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pro vyhledávání: '"P V, Uldall"'
Autor:
P V, Uldall
Publikováno v:
Ugeskrift for laeger. 161(7)
Autor:
P V, Uldall, F J, Hansen, B, Beck, J M, Buchholt, F U, Knudsen, L B, Lassen, K, Lee, K, Taudorf
Publikováno v:
Ugeskrift for laeger. 160(39)
Publikováno v:
Ugeskrift for laeger. 160(29)
The congenital bilateral perisylvian syndrome is characterized by pseudobulbar palsy, moderate delay in mental and motor development and epilepsy. Three characteristic case stories are presented. Epileptic seizures are most frequently generalized: to
Autor:
P V, Uldall, B, Sommer
Publikováno v:
Ugeskrift for laeger. 158(14)
Fifty-two children with intractable epilepsy received lamotrigine as add-on therapy on a compassionate basis. The results were reviewed after three and six months of treatment in order to evaluate the efficacy in different epilepsy syndromes. Mental
Autor:
P V, Uldall
Publikováno v:
Ugeskrift for laeger. 158(14)
Publikováno v:
Ugeskrift for laeger. 157(6)
The aim of The Cerebral Palsy Register is to follow the development of cerebral palsy in East Denmark as reported from the children's departments within the area. The prevalence among Danish children born in 1971-1982 is reported. Postnatal cases hav
Publikováno v:
Ugeskrift for laeger. 153(13)
Pseudoepileptic seizures (pseudoseizures) are defined as episodic disturbances of behaviour with elements of epileptic seizures, but with atypical features and not accompanied by abnormal EEG discharges. They are frequently seen in patients with epil