Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Alzheimer type II astrocyte"'
Akademický článek
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Autor:
Nagarajarao Shamaladevi, Michael D. Norenberg, Arumugam Jayakumar, Taherian Mehran, Anis Ahmad, Xiaoying Tong, Jennifer Arcuri
Publikováno v:
American Journal of Gastroenterology. 114:S38-S39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cd5f107b2f905487e82d4b856bb92e4
https://doi.org/10.14309/01.ajg.0000582288.72427.46
https://doi.org/10.14309/01.ajg.0000582288.72427.46
Akademický článek
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Publikováno v:
Gastroenterology Week; 11/15/2024, p562-562, 1p
Autor:
Philomena Frances Foley
Hepatic encephalopathy (HE) is a serious neurological consequence of major liver failure for which the underlying pathogenic process is not well understood. It is a frequent concomitant of alcoholic liver disease as well as of other forms of cirrhosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90e7d9fa6cf2112db99a2ad6167af5ac
https://doi.org/10.14264/105580
https://doi.org/10.14264/105580
Autor:
Kimura, Noriyuki1 noriyuki@med.oita-u.ac.jp, Kumamoto, Toshihide1, Hanaoka, Takuya1, Nakamura, Kenichiro1, Hazama, Yusuke1, Arakawa, Ryuki1
Publikováno v:
Neuropathology. Dec2008, Vol. 28 Issue 6, p627-632. 6p. 1 Color Photograph, 1 Black and White Photograph.
Publikováno v:
Neuroscience letters. 396(3)
Exposure to manganese in an industrial or clinical setting can lead to manganism, a neurological disorder with similarities to Parkinson's disease. Although the pathogenetic basis of this disorder is unclear, studies indicate this metal is highly acc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9926bb62304634873ff90051ed5ce4e3
https://pubmed.ncbi.nlm.nih.gov/16384640
https://pubmed.ncbi.nlm.nih.gov/16384640
Autor:
Yusuke Hazama, Toshihide Kumamoto, Takuya Hanaoka, Kenichiro Nakamura, Noriyuki Kimura, Ryuki Arakawa
Publikováno v:
Neuropathology. :080401034624438
We report herein an autopsy case of portal-systemic encephalopathy (PSE) presenting with diffuse tissue rarefaction in the cerebral deep white matter. Clinically, the patient showed recurrent episodes of unconsciousness, abnormal behavior and urinary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ea350093e111f89c6bec675d1c3dad7
https://doi.org/10.1111/j.1440-1789.2008.00898.x
https://doi.org/10.1111/j.1440-1789.2008.00898.x
Autor:
Y. Edward Hsia
Publikováno v:
Gastroenterology. 67:347-374
The term congenital hyperammonemia is generic, and the condition can be caused by inborn deficiencies of urea cycle enzymes, by some disorders of ornithine and lysine metabolism, and by some inborn errors of branched-chain amino acid catabolism. Ammo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcb450dcb44f193664a1c1e04c006b21
https://doi.org/10.1016/s0016-5085(19)32902-6
https://doi.org/10.1016/s0016-5085(19)32902-6
Autor:
Michael D. Norenberg
Publikováno v:
Neurochemical pathology. 6(1-2)
The Alzheimer type II astrocyte change is the distinctive morphologic alteration in brain of humans and experimental animals succumbing to hepatic encephalopathy (HE). Whether this change is a primary event in the pathogenesis of HE or whether it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b89bb06b44b86564e6567823d89af021
https://pubmed.ncbi.nlm.nih.gov/3306480
https://pubmed.ncbi.nlm.nih.gov/3306480