Displaying publications 41 - 60 of 1521 in total

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  1. Sinniah D
    Intern Med J, 2015 Apr;45(4):467-8.
    PMID: 25827521 DOI: 10.1111/imj.12715
    Matched MeSH terms: Restless Legs Syndrome/blood; Restless Legs Syndrome/diagnosis*; Restless Legs Syndrome/etiology*
  2. Fook CW
    Med J Malaya, 1970 Sep;25(1):58-60.
    PMID: 4250313
    Matched MeSH terms: Meigs Syndrome/diagnosis*; Meigs Syndrome/pathology; Meigs Syndrome/radiography
  3. Nurul Adzlyana Mohd Saadon, Rosma Mohd Dom, Nurazzah Abd Rahman
    MyJurnal
    Clustering refers to reducing selected features involved in determining the clusters. Raw data might come with a lot of features, including unimportant ones. A hybrid similarity measure (discovered in 2014) used in selecting features can be improvised as it might select all the attributes, including insignificant ones. This paper suggests Fuzzy Lambda-Max to be used as a feature selection method since Lambda-Max is normally used in ranking of alternatives. A set of AIDS data is used to measure the performance. Results show that Fuzzy Lambda-Max has the ability to determine criteria weights and ranking the criteria. Hence, feature selection can be done by choosing only the important criteria.
    Matched MeSH terms: Acquired Immunodeficiency Syndrome
  4. Nor Azizah A, Thong SP, Hung LC
    Med J Malaysia, 2018 08;73(4):257-259.
    PMID: 30121692 MyJurnal
    Kawasaki disease (KD) is an acute systemic vasculitis usually affecting children <5 years old. We report a 44-dayold baby who had persistent fever despite being on antibiotics for presumed sepsis. Erythema of Bacillus Calmette-Guerin (BCG) scar and thrombocytosis were noted on day-2 of illness. Diagnosis of incomplete KD was made on the 10th day of illness. Her fever resolved with intravenous immunoglobulin, but echocardiogram revealed coronary artery aneurysm. High index of suspicion is required to diagnose KD in infants ≤3 months since it is rare and commonly presents with incomplete clinical features. The presence of unexplained fever for ≥5 days with erythema of BCG scar or thrombocytosis in infants should alert the clinicians of KD.
    Matched MeSH terms: Mucocutaneous Lymph Node Syndrome/complications; Mucocutaneous Lymph Node Syndrome/diagnosis*; Mucocutaneous Lymph Node Syndrome/pathology
  5. Dunlop GA
    Lancet, 1928;212:500.
    DOI: 10.1016/S0140-6736(00)83930-6
    Matched MeSH terms: Cervical Rib Syndrome
  6. Cheong IKS
    Family Physician, 1993;5:35-36.
    Matched MeSH terms: Acquired Immunodeficiency Syndrome
  7. Hafizzi Awang NMS, Mohd Noor R, Ramli R, Abdullah B
    Gulf J Oncolog, 2022 Jan;1(38):78-81.
    PMID: 35156648
    BACKGROUND: The infratemporal fossa poses a great challenge to surgeons due to its complex anatomy and communications to many surrounding areas. The disorders that arise from this area can be infections and neoplasms. They can cause varieties of complications due to the extension of the pathologies and compression effect to the other adjacent structures. Inflammatory pseudotumor of the infratemporal fossa is one of the rare disorders of the head and neck.

    CASE PRESENTATION: We report a patient with a pseudotumor of infratemporal fossa that extends to the orbital area and cavernous sinus, causing orbital apex syndromes. The diagnostic imaging, different surgical approaches of the biopsy and methods of treatment of this case are discussed.

    DISCUSSION AND CONCLUSION: Radiological imaging and immunohistopathology are essential in establishing the diagnosis and determine the complications. The surgeons must well understand the characteristics and the impact of the disorders on the adjacent structure and give prompt decision to provide definitive treatments.

    Matched MeSH terms: Syndrome
  8. Zulkipli NS, Satari SZ, Hariri F, Abdullah NA, Wan Yusoff WNS, Hussin AG
    Cleft Palate Craniofac J, 2023 Nov;60(11):1484-1493.
    PMID: 35711157 DOI: 10.1177/10556656221107524
    INTRODUCTION: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndromic craniosynostosis (SC), whereby it is a congenital defect that occurs when the cranial growth is distorted. Identifying cranial angles associated with these 3 syndromes may assist the surgical team to focus on a specific cranial part during the intervention planning, thus optimizing surgical outcomes and reducing potential morbidity.

