Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease.
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Biomarkers for diagnosis of Wilson's diseasePersistent hypertransaminasemia in asymptomatic children: a stepwise approachA review and current perspective on Wilson disease.Neurological features and management of Wilson disease in children: an evaluation of 12 casesZinc and Copper in Alzheimer's Disease.Zinc monotherapy is effective in Wilson's disease patients with mild liver disease diagnosed in childhood: a retrospective study.Wilson's disease and other neurological copper disorders.Clinical presentation and mutations in Danish patients with Wilson disease.Prospective evaluation of the diagnostic accuracy of hepatic copper content, as determined using the entire core of a liver biopsy sample.A genetic study of Wilson's disease in the United KingdomUpdate on the clinical management of Wilson's disease.Evolving perspectives in Wilson disease: diagnosis, treatment and monitoring.Application of exome sequencing in the search for genetic causes of rare disorders of copper metabolism.Genetics of Wilson's disease: a clinical perspective.Pathogenesis and management of Wilson disease.Pediatric liver diseases: current challenges and future perspectives.Wilson's disease and diagnostic conundrum in a low income countryWilson disease in a Nigerian child: a case reportCommentary: The Case for Abandoning Therapeutic Chelation of Copper Ions in Alzheimer's Disease.The genetics of Wilson disease.Recommendations for provoked challenge urine testing.Insights into the management of Wilson's disease.Cholestatic liver disease masquerading as Wilson disease.Plasma exchange and chelator therapy rescues acute liver failure in Wilson disease without liver transplantation.Relative exchangeable copper: A valuable tool for the diagnosis of Wilson disease.The optimal threshold of serum ceruloplasmin in the diagnosis of Wilson's disease: A large hospital-based study.Never forget aceruloplasminemia in case of highly suggestive Wilson's disease score.Idiopathic acute liver injury in paediatric outpatients: incidence and signal detection in two European countries.Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.Psychological Signs as the Only Presentation of Wilson's Disease in an 11-Year-Old Boy.Functional Characterization of Novel ATP7B Variants for Diagnosis of Wilson Disease.
P2860
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P2860
Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Re-evaluation of the diagnosti ...... ldren with mild liver disease.
@en
Re-evaluation of the diagnosti ...... ldren with mild liver disease.
@nl
type
label
Re-evaluation of the diagnosti ...... ldren with mild liver disease.
@en
Re-evaluation of the diagnosti ...... ldren with mild liver disease.
@nl
prefLabel
Re-evaluation of the diagnosti ...... ldren with mild liver disease.
@en
Re-evaluation of the diagnosti ...... ldren with mild liver disease.
@nl
P50
P356
P1433
P1476
Re-evaluation of the diagnosti ...... ldren with mild liver disease.
@en
P2093
Angela Vegnente
Giusy Ranucci
P304
P356
10.1002/HEP.23910
P407
P577
2010-10-21T00:00:00Z