Long-term neurological and functional outcome in Nipah virus infection

Objective Nipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case‐fatality. Long‐term neurological assessments of survivors are limited. We assessed long‐term neurologic and functional outcomes of 22 patients surviving NiV illness in Bangladesh. Meth...

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Published inAnnals of neurology Vol. 62; no. 3; pp. 235 - 242
Main Authors Sejvar, James J., Hossain, Jahangir, Saha, Sankar Kama, Gurley, Emily S., Banu, Shakila, Hamadani, Jena D., Faiz, Mohammed Abdul, Siddiqui, F. M., Mohammad, Quazi Deen, Mollah, Abid Hossain, Uddin, Rafique, Alam, Rajibul, Rahman, Ridwanur, Tan, Chong Tin, Bellini, William, Rota, Paul, Breiman, Robert F., Luby, Stephen P.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2007
Willey-Liss
Subjects
Online AccessGet full text
ISSN0364-5134
1531-8249
DOI10.1002/ana.21178

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Abstract Objective Nipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case‐fatality. Long‐term neurological assessments of survivors are limited. We assessed long‐term neurologic and functional outcomes of 22 patients surviving NiV illness in Bangladesh. Methods During August 2005 and May 2006, we administered a questionnaire on persistent symptoms and functional difficulties to 22 previously identified NiV infection survivors. We performed neurologic evaluations and brain magnetic resonance imaging (MRI). Results Twelve (55%) subjects were male; median age was 14.5 years (range 6–50). Seventeen (77%) survived encephalitis, and 5 survived febrile illness. All but 1 subject had disabling fatigue, with a median duration of 5 months (range, 8 days–8 months). Seven encephalitis patients (32% overall), but none with febrile illness had persistent neurologic dysfunction, including static encephalopathy (n = 4), ocular motor palsies (2), cervical dystonia (2), focal weakness (2), and facial paralysis (1). Four cases had delayed‐onset neurologic abnormalities months after acute illness. Behavioral abnormalities were reported by caregivers of over 50% of subjects under age 16. MRI abnormalities were present in 15, and included multifocal hyperintensities, cerebral atrophy, and confluent cortical and subcortical signal changes. Interpretation Although delayed progression to neurologic illness following Nipah fever was not observed, persistent fatigue and functional impairment was frequent. Neurologic sequelae were frequent following Nipah encephalitis. Neurologic dysfunction may persist for years after acute infection, and new neurologic dysfunction may develop after acute illness. Survivors of NiV infection may experience substantial long‐term neurologic and functional morbidity. Ann Neurol 2007
AbstractList Nipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case-fatality. Long-term neurological assessments of survivors are limited. We assessed long-term neurologic and functional outcomes of 22 patients surviving NiV illness in Bangladesh.OBJECTIVENipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case-fatality. Long-term neurological assessments of survivors are limited. We assessed long-term neurologic and functional outcomes of 22 patients surviving NiV illness in Bangladesh.During August 2005 and May 2006, we administered a questionnaire on persistent symptoms and functional difficulties to 22 previously identified NiV infection survivors. We performed neurologic evaluations and brain magnetic resonance imaging (MRI).METHODSDuring August 2005 and May 2006, we administered a questionnaire on persistent symptoms and functional difficulties to 22 previously identified NiV infection survivors. We performed neurologic evaluations and brain magnetic resonance imaging (MRI).Twelve (55%) subjects were male; median age was 14.5 years (range 6-50). Seventeen (77%) survived encephalitis, and 5 survived febrile illness. All but 1 subject had disabling fatigue, with a median duration of 5 months (range, 8 days-8 months). Seven encephalitis patients (32% overall), but none with febrile illness had persistent neurologic dysfunction, including static encephalopathy (n = 4), ocular motor palsies (2), cervical dystonia (2), focal weakness (2), and facial paralysis (1). Four cases had delayed-onset neurologic abnormalities months after acute illness. Behavioral abnormalities were reported by caregivers of over 50% of subjects under age 16. MRI abnormalities were present in 15, and included multifocal hyperintensities, cerebral atrophy, and confluent cortical and subcortical signal changes.RESULTSTwelve (55%) subjects were male; median age was 14.5 years (range 6-50). Seventeen (77%) survived encephalitis, and 5 survived febrile illness. All but 1 subject had disabling fatigue, with a median duration of 5 months (range, 8 days-8 months). Seven encephalitis patients (32% overall), but none with febrile illness had