Results 301 to 310 of about 13,679,770 (330)
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Archives of Neurology, 1988
To the Editor. —Our experience with both penicillamine and/or zinc worsening neurologic symptoms agrees with that of Brewer et al. 1 The exact cause of this initial exacerbation of symptoms is different with these two types of therapy, as we know from 22 years of experience using penicillamine and trace elements as therapy.
C C, Pfeiffer, B, Camo
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To the Editor. —Our experience with both penicillamine and/or zinc worsening neurologic symptoms agrees with that of Brewer et al. 1 The exact cause of this initial exacerbation of symptoms is different with these two types of therapy, as we know from 22 years of experience using penicillamine and trace elements as therapy.
C C, Pfeiffer, B, Camo
openaire +2 more sources
Parkinsonism & Related Disorders, 2009
Wilson’s disease (WD), also called progressive hepatolenticular degeneration, is a rare autosomal recessive inborn error of metabolism, first described by S.A.K. Wilson in 1912 [1]. The consequences of this disorder, related to copper deposition in various tissues, are treatable and preventable.
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Wilson’s disease (WD), also called progressive hepatolenticular degeneration, is a rare autosomal recessive inborn error of metabolism, first described by S.A.K. Wilson in 1912 [1]. The consequences of this disorder, related to copper deposition in various tissues, are treatable and preventable.
openaire +2 more sources
Current Treatment Options in Gastroenterology, 1999
Early diagnosis permits preventive therapy to preempt development of organ damage. In all diagnosed patients, both symptomatic and asymptomatic, pharmacologic therapy is lifelong, and maintenance treatment to prevent copper toxicity is mandatory. Patients with either fulminant hepatic failure or hepatic insufficiency unresponsive to medical therapy ...
, Tavill, , Schilsky
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Early diagnosis permits preventive therapy to preempt development of organ damage. In all diagnosed patients, both symptomatic and asymptomatic, pharmacologic therapy is lifelong, and maintenance treatment to prevent copper toxicity is mandatory. Patients with either fulminant hepatic failure or hepatic insufficiency unresponsive to medical therapy ...
, Tavill, , Schilsky
openaire +2 more sources
EASL-ERN Clinical Practice Guidelines on Wilson's disease.
Journal of HepatologyWilson's disease is an autosomal recessive disorder of copper metabolism which affects the liver, brain and other organs. Diagnosis is based on: clinical features; biochemical tests, including plasma ceruloplasmin concentration, 24-h urinary copper ...
P. Socha +11 more
semanticscholar +1 more source
The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
Nature Genetics, 1993Peter Bull +4 more
semanticscholar +1 more source
Efficacy and Safety of Oral Chelators in Treatment of Patients With Wilson Disease
Clinical Gastroenterology and Hepatology, 2013Karl Heinz Weiss +2 more
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