoperable tumours. The prognosis was poor even with adjuvant chemoradiotherapy. The main surgical approach was the anterior transabdominal route. There was no operative mortality or morbidity in all operated cases.
- Published
- 1996
75. Thyroid function and pubertal development in malnutrition.
- Author
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Ali O, Tan TT, Sakinah O, Khalid BA, Wu LL, Wan Nazaimoon WM, and Ng ML
- Subjects
- Adolescent, Adult, Asian People, Body Mass Index, Child, Female, Goiter ethnology, Humans, Malaysia epidemiology, Male, Native Hawaiian or Other Pacific Islander, Nutrition Disorders ethnology, Nutritional Status, Puberty ethnology, Racial Groups, Regression Analysis, Risk Factors, Goiter physiopathology, Nutrition Disorders physiopathology, Puberty physiology, Thyroid Gland physiopathology, Thyroid Hormones blood
- Abstract
Thyroid function and pubertal development of aborigines (Orang Asli) and Malays at different socioeconomic strata were assessed among 1136 subjects aged 7 years and above. Anthropometric measurements, goitre and pubertal staging were done. Serum thyroxine (T4), triiodothyronine (T3) and growth hormone were measured using radioimmunoassays (RIA) and serum thyroid stimulating hormone (TSH) by immunoradiometric assays (IRMA). It was found that serum T3 in children was significantly higher in Malays from rural areas, girls and children aged less than 13 years. However, in adults, T3 was significantly associated with anthropometric indices. On the contrary, serum T4 levels were higher among children from urban areas. In adults, serum T4 levels were significantly related to nutritional status and they increased according to the levels of social development, being lowest in remote areas and highest in urban areas. However, serum TSH levels were significantly higher in Orang Asli at all ages and among malnourished children. By using multiple regression, apart from age, gender and ethnicity, nutritional status was a significant predictor for T3 levels in children and adults. Presence of goitre was an important factor which determined the T4 levels in children and adults after controlling for other factors. It was also a predictor for TSH levels in children but not in adults. Fasting serum growth hormone (GH) levels were significantly higher among less privileged groups and decreased according to social development. Serum growth hormone was negatively correlated with anthropometric indices and had a significant association with malnutrition.(ABSTRACT TRUNCATED AT 250 WORDS)
- Published
- 1994
76. ANF(1-28) is a potent suppressor of pro-opiomelanocortin (POMC) mRNA but a weak inhibitor of beta EP-LI release from AtT-20 cells.
- Author
-
Tan TT, Yang Z, Huang W, and Lim AT
- Subjects
- Animals, Blotting, Northern, Dibutyryl Cyclic GMP pharmacology, Dose-Response Relationship, Drug, Mice, Nitroprusside pharmacology, RNA, Messenger metabolism, Tumor Cells, Cultured drug effects, Tumor Cells, Cultured metabolism, Atrial Natriuretic Factor pharmacology, Gene Expression Regulation, Pituitary Neoplasms metabolism, Pro-Opiomelanocortin genetics, beta-Endorphin metabolism
- Abstract
Controversies remain whether atrial natriuretic factor (ANF) may play a role in modulating the release of POMC derived peptides from pituitary corticotrophs. Employing AtT-20 mouse pituitary tumour cells, we report here the effects of rat ANF(1-28) and sodium nitroprusside (SNP), both of which augment cellular levels of cGMP through activating particulate and soluble guanylyl cyclases respectively, on the expression of POMC mRNA abundance. Furthermore, the cellular contents and secretion of (beta endorphin-like immunoreactivity) beta EP-LI from these cultures were also examined. Whereas the abundance of POMC mRNA was found to be markedly suppressed following 4h of incubation with rANP(1-28) (0.01 to 1 microM), SNP (0.1 to 10 microM) and dibutyryl-cGMP (1 to 100 microM) in a dose related manner, only a modest reduction in the release and cell contents of beta EP-LI was found in some of these cultures. It is also of interest to note that in all the cases examined, the inhibitory effect was associated with a significant suppression of cAMP levels in the cultures. Taken together, our present findings suggest that ANF may play a more important role in suppressing the production than the release of POMC related peptides from AtT-20 cells. Thus, it raises the possibility that hypothalamic ANF may likewise modulate the function of the pituitary-adrenal axis through exerting a greater effect on inhibiting the production than the secretion of pituitary ACTH.
