Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Ziad Albahri"'
Autor:
Ziad Albahri, Eliška Marklová, Hubert Vaníček, Lenka Minxová, Petr Dědek, Sylva Skálová, Marika Talábová, Jaroslava Vávrová, Eva Rencová
Publikováno v:
Acta Medica, Vol 47, Iss 4, Pp 267-272 (2004)
The aim of this study is to report our 3years experience with the screening of congenital disorders of glycosylation. A common isoelectric focusing method with immunofixation was used for analysis of serum transferrin and α1-antitrypsin, apart from
Externí odkaz:
https://doaj.org/article/10cb0e0e5ddc440ba60e6d1d45ceeb56
Publikováno v:
Intervenční a akutní kardiologie. 16:6-10
Cilem nasi studie bylo ukazat, do jake miry přimý transport pacientů se STEMI z terenu do katetrizacni laboratoře ovlivňuje zkraceni casu do provedeni reperfuze pomoci p-PCI a jaký ma vliv na jejich mortalitu. Přestože se v poslednich letech
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::426180c5b3d2b3607f3bb713acc25b03
https://doi.org/10.36290/kar.2017.003
https://doi.org/10.36290/kar.2017.003
Autor:
Eliška Marklová, Ziad Albahri
Publikováno v:
Journal of Clinical Laboratory Analysis. 23:77-81
Congenital disorders of glycosylation are a rapidly growing group of inherited (neuro)metabolic disorders characterized by defects in glycosylation of proteins and lipids. This study discusses an analytical problem in the differentiation between hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da5bc4b8a73aec4a4746b248ccd5177
https://doi.org/10.1002/jcla.20293
https://doi.org/10.1002/jcla.20293
Publikováno v:
Journal of Inherited Metabolic Disease. 31:457-461
Genetic polymorphism of serum transferrin (Tf) was studied in order to differentiate between protein genetic variants and congenital disorders of glycosylation (CDG), further focusing on unusual findings.Screening of Tf hypoglycosylation was carried
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8401fbafa8009c684037b71aaef176
https://doi.org/10.1007/s10545-008-0733-0
https://doi.org/10.1007/s10545-008-0733-0
Akademický článek
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Publikováno v:
American Journal of Pediatrics. 3:1
Ischemic stroke is an infrequent disease of pediatric patients. We report a case of 2 year old child with neurofibromatosis, who had acute hemiplegia and severe hypertension (required artery angioplasty) due to both cerebral vascular disease and rena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b67a1b81aa74723f1c7d52bc2f123e8b
https://doi.org/10.11648/j.ajp.20170301.11
https://doi.org/10.11648/j.ajp.20170301.11
Publikováno v:
Journal of child neurology. 29(10)
Churg-Strauss syndrome is a rare form of small-vessel vasculitis. In the current report, we describe the case of a 17-year-old Czech girl predominantly characterized by peripheral neuropathy, the presence of cardiac and pulmonary involvement, hypereo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7aef65223e8b6b75739527eb89eac0f
https://pubmed.ncbi.nlm.nih.gov/24170259
https://pubmed.ncbi.nlm.nih.gov/24170259
Autor:
Ziad Albahri, Antonín Lukeš
Publikováno v:
American Journal of Pediatrics. 2:1
We report a case of a male newborn who was evaluated due to persistent jaundice. Evaluation showed hypothyroidism associated with infantile hemangioma of the liver. Euthyroidism and regression of the hepatic hemangiomas were obtained with L-thyroxin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c757f3527c0c328d9c940baa7b1b772c
https://doi.org/10.11648/j.ajp.20160201.11
https://doi.org/10.11648/j.ajp.20160201.11
Publikováno v:
American Journal of Internal Medicine. 4:75
In ST-elevation myocardial infarction (STEMI), the pre-hospital phase is the most critical and appropriate treatment in a timely manner which is instrumental for mortality reduction. STEMI systems of care based on networks of medical institutions con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fc3b5b125695c3e07296fa38bb2441e
https://doi.org/10.11648/j.ajim.20160404.13
https://doi.org/10.11648/j.ajim.20160404.13
Publikováno v:
Journal of the neurological sciences. 314(1-2)
article Background: Participation of protein polymorphism is often considered in the pathogenesis of various diseases. Aberrant protein glycosylation has been recognized to play major roles in human disorders, including neurodegenerative diseases. Ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3733894b46341dd05e69ab3684be782f
https://pubmed.ncbi.nlm.nih.gov/22118861
https://pubmed.ncbi.nlm.nih.gov/22118861