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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Child's nervous system 9 (1993), S. 458-461 
    ISSN: 1433-0350
    Keywords: Paroxysmal dystonia ; Nocturnal seizures ; Sleep disorder
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The authors describe a case of a 15-year-old girl who presented with a progressive sequence of nocturnal dystonic episodes, generalized seizures, and diurnal dystonic episodes. A diagnosis of nocturnal paroxysmal dystonia has been proposed in view of the association between nocturnal episodes and epileptic seizures, while the diurnal episodes are atypical. Neurophysiological data recorded during critical episodes are reported. A linkage between dystonic attacks and epilepsy is hypothesized.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 13 (1992), S. 617-619 
    ISSN: 1590-3478
    Keywords: Metachromatic leukodystrophy ; CSF protein ; motor conduction velocity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Gli autori descrivono un caso atipico di Leucodistrofia Metacromatica di tipo giovanile. A 3 anni di distanza dall'esordio clinico la VdC motoria è risultata ancora nella norma, in contrasto con quanto comunemente osservabile in tale patologia. Altro dato inusuale è la normalità del livello delle proteine nel CFS. Tali dati vengono discussi anche alla luce dei risultati della biopsia di nervo surale, che rivela solo modesta compromissione.
    Notes: Abstract We describe an atypical case of juvenile metachromatic leukodystrophy. Motor conduction velocity was still within the normal range 3 years after clinical onset, in contrast to what is commonly found in this disease. Another unusual feature is the normal level of CSF protein. These data are discussed in the light of the sural nerve biopsy findings, which revealed only slight impairment.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of autism and developmental disorders 25 (1995), S. 553-555 
    ISSN: 1573-3432
    Source: Springer Online Journal Archives 1860-2000
    Topics: Psychology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of autism and developmental disorders 27 (1997), S. 493-496 
    ISSN: 1573-3432
    Source: Springer Online Journal Archives 1860-2000
    Topics: Psychology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 18 (1997), S. 283-288 
    ISSN: 1590-3478
    Keywords: Periodic syndrome ; Childhood ; Adolescence ; Migraine ; Psychosomatic pathology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Molti studi in letteratura confermano l'ipotesi che vede la sindrome periodica come un precursore o un equivalente dell'emicrania. Lo scopo di questo studio è di dimostrare la prevalenza della sindrome periodica in un gruppo di bambini e adolescenti cefalalgici confrontati con un gruppo di controllo. Sono stati considerati 7 sintomi: vomiti ricorrenti e dolori addominali, dolori migranti, febbri ricorrenti senza una causa dimostrata, vertigine, disturbi del sonno e dell'alimentazione. Sono stati studiati 171 bambini divisi in 4 gruppi: 42 emicranici, 37 soggetti con patologia cronica a carico del sistema nervoso, 46 soggetti affetti da patologia a genesi psicosomatica, 46 soggetti sani. La prevalenza dei sintomi è risultata differente rispetto al gruppo di controllo e mostra un pattern simile per gli emicranici e il gruppo di pazienti psicosomatici rispetto all'altro gruppo di controllo. La sindrome periodica può quindi essere considerata predittiva rispetto al seguente sviluppo di una patologia psicosomatica.
    Notes: Abstract Many reports in the literature seem to confirm the hypothesis that the symptoms of periodic syndrome are precursors or the equivalent of migraine: the aim of this study was to assess the prevalence of periodic syndrome in a group of children and adolescents suffering from migraine in comparison with that observed in various control groups. We considered seven symptoms: recurrent vomiting and abdominal pain, migrating limb pain, vertigo, recurrent hyperthermia with no visible cause, sleep disturbances and eating disorders. The study involved 171 children divided into four groups: 42 migraineurs; 37 subjects with chronic nervous pathologies but no psychosomatic symptoms; 46 subjects with a known psychosomatic disease, and 46 healthy subjects. The prevalence of the symptoms in the different control groups was different, although the pattern was more similar in the migraineurs and psychosomatic patients than in the other control groups. The development continuum of the syndrome may support the view that periodic syndrome is predictive of the subsequent development of a psychosomatic pathology.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 12 (1991), S. 475-478 
    ISSN: 1590-3478
    Keywords: Dystonia-parkinsonism ; L-dopa treatment ; follow-up
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Gli autori descrivono due casi sporadici di Distonia-parkinsonismo in differenti stadi di progressione della malattia. Si tratta di due ragazze viste per la prima volta rispettivamente a 10 e 12 anni e seguite per 9 e 2 anni. Dosi di 60mg di L-dopa+6mg di Carbidopa hanno determinato in entrambe una regressione pronta e completa dei sintomi che persiste a tutt'oggi. I livelli di HVA e 5HIAA sono risultati abbassati sia a livello liquorale che urinario in un caso e si sononormalizzati con la terapia. Questo dato potrebbe costituire un indice sufficientemente valido di predizione dell'efficacia della cura con L-dopa.
    Notes: Abstract We describe two sporadic cases of dystonia-parkinsonism at different stages of disease progression. The two girls, first seen at the ages of 10 and 12 years, have been followed for 9 and 2 years respectively. In both patients L-dopa 60 mg+carbidopa 6 mg brought about a swift remission of symptoms, which persists to date. All examinations, including CT and MR brainscans, were normal. The CSF and urine levels of HVA and 5 HIAA were low in one case and normalized with treatment. This finding might provide a fairly valid predictive index of responsiveness to L-dopa.
    Type of Medium: Electronic Resource
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