persistent neurologic dysfunction, including static encephalopathy (n = 4), ocular motor palsies (2), cervical dystonia (2), focal weakness (2), and facial paralysis (1). Four cases had delayed-onset neurologic abnormalities months after acute illness. Behavioral abnormalities were reported by caregivers of over 50% of subjects under age 16. MRI abnormalities were present in 15, and included multifocal hyperintensities, cerebral atrophy, and confluent cortical and subcortical signal changes.Although delayed progression to neurologic illness following Nipah fever was not observed, persistent fatigue and functional impairment was frequent. Neurologic sequelae were frequent following Nipah encephalitis. Neurologic dysfunction may persist for years after acute infection, and new neurologic dysfunction may develop after acute illness. Survivors of NiV infection may experience substantial long-term neurologic and functional morbidity.INTERPRETATIONAlthough delayed progression to neurologic illness following Nipah fever was not observed, persistent fatigue and functional impairment was frequent. Neurologic sequelae were frequent following Nipah encephalitis. Neurologic dysfunction may persist for years after acute infection, and new neurologic dysfunction may develop after acute illness. Survivors of NiV infection may experience substantial long-term neurologic and functional morbidity.
Objective Nipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case‐fatality. Long‐term neurological assessments of survivors are limited. We assessed long‐term neurologic and functional outcomes of 22 patients surviving NiV illness in Bangladesh. Methods During August 2005 and May 2006, we administered a questionnaire on persistent symptoms and functional difficulties to 22 previously identified NiV infection survivors. We performed neurologic evaluations and brain magnetic resonance imaging (MRI). Results Twelve (55%) subjects were male; median age was 14.5 years (range 6–50). Seventeen (77%) survived encephalitis, and 5 survived febrile illness. All but 1 subject had disabling fatigue, with a median duration of 5 months (range, 8 days–8 months). Seven encephalitis patients (32% overall), but none with febrile illness had persistent neurologic dysfunction, including static encephalopathy (n = 4), ocular motor palsies (2), cervical dystonia (2), focal weakness (2), and facial paralysis (1). Four cases had delayed‐onset neurologic abnormalities months after acute illness. Behavioral abnormalities were reported by caregivers of over 50% of subjects under age 16. MRI abnormalities were present in 15, and included multifocal hyperintensities, cerebral atrophy, and confluent cortical and subcortical signal changes. Interpretation Although delayed progression to neurologic illness following Nipah fever was not observed, persistent fatigue and functional impairment was frequent. Neurologic sequelae were frequent following Nipah encephalitis. Neurologic dysfunction may persist for years after acute infection, and new neurologic dysfunction may develop after acute illness. Survivors of NiV infection may experience substantial long‐term neurologic and functional morbidity. Ann Neurol 2007
Nipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case-fatality. Long-term neurological assessments of survivors are limited. We assessed long-term neurologic and functional outcomes of 22 patients surviving NiV illness in Bangladesh. During August 2005 and May 2006, we administered a questionnaire on persistent symptoms and functional difficulties to 22 previously identified NiV infection survivors. We performed neurologic evaluations and brain magnetic resonance imaging (MRI). Twelve (55%) subjects were male; median age was 14.5 years (range 6-50). Seventeen (77%) survived encephalitis, and 5 survived febrile illness. All but 1 subject had disabling fatigue, with a median duration of 5 months (range, 8 days-8 months). Seven encephalitis patients (32% overall), but none with febrile illness had persistent neurologic dysfunction, including static encephalopathy (n = 4), ocular motor palsies (2), cervical dystonia (2), focal weakness (2), and facial paralysis (1). Four cases had delayed-onset neurologic abnormalities months after acute illness. Behavioral abnormalities were reported by caregivers of over 50% of subjects under age 16. MRI abnormalities were present in 15, and included multifocal hyperintensities, cerebral atrophy, and confluent cortical and subcortical signal changes. Although delayed progression to neurologic illness following Nipah fever was not observed, persistent fatigue and functional impairment was frequent. Neurologic sequelae were frequent following Nipah encephalitis. Neurologic dysfunction may persist for years after acute infection, and new neurologic dysfunction may develop after acute illness. Survivors of NiV infection may experience substantial long-term neurologic and functional morbidity.
