- Wilson's
disease (also
called Hepatolenticular degeneration) is a
genetic disorder characterized by the
excess build-up of
copper in the body. Symptoms...
- 12, 1937) was an American-born
British neurologist. His
research of
hepatolenticular degeneration led the
disease to be
named after him as Wilson's disease...
-
Samuel Alexander Kinnier Wilson (1878–1937),
neurologist who
described hepatolenticular degeneration, a
copper metabolism disorder affecting the
liver and...
- a blue
discoloration of the lunulae, seen in
argyria and
cases of
hepatolenticular degeneration (Wilson's disease), also
having been
reported in hemoglobin...
-
Gitlin D (Oct 1952). "Deficiency of
ceruloplasmin in
patients with
hepatolenticular degeneration (Wilson's disease)". Science. 116 (3018): 484–5. Bibcode:1952Sci...
- Kayser,
Bruno Fleischer neurology,
gastroenterology Wilson's
disease (
hepatolenticular degeneration) ring of
brownish copper deposit at corneo-scleral junction...
- thalamus) of the
brains of
people with
Wilson disease and
acquired hepatolenticular degeneration.
Opalski cells was
described by Adam Opalski,
Polish neurologist...
-
African porphyria)
Verruciform xanthoma Waxy skin Wilson's
disease (
hepatolenticular degeneration)
Xanthelasma palpebrarum (xanthelasma)
Xanthoma diabeticorum...
-
Samuel Alexander Kinnier Wilson (1878–1937),
neurologist who
described hepatolenticular degeneration, a
copper metabolism disorder affecting the
liver and...
- S2CID 41967295. GeneReviews/NIH/NCBI/UW
entry on
Wilson Disease or
Hepatolenticular Degeneration Wilson+disease+protein at the U.S.
National Library of...
