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 in | Annals of neurology Vol. 62; no. 3; pp. 235 - 242 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.09.2007
Willey-Liss |
Subjects | |
Online Access | Get full text |
ISSN | 0364-5134 1531-8249 |
DOI | 10.1002/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 |
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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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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. 2002; 17 2001; 71 2001; 344 2005; 294 2006; 12 1995; 38 2002; 50 2002; 51 2002; 34 2002; 78 2004; 8 2004; 25 2000; 22 1999; 48 2004; 24 1999; 46 2002; 4 2005; 65 2003; 18 1999; 6 2003; 74 2007; 28 2004; 10 1968; 18 2002; 161 2000; 19 2000; 15 2004; 16 2006; 66 2002; 222 2004; 79 2002; 128 2001; 3 2000; 342 1999; 354 2000; 288 2003; 60 2005; 11 2001; 30 2000; 181 e_1_2_6_31_2 e_1_2_6_30_2 Sener RN (e_1_2_6_40_2) 2004; 25 e_1_2_6_18_2 e_1_2_6_19_2 (e_1_2_6_20_2) 2004; 79 e_1_2_6_12_2 e_1_2_6_35_2 e_1_2_6_13_2 e_1_2_6_34_2 e_1_2_6_10_2 e_1_2_6_33_2 e_1_2_6_11_2 e_1_2_6_16_2 e_1_2_6_39_2 e_1_2_6_17_2 e_1_2_6_38_2 e_1_2_6_14_2 e_1_2_6_37_2 e_1_2_6_15_2 e_1_2_6_36_2 e_1_2_6_42_2 e_1_2_6_41_2 e_1_2_6_8_2 e_1_2_6_7_2 e_1_2_6_9_2 e_1_2_6_29_2 e_1_2_6_4_2 e_1_2_6_3_2 e_1_2_6_6_2 (e_1_2_6_2_2) 1999; 48 e_1_2_6_5_2 e_1_2_6_24_2 e_1_2_6_23_2 e_1_2_6_22_2 Cubo E (e_1_2_6_32_2) 2003; 18 e_1_2_6_21_2 e_1_2_6_28_2 e_1_2_6_43_2 e_1_2_6_27_2 e_1_2_6_44_2 e_1_2_6_26_2 e_1_2_6_45_2 e_1_2_6_25_2 |
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. 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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 – volume: 18 start-page: 30 year: 2003 end-page: 33 article-title: Movement disorders in adult‐onset measles encephalitis publication-title: Neurologia – volume: 18 start-page: 1023 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 start-page: 77 year: 2000 end-page: 80 article-title: Severe La Crosse encephalitis with significant neurologic sequelae publication-title: Pediatr Infect Dis J – volume: 51 start-page: 703 year: 2002 end-page: 708 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 start-page: 25 year: 2002 end-page: 29 article-title: Subacute sclerosing panencephalitis: clinical and magnetic resonance imaging evaluation of 36 patients publication-title: J Child Neurol – volume: 8 start-page: 89 year: 2004 end-page: 94 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 – volume: 3 start-page: 289 year: 2001 end-page: 295 article-title: Laboratory diagnosis of Nipah and Hendra virus infections publication-title: Microbes Infect – volume: 38 start-page: 269 year: 1995 end-page: 273 article-title: Antibody responses to Epstein‐Barr virus, human herpesvirus 6 and human herpesvirus 7 in patients with chronic fatigue syndrome publication-title: Intervirology – volume: 74 start-page: 131 year: 2003 end-page: 133 article-title: Late clinical and magnetic resonance imaging follow up of Nipah virus infection publication-title: J Neurol Neurosurg Psychiatry – volume: 6 start-page: 216 year: 1999 end-page: 223 article-title: Human herpesviruses in chronic fatigue syndrome publication-title: Clin Diagn Lab Immunol – volume: 78 start-page: 238 year: 2002 end-page: 241 article-title: Prognosis of Japanese encephalitis patients with dystonia compared to those with parkinsonian features only publication-title: Postgrad Med J – volume: 46 start-page: 428 year: 1999 end-page: 432 article-title: The neurological manifestations of Nipah virus encephalitis, a novel paramyxovirus publication-title: Ann Neurol – volume: 354 start-page: 1253 year: 1999 end-page: 1256 article-title: Outbreak of Nipah‐virus infection among abattoir workers in Singapore publication-title: Lancet – volume: 34 start-page: S48 issue: suppl 2 year: 2002 end-page: S51 article-title: Nipah virus encephalitis outbreak in Malaysia publication-title: Clin Infect Dis – volume: 128 start-page: 93 year: 2002 end-page: 98 article-title: A survey of Nipah virus infection among various risk groups in Singapore publication-title: Epidemiol Infect – volume: 66 start-page: 1599 year: 2006 end-page: 1600 article-title: Transient downbeat nystagmus from West Nile virus encephalomyelitis publication-title: Neurology – volume: 294 start-page: 2188 year: 2005 end-page: 2194 article-title: Neurological and neuromuscular disease as a risk factor for respiratory failure in children hospitalized with influenza infection publication-title: JAMA – volume: 71 start-page: 552 year: 2001 end-page: 554 article-title: Late presentation of Nipah virus encephalitis and kinetics of the humoral immune response publication-title: J Neurol Neurosurg Psychiatry – volume: 18 start-page: 269 year: 2003 end-page: 273 article-title: Behavioural disturbances following Japanese B encephalitis publication-title: Eur Psychiatry – volume: 30 start-page: 1017 year: 2001 end-page: 1020 article-title: Nipah virus infection among abattoir workers in Malaysia, 1998‐1999 publication-title: Int J Epidemiol – volume: 342 start-page: 1229 year: 2000 end-page: 1235 article-title: Clinical features of Nipah virus encephalitis among pig farmers in Malaysia publication-title: N Engl J Med – volume: 222 start-page: 219 year: 2002 end-page: 226 article-title: Nipah virus encephalitis: serial MR study of an emerging disease publication-title: Radiology – volume: 22 start-page: 451 year: 2000 end-page: 453 article-title: Diagnostic usefulness of diffusion‐weighted magnetic resonance imaging in influenza‐associated acute encephalopathy or encephalitis publication-title: Brain Dev – volume: 161 start-page: 2153 year: 2002 end-page: 2167 article-title: Nipah virus infection: pathology and pathogenesis of an emerging paramyxoviral zoonosis publication-title: Am J Pathol – volume: 65 start-page: 1145 year: 2005 end-page: 1146 article-title: Subacute sclerosing panencephalitis in the differential diagnosis of encephalitis publication-title: Neurology – ident: 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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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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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