- Published
- 1994
- Full Text
- View/download PDF
77. State of mutational alterations of p53 and retinoblastoma susceptibility genes in papillomavirus-negative small cell cervical carcinomas.
- Author
-
Pao CC, Kao SM, Chen JH, Tang GC, Chang PY, and Tan TT
- Subjects
- Base Sequence, Carcinoma, Small Cell virology, Chromosome Aberrations, DNA Mutational Analysis, DNA Primers, False Positive Reactions, Female, Humans, Molecular Sequence Data, Mutation, Papillomaviridae isolation & purification, Polymerase Chain Reaction, Polymorphism, Single-Stranded Conformational, Uterine Cervical Neoplasms virology, Carcinoma, Small Cell genetics, Genes, Retinoblastoma genetics, Genes, p53 genetics, Uterine Cervical Neoplasms genetics
- Abstract
Genetic aberrations were examined to assess the possible roles that p53 and retinoblastoma susceptibility genes might have played in the development of small cell cervical carcinomas. Cervical cancer tissues from 12 patients with small cell cervical carcinoma that were free of human papillomavirus were analyzed. The presence of mutational alterations were examined by polymerase chain reaction-single-strand conformation polymorphism and by direct DNA sequencing. None of 12 small cell cervical carcinomas were found to contain mutations in regions of p53 and retinoblastoma susceptibility genes that were functionally important and where most mutations, in human tumors have been found. Furthermore, there was no evidence indicative of loss of heterozygosity of chromosome region 17p13 (in which p53 is located) in these tumors. These data seem to suggest that whereas mutant type of p53 and retinoblastoma susceptibility genes may exhibit "oncogenic" function in many human tumors, mutational inactivation of these genes may not be an important feature in the carcinogenic development of human papillomavirus-negative small cell cervical carcinomas.
- Published
- 1994
- Full Text
- View/download PDF
78. Low incidence of hypercalcaemia in tuberculosis in Malaysia.
- Author
-
Tan TT, Lee BC, and Khalid BA
- Subjects
- Adult, Female, Humans, Hypercalcemia epidemiology, Incidence, Malaysia epidemiology, Male, Middle Aged, Hypercalcemia etiology, Tuberculosis complications
- Abstract
In this study we examined the incidence of hypercalcaemia among patients with tuberculosis in Malaysia. Serum calcium concentration and other calcium metabolism parameters were studied in 43 newly diagnosed tuberculous patients from the Kuala Lumpur General Hospital and the National Tuberculosis Centre. Forty-four patients admitted to the medical wards of the General Hospital, Kuala Lumpur were recruited as controls. The incidence of hypercalcaemia was found to be only 1/43 (2.3%). There was no significant difference between the mean serum calcium and other calcium metabolism parameters between the patients and the controls. Despite earlier reported incidences of 30-50%, this study showed that hypercalcaemia in tuberculosis is uncommon in Malaysia.
- Published
- 1993
79. Effect of gender and age on fasting serum growth hormone levels in normal subjects.
- Author
-
Nazaimoon WM, Ng ML, Osman A, Tan TT, Wu LL, and Khalid BA
- Subjects
- Adolescent, Adult, Age Factors, Aged, Aged, 80 and over, Child, Fasting, Female, Humans, Male, Middle Aged, Sex Factors, Growth Hormone blood
- Abstract
Fasting growth hormone (GH) level is an important reference level in dynamic tests of GH secretion. Other studies have demonstrated sex and age variation in the rate of GH secretion. We analysed fasting serum samples from 377 normal subjects (193 males and 184 females, age range 6 to 81 years old), using our in-house enzyme immunoassay. We found sex differences in fasting GH levels to be only significant in the prepubertal children (Tanner stage I), being higher in girls than in age-matched boys (p < 0.05). Both sexes showed age-dependent changes in fasting GH levels (p < 0.001); highest levels were achieved at puberty and subsequently declined with advancing age. Hence, the physiological sex difference and age-dependency in GH secretion can also be demonstrated in single fasting samples.
