Zobrazeno 41 - 50
of 284
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Autor:
Claudio Zucca, Francesca Ragona, Renato Borgatti, Giovanna Zorzi, Filippo Arrigoni, Erika Tenderini, Maria Teresa Bassi, Romina Romaniello
Publikováno v:
Journal of Child Neurology. 29:249-253
Mutations in STXBP1 gene, encoding the syntaxin binding protein 1, have been recently described in Ohtahara syndrome, or early infantile epileptic encephalopathy with suppression-burst pattern, and in other early-onset epileptic encephalopathies. A 3
Publikováno v:
Journal of Child Neurology. 29:NP40-NP46
Propofol infusion syndrome is a recognized complication of prolonged propofol use in the pediatric population, but little is reported on other metabolic effects of propofol, especially in children with mitochondrial disorders. We report on a child wi
Publikováno v:
Journal of Child Neurology. 28:1159-1168
The neuronal ceroid lipofuscinoses, a family of neurodegenerative lysosomal storage disorders, represent the most common cause of pediatric-onset neurodegeneration. The infantile form has a devastatingly early onset and one of the fastest-progressing
Autor:
Karen Margallo, Julia Lockhart, Nancy Goldie, Adrienne Harvey, Ronit Mesterman, Jenny McEwen-Hill, Jan Willem Gorter
Publikováno v:
Journal of Child Neurology. 29:210-213
This retrospective cohort study reviewed set goals and their outcomes of children and adolescents with severe cerebral palsy who received botulinum toxin A in 2008 and 2009. Sixty children (36 male, mean age 9 years) were included. They received on a
Publikováno v:
Journal of Child Neurology. 28:1320-1341
The authors conducted a systematic literature review of preventive pharmacological treatments for episodic childhood migraines searching several databases through May 20, 2012. Episodic migraine prevention was examined in 24 publications of randomize
Autor:
Debabrata Ghosh, Shalaka Indulkar
Publikováno v:
Journal of Child Neurology. 28:1418-1422
Primary myoclonus-dystonia is a childhood-onset autosomal-dominant movement disorder with myoclonic jerks and dystonia. The authors report 9 children (4 boys, 5 girls) with myoclonus-dystonia from 8 families seen over a 4-year period at Cleveland Cli
Autor:
Alfredo Onofri, Federica Deodato, Giorgia Grutter, Virginia Maria Ginocchio, Carlo Dionisi-Vici, Alessandro Germani
Publikováno v:
Journal of Child Neurology. 29:850-854
Infantile Pompe disease, resulting from deficiency of lysosomal acid α-glucosidase, requires enzyme replacement therapy with recombinant human acid α-glucosidase. Most patients develop antirecombinant human acid α-glucosidase antibodies, leading t
Autor:
Mary Jo Elgie, Jimmy Schiemann-Delgado, Nathalie Toublanc, Armel Stockis, Danielle Gerard, Yuval Karmon, Arie Weinstock, Deanne Dilley, Matilde Ruiz, Osman Farooq
Publikováno v:
Journal of Child Neurology. 28:1423-1429
Levetiracetam given via intravenous administration has been shown to be an effective alternative in adults with epilepsy when oral administration is not feasible. This study was a prospective single-arm, multicenter study to assess tolerability, safe
Autor:
Chuanjun Zhuo, Li Li
Publikováno v:
Journal of Child Neurology. 29:965-968
We aimed to examine the effectiveness of combined neurofeedback therapy and imagery training in adolescent patients with refractory Tourette syndrome. Two patients, aged respectively 14 and 16 years, had been treated with haloperidol and tiapride; ho
Autor:
Rita Christopher, George Tomy Mampilly, Tomy Kochuvareed Mampilly, Vijayalakshmy Janaki, Neeradha Chandramohan
Publikováno v:
Journal of Child Neurology. 29:833-836
Certain drugs are known to cause metabolic changes resulting in altered metabolic profiles. We report here a case where a combination of antiepileptic drugs resulted in a profile that mimicked a metabolic disorder. A 16month-old female child on antie