Author Sejvar, James J.
Tan, Chong Tin
Rahman, Ridwanur
Hossain, Jahangir
Faiz, Mohammed Abdul
Luby, Stephen P.
Gurley, Emily S.
Hamadani, Jena D.
Uddin, Rafique
Bellini, William
Rota, Paul
Breiman, Robert F.
Siddiqui, F. M.
Alam, Rajibul
Saha, Sankar Kama
Mohammad, Quazi Deen
Banu, Shakila
Mollah, Abid Hossain
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  organization: Department of Medicine, Begum Khaleda Zia Medical College, Dhaka, Bangladesh
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  organization: Department of Medicine, University of Malaya, Kuala Lumpur, Malaysia
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  organization: Division of Viral Diseases, National Center for Immunizations and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta GA
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  surname: Luby
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  organization: Institute for Diarrhoeal Disease and Research, Bangladesh
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https://www.ncbi.nlm.nih.gov/pubmed/17696217$$D View this record in MEDLINE/PubMed
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Keywords Infection
Nervous system diseases
Prognosis
Long term
Viral disease
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References Tan CT, Goh KJ, Wong KT, et al. Relapsed and late-onset Nipah encephalitis. Ann Neurol 2002; 51: 703-708.
Lim CC, Lee WL, Leo YS, et al. Late clinical and magnetic resonance imaging follow up of Nipah virus infection. J Neurol Neurosurg Psychiatry 2003; 74: 131-133.
Nipah virus outbreak(s) in Bangladesh, January-April 2004. Wkly Epidemiol Rec 2004; 79: 168-171.
Chan KP, Rollin PE, Ksiazek TG, et al. A survey of Nipah virus infection among various risk groups in Singapore. Epidemiol Infect 2002; 128: 93-98.
Wong KT, Shieh WJ, Kumar S, et al. Nipah virus infection: pathology and pathogenesis of an emerging paramyxoviral zoonosis. Am J Pathol 2002; 161: 2153-2167.
Bellini WJ, Harcourt BH, Bowden N, Rota PA. Nipah virus: an emergent paramyxovirus causing severe encephalitis in humans. J Neurovirol 2005; 11: 481-487.
Misra UK, Kalita J. Prognosis of Japanese encephalitis patients with dystonia compared to those with parkinsonian features only. Postgrad Med J 2002; 78: 238-241.
Ross JJ, Worthington MG. Bilateral sixth nerve palsy in West Nile meningoencephalitis. J Neuroophthalmol 2004; 24: 97-98.
Wong SC, Ooi MH, Wong MN, et al. Late presentation of Nipah virus encephalitis and kinetics of the humoral immune response. J Neurol Neurosurg Psychiatry 2001; 71: 552-554.
Ozturk A, Gurses C, Baykan B, et al. Subacute sclerosing panencephalitis: clinical and magnetic resonance imaging evaluation of 36 patients. J Child Neurol 2002; 17: 25-29.
McJunkin JE, de los Reyes EC, Irazuzta JE, et al. La Crosse encephalitis in children. N Engl J Med 2001; 344: 801-807.
Dubois B, Lemmens R, Laffut W, Van Ranst M. Subacute sclerosing panencephalitis in the differential diagnosis of encephalitis. Neurology 2005; 65: 1145-1146.
Sairenji T, Yamanishi K, Tachibana Y, et al. Antibody responses to Epstein-Barr virus, human herpesvirus 6 and human herpesvirus 7 in patients with chronic fatigue syndrome. Intervirology 1995; 38: 269-273.
Tokunaga Y, Kira R, Takemoto M, et al. Diagnostic usefulness of diffusion-weighted magnetic resonance imaging in influenza-associated acute encephalopathy or encephalitis. Brain Dev 2000; 22: 451-453.