    OBJECTIVE: The aim of this study is to identify the cranial angles, which are associated with Apert, Crouzon, and Pfeiffer syndromes.

    METHODS: The cranial computed tomography scan images of 17 patients with SC and 22 control groups aged 0 to 12 years who were treated in the University Malaya Medical Centre were obtained, while 12 angular measurements were attained using the Mimics software. The angular data were then divided into 2 groups (patients aged 0 to 24 months and >24 months). This work proposes a 95% confidence interval (CI) for angular mean to detect the abnormality in patient's cranial growth for the SC syndromes.

    RESULTS: The 95% CI of angular mean for the control group was calculated and used as an indicator to confirm the abnormality in patient's cranial growth that is associated with the 3 syndromes. The results showed that there are different cranial angles associated with these 3 syndromes.

    CONCLUSIONS: All cranial angles of the patients with these syndromes lie outside the 95% CI of angular mean of control group, indicating the reliability of the proposed CI in the identification of abnormality in the patient's cranial growth.

    Matched MeSH terms: Syndrome
  9. Ng ZQ, Tan HCL, Tan JH
    J Gastrointest Surg, 2023 Apr;27(4):836-837.
    PMID: 36658386 DOI: 10.1007/s11605-023-05597-w
    Matched MeSH terms: Syndrome
  10. Su AT, Darus A, Bulgiba A, Maeda S, Miyashita K
    J Occup Health, 2012;54(5):349-60.
    PMID: 22863899
    The internationally accepted limit values and the health effects of hand-transmitted vibration exposure have been described extensively in the literature from temperate climate countries but not from a tropical climate environment.

    OBJECTIVES: We conducted a systematic review of the health effects of hand-transmitted vibration exposure in tropical countries to determine the characteristics of hand-arm vibration syndrome in a warm environment and compared the findings with the results of the systematic reviews published by the US NIOSH.

    METHODS: We searched major medical databases including MEDLINE, PubMed, Embase, CINAHL, Ovid and Cochrane based on the terms "hand arm vibration syndrome," "hand transmitted vibration," "vibration white finger" and "Raynaud" up to January 2011. Only studies conducted in a tropical or subtropical environment were selected for the review. The quality of the selected papers was assessed independently by two investigators using predefined criteria. A standard set of information was abstracted from the papers for review.

    RESULTS: Only six papers from tropical countries and three papers from subtropical countries were available in the literature. No vibration white finger was reported in the tropical countries. Neurological symptoms were prevalent in the vibration-exposed workers. Finger coldness seems to be an important surrogate for vascular disorder in a tropical environment. Meta-analysis could not be performed due to inadequacy of the information reported in these papers.

    CONCLUSIONS: The current dose-response relationship in ISO5349-1 for hand-transmitted vibration exposure is not applicable to a tropical environment. Further studies on hand-arm vibration syndromes in tropical countries are needed.

