Displaying publications 41 - 60 of 261 in total

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  1. POND WL, RUSS SB, LANCASTER WE, AUDY JR, SMADEL JE
    Am J Hyg, 1954 Jan;59(1):17-25.
    PMID: 13124320
    Matched MeSH terms: Encephalitis, Japanese/immunology*
  2. Lih Shan Lim, Suk Fun Chin, Suh Cem Pang, Magdline Sia Henry Sum, David Perera
    Sains Malaysiana, 2017;46:2447-2454.
    A novel silver nanoparticles (Ag NPs)-based optical sensing probe has been developed for the detection of Japanese Encephalitis virus (JEV). Ag NPs were initially deposited onto amine functionalized glass slides. Subsequently, JEV antibodies were self-assembled onto surfaces of Ag NPs to form optical sensing probes. The detection of JEV antigen was observed via changes in light absorbance by Ag NPs upon occurrence of JEV antigen-antibody bindings. A highly sensitive and rapid optical sensing probe for JEV antigen with a detection limit of 12.8 ng/mL (for S/N ratio = 3) and an analysis assay time of 1 h had been demonstrated.
    Matched MeSH terms: Encephalitis Virus, Japanese; Encephalitis, Japanese
  3. Li MH, Fu SH, Chen WX, Wang HY, Guo YH, Liu QY, et al.
    PLoS Negl Trop Dis, 2011 Jul;5(7):e1231.
    PMID: 21750744 DOI: 10.1371/journal.pntd.0001231
    Japanese encephalitis (JE) is a global public health issue that has spread widely to more than 20 countries in Asia and has extended its geographic range to the south Pacific region including Australia. JE has become the most important cause of viral encephalitis in the world. Japanese encephalitis viruses (JEV) are divided into five genotypes, based on the nucleotide sequence of the envelope (E) gene. The Muar strain, isolated from patient in Malaya in 1952, is the sole example of genotype V JEV. Here, the XZ0934 strain of JEV was isolated from Culex tritaeniorhynchus, collected in China. The complete nucleotide and amino acid sequence of XZ0934 strain have been determined. The nucleotide divergence ranged from 20.3% to 21.4% and amino acid divergence ranged from 8.4% to 10.0% when compared with the 62 known JEV isolates that belong to genotype I-IV. It reveals low similarity between XZ0934 and genotype I-IV JEVs. Phylogenetic analysis using both complete genome and structural gene nucleotide sequences demonstrates that XZ0934 belongs to genotype V. This, in turn, suggests that genotype V JEV is emerging in JEV endemic areas. Thus, increased surveillance and diagnosis of viral encephalitis caused by genotype V JEV is an issue of great concern to nations in which JEV is endemic.
    Matched MeSH terms: Encephalitis Viruses, Japanese/classification*; Encephalitis Viruses, Japanese/genetics*; Encephalitis Viruses, Japanese/isolation & purification
  4. Looi LM, Chua KB
    Malays J Pathol, 2007 Dec;29(2):63-7.
    PMID: 19108397 MyJurnal
    The Nipah virus outbreak in Malaysia (September 1998 to May 1999) resulted in 265 cases of acute encephalitis with 105 deaths, and near collapse of the billion-dollar pig-farming industry. Because it was initially attributed to Japanese encephalitis, early control measures were ineffective, and the outbreak spread to other parts of Malaysia and nearby Singapore. The isolation of the novel aetiological agent, the Nipah virus (NiV), from the cerebrospinal fluid of an outbreak victim was the turning point which led to outbreak control 2 months later. Together with the Hendra virus, NiV is now recognised as a new genus, Henipavirus (Hendra + Nipah), in the Paramyxoviridae family. Efforts of the local and international scientific community have since elucidated the epidemiology, clinico-pathophysiology and pathogenesis of this new disease. Humans contracted the infection from close contact with infected pigs, and formed the basis for pig-culling that eventually stopped the outbreak. NiV targeted medium-sized and small blood vessels resulting in endothelial multinucleated syncytia and fibrinoid necrosis. Autopsies revealed disseminated cerebral microinfarctions resulting from vasculitis-induced thrombosis and direct neuronal involvement. The discovery of NiV in the urine and saliva of Malaysian Island flying foxes (Pteropus hypomelanus and Petropus vampyrus) implicated these as natural reservoir hosts of NiV. It is probable that initial transmission of NiV from bats to pigs occurred in late 1997/early 1998 through contamination of pig swill by bat excretions, as a result of migration of these forest fruitbats to cultivated orchards and pig-farms, driven by fruiting failure of forest trees during the El Nino-related drought and anthropogenic fires in Indonesia in 1997-1998. This outbreak emphasizes the need for sharing information of any unusual illnesses in animals and humans, an open-minded approach and close collaboration and co-ordination between the medical profession, veterinarians and wildlife specialists in the investigation of such illnesses. Environmental mismanagement (such as deforestation and haze) has far-reaching effects, including encroachment of wildlife into human habitats and the introduction of zoonotic infections into domestic animals and humans.