Sener RN. Subacute sclerosing panencephalitis findings at MR imaging, diffusion MR imaging, and proton MR spectroscopy. AJNR Am J Neuroradiol 2004; 25: 892-894.
Daniels P, Ksiazek T, Eaton BT. Laboratory diagnosis of Nipah and Hendra virus infections. Microbes Infect 2001; 3: 289-295.
Keren R, Zaoutis TE, Bridges CB, et al. Neurological and neuromuscular disease as a risk factor for respiratory failure in children hospitalized with influenza infection. JAMA 2005; 294: 2188-2194.
Ng BY, Lim CC, Yeoh A, Lee WL. Neuropsychiatric sequelae of Nipah virus encephalitis. J Neuropsychiatry Clin Neurosci 2004; 16: 500-504.
Chua KB, Goh KJ, Wong KT, et al. Fatal encephalitis due to Nipah virus among pig-farmers in Malaysia. Lancet 1999; 354: 1257-1259.
Lessell S, Collins TE. Ophthalmoplegia in Powassan encephalitis. Neurology 2003; 60: 1726-1727.
Parashar UD, Sunn LM, Ong F, et al. Case-control study of risk factors for human infection with a new zoonotic paramyxovirus, Nipah virus, during a 1998-1999 outbreak of severe encephalitis in Malaysia. J Infect Dis 2000; 181: 1755-1759.
Matthews CG, Chun RW, Grabow JD, Thompson WH. Psychological sequelae in children following California arbovirus encephalitis. Neurology 1968; 18: 1023-1030.
Harcourt BH, Lowe L, Tamin A, et al. Genetic characterization of Nipah virus, Bangladesh, 2004. Emerg Infect Dis 2005; 11: 1594-1597.
Lam SK, Chua KB. Nipah virus encephalitis outbreak in Malaysia. Clin Infect Dis 2002; 34(suppl 2): S48-S51.
Paton NI, Leo YS, Zaki SR, et al. Outbreak of Nipah-virus infection among abattoir workers in Singapore. Lancet 1999; 354: 1253-1256.
Bojinova VS, Dimova PS, Belopitova LD, et al. Clinical and epidemiological characteristics of subacute sclerosing panencephalitis in Bulgaria during the past 25 years (1978-2002). Eur J Paediatr Neurol 2004; 8: 89-94.
Chadha MS, Comer JA, Lowe L, et al. Nipah virus-associated encephalitis outbreak, Siliguri, India. Emerg Infect Dis 2006; 12: 235-240.
Oga T, Ikeda A, Nagamine T, et al. Implication of sensorimotor integration in the generation of periodic dystonic myoclonus in subacute sclerosing panencephalitis (SSPE). Mov Disord 2000; 15: 1173-1183.
Hsu VP, Hossain MJ, Parashar UD, et al. Nipah virus encephalitis reemergence, Bangladesh. Emerg Infect Dis 2004; 10: 2082-2087.
Prasad S, Brown MJ, Galetta SL. Transient downbeat nystagmus from West Nile virus encephalomyelitis. Neurology 2006; 66: 1599-1600.
Balkhy HH, Schreiber JR. Severe La Crosse encephalitis with significant neurologic sequelae. Pediatr Infect Dis J 2000; 19: 77-80.
Goh KJ, Tan CT, Chew NK, et al. Clinical features of Nipah virus encephalitis among pig farmers in Malaysia. N Engl J Med 2000; 342: 1229-1235.
Wallace HL 2nd, Natelson B, Gause W, Hay J. Human herpesviruses in chronic fatigue syndrome. Clin Diagn Lab Immunol 1999; 6: 216-223.
Chua KB, Bellini WJ, Rota PA, et al. Nipah virus: a recently emergent deadly paramyxovirus. Science 2000; 288: 1432-1435.
Wacharapluesadee S, Lumlertdacha B, Boongird K, et al. Bat Nipah virus, Thailand. Emerg Infect Dis 2005; 11: 1949-1951.
Gurley ES, Montgomery JM, Hossain MJ, et al. Risk of Nosocomial Transmission of Nipah Virus in a Bangladesh Hospital. Infect Control Hosp Epidemiol 2007; 28: 740-742.