    Matched MeSH terms: Hand-Arm Vibration Syndrome/physiopathology*
  11. Idris N, Aznal SS, Chin SP, Wan Ahmad WA, Rosman A, Jeyaindran S, et al.
    Int J Womens Health, 2011;3:375-80.
    PMID: 22140324 DOI: 10.2147/IJWH.S15825
    There is scarce or no data on prevalence and presentation of acute coronary syndrome (ACS) among women of reproductive age. Furthermore, whether women of reproductive age presenting with ACS have the same risk factors as men and older women is not known.
    Matched MeSH terms: Acute Coronary Syndrome*
  12. Shahrizaila N, Goh KJ, Kokubun N, Abdullah S, Yuki N
    J Neurol Sci, 2011 Oct 15;309(1-2):26-30.
    PMID: 21849173 DOI: 10.1016/j.jns.2011.07.042
    The electrodiagnosis of Guillain-Barré syndrome (GBS) can be broadly divided into acute inflammatory demyelinating polyneuropathy (AIDP) and acute motor axonal neuropathy (AMAN). Fisher syndrome (FS) is a variant of GBS, although the underlying neuropathy of FS has yet to be established. Serial nerve conduction studies (NCS) can provide further insight into the likely pathophysiology by further subtyping of GBS and FS. We present a patient with an initial diagnosis of AIDP in whom repeated NCS revealed the AMAN variant. This led us to investigate serial NCS in five patients with GBS, FS and FS/GBS overlap presenting over a period of a year. Three patients with AIDP showed a gradual increase in distal motor latencies during the acute phase of illness. NCS of two patients with FS and FS/GBS overlap showed no demyelinating features suggesting underlying axonal neuropathy in this group of patients. The importance of serial NCS in establishing the underlying pattern of neuropathy in GBS and FS is further emphasized in this study. Larger studies incorporating serial NCS are required to confirm the observations seen in our case series especially when pathological studies are often not justified in this group of patients.
    Matched MeSH terms: Miller Fisher Syndrome/diagnosis*; Miller Fisher Syndrome/pathology; Miller Fisher Syndrome/physiopathology*; Guillain-Barre Syndrome/diagnosis*; Guillain-Barre Syndrome/pathology; Guillain-Barre Syndrome/physiopathology*
  13. Das Gupta E
    Malays Fam Physician, 2008;3(1):51.
    PMID: 25606113
    Matched MeSH terms: Guillain-Barre Syndrome*
  14. Loh YC, Trail IA
    Med J Malaysia, 2002 Jun;57(2):205-8.
    PMID: 24326652
    Fourteen fit and healthy patients underwent arthroscopic subacromial decompression (ASD) of shoulder for rotator cuff impingement. Their blood chemistry was analysed pre-operatively, 24 hours post-operatively and 2-3 weeks post-operatively. Levels of haematocrit, sodium, potassium, creatinine and urea were measured. The blood chemistry returned almost to the pre-operative level at 2-3 weeks post-operatively. There was no statistically significant differences found. This study concludes that arthroscopic subacromial decompression is a safe technique when considering the blood parameters despite the haemodilution seen in all patients.
    Matched MeSH terms: Shoulder Impingement Syndrome*
  15. Robinson AJ, Waugh MA
    Genitourin Med, 1992 Apr;68(2):139-40.
    PMID: 1582659
    Matched MeSH terms: Acquired Immunodeficiency Syndrome*
  16. Krishnaswamy S, Mohamed M
    Med J Malaysia, 1985 Dec;40(4):330-2.
    PMID: 3842735
    A case of the Klippel-Feil syndrome presenting with schizophrenia is described. The Klippel-Feil syndrome is reported to be associated with abnormalities in many systems of the body, but its association with a schizophrenic illness has not been described.
    Matched MeSH terms: Klippel-Feil Syndrome/complications*
  17. Tan CY, Razali SNO, Goh KJ, Shahrizaila N
    J Peripher Nerv Syst, 2019 06;24(2):168-173.
    PMID: 31001904 DOI: 10.1111/jns.12320
    Guillain-Barré syndrome (GBS) is an acute immune-mediated neuropathy that has variable disease course and outcome. The Erasmus GBS outcome score (EGOS), modified EGOS (mEGOS), and Erasmus GBS respiratory insufficiency score (EGRIS) are prognostic models designed to predict the functional outcome of GBS patients at 6 months (EGOS and mEGOS) and the need for mechanical ventilation within a week of admission (EGRIS). The models were primarily developed in the Dutch GBS population, and thus the usefulness of these models in other GBS cohorts is less clear. In the current study, we aimed to validate mEGOS, EGOS, and EGRIS in Malaysian GBS patients. A total of 107 patients with GBS and its variants were consecutively recruited. Patients with GBS and Miller Fisher syndrome (MFS) were analysed separately. In the GBS cohort, high mEGOS and EGOS scores were significantly correlated with poor outcome at 6 months (mEGOS on admission: r = .381, P = .005; mEGOS at day 7 of admission: r = .507, P 
    Matched MeSH terms: Miller Fisher Syndrome/diagnosis*; Miller Fisher Syndrome/physiopathology; Miller Fisher Syndrome/therapy; Guillain-Barre Syndrome/diagnosis*; Guillain-Barre Syndrome/physiopathology; Guillain-Barre Syndrome/therapy
  18. Wong JJM, Lee SW, Lee JH
    Pediatr Crit Care Med, 2020 09;21(9):855-856.
    PMID: 32890097 DOI: 10.1097/PCC.0000000000002446
    Matched MeSH terms: Respiratory Distress Syndrome, Adult*
  19. Chan JCN, Lim LL, Shaw JE, Aguilar-Salinas CA, Gregg EW, Lancet Commission on diabetes
    Lancet, 2021 06 05;397(10290):2150.
    PMID: 34090602 DOI: 10.1016/S0140-6736(21)00664-4
    Matched MeSH terms: Respiratory Distress Syndrome, Adult*
  20. Anuar M, Ng KK, Chong KF
    Med J Malaysia, 1977 Mar;31(3):244-6.
    PMID: 904521
    Matched MeSH terms: Empty Sella Syndrome/radiography*
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