- Published
- 1993
80. Iodine content in drinking water not an important determinant of endemic goitre.
- Author
-
Osman A, Khalida M, Azman AB, Jamil R, Tan TT, Wu LL, Sakinah SO, and Khalid BA
- Abstract
The prevalence of goitre was determined in several communities in rural parts of Pahang. Urine specimens were collected randomly among the participants. Drinking water from various sources such as river and spring, and water from gravity feed systems was also collected to determine the iodine content by using the ashing method. The results were compared to that of Kuala Lumpur City. lt was found that the prevalence of goitre in rural areas was between 20 and 70% depending on village, ethnic group, age and gender. The interior parts of the jungle where Aborigines lived was moderately endemic with goitre prevalence of goitre more than 20% and urinary iodine content 2.0-5.0 μg I/dl). A nearby Malay traditional village which was studied had mild endemia (prevalence 10-30% and urinary iodine content 5.0-10.0 μg I/dl) while a Felda Malay resettlement scheme and Kuala Lumpur City did not have endemic goitre. Endemic goitre in rural areas was associated with low iodine content in drinking water. Even though Kuala Lumpur had low iodine content in its drinking water there was no endemic goitre, indicating that other factors were more important.
- Published
- 1993
81. Thyroid hormones and autoantibodies in pregnant patients with thyroid diseases.
- Author
-
Goh KH, Ng ML, Roslan BA, Tan TT, Nasri BN, and Khalid BA
- Subjects
- Adult, Cross-Sectional Studies, Female, Gestational Age, Humans, Pregnancy, Pregnancy Complications immunology, Reference Values, Singapore, Thyrotropin blood, Thyroxine blood, Triiodothyronine blood, Autoantibodies blood, Pregnancy Complications diagnosis, Thyroid Gland immunology, Thyroid Hormones blood
- Abstract
Serum concentrations of thyroid stimulating hormone (TSH) and thyroid autoantibodies in pregnant patients with thyroid disease at various stages of pregnancy were determined by in-house ELISAs. In normal pregnancy, serum TSH levels were significantly elevated (p < 0.05) from 13 weeks of gestation. The normal reference ranges for TSH for the second (0.6-5.0 mIU/l) and third trimester (0.6-5.6 mIU/l) were significantly higher (p < 0.05; p < 0.01 respectively) compared to 0.4-4.5 mIU/l for the first trimester. In pregnant thyroid patients, serum TSH levels correlated highly (p < 0.001) to T4 (r = 0.740), FT4I (r = 0.683) and MicAb (microsomal antibodies) (r = 0.825) but weaker (p < 0.01) to T3 (r = -0.512), FT3I (r = 0.520) and TgAb (thyroglobulin antibodies) (r = 0.618). Thus, measurement of TSH with the highly sensitive ELISA (enzyme linked immunosorbent assay) would form a useful first line test for thyroid dysfunction in pregnancy while measurement of thyroid autoantibodies would aid in the diagnosis of autoimmune hypothyroidism.
- Published
- 1993
82. Usefulness and limitations of thyrotropin measurements as a first-line test for follow-up of Graves' patients.
- Author
-
Ng ML, Tan TT, Roslan BA, Rajna A, and Khalid BA
- Subjects
- Adolescent, Adult, Antithyroid Agents therapeutic use, Autoantibodies blood, Female, Follow-Up Studies, Graves Disease drug therapy, Graves Disease immunology, Humans, Hyperthyroidism diagnosis, Hyperthyroidism drug therapy, Hyperthyroidism immunology, Hypothyroidism diagnosis, Hypothyroidism drug therapy, Hypothyroidism immunology, Male, Middle Aged, Thyroid Function Tests, Thyroiditis, Autoimmune diagnosis, Thyroiditis, Autoimmune drug therapy, Thyroiditis, Autoimmune immunology, Graves Disease diagnosis, Thyrotropin blood
- Abstract
We evaluated the usefulness of sensitive thyrotrophin hormone (TSH) measurements in determining the thyroid status in the follow-up of Graves' patients undergoing medical treatment with thionamides. Out of a total of 186 serum samples tested, TSH levels were suppressed in 123 (66.1%), normal in 32 (17.2%) and elevated in 31 (16.7%) cases. Total T4, or T3 or both were elevated only in 97 (74.8%) cases of TSH-suppressed patients, indicating that TSH is less discriminatory as a first-line test for patients under treatment due to the hypothalamic-pituitary lag period. No comparisons with free T4 or free T3 were done in this study. Both total T4 (120 +/- 28 nmol/l) and TBII (23 +/- 21%) levels were significantly greater (p < 0.02) in the euthyroid group with suppressed TSH. This may suggest that persistence of a thyrotoxic state may still be present.
