The Experts below are selected from a list of 39 Experts worldwide ranked by ideXlab platform
C Paolozzi - One of the best experts on this subject based on the ideXlab platform.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
A Guizzaro - One of the best experts on this subject based on the ideXlab platform.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
F Bravaccio - One of the best experts on this subject based on the ideXlab platform.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
R Cotrufo - One of the best experts on this subject based on the ideXlab platform.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
E Volpe - One of the best experts on this subject based on the ideXlab platform.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.
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progressive rubella panencephalitis follow up eeg study of a case
Acta neurologica, 1992Co-Authors: A Guizzaro, E Volpe, F Bravaccio, R Cotrufo, C PaolozziAbstract:: Progressive rubella panencephalitis is a very rare Slow Virus Disease of the nervous system. The authors present a case, concerning a young man, aged 20 years, died 11 months after the onset of the Disease. The following peculiarities of the case are emphasized: 1) the clinical symptomatology and the evolution (myoclonus, lack of cerebellar impairment) could suggest the diagnosis of SSPE; 2) the EEG recordings showed epileptiform abnormalities, long latency diffuse periodic complexes and--during interferon therapy and simultaneously with a temporary clinical improvement--the appearance of short latency anterior periodic complexes.