Cubo E. [ Movement disorders in adult-onset measles encephalitis]. Neurologia 2003; 18: 30-33.
Monnet FP. Behavioural disturbances following Japanese B encephalitis. Eur Psychiatry 2003; 18: 269-273.
Update: outbreak of Nipah virus-Malaysia and Singapore, 1999. MMWR Morb Mortal Wkly Rep 1999; 48: 335-337.
Lee KE, Umapathi T, Tan CB, et al. The neurological manifestations of Nipah virus encephalitis, a novel paramyxovirus. Ann Neurol 1999; 46: 428-432.
Chua KB, Koh CL, Hooi PS, et al. Isolation of Nipah virus from Malaysian Island flying-foxes. Microbes Infect 2002; 4: 145-151.
Lim CC, Lee KE, Lee WL, et al. Nipah virus encephalitis: serial MR study of an emerging disease. Radiology 2002; 222: 219-226.
Sahani M, Parashar UD, Ali R, et al. Nipah virus infection among abattoir workers in Malaysia, 1998-1999. Int J Epidemiol 2001; 30: 1017-1020.
Berner YN, Lang R, Chowers MY. Outcome of West Nile fever in older adults. J Am Geriatr Soc 2002; 50: 1844-1846.
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References_xml – reference: Ng BY, Lim CC, Yeoh A, Lee WL. Neuropsychiatric sequelae of Nipah virus encephalitis. J Neuropsychiatry Clin Neurosci 2004; 16: 500-504.
– reference: Goh KJ, Tan CT, Chew NK, et al. Clinical features of Nipah virus encephalitis among pig farmers in Malaysia. N Engl J Med 2000; 342: 1229-1235.
– reference: Update: outbreak of Nipah virus-Malaysia and Singapore, 1999. MMWR Morb Mortal Wkly Rep 1999; 48: 335-337.
– reference: Tan CT, Goh KJ, Wong KT, et al. Relapsed and late-onset Nipah encephalitis. Ann Neurol 2002; 51: 703-708.
– reference: Lim CC, Lee KE, Lee WL, et al. Nipah virus encephalitis: serial MR study of an emerging disease. Radiology 2002; 222: 219-226.
– reference: Sahani M, Parashar UD, Ali R, et al. Nipah virus infection among abattoir workers in Malaysia, 1998-1999. Int J Epidemiol 2001; 30: 1017-1020.
– reference: Lim CC, Lee WL, Leo YS, et al. Late clinical and magnetic resonance imaging follow up of Nipah virus infection. J Neurol Neurosurg Psychiatry 2003; 74: 131-133.
– reference: Paton NI, Leo YS, Zaki SR, et al. Outbreak of Nipah-virus infection among abattoir workers in Singapore. Lancet 1999; 354: 1253-1256.
– reference: Keren R, Zaoutis TE, Bridges CB, et al. Neurological and neuromuscular disease as a risk factor for respiratory failure in children hospitalized with influenza infection. JAMA 2005; 294: 2188-2194.
– reference: Wong KT, Shieh WJ, Kumar S, et al. Nipah virus infection: pathology and pathogenesis of an emerging paramyxoviral zoonosis. Am J Pathol 2002; 161: 2153-2167.
– reference: Bojinova VS, Dimova PS, Belopitova LD, et al. Clinical and epidemiological characteristics of subacute sclerosing panencephalitis in Bulgaria during the past 25 years (1978-2002). Eur J Paediatr Neurol 2004; 8: 89-94.
– reference: Nipah virus outbreak(s) in Bangladesh, January-April 2004. Wkly Epidemiol Rec 2004; 79: 168-171.
– reference: Misra UK, Kalita J. Prognosis of Japanese encephalitis patients with dystonia compared to those with parkinsonian features only. Postgrad Med J 2002; 78: 238-241.
– reference: McJunkin JE, de los Reyes EC, Irazuzta JE, et al. La Crosse encephalitis in children. N Engl J Med 2001; 344: 801-807.
– reference: Monnet FP. Behavioural disturbances following Japanese B encephalitis. Eur Psychiatry 2003; 18: 269-273.
– reference: Cubo E. [ Movement disorders in adult-onset measles encephalitis]. Neurologia 2003; 18: 30-33.
