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1 lsive status epilepticus, endocrinopathy, or thiamine deficiency.
2 chanism, which appears to be up-regulated in thiamine deficiency.
4 occur during the acute and chronic phases of thiamine deficiency and describe how rodent models of We
5 extending the focus from lethal to sublethal thiamine deficiency, and by linking biochemical alterati
7 mical and cognitive deficits associated with thiamine deficiency as well as proven useful toward grea
8 us on day 10 of PTD treatment, a duration of thiamine deficiency associated with perivascular edema i
9 ley rats were assigned to one of 4 stages of thiamine deficiency based on behavioral symptoms: pre-sy
10 ignificantly, these results demonstrate that thiamine deficiency causes selective cholinergic dysfunc
12 rrier (BBB) breakdown in the pathogenesis of thiamine deficiency encephalopathy was investigated in R
14 Primary and secondary conditions leading to thiamine deficiency have overlapping features in childre
19 iovascular traits previously associated with thiamine deficiency, including elevated cardiac stroke v
20 ces from granulocytes may be responsible for thiamine deficiency-induced vascular breakdown and periv
23 effects, we demonstrate that the problem of thiamine deficiency is considerably more widespread and
28 ith the thalamus of the pyrithiamine-induced thiamine deficiency (PTD) rat model of Wernicke's enceph
31 f diencephalic amnesia, pyrithiamine-induced thiamine deficiency (PTD), was used to investigate dienc
32 iberi, a potentially fatal disease caused by thiamine deficiency, remains a public health concern in
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