- Published
- 1993
83. Serum thyroid stimulating hormone (TSH) in malnutrition: preliminary results.
- Author
-
Osman A, Khalid BA, Tan TT, Wan Nazaimoon WM, Wu LL, and Ng ML
- Subjects
- Adolescent, Alanine Transaminase blood, Blood Glucose analysis, Body Mass Index, Calcium blood, Child, Cross-Sectional Studies, Female, Growth Hormone blood, Humans, Hydrocortisone blood, Male, Nutrition Assessment, Thyroxine blood, Triiodothyronine blood, Nutrition Disorders blood, Thyrotropin blood
- Abstract
This is a report of a cross sectional study involving 3 groups of children, moderately malnourished (BMI < 15), mildly malnourished (BMI 15-18) and well nourished (BMI > 18) to determine the differences in hormonal and biochemical parameters between the groups. The children were of age range from 7-17 years old. The children were from the same area with exposure to the same food, drinking water and environment. There were significant differences in the nutritional indices between the three groups. No differences were observed in levels of triiodothyronine (T3), thyroxine (T4) and T3:T4 ratio. Significant difference however was found in the TSH levels using highly sensitive IRMA TSH assays. Moderately malnourished children had higher TSH levels (p < 0.05) compared to mildly malnourished and well-nourished children. No difference was found between the mildly malnourished and well-nourished groups. There were no significant differences in serum cortisols done at similar times, fasting growth hormone and calcium. Serum alanine transminase (ALT) however was higher in moderately malnourished than in well-nourished children. Thus using highly sensitive IRMA TSH assays, we were able to detect differences in TSH levels even though T3, T4 and T3:T4 ratio, cortisol, growth hormone and calcium were normal, implying in moderately malnourished children, a higher TSH drive to maintain euthyroid state.
- Published
- 1993
84. Insulin-like growth factor-I and fast growth-hormone levels in mild and moderately malnourished children.
- Author
-
Wan Nazaimoona WM, Osman A, Ng ML, Tan TT, Wu LL, Sakinah O, and Khalid AK
- Abstract
Insulin-like growth factor-I (IGF-I)and fasting growth hormone levels were measured in a group of 255 children (163 males and 92 females. age ranged 6-17 years) of varying pubertal development and body mass index (BMI); well-nourished (BMI> 18). mildly-malnourished (BMI = 15-18) and moderately-malnourished (BMI<15). In well-nourished children IGF-I levels increased significantly (P = 0.02) with pubertal development. where girls at Tanner 5 had significantly higher (p = 0.03) IGF-I levels than the boys. Whilst there was no change in fasting GH levels with nutritional status, IGF-I levels of prepubertal boys and girls decreased significantly with BMI (P<0.001 and P = 0.01 respectively). Hence. measurement of IGF-I levels is a sensitive biochemical index in the assessment of mild and moderate form of malnutrition in prepubertal children.