– reference: Harcourt BH, Lowe L, Tamin A, et al. Genetic characterization of Nipah virus, Bangladesh, 2004. Emerg Infect Dis 2005; 11: 1594-1597.
– reference: Prasad S, Brown MJ, Galetta SL. Transient downbeat nystagmus from West Nile virus encephalomyelitis. Neurology 2006; 66: 1599-1600.
– reference: Sairenji T, Yamanishi K, Tachibana Y, et al. Antibody responses to Epstein-Barr virus, human herpesvirus 6 and human herpesvirus 7 in patients with chronic fatigue syndrome. Intervirology 1995; 38: 269-273.
– reference: Chan KP, Rollin PE, Ksiazek TG, et al. A survey of Nipah virus infection among various risk groups in Singapore. Epidemiol Infect 2002; 128: 93-98.
– reference: Wong SC, Ooi MH, Wong MN, et al. Late presentation of Nipah virus encephalitis and kinetics of the humoral immune response. J Neurol Neurosurg Psychiatry 2001; 71: 552-554.
– reference: Balkhy HH, Schreiber JR. Severe La Crosse encephalitis with significant neurologic sequelae. Pediatr Infect Dis J 2000; 19: 77-80.
– reference: Chua KB, Bellini WJ, Rota PA, et al. Nipah virus: a recently emergent deadly paramyxovirus. Science 2000; 288: 1432-1435.
– reference: Sener RN. Subacute sclerosing panencephalitis findings at MR imaging, diffusion MR imaging, and proton MR spectroscopy. AJNR Am J Neuroradiol 2004; 25: 892-894.
– reference: Chua KB, Goh KJ, Wong KT, et al. Fatal encephalitis due to Nipah virus among pig-farmers in Malaysia. Lancet 1999; 354: 1257-1259.
– reference: Wallace HL 2nd, Natelson B, Gause W, Hay J. Human herpesviruses in chronic fatigue syndrome. Clin Diagn Lab Immunol 1999; 6: 216-223.
– reference: Hsu VP, Hossain MJ, Parashar UD, et al. Nipah virus encephalitis reemergence, Bangladesh. Emerg Infect Dis 2004; 10: 2082-2087.
– reference: Chadha MS, Comer JA, Lowe L, et al. Nipah virus-associated encephalitis outbreak, Siliguri, India. Emerg Infect Dis 2006; 12: 235-240.
– reference: Dubois B, Lemmens R, Laffut W, Van Ranst M. Subacute sclerosing panencephalitis in the differential diagnosis of encephalitis. Neurology 2005; 65: 1145-1146.
– reference: Matthews CG, Chun RW, Grabow JD, Thompson WH. Psychological sequelae in children following California arbovirus encephalitis. Neurology 1968; 18: 1023-1030.
– reference: Lam SK, Chua KB. Nipah virus encephalitis outbreak in Malaysia. Clin Infect Dis 2002; 34(suppl 2): S48-S51.
– reference: Gurley ES, Montgomery JM, Hossain MJ, et al. Risk of Nosocomial Transmission of Nipah Virus in a Bangladesh Hospital. Infect Control Hosp Epidemiol 2007; 28: 740-742.
– reference: Berner YN, Lang R, Chowers MY. Outcome of West Nile fever in older adults. J Am Geriatr Soc 2002; 50: 1844-1846.
– reference: Parashar UD, Sunn LM, Ong F, et al. Case-control study of risk factors for human infection with a new zoonotic paramyxovirus, Nipah virus, during a 1998-1999 outbreak of severe encephalitis in Malaysia. J Infect Dis 2000; 181: 1755-1759.
– reference: Tokunaga Y, Kira R, Takemoto M, et al. Diagnostic usefulness of diffusion-weighted magnetic resonance imaging in influenza-associated acute encephalopathy or encephalitis. Brain Dev 2000; 22: 451-453.
– reference: Ozturk A, Gurses C, Baykan B, et al. Subacute sclerosing panencephalitis: clinical and magnetic resonance imaging evaluation of 36 patients. J Child Neurol 2002; 17: 25-29.
