[The diagnostic and prognostic significance of enzyme findings in hepatolenticular degeneration]. 1961

H TSCHABITSCHER, and H SCHINKO

UI MeSH Term Description Entries
D004798 Enzymes Biological molecules that possess catalytic activity. They may occur naturally or be synthetically created. Enzymes are usually proteins, however CATALYTIC RNA and CATALYTIC DNA molecules have also been identified. Biocatalyst,Enzyme,Biocatalysts
D006527 Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. Cerebral Pseudosclerosis,Neurohepatic Degeneration,Pseudosclerosis,Wilson Disease,Copper Storage Disease,Hepatic Form of Wilson Disease,Hepato-Neurologic Wilson Disease,Hepatocerebral Degeneration,Hepatolenticular Degeneration Syndrome,Kinnier-Wilson Disease,Progressive Lenticular Degeneration,Westphal-Strumpell Syndrome,Wilson Disease, Hepatic Form,Wilson's Disease,Cerebral Pseudoscleroses,Copper Storage Diseases,Degeneration Syndrome, Hepatolenticular,Degeneration Syndromes, Hepatolenticular,Degeneration, Hepatocerebral,Degeneration, Hepatolenticular,Degeneration, Neurohepatic,Degeneration, Progressive Lenticular,Degenerations, Hepatocerebral,Degenerations, Neurohepatic,Disease, Copper Storage,Diseases, Copper Storage,Diseases, Hepato-Neurologic Wilson,Diseases, Kinnier-Wilson,Hepato Neurologic Wilson Disease,Hepato-Neurologic Wilson Diseases,Hepatocerebral Degenerations,Hepatolenticular Degeneration Syndromes,Kinnier Wilson Disease,Kinnier-Wilson Diseases,Lenticular Degeneration, Progressive,Neurohepatic Degenerations,Pseudoscