Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Icagasioglu D"'
Intracranial epidermoid cysts can closely mimic cerebrospinal fluid on magnetic resonance imaging and computed tomography. Epidermoid cysts are isointense to slightly hyperintense relative to cerebrospinal fluid on T1-, T2-, and proton density-weight
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3104::c3196012f659c103100d673db3de89ed
https://hdl.handle.net/20.500.12418/4350
https://hdl.handle.net/20.500.12418/4350
[No abstract available]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3104::00f70411e689c917158285c90741d5bb
https://hdl.handle.net/20.500.12418/4692
https://hdl.handle.net/20.500.12418/4692
Publikováno v:
Scopus-Elsevier
We investigated the effect of antibiotic or G-CSF plus antibiotic therapy given to E. coli septic rats. In our study, 80 rats were inoculated transperitoneally with 1 ml of a solution containing 10 colony forming units per milliliter of E. coli. Rats
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2269029c1f4d54c4279adf6ad89109fa
https://hdl.handle.net/20.500.12418/4691
https://hdl.handle.net/20.500.12418/4691
Autor:
Cevit O., Toksoy H.B., Bakici M.Z., Icagasioglu D., Sutcu I., Turkay S., Ergur A.T., Kafali G.
Group A streptococcus is the most common cause bacterial pharyngitis in childhood. Streptococcal pharyngitis has been usually treated by penicillins. Recent reports suggest that non-group A streptococci has been increasingly described as the cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3104::ad21015c6a844027e947913e92c0fccd
https://hdl.handle.net/20.500.12418/4736
https://hdl.handle.net/20.500.12418/4736
Akademický článek
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Do we consider Andermann syndrome in infants with agenesis of corpus callosum: Andermann syndrome is characterized by agenesis of corpus callosum, anterior horn cell disease, a mixed sensory and motor neuropathy, and facial dysmorphism, and is inheri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10157::81b61374a3b460ab4f9b0d98452380c1
https://avesis.yyu.edu.tr/publication/details/71da43c3-a09d-4b66-9f52-9e9ef741cdbb/oai
https://avesis.yyu.edu.tr/publication/details/71da43c3-a09d-4b66-9f52-9e9ef741cdbb/oai
WOS: 000185736200012
PubMed ID: 14531762
Objective: Hallervorden - Spatz disease is a rare autosomal recessive condition, with early onset of predominantly extrapyramidal dysfunction. The symptoms of the disease are dystonia, rigidity, chor
PubMed ID: 14531762
Objective: Hallervorden - Spatz disease is a rare autosomal recessive condition, with early onset of predominantly extrapyramidal dysfunction. The symptoms of the disease are dystonia, rigidity, chor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3104::e40dc23c680f55b220be9cb1a625afde
https://hdl.handle.net/20.500.12418/11318
https://hdl.handle.net/20.500.12418/11318
A fatal case of cerebellar hypoplasia associated with anterior horn cell disease: A 27-month-old girl was admitted with inability to walk and speak. The pregnancy, labor and delivery were unremarkable. She was the second child of first degree consang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10157::143dc26f0765e9350263494a41d785ef
https://avesis.yyu.edu.tr/publication/details/9e6589fd-353e-4f32-86b7-18f000bda13a/oai
https://avesis.yyu.edu.tr/publication/details/9e6589fd-353e-4f32-86b7-18f000bda13a/oai
WOS: A1996UU55500017
PubMed ID: 8819632
Guillain-Barre syndrome (GBS) is the most common muse of acute generalized paralysis. Although the muse and pathogenesis of GBS remain unknown, there is increasing evidence to suggest that this syndro
PubMed ID: 8819632
Guillain-Barre syndrome (GBS) is the most common muse of acute generalized paralysis. Although the muse and pathogenesis of GBS remain unknown, there is increasing evidence to suggest that this syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3104::cf982e088fe0c0cb9948b25a9b0c19b6
https://hdl.handle.net/20.500.12418/11903
https://hdl.handle.net/20.500.12418/11903
WOS: A1996VK96400018
PubMed ID: 8827912
Achalasia is a motility disorder of the esophagus characterized by absence of normal peristalsis and failure of relaxation of the lower esophageal sphincter. Among the most common clinical findings ar
PubMed ID: 8827912
Achalasia is a motility disorder of the esophagus characterized by absence of normal peristalsis and failure of relaxation of the lower esophageal sphincter. Among the most common clinical findings ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3104::e6083c701c7b8e1510e916ac54e43dd1
https://hdl.handle.net/20.500.12418/11881
https://hdl.handle.net/20.500.12418/11881