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pro vyhledávání: '"H P, Hakola"'
Autor:
H P, Hakola
Publikováno v:
The Journal of clinical psychiatry. 51(1)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLO-SL) is a rare hereditary disease affecting both brain and bones. Skeletal symptoms begin in early adulthood and neuropsychiatric symptoms at approximately age 30. Progr
Autor:
H P Hakola, V S Partanen
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 46:515-520
17 patients suffering from the presenile dementia characterised by polycystic lipomenbranous osteodysplasia and sclerosing leukoencephalopathy were studied neurophysiologically. Noteworthy findings were diffuse slowing, the accentuation of 6-8 Hz par
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 90(2)
Autor:
H P, Hakola, J J, Puittinen
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 93(9)
Publikováno v:
Acta neurologica Scandinavica. 46(S43)
Autor:
H P, Hakola
Publikováno v:
Acta psychiatrica Scandinavica. Supplementum. 232