- Published
- 1992
85. Protein energy malnutrition, thyroid hormones and goitre among Malaysian Aborigines and Malays.
- Author
-
Osman A, Khalid B, Tan TT, Wu LL, and Ng ML
- Abstract
The relationship between malnutrition, goitre and thyroid hormones was studied among Aborigines and Malays in Ulu Langat, Malaysia. Fifty Aborigines aged >=7years were selected randomly for anthropometric, clinical and hormonal assessment. Fifty Malays of similar age from the nearby Malay village were chosen as controls. The Aborigines had a higher prevalence of malnutrition and goitre compared to the Malays. The prevalence of goitre was 26.5% amongst Aborigines and 19.6% among the Malays. All the nutritional indexes measured were significantly different between the two communities, especially among females. The differences corresponded to significant differences in levels of thyroid-stimulating hormone (TSH) measured using a highly sensitive TSH assay. By univariate analysis the increase in TSH corresponded to the decrease in body mass index (BMI). On the other hand, no association was found between BMI and goitres. No thyroid autoantibodies were detected and all subjects were clinically euthyroid and had normal thyroxine and triidothyronine levels. However, consumption of cassava conferred a four-fold risk of developing goitres. The high prevalence of goitres in malnourished subjects in this region which is not known to be iodine deficient could be due to cassava consumption.
- Published
- 1992
86. Primary hyperparathyroidism--a surgical review of 12 cases.
- Author
-
Meah FA, Tan TT, Taha A, and Khalid BA
- Subjects
- Adenoma diagnosis, Adenoma surgery, Adolescent, Adult, Child, Female, Humans, Hyperparathyroidism surgery, Male, Middle Aged, Parathyroid Neoplasms diagnosis, Parathyroid Neoplasms surgery, Hyperparathyroidism diagnosis
- Abstract
Twelve cases of primary hyperparathyroidism operated by the Universiti Kebangsaan Malaysia Surgical Team from 1978 to 1989 were reviewed. There was a preponderance of Indian females in this series. The majority of the cases presented late and with complications. Renal calculi and bone disease were the commonest complications noted. Of the 12 patients, 9 had single parathyroid adenoma of which 4 were ectopically located, and 2 had hyperplasia of the parathyroids. These were all successfully operated. The remaining patient had 2 failed neck explorations. Failure at initial exploration was due to ectopic location of the glands. Meticulous surgical technique, knowledge of the anatomical variations of location of the parathyroid glands and availability of frozen section facility are essential for successful outcome.
- Published
- 1991
87. Hypercalcemia in a patient with tuberculous mediastinal lymphadenopathy.
- Author
-
Tan TT, Lee BC, Zainuddin BM, Wong KT, Samad A, and Khalid BA
- Subjects
- Female, Humans, Hypercalcemia diagnosis, Malaysia, Mediastinal Diseases diagnostic imaging, Mediastinal Diseases therapy, Middle Aged, Radiography, Tuberculosis, Lymph Node diagnostic imaging, Tuberculosis, Lymph Node therapy, Hypercalcemia etiology, Mediastinal Diseases complications, Tuberculosis, Lymph Node complications
- Abstract
We describe the case of a 48 year old Indian female with hypercalcemia due to tuberculosis. She presented with symptoms of hypercalcemia and chest radiographs showed bilateral hilar lymphadenopathy with normal lung fields. The diagnosis of tuberculosis was made histologically from biopsy of the enlarged hilar nodes. Her hypercalcemia resolved following one month of anti-tuberculous treatment. The prevalence of hypercalcemia in tuberculosis has been reported to be high in western series. There is, however, a paucity of local data on the subject. The presence of 1-alpha-hydroxylase-like activity in pulmonary alveolar macrophages with resulting increased formation of active vitamin D metabolites is the postulated mechanism of tuberculosis associated hypercalcemia.
- Published
- 1991
88. Adrenal histoplasmosis in Cushing's syndrome with bilateral adrenocortical nodular hyperplasia.
- Author
-
Tan TT, Choy YW, Norizan MA, Meah F, and Khalid BA
- Subjects
- Adrenal Gland Diseases surgery, Adrenalectomy, Cushing Syndrome surgery, Histoplasmosis surgery, Humans, Hyperplasia pathology, Male, Middle Aged, Adrenal Gland Diseases complications, Adrenal Glands pathology, Cushing Syndrome complications, Histoplasmosis complications
- Abstract
Adrenal histoplasmosis in Cushing's syndrome of adrenal origin is rare. A patient with Cushing's disease with bilateral nodular hyperplasia and histoplasmosis of both the adrenal glands is described. The diagnosis of histoplasmosis was only made post operatively as the constitutional manifestations, besides being partially masked by hypercortisolism also resemble those of tuberculosis.