    Matched MeSH terms: Encephalitis, Viral/epidemiology*; Encephalitis, Viral/pathology; Encephalitis, Viral/transmission
  5. Lo MK, Rota PA
    J Clin Virol, 2008 Dec;43(4):396-400.
    PMID: 18835214 DOI: 10.1016/j.jcv.2008.08.007
    Nipah virus first emerged in Malaysia and Singapore between 1998 and 1999, causing severe febrile encephalitis in humans with a mortality rate of close to 40%. In addition, a significant portion of those recovering from acute infection had relapse encephalitis and long-term neurological defects. Since its initial outbreak, there have been numerous outbreaks in Bangladesh and India, in which the mortality rate rose to approximately 70%. These subsequent outbreaks were distinct from the initial outbreak, both in their epidemiology and in their clinical presentations. Recent developments in diagnostics may expedite disease diagnosis and outbreak containment, while progress in understanding the molecular biology of Nipah virus could lead to novel therapeutics and vaccines for this deadly pathogen.
    Matched MeSH terms: Encephalitis, Viral/mortality; Encephalitis, Viral/epidemiology*; Encephalitis, Viral/virology
  6. Wong SC, Ooi MH, Wong MN, Tio PH, Solomon T, Cardosa MJ
    J Neurol Neurosurg Psychiatry, 2001 Oct;71(4):552-4.
    PMID: 11561048
    Nipah virus is a newly discovered paramyxovirus transmitted directly from pigs to humans. During a large encephalitis outbreak in Malaysia and Singapore in 1998-9, most patients presented acutely. A 12 year old child is described who developed encephalitis 4 months after exposure to the virus. She was diagnosed by a new indirect IgG enzyme linked immunosorbent assay (ELISA), which is also described. The late presentation and IgG subclass responses had similarities to subacute sclerosing panencephalitis. Nipah virus should be considered in patients with encephalitis even months after their possible exposure.
    Matched MeSH terms: Encephalitis, Viral/diagnosis; Encephalitis, Viral/immunology*; Encephalitis, Viral/transmission
  7. Farrar JJ
    Lancet, 1999 Oct 9;354(9186):1222-3.
    PMID: 10520625
    Matched MeSH terms: Encephalitis, Viral/diagnosis; Encephalitis, Viral/mortality; Encephalitis, Viral/epidemiology*
  8. Tan CT, Wong KT
    Ann Acad Med Singap, 2003 Jan;32(1):112-7.
    PMID: 12625108
    INTRODUCTION: Between September 1998 and June 1999, there was a severe outbreak of viral encephalitis among the pig farm workers in Malaysia.

    METHODS: This is a review of the published literature related to the outbreak with the focus on human diseases.

