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Physostigmine in Wilson disease.
Hepatobiliary malignancies in Wilson disease.
Cholestatic liver disease masquerading as Wilson disease.
The genetics of Wilson disease.
DNA-based presymptomatic diagnosis of Wilson disease.
Metal storage disorders: Wilson disease and hemochromatosis.
Hirschsprung's disease associated with Mowat-Wilson syndrome.
Worsening of Wilson disease following penicillamine therapy.
Wilson disease: clinical presentation, treatment, and survival.
Brain cholesterol homeostasis in Wilson disease.
Plasma exchange for fulminant Wilson disease.
Kayser-Fleischer ring and sunflower cataract in Wilson disease.
A century for progress in the diagnosis of Wilson disease.
Long-term outcome for Wilson disease: 85% good.
Whom and how to screen for Wilson disease.
Successful treatment of Wilson disease-associated IgA pemphigus with IVIG.
Increased Prevalence of Subcutaneous Lipomas in Patients With Wilson Disease.
Juvenile Wilson disease: histologic and functional studies during penicillamine therapy.
Influence of Liver Transplantation on Neuropsychiatric Manifestations of Wilson Disease.
Clinical zinc deficiency as early presentation of Wilson disease.
Wilson disease: a matter of copper, but also of zinc.
Mutational analysis of ATP7B in Chinese Wilson disease patients.
Pyoderma Gangrenosum-A New Manifestation of Wilson Disease?
Hirschsprung's disease in children with Mowat-Wilson syndrome.
Wilson disease.
Wilson disease is an inherited disorder of copper metabolism. Progress has been made in establishing the location of the gene on the long arm of chrom...
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Recommend Documents
Physostigmine in Wilson disease.
Hepatobiliary malignancies in Wilson disease.
Cholestatic liver disease masquerading as Wilson disease.
The genetics of Wilson disease.
DNA-based presymptomatic diagnosis of Wilson disease.
Metal storage disorders: Wilson disease and hemochromatosis.
Hirschsprung's disease associated with Mowat-Wilson syndrome.
Worsening of Wilson disease following penicillamine therapy.
Wilson disease: clinical presentation, treatment, and survival.
Brain cholesterol homeostasis in Wilson disease.
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