Results 171 to 180 of about 5,749 (189)
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Subacute Sclerosing Panencephalitis

Neurologic Clinics, 1984
SSPE is a rare, late manifestation of measles-virus infection. Discussed are its clinical features, laboratory findings, pathology, epidemiology, pathogenesis, and treatment.
openaire   +2 more sources

Isoprimosine in subacute sclerosing panencephalitis

Neurology, 1979
An open therapeutic trial of isoprinosine was conducted in 15 patients with subacute sclerosing panencephalitis (SSPE). Long-term remissions occurred in 5 (33 percent), with documented improvement sustained for 2 or more years. Another patient was in remission 9 months after starting treatment, and three patients had transient remissions or ...
P R, Huttenlocher, R H, Mattson
openaire   +2 more sources

Subacute sclerosing panencephalitis

Seminars in Pediatric Neurology, 1996
Subacute sclerosing panencephalitis (SSPE), a neurodegenerative disease caused by a persistent "slow virus infection" with a mutated measles virus, is endemic in much of the developing world. Its incidence will increase in the USA, not only in immigrants, but also because of the 1988-1990 measles epidemic. This report reviews the pathogenesis, clinical
openaire   +2 more sources

Subacute Sclerosing Panencephalitis

1989
Subacute sclerosing panencephalitis (SSPE) is one of the slow virus infections of the CNS. It is a rare disorder, but it is the commonest of the chronic virus infections to affect children. It is caused by measles virus. SSPE is a disease of childhood and adolescence, with an age range of 4–20 years and a peak incidence at 7–10 years. There is a racial
Jacob Valk, Marjo S. van der Knaap
openaire   +1 more source

Subacute sclerosing panencephalitis.

The Journal of the Association of Physicians of India, 1992
A retrospective study of 36 confirmed cases of subacute sclerosing panencephalitis (SSPE) was carried out to detect any variation in the clinical and EEG patterns previously described. There were 31 males and 5 females, aged 4 to 24 years. Onset of SSPE at or after 15 years of age was observed in 22.2% of cases.
G A, Khwaja, M, Gupta, D K, Sharma
openaire   +1 more source

Subacute sclerosing panencephalitis

The Pediatric Infectious Disease Journal, 1991
openaire   +2 more sources

SUBACUTE SCLEROSING PANENCEPHALITIS

Medical Journal of Australia, 1971
openaire   +2 more sources

Subacute sclerosing panencephalitis

Neurology, 1993
Generoso G. Gascon   +3 more
openaire   +1 more source

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