    RESULTS: The encephalitis was caused by a newly discovered paramyxovirus related to Hendra virus, later named Nipah virus. There were 265 patients with acute encephalitis. The disease is thought to spread from pig to man through close contact. The risk of human-to-human spread is thought to below. The disease affected mainly adult Chinese males, half of whom had affected family members. The disease presented mainly as acute encephalitis with a short incubation period of less than two weeks, with the main symptoms of fever, headache, and giddiness followed by coma. Distinctive clinical signs include segmental myoclonus, areflexia and hypotonia, hypertension, and tachycardia. Initial cerebrospinal fluid was abnormal in 75% of patients. Serology was helpful in confirming the diagnosis. Magnetic resonance imaging showed distinctive changes of multiple, discrete, and small high signal lesions, best seen with fluid-attenuated inversion recovery (FLAIR) sequences. Mortality was high at 40% and death was probably due to severe brainstem involvement. The main necropsy finding in acute encephalitis was that of disseminated microinfarction associated with vasculitis and direct neuronal involvement. Ribavirin was able to reduce the mortality by 36%. Relapse encephalitis was seen in 7.5% of those who recovered from acute encephalitis, and late-onset encephalitis in 3.4% of those with initial non-encephalitic or asymptomatic diseases. The mean interval between initial illness and the onset of the complication was 8.4 months. The relapse and late-onset encephalitis which manifested as focal encephalitis arose from recurrent infection.

    CONCLUSION: Nipah virus, a recently discovered paramyxovirus, causes a unique encephalitis with high mortality as well as relapse and late-onset encephalitis. The infection is mainly spread from pigs to man.

    Matched MeSH terms: Encephalitis, Viral/epidemiology*; Encephalitis, Viral/transmission; Encephalitis, Viral/virology*
  9. Poidinger M, Hall RA, Mackenzie JS
    Virology, 1996 Apr 15;218(2):417-21.
    PMID: 8610471
    The Japanese encephalitis (JE) serocomplex of flaviviruses comprises 10 members, 9 of which: Alfuy (ALF); Koutango (KOU); Kokobera (KOK); Kunjin (KUN); Murray Valley encephalitis (MVE); JE; Stratford (STR); Usutu (USU); and West Nile (WN) have been isolated from Africa, southern Europe, Middle East, Asia, and Australia. The tenth member, St. Louis encephalitis (SLE) virus, is confined to North, Central, and South America. For ALF, KOK, KOU, STR, and USU, no sequence data have as yet been reported, and little molecular phylogeny has been determined for this complex as a whole. Using a rapid, one-step RT-PCR and universal primers, we have amplified and sequenced a 450-600 base pair region of the virus genome encompassing the N terminus of the nonstructural protein NS5 and the 5' end of the 3' noncoding region, for several strains of all of these viruses, except USU and SLE viruses. These data, as well as published sequence data for other flaviviruses, were analyzed with the ClustalW and Phylip computer packages. The resultant phylogenetic data were consistent with some of the current flavivirus serological classification, showing a close relationship between ALF and MVE viruses and between KOK and STR viruses, but suggested that KOK and STR are distantly related to the other viruses and should perhaps be reclassified in their own serocomplex. The data also confirmed the close relationship between KUN and WN viruses and showed that an isolate of KUN virus from Sarawak may represent a "link" between these two virus species. In addition, the primary sequence data revealed a polymorphic region just downstream of the stop codon in the 3' end of the viral genomes.
    Matched MeSH terms: Encephalitis, Arbovirus/virology; Encephalitis Viruses, Japanese/genetics*
  10. Fang R, Hsu DR, Lim TW
    Malays J Pathol, 1980 Aug;3:23-30.
    PMID: 6312203
    Matched MeSH terms: Encephalitis, Japanese/diagnosis; Encephalitis, Japanese/epidemiology*; Encephalitis, Japanese/transmission
  11. Vythilingam I, Singh KI, Mahadevan S, Zaridah MS, Ong KK, Abidin MH
    J Am Mosq Control Assoc, 1993 Dec;9(4):467-9.
    PMID: 8126485
    Mosquito collections were carried out from May to June 1992 and from September to December 1992 in an area where a case of Japanese encephalitis was confirmed. A total of 40,072 mosquitoes belonging to 35 species and 8 genera were collected. The dominant species in that locality were Culex vishnui, Culex tritaeniorhynchus, Culex pseudovishnui, Culex gelidus, Aedes butleri, and Mansonia uniformis.
