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pro vyhledávání: '"Z Liptai"'
Akademický článek
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Publikováno v:
European Journal of Paediatric Neurology. 21:e19-e20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1144e014a21616de6dc9d3987b88fe0
https://doi.org/10.1016/j.ejpn.2017.04.985
https://doi.org/10.1016/j.ejpn.2017.04.985
Publikováno v:
Neuropediatrics. 38(1)
Progressive multifocal leukoencephalopathy is an infection of the immunosuppressed, especially of AIDS, patients. The disease is caused by the JC virus and is exceptionally rare in children. The diagnosis is based on MRI and on the detection of JC vi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b1ea731c31977c83cdee04898a855bd
https://pubmed.ncbi.nlm.nih.gov/17607602
https://pubmed.ncbi.nlm.nih.gov/17607602
Publikováno v:
Neuropediatrics. 36(2)
Bilateral striatal lesion is characterised by a specific clinical syndrome (encephalopathy with rigidity, irritability, variable pyramidal, and extrapyramidal symptoms, speech abnormalities) and symmetrical lesion of the basal ganglia including the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4802783f020e8b1e457b47b757f80457
https://pubmed.ncbi.nlm.nih.gov/15822026
https://pubmed.ncbi.nlm.nih.gov/15822026
Publikováno v:
European Journal of Paediatric Neurology. 17:S9-S10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3275545299308a0ef942cb40e3e8b8ac
https://doi.org/10.1016/s1090-3798(13)70031-x
https://doi.org/10.1016/s1090-3798(13)70031-x
Publikováno v:
Archives of Disease in Childhood. 99:A322.3-A322
CGD is an immunodeficiency caused by mutations in genes encoding subunits of the NADPH oxidase complex. Normally, assembly of the NADPH oxidase complex in phagosomes of phagocytic cells leads to a “respiratory burst” essential for the clearance o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5b52029818851971db16038c8c0a874
https://doi.org/10.1136/archdischild-2014-307384.890
https://doi.org/10.1136/archdischild-2014-307384.890
Akademický článek
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Publikováno v:
Orvosi hetilap. 139(43)
Authors report the case of a white male patient suffering from a rare neurocutaneous dysplasia. Macrocrania and right ventricular dilation of the brain were present at birth. Motor milestones were delayed and epilepsy with staring spells started at t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da88b06e54be7a41cebcd66d5335f2f1
https://pubmed.ncbi.nlm.nih.gov/9825649
https://pubmed.ncbi.nlm.nih.gov/9825649
Publikováno v:
Orvosi hetilap. 138(5)
Ten patients with infantile spasms were treated with low dose ACTH therapy during the last five years. The etiology, EEG, the clinical features and the efficacy of the treatment were found to be similar to the data published in the literature. The ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3419821bd870265c4797ff987f71f40c
https://pubmed.ncbi.nlm.nih.gov/9064632
https://pubmed.ncbi.nlm.nih.gov/9064632
Publikováno v:
Orvosi hetilap. 137(31)
Authors report a rare central nervous system malformation on giving account of three of their cases. The possibility of septo-optic dysplasia should be raised in children with unilateral or bilateral hypoplasia of the optic nerve. The use of neuroima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a0a108a541ba1c625c79e4c16e4fd81
https://pubmed.ncbi.nlm.nih.gov/8992420
https://pubmed.ncbi.nlm.nih.gov/8992420