- Published
- 1990
89. Massive pericardial effusion in primary hypothyroidism.
- Author
-
Hanip MR, Ong SB, Tan TT, and Khalid BA
- Subjects
- Adult, Female, Galactorrhea etiology, Humans, Hyperprolactinemia etiology, Hypertension etiology, Hypothyroidism complications, Pericardial Effusion etiology
- Abstract
A 44 year old lady with primary hypothyroidism presented with massive pericardial effusion without cardiac tamponade. Pericardial tap was done twice and the effusion resolved as the hypothyroid state improved. She remained hypertensive despite the euthyroid state. She was discharged well with L-thyroxine and anti-hypertensive therapy.
- Published
- 1989
90. Sporadic adult-onset hypophosphatemic osteomalacia--a report of two cases.
- Author
-
Tan TT, Raymond AA, Cheong I, and Khalid BA
- Subjects
- Adult, Bone and Bones diagnostic imaging, Female, Humans, Male, Middle Aged, Osteomalacia etiology, Radionuclide Imaging, Osteomalacia blood, Phosphates blood
- Abstract
Two cases of sporadic adult onset hypophosphatemic osteomalacia are described. Both patients initially presented with intractable low backache and had lumbar laminectomies. In retrospect, they both had typical clinical and biochemical features of hypophosphatemic osteomalacia prior to surgery. Medical treatment resulted in rapid relief of symptoms in both patients.
- Published
- 1989
91. [Results of surgical treatment of carcinoma of uterine cervix in 1962-1977 (author's transl)].
- Author
-
Tan TT
- Subjects
- Adult, Aged, Female, Humans, Lymphatic Metastasis, Middle Aged, Pregnancy, Pregnancy Complications surgery, Time Factors, Uterine Cervical Neoplasms surgery
- Published
- 1979
92. Luteotropic activity in serum of women following embryo or gamete transfer in a program of assisted conception.
- Author
-
Stone BA, Tan TT, Koopersmith TB, Quinn K, and Marrs RP
- Subjects
- Chorionic Gonadotropin blood, Chorionic Gonadotropin metabolism, Female, Humans, Iodine Radioisotopes, Luteinizing Hormone blood, Oocytes, Pregnancy, Radioimmunoassay, Testosterone analysis, Embryo Transfer, Fertilization in Vitro, Luteinizing Hormone metabolism
- Abstract
In an attempt to track the proliferation/demise of trophoblastic tissues in women following gamete transfer (GT) or in vitro fertilization/embryo transfer (IVF/ET), we have measured levels of human chorionic gonadotropin (hCG) in serum of 180 patients on days 7 and 14 following oocyte pickup (OPU). Serum hCG levels were measured by immunoassay and by a bioassay based on the capacity of the sample to stimulate testosterone secretion by cultured mouse Leydig cells. Based on determinations of bioactive and immunoactive hCG in serum from 18 of 180 patients who subsequently delivered (12 of 73 GT, 6 of 107 IVF/ET; P less than 0.05) and classification of patients in accord with their compliance or noncompliance with these ranges of values, about 70% of all patients in the present study were classified as "pregnant" 7 days following OPU. Based on these same criteria, about 23% were pregnant 7 days later. Biochemical pregnancy rates on days 7 and 14 following GT (near 73 and 27%, respectively) were not different from the respective values following IVF/ET (near 68 and 20%, respectively; P greater than 0.05). The luteotropin bioassay described is highly sensitive to hCG (to 0.02 mIU/ml serum) and appears appropriate to the characterization of proliferation/demise of embryonic tissues during the 14 days after gamete/embryo transfer. In addition, through its representation of the cumulative luteotropic properties of human serum and its insensitivity to biologically inactive hCG subunits, this bioassay appears more appropriate than hCG immunoassay in the monitoring of early embryonic signalling following assisted (or spontaneous) conception in the woman.