    Matched MeSH terms: Encephalitis Virus, Japanese/physiology; Encephalitis, Japanese/transmission*
  12. Mohd Fauzi NA, Abdullah S, Tan AH, Mohd Ramli N, Tan CY, Lim SY
    Parkinsonism Relat Disord, 2020 06;75:110-113.
    PMID: 30846242 DOI: 10.1016/j.parkreldis.2019.02.025
    We report a case of relapsing-remitting opsoclonus-myoclonus-ataxia syndrome (OMAS) in a patient with Hashimoto's encephalopathy, diagnosed after comprehensive evaluation. OMAS as a manifestation of Hashimoto's encephalopathy has been reported once previously. It is hoped that recognition of this entity and early initiation of immunotherapy will improve clinical outcomes for patients.
    Matched MeSH terms: Encephalitis/complications*; Encephalitis/diagnosis; Encephalitis/drug therapy
  13. Wong CK, Hor JY, Loo YP, Heng HS, Lee S, Perianen PP, et al.
    J Neuroimmunol, 2021 07 15;356:577584.
    PMID: 33933821 DOI: 10.1016/j.jneuroim.2021.577584
    NMDAR encephalitis may be more common among non-Caucasians. A population-based study was conducted to estimate its incidence in Sabah, Malaysia, where the population consists predominantly of Austronesians (84%), and with a Chinese minority. Registries of NMDAR encephalitis at neurology referral centers were reviewed for case ascertainment. The annual incidence was 2.29/million (Austronesians: 2.56/million, Chinese: 1.31/million). Among pediatric population, the incidence was: Austronesians: 3.63/million, Chinese: 2.59/million. Our study demonstrated a higher incidence of NMDAR encephalitis among Austronesians than the predominantly Caucasian populations in Europe (0.5-0.9/million; pediatric: 0.7-1.5/million). Racial and genetic factors may contribute to risks of developing NMDAR encephalitis.
    Matched MeSH terms: Anti-N-Methyl-D-Aspartate Receptor Encephalitis/diagnosis*; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/genetics; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/epidemiology*
  14. Mohd Farid Md Yusof, Shalisah Sharip, Suriati Mohamed Saini, Fairuz Nazri Abdul Rahman, Hamid Abdul Rahman, Raihanah Abdul Khalid
    MyJurnal
    A Severe encephalitis with an uncontrolled seizure may produce impairment in a variety
    of cognitive functions. The appropriate treatment for cognitive impairment postencephalitisis
    are currently unknown. We are reporting a case of depression and cognitive impairment post- encephalitis with an uncontrolled seizure. (Copied from article).
    Matched MeSH terms: Encephalitis
  15. Mohammad Farris Iman Leong Abdullah, Rizal Abu Bakar
    MyJurnal
    Objective: This case reported highlighted psychotic disorder due to dengue fever
    is rare. Hence we describe a case which clearly presented with psychotic
    symptoms during the illness.

    Methods: We reported a case of psychotic disorder
    due to dengue fever who presented with psychotic symptoms of auditory and
    visual hallucination, and persecutory delusion, which had significant temporal
    correlation with dengue fever symptoms. There were no neurological deficits
    noted, no altered sensorium and cognitive impairment during the episode. He
    has no past and family history of mental illness and there was no evidence of
    encephalitis and metabolic disturbances.

    Results: Our case suggests that
    prominent psychotic symptoms can occur during an episode of dengue fever,
    which remitted when one recovering from dengue fever.

    Conclusion: We
    demonstrated that patients who presented with the acute onset of psychosis
    accompanied by symptoms of viral fever should be screened for dengue fever,
    particularly if the person lived in or visited the area where dengue fever is
    endemic.
    Matched MeSH terms: Encephalitis
  16. Portelly J
    Matched MeSH terms: Encephalitis
  17. Low JM
    Med J Malaysia, 2017 10;72(5):306-307.
    PMID: 29197887 MyJurnal
    Anti-N-Methyl-D-Aspartate receptor (NMDAR) encephalitis is an immune mediated condition, which remains relatively unknown in Malaysia outside tertiary hospitals with neurology unit. It is often misdiagnosed as a psychiatric illness before definitive treatment is instituted. We report here an 18-year-old man who initially presented to the psychiatry unit before he was subsequently diagnosed as having anti-NMDAR encephalitis. To our knowledge, this is the first reported case of anti-NMDAR encephalitis in the east coast of Peninsular Malaysia.
