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Pathogenesis of varicella-zoster angiitis in the CNS.
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Experimental cerebrovascular lesions in congenital and neonatal rubella-virus infections of ferrets.
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Virulence and persistence of three prototype strains of mumps virus in newborn hamsters.
Arch Virol. 1978;57(4):355-9
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Differential effects of cyclophosphamide on the B and T cell compartments of adult mice.
J Immunol. 1973 Jan;110(1):277-82
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Reovirus-induced aqueductal stenosis in hamsters. Phase contrast and electron microscopic studies.
Lab Invest. 1972 Dec;27(6):531-7
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Poliomyelitis: immunoglobulin-containing cells in the central nervous system in acute and convalescent phases of the human disease.
Clin Exp Immunol. 1980 Apr;40(1):42-8
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Pathology of the congenital rubella syndrome.
J Pediatr. 1967 Nov;71(5):665-75
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Viruslike particles in granulomatous angiitis of the central nervous system.
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Genetic factors in resistance against virus infections.
Arch Gesamte Virusforsch. 1965;17(2):280-94
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Viral models of demyelination.
Neurology. 1978 Sep;28(9 Pt 2):111-4
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Immunopathology of mouse hepatitis virus type 3 infection. III. Clinical and virologic observation of a persistent viral infection.
J Immunol. 1975 Sep;115(3):640-3
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Hydrocephalus and viral infections.
Dev Med Child Neurol. 1975 Dec;17(6):807-16
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Infectious leukoencephalitis. A critical comparison of certain experimental and naturally-occurring viral leukoencephalitides with experimental allergic encephalomyelitis.
J Neuropathol Exp Neurol. 1962 Oct;21:491-518
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Temperature-sensitive mutants of mouse hepatitis virus produce a high incidence of demyelination.
Proc Natl Acad Sci U S A. 1978 Aug;75(8):4033-6
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Nervous system lesions in the congenital rubella syndrome.
Arch Otolaryngol. 1973 Oct;98(4):249-51
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Granulomatous angiitis of the central nervous system.
Arch Neurol. 1968 Nov;19(5):510-24
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Mouse hepatitis virus-induced recurrent demyelination. A preliminary report.
Arch Neurol. 1975 Jan;32(1):32-5
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Macrophages and age-dependent resistance to Herpes simplex virus in mice.
J Immunol. 1970 May;104(5):1160-5
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Chronic central nervous system demyelination in mice after JHM virus infection.
Neurology. 1981 Jan;31(1):38-44
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Pathogenesis of demyelination induced by a mouse hepatitis.
Arch Neurol. 1973 May;28(5):298-303
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Neonatal susceptibility to MHV3 infection in mice. II. Role of natural effector marrow cells in transfer of resistance.
J Immunol. 1980 Jan;124(1):418-23
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Mechanism of demyelination in JHM virus encephalomyelitis. Electron microscopic studies.
Acta Neuropathol. 1973 Mar 30;24(1):76-85
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Pathogenesis of reovirus type 1 hydrocephalus in mice. Significance of aqueductal changes.
Arch Neurol. 1977 Jan;34(1):18-28
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Immunopathology of mouse hepatitis virus type 3mii. effect of immunosuppression in resistant mice.
J Immunol. 1975 Jan;114(1 Pt 1):226-30
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Neuropathological effects of persistent infection of mice by mouse hepatitis virus.
Infect Immun. 1975 Nov;12(5):1127-40
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Cerebral lesions in congenital rubella syndrome.
J Pediatr. 1967 Feb;70(2):243-55
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Hydrocephalus following viral infection: the pathology of aqueductal stenosis developing after experimental mumps virus infection.
J Neuropathol Exp Neurol. 1968 Oct;27(4):591-606
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Virus-induced hydrocephalus: development of aqueductal stenosis in hamsters after mumps infection.
Science. 1967 Sep 1;157(3792):1066-7
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Granulomatous angiitis of the nervous system in cases of herpes zoster and lymphosarcoma.
Neurology. 1972 Apr;22(4):348-54
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Immunopathology of mouse hepatitis virus type 3 infection. Role of humoral and cell-mediated immunity in resistance mechanisms.
J Immunol. 1975 Jan;114(1 Pt 1):221-5
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Mumps virus-induced hydrocephalus in hamsters. Ultrastructure of the chronic infection.
Lab Invest. 1977 Sep;37(3):229-36
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Genetic study of mouse sensitivity to MHV3 infection: influence of the H-2 complex.
J Immunol. 1979 Apr;122(4):1359-62
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Effect of cyclophosphamide on the genetic resistance of C 3 H mice to mouse hepatitis virus.
Proc Soc Exp Biol Med. 1973 Mar;142(3):762-6
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THE PATHOGENESIS OF HERPES VIRUS ENCEPHALITIS. I. VIRUS PATHWAYS TO THE NERVOUS SYSTEM OF SUCKLING MICE DEMONSTRATED BY FLUORESCENT ANTIBODY STAINING.
J Exp Med. 1964 Feb 1;119:343-56
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Molecular basis of reovirus virulence: role of the S1 gene.
Proc Natl Acad Sci U S A. 1977 Dec;74(12):5744-8
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