Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Gabor Barabas"'
Autor:
Márta Font, Gábor Barabás
A figure of crucial importance to scholarship on western and eastern Europe alike, King Coloman (1208–1241) here receives long-overdue scholarly treatment as a key figure of the thirteenth century. The Árpád prince ruled over a vast area in Centr
Publikováno v:
Developmental Medicine & Child Neurology. 37:715-722
SUMMARY The present study represents the first effort to assess systematically the cognitive functioning of a population of individuals with Lesch-Nyhan syndrome using standardized psychometric instruments. Seven residents from a special hospital set
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91ac39430b2755e9e5ab82089ec14340
https://doi.org/10.1111/j.1469-8749.1995.tb15017.x
https://doi.org/10.1111/j.1469-8749.1995.tb15017.x
Publikováno v:
Developmental Medicine & Child Neurology. 26:457-460
SUMMARY A total of 171 children, 57 with Tourette syndrome, 57 with learning disabilities and the rest with seizure disorders, were studied to discover the incidence of somnambulism. Of the 13 identified sleepwalkers, 10 had Tourette syndrome. It is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e6c3aa444e938194c4a3cff1afed83
https://doi.org/10.1111/j.1469-8749.1984.tb04471.x
https://doi.org/10.1111/j.1469-8749.1984.tb04471.x
Publikováno v:
Developmental Medicine & Child Neurology. 45:167-171
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bd5e4be82fa5b03b360bd99a035e42e
https://doi.org/10.1111/j.1469-8749.2003.tb00925.x
https://doi.org/10.1111/j.1469-8749.2003.tb00925.x
Autor:
James C. Harris, Isabelle Desguerre, Jasper E. Visser, Gary E. Eddey, Juan G. Puig, Laura E. Laróvere, Olivier Dulac, Vladimir Neychev, Irène Ceballos-Picot, Kenneth L. Robey, Bastiaan R. Bloem, Stephen G. Reich, Gabor Barabas, Hyder A. Jinnah, Alfonso Verdu, Rosa J. Torres, David J. Schretlen, Raquel Dodelson de Kremer, Pedro Gonzalez-Alegre, William L. Nyhan
Publikováno v:
Brain, 129, 1201-17
Brain, 129, Pt 5, pp. 1201-17
Brain, 129, Pt 5, pp. 1201-17
Contains fulltext : 51161.pdf (Publisher’s version ) (Open Access) Lesch-Nyhan disease (LND) is caused by deficiency of the purine salvage enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT). Affected individuals exhibit over-production of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6768d376f4a44ff73cd714a990cfe5bf
https://doi.org/10.1093/brain/awl056
https://doi.org/10.1093/brain/awl056
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 23:1161-1164
Reports describing the neurological features of Lesch-Nyhan disease (LND) vary widely, thereby implying the involvement of different neurological substrates. The movement abnormalities in 20 patients with LND were investigated. Dystonia was the most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82a9f7c7f8188eec808dc8b777b23b5f
https://doi.org/10.1081/ncn-200027432
https://doi.org/10.1081/ncn-200027432
Autor:
Gabor Barabas, Wendy S. Matthews
Publikováno v:
Journal of Developmental and Physical Disabilities. 9:337-346
The palmo-mental reflex (PMR) is a neurological sign found in normal children under the age of 3 years, but disappearing with age. A study population consisting of 45 children with cerebral palsy (CP) and control populations of 136 children with atte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcfe6f58d98203b940abee72fec7fdb0
https://doi.org/10.1023/a:1024977911950
https://doi.org/10.1023/a:1024977911950
Autor:
Gábor Barabás
Publikováno v:
Zeitschrift für Ostmitteleuropa-Forschung, Vol 70, Iss 2, Pp 187-226 (2021)
Externí odkaz:
https://doaj.org/article/da9b248670a2473695b95ad0fad478f2
Publikováno v:
ChemInform. 36
Reports describing the neurological features of Lesch‐Nyhan disease (LND) vary widely, thereby implying the involvement of different neurological substrates. The movement abnormalities in 20 patients with LND were investigated. Dystonia was the mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ce10272b179d2e4d301a61bf3959804
https://doi.org/10.1002/chin.200509217
https://doi.org/10.1002/chin.200509217
Publikováno v:
Developmental Medicine & Child Neurology. 45
Lesch-Nyhan disease (LND) is a rare X-linked recessive genetic disorder associated with cognitive impairment, choreoathetosis, hyperuricemia, and the hallmark symptom of severe and involuntary self-mutilation. This study examines data gathered from a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc9236e02c94ab5f3f9ba154e2e9678c
https://doi.org/10.1017/s001216220300032x
https://doi.org/10.1017/s001216220300032x