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Akademický článek
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Autor:
V. Váradi, György Várallyay, György Bozsik, Ildikó Vastagh, Kristóf Szőke, Gábor Rudas, T. Rab, Dániel Bereczki
Publikováno v:
Journal of the Neurological Sciences. 333:e180
WCN 2013 No: 950 Topic: 3 — Stroke Internuclear ophthalmoplegia caused by an isolated ischemic lesion affecting the medial longitudinal fascicle T. Rab, I. Vastagh, V. Varadi, K. Szőke, G. Bozsik, G. Varallyay, G. Rudas, D. Bereczki. Department of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9459c5f334dbe4a47730a252c3d7587
https://doi.org/10.1016/j.jns.2013.07.735
https://doi.org/10.1016/j.jns.2013.07.735
Publikováno v:
Orvosi hetilap. 136(8)
Authors reported about their experiences with newborn infants, who had transient myasthenia gravis; one disease developed in the fetal, others 10 in the early neonatal age. Direct correlation was found between the development of maternal polyhydramni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df181db5c5ddb55c279e606cf5348478
https://pubmed.ncbi.nlm.nih.gov/7885685
https://pubmed.ncbi.nlm.nih.gov/7885685
Publikováno v:
Acta paediatrica Hungarica. 30(1)
Periventricular leukomalacia is a form of hypoxic-ischaemic encephalopathy developing in preterm babies. During the last year among 387 sonographically screened neonates 11 periventricular neonatal leukomalacia cases were found. Analysing their cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d849c5a5195275f762ce796777598ed
https://pubmed.ncbi.nlm.nih.gov/2180453
https://pubmed.ncbi.nlm.nih.gov/2180453
Publikováno v:
Acta paediatrica Hungarica. 30(1)
On the basis of eleven own cases sonographic features of infant meningoencephalitis and ventriculitis are discussed. The characteristic findings are as follows: abnormal parenchymal echogenicity of brain, changes of the size and wall echogenicity of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f3fd586e7f4b91e213335fa457743e1
https://pubmed.ncbi.nlm.nih.gov/2180454
https://pubmed.ncbi.nlm.nih.gov/2180454
Publikováno v:
Orvosi hetilap. 127(50)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d258b8614d906ed375640d0884167a7
https://pubmed.ncbi.nlm.nih.gov/3540789
https://pubmed.ncbi.nlm.nih.gov/3540789
Publikováno v:
Orvosi hetilap. 128(30)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f0bb24bb7a28af32ebc8c41beaf852f
https://pubmed.ncbi.nlm.nih.gov/3302825
https://pubmed.ncbi.nlm.nih.gov/3302825
Publikováno v:
Orvosi hetilap. 130(5)
The defect of the enzyme heparan sulfamidase is the cause of Sanfilippo A syndrome (mucopolysaccharidosis IIIA) which is an autosomal recessive inherited disease. Three children of a marriage couple who attended our genetical counselling died of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::701c41e0970a9e3dc6450f12ef90f490
https://pubmed.ncbi.nlm.nih.gov/2492654
https://pubmed.ncbi.nlm.nih.gov/2492654
Publikováno v:
Orvosi hetilap. 127(39)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dcabc594cb90514209b421973656a47f
https://pubmed.ncbi.nlm.nih.gov/3095766
https://pubmed.ncbi.nlm.nih.gov/3095766