– reference: Ross JJ, Worthington MG. Bilateral sixth nerve palsy in West Nile meningoencephalitis. J Neuroophthalmol 2004; 24: 97-98.
– reference: Wacharapluesadee S, Lumlertdacha B, Boongird K, et al. Bat Nipah virus, Thailand. Emerg Infect Dis 2005; 11: 1949-1951.
– reference: Lessell S, Collins TE. Ophthalmoplegia in Powassan encephalitis. Neurology 2003; 60: 1726-1727.
– reference: Lee KE, Umapathi T, Tan CB, et al. The neurological manifestations of Nipah virus encephalitis, a novel paramyxovirus. Ann Neurol 1999; 46: 428-432.
– reference: Oga T, Ikeda A, Nagamine T, et al. Implication of sensorimotor integration in the generation of periodic dystonic myoclonus in subacute sclerosing panencephalitis (SSPE). Mov Disord 2000; 15: 1173-1183.
– reference: Chua KB, Koh CL, Hooi PS, et al. Isolation of Nipah virus from Malaysian Island flying-foxes. Microbes Infect 2002; 4: 145-151.
– reference: Bellini WJ, Harcourt BH, Bowden N, Rota PA. Nipah virus: an emergent paramyxovirus causing severe encephalitis in humans. J Neurovirol 2005; 11: 481-487.
– reference: Daniels P, Ksiazek T, Eaton BT. Laboratory diagnosis of Nipah and Hendra virus infections. Microbes Infect 2001; 3: 289-295.
– volume: 79
  start-page: 168
  year: 2004
  end-page: 171
  article-title: Nipah virus outbreak(s) in Bangladesh, January‐April 2004
  publication-title: Wkly Epidemiol Rec
– volume: 28
  start-page: 740
  year: 2007
  end-page: 742
  article-title: Risk of Nosocomial Transmission of Nipah Virus in a Bangladesh Hospital
  publication-title: Infect Control Hosp Epidemiol
– volume: 50
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  year: 2002
  end-page: 1846
  article-title: Outcome of West Nile fever in older adults
  publication-title: J Am Geriatr Soc
– volume: 4
  start-page: 145
  year: 2002
  end-page: 151
  article-title: Isolation of Nipah virus from Malaysian Island flying‐foxes
  publication-title: Microbes Infect
– volume: 181
  start-page: 1755
  year: 2000
  end-page: 1759
  article-title: Case‐control study of risk factors for human infection with a new zoonotic paramyxovirus, Nipah virus, during a 1998‐1999 outbreak of severe encephalitis in Malaysia
  publication-title: J Infect Dis
– volume: 60
  start-page: 1726
  year: 2003
  end-page: 1727
  article-title: Ophthalmoplegia in Powassan encephalitis
  publication-title: Neurology
– volume: 11
  start-page: 1949
  year: 2005
  end-page: 1951
  article-title: Bat Nipah virus, Thailand
  publication-title: Emerg Infect Dis
– volume: 25
  start-page: 892
  year: 2004
  end-page: 894
  article-title: Subacute sclerosing panencephalitis findings at MR imaging, diffusion MR imaging, and proton MR spectroscopy
  publication-title: AJNR Am J Neuroradiol
– volume: 15
  start-page: 1173
  year: 2000
  end-page: 1183
  article-title: Implication of sensorimotor integration in the generation of periodic dystonic myoclonus in subacute sclerosing panencephalitis (SSPE)
  publication-title: Mov Disord
– volume: 12
  start-page: 235
  year: 2006
  end-page: 240
  article-title: Nipah virus‐associated encephalitis outbreak, Siliguri, India
  publication-title: Emerg Infect Dis
– volume: 354
  start-page: 1257
  year: 1999
  end-page: 1259
  article-title: Fatal encephalitis due to Nipah virus among pig‐farmers in Malaysia
  publication-title: Lancet
– volume: 24
  start-page: 97
  year: 2004
  end-page: 98
  article-title: Bilateral sixth nerve palsy in West Nile meningoencephalitis
  publication-title: J Neuroophthalmol
– volume: 288
  start-page: 1432
  year: 2000
  end-page: 1435
  article-title: Nipah virus: a recently emergent deadly paramyxovirus
  publication-title: Science
– volume: 344
  start-page: 801
  year: 2001
  end-page: 807
  article-title: La Crosse encephalitis in children
  publication-title: N Engl J Med
– volume: 10
  start-page: 2082
  year: 2004
  end-page: 2087
  article-title: Nipah virus encephalitis reemergence, Bangladesh
  publication-title: Emerg Infect Dis
– volume: 16
  start-page: 500
  year: 2004
  end-page: 504
  article-title: Neuropsychiatric sequelae of Nipah virus encephalitis
  publication-title: J Neuropsychiatry Clin Neurosci
– volume: 11
  start-page: 481
  year: 2005
  end-page: 487
  article-title: Nipah virus: an emergent paramyxovirus causing severe encephalitis in humans
  publication-title: J Neurovirol
