Manganese encephalopathy: an under-recognized condition in the intensive care unit.
about
Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in manMutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.Inverse association of intellectual function with very low blood lead but not with manganese exposure in Italian adolescents.Manganese efflux in Parkinsonism: insights from newly characterized SLC30A10 mutationsKnown and potential roles of transferrin in iron biology.Zebrafish slc30a10 deficiency revealed a novel compensatory mechanism of Atp2c1 in maintaining manganese homeostasis.Manganese Provision in Parenteral Nutrition: An Update.Manganese toxicity in critical care: Case report, literature review and recommendations for practice
P2860
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P2860
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
@ast
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
@en
type
label
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
@ast
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
@en
prefLabel
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
@ast
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
@en
P2093
P2860
P1433
P1476
Manganese encephalopathy: an under-recognized condition in the intensive care unit.
@en
P2093
Angela Hays
Julio A Chalela
Leo Bonillha
Ron Neyens
P2860
P2888
P304
P356
10.1007/S12028-010-9476-5
P577
2011-06-01T00:00:00Z
P6179
1015398525