    Matched MeSH terms: Anti-N-Methyl-D-Aspartate Receptor Encephalitis/diagnosis*; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/drug therapy; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/physiopathology*
  18. Nissapatorn V, Lee CK, Khairul AA
    Singapore Med J, 2003 Apr;44(4):194-6.
    PMID: 12952031
    Four hundred and six AIDS patients were recruited in this retrospective study. The seroprevalence of toxoplasmosis among 406 AIDS patients was 208 (51.2%). Their age ranged from 17 to 74 years with a median of 35 years. The majority of patients were males 172 (82.6%), Malays 99 (47.5%), single 109 (52.4%), unemployed 99 (47.6%) and heterosexual with commercial sex workers (CSW) 97 (46.6%) as the risk marker to HIV infection. Thirty-one (14.9%) of 208 AIDS-related toxoplasmosis were diagnosed as active toxoplasmic encephalitis. The most common clinical manifestation was headache (67.7%). The CT scan findings showed most lesions to be multiple (87.5%), hypodense (66.7%), and in frontal region (41.7%). Twenty-two (71%) patients had chronic (latent) Toxoplasma infection as evidenced by seropositivity for anti-Toxoplasma (IgG) antibody. They were statistically significant in the association between CD4 count and toxoplasmic encephalitis (P = 0.019; OR = 2.6; 95% CI = 1.14-6.02). After the initial six weeks of anti-TE therapy, relapsing toxoplasmic encephalitis was detected in 9.7% in this study.
    Matched MeSH terms: Encephalitis/epidemiology; Encephalitis/parasitology; Encephalitis/radiography
  19. Caplan CE
    CMAJ, 1999 Jun 15;160(12):1697.
    PMID: 10410627
    Matched MeSH terms: Encephalitis, Viral/epidemiology; Encephalitis, Viral/transmission; Encephalitis, Viral/virology*
  20. Prow NA, Setoh YX, Biron RM, Sester DP, Kim KS, Hobson-Peters J, et al.
    J Virol, 2014 Sep 1;88(17):9947-62.
    PMID: 24942584 DOI: 10.1128/JVI.01304-14
    The mosquito-borne West Nile virus (WNV) is responsible for outbreaks of viral encephalitis in humans, horses, and birds, with particularly virulent strains causing recent outbreaks of disease in eastern Europe, the Middle East, North America, and Australia. Previous studies have phylogenetically separated WNV strains into two main genetic lineages (I and II) containing virulent strains associated with neurological disease. Several WNV-like strains clustering outside these lineages have been identified and form an additional five proposed lineages. However, little is known about whether these strains have the potential to induce disease. In a comparative analysis with the highly virulent lineage I American strain (WNVNY99), the low-pathogenicity lineage II strain (B956), a benign Australian strain, Kunjin (WNVKUN), the African WNV-like Koutango virus (WNVKOU), and a WNV-like isolate from Sarawak, Malaysia (WNVSarawak), were assessed for neuroinvasive properties in a murine model and for their replication kinetics in vitro. While WNVNY99 replicated to the highest levels in vitro, in vivo mouse challenge revealed that WNVKOU was more virulent, with a shorter time to onset of neurological disease and higher morbidity. Histological analysis of WNVKOU- and WNVNY99-infected brain and spinal cords demonstrated more prominent meningoencephalitis and the presence of viral antigen in WNVKOU-infected mice. Enhanced virulence of WNVKOU also was associated with poor viral clearance in the periphery (sera and spleen), a skewed innate immune response, and poor neutralizing antibody development. These data demonstrate, for the first time, potent neuroinvasive and neurovirulent properties of a WNV-like virus outside lineages I and II.
    Matched MeSH terms: Encephalitis, Arbovirus/immunology; Encephalitis, Arbovirus/pathology*; Encephalitis, Arbovirus/virology; Encephalitis Viruses, Japanese/immunology*; Encephalitis Viruses, Japanese/pathogenicity*
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