- Published
- 1988
- Full Text
- View/download PDF
93. Cerebral metastatic choriocarcinoma in the People's Republic of China.
- Author
-
Liu TL, Deppe G, Chang QT, and Tan TT
- Subjects
- Adult, Brain Neoplasms drug therapy, China, Choriocarcinoma drug therapy, Drug Therapy, Combination, Female, Humans, Middle Aged, Neoplasm Metastasis, Phytotherapy, Pregnancy, Prognosis, Uterine Neoplasms, Antineoplastic Agents administration & dosage, Brain Neoplasms secondary, Choriocarcinoma secondary
- Abstract
Thirty-four patients with cerebral metastases from choriocarcinoma were treated between 1964 and 1978 by the Department of Gynecology of the Tumor Hospital Chung Shan Medical College, Kwongchow, People's Republic of China. Disease in 20.5% (7 of 34 patients) is currently in remission (12 to 120 months). Treatment was primarily by chemotherapy and Chinese herbs, with adjunctive craniotomy in selected patients. Myelosuppression was the main side effect.
- Published
- 1983
- Full Text
- View/download PDF
94. Clinical and endocrine profiles of 62 Malaysian women with polycystic ovary syndrome.
- Author
-
Tan TT, Lui SK, Satgunasingam N, and Khalid BA
- Subjects
- Acanthosis Nigricans etiology, Adult, Female, Hormones blood, Humans, Hyperinsulinism etiology, Polycystic Ovary Syndrome blood, Polycystic Ovary Syndrome diagnosis, Testosterone blood, Polycystic Ovary Syndrome etiology
- Abstract
62 cases of polycystic ovary syndrome (PCO) were reviewed with regards to their clinical and endocrine features. The subgroup of patients with acanthosis nigricans (AN) was further studied in detail. The prevalence of the syndrome was significantly higher in the Indian (35.5% of cases). Obesity, AN, hirsutism, non-insulin dependent diabetes mellitus (NIDDM) and raised level of serum testosterone were present in 77.1%, 74%, 79%, 21% and 48% of the cases respectively. Patients with AN was associated with higher body mass index, serum testosterone level, and prevalence of hirsutism and NIDDM than patients without AN. These observations are in keeping with the hypothesis that hyperinsulinemia may be of importance in the pathogenesis of a sub-group of PCO associated with insulin resistant states.
- Published
- 1989
95. Rates and effects of foot marches.
- Author
-
Tan TT, Chow KK, Anantharaman V, Seet LC, Giam CK, and Teh KC
- Subjects
- Heart Rate, Humans, Physical Endurance, Physical Exertion, Gait, Locomotion, Military Medicine
- Published
- 1979
96. Mesenteric cyst--a case report and review of the literature.
- Author
-
Vellayappan K, Teo J, and Tan TT
- Subjects
- Child, Preschool, Humans, Male, Mesenteric Cyst pathology, Mesenteric Cyst surgery, Mesenteric Cyst diagnosis
- Published
- 1980
97. Hyperthyroid graves disease--a 5 year retrospective study.
- Author
-
Tan TT, Ng ML, Wu LL, and Khalid BA
- Subjects
- Adolescent, Adult, Age Factors, Child, Female, Graves Disease epidemiology, Graves Disease therapy, Humans, Malaysia epidemiology, Male, Middle Aged, Retrospective Studies, Graves Disease diagnosis
- Abstract
The clinical, biochemical and immunological features of 180 patients with hyperthyroid Graves' disease managed at the Universiti Kebangsaan Malaysia (UKM) Endocrine Clinic from 1983 to 1987 were examined. The prevalence of the disease is highest in Chinese and lowest in Indians. The female: male ratio is 2.8:1. Hypokalaemic periodic paralysis and hypercalcaemia were present in 5.0% and 1.7% of the cases respectively. Pretibial myxoedema was extremely rare. Thyrotropin - binding inhibitory immunoglobulins, anti-thyroglobulin and anti-microsome antibodies were positive in 61.5%, 25.8% and 42.3% of the patients respectively. A eumetabolic state could be achieved in the majority of patients with antithyroid drugs alone. Definitive therapy with subtotal thyroidectomy or radioiodine were needed in 31.3% of cases.
- Published
- 1989
98. [Multiple cartilaginous exostoses and multiple enchondromatoses].
- Author
-
LIEM TD and TAN TT
- Subjects
- Humans, Chondroma, Enchondromatosis, Exostoses, Multiple Hereditary, Osteochondrodysplasias
- Published
- 1960
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