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  year: 2003
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  article-title: Movement disorders in adult‐onset measles encephalitis
  publication-title: Neurologia
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  year: 1968
  end-page: 1030
  article-title: Psychological sequelae in children following California arbovirus encephalitis
  publication-title: Neurology
– volume: 11
  start-page: 1594
  year: 2005
  end-page: 1597
  article-title: Genetic characterization of Nipah virus, Bangladesh, 2004
  publication-title: Emerg Infect Dis
– volume: 19
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  year: 2000
  end-page: 80
  article-title: Severe La Crosse encephalitis with significant neurologic sequelae
  publication-title: Pediatr Infect Dis J
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  year: 2002
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  article-title: Relapsed and late‐onset Nipah encephalitis
  publication-title: Ann Neurol
– volume: 48
  start-page: 335
  year: 1999
  end-page: 337
  article-title: Update: outbreak of Nipah virus—Malaysia and Singapore, 1999
  publication-title: MMWR Morb Mortal Wkly Rep
– volume: 17
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  year: 2002
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  article-title: Subacute sclerosing panencephalitis: clinical and magnetic resonance imaging evaluation of 36 patients
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  article-title: Clinical and epidemiological characteristics of subacute sclerosing panencephalitis in Bulgaria during the past 25 years (1978‐2002)
  publication-title: Eur J Paediatr Neurol
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  article-title: Antibody responses to Epstein‐Barr virus, human herpesvirus 6 and human herpesvirus 7 in patients with chronic fatigue syndrome
  publication-title: Intervirology
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  year: 2003
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  publication-title: J Neurol Neurosurg Psychiatry
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  publication-title: Clin Diagn Lab Immunol
– volume: 78
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  year: 1999
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  end-page: 1256
  article-title: Outbreak of Nipah‐virus infection among abattoir workers in Singapore
  publication-title: Lancet
– volume: 34
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  issue: suppl 2
  year: 2002
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  article-title: Nipah virus encephalitis outbreak in Malaysia
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Snippet Objective Nipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case‐fatality. Long‐term neurological...
Nipah virus (NiV) is an emerging zoonosis. Central nervous system disease frequently results in high case-fatality. Long-term neurological assessments of...
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StartPage 235
SubjectTerms Adolescent
Adult
Bangladesh
Biological and medical sciences
Brain - pathology
Child, Preschool
Disease Progression
Electroencephalography
Encephalitis - pathology
Encephalitis - physiopathology
Enzyme-Linked Immunosorbent Assay
Fatigue - etiology
Female
Follow-Up Studies
Henipavirus Infections - cerebrospinal fluid
Henipavirus Infections - pathology
Henipavirus Infections - physiopathology
Human viral diseases
Humans
Immunoglobulin G - analysis
Infectious diseases
Magnetic Resonance Imaging
Male
Medical sciences
Middle Aged
Muscle Weakness - etiology
Nervous System Diseases - etiology
Nervous System Diseases - pathology
Nervous System Diseases - physiopathology
Neurologic Examination
Neurology
Nipah Virus
Recurrence
Reverse Transcriptase Polymerase Chain Reaction
Surveys and Questionnaires
Survivors
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral diseases of the nervous system
Title Long-term neurological and functional outcome in Nipah virus infection
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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fana.21178
https://www.ncbi.nlm.nih.gov/pubmed/17696217
https://www.proquest.com/docview/68336636
Volume 62
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