Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
about
Oxidative Stress Implications in the Affective Disorders: Main Biomarkers, Animal Models Relevance, Genetic Perspectives, and Antioxidant ApproachesMottled Mice and Non-Mammalian Models of Menkes DiseaseTreatment of nongout joint deposition diseases: an updateMetals, oxidative stress and neurodegeneration: a focus on iron, manganese and mercuryMolecular basis of neurodegeneration and neurodevelopmental defects in Menkes diseaseElemental and chemically specific X-ray fluorescence imaging of biological systemsHypocupremia: a possible association with late cortical cerebellar atrophy.The T1048I mutation in ATP7A gene causes an unusual Menkes disease presentation.The Features of Copper Metabolism in the Rat Liver during DevelopmentCeliac disease markers in patients with liver diseases: a single center large scale screening study.Diagnostic copper imaging of Menkes disease by synchrotron radiation-generated X-ray fluorescence analysisEffects of ATP7A overexpression in mice on copper transport and metabolism in lactation and gestationInborn errors of metabolism causing epilepsy.Pathological mitochondrial copper overload in livers of Wilson's disease patients and related animal models.What has fluorescent sensing told us about copper and brain malfunction?Possible role of trace elements in epilepsy and febrile seizures: a meta-analysis.Psychiatric comorbidity in Wilson's disease.Drosophila melanogaster Models of Metal-Related Human Diseases and Metal Toxicity.Reduced glutathione biosynthesis in Drosophila melanogaster causes neuronal defects linked to copper deficiency.Wilson's disease in association with anetoderma.Characterization of ATP7A missense mutants suggests a correlation between intracellular trafficking and severity of Menkes diseaseCopper deficiency, a new triad: anemia, leucopenia, and myeloneuropathy.The Extracellular Domain of Human High Affinity Copper Transporter (hNdCTR1), Synthesized by E. coli Cells, Chelates Silver and Copper Ions In Vivo.Novel mutations and clinical outcomes of copper-histidine therapy in Menkes disease patients.Spontaneous retroperitoneal hemorrhage in Menkes disease: A rare case report.Toxic effects of copper sulfate on the brains of term Hubbard broiler chicks: a stereological and biochemical study.Menkes disease: importance of diagnosis with molecular analysis in the neonatal period
P2860
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P2860
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
description
2012 nî lūn-bûn
@nan
2012 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մարտին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@ast
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@en
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@nl
type
label
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@ast
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@en
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@nl
prefLabel
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@ast
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@en
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@nl
P2093
P2860
P921
P1476
Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.
@en
P2093
Chie Fujisawa
Hiroko Kodama
Wattanaporn Bhadhprasit
P2860
P304
P356
10.2174/138920012799320455
P407
P5008
P577
2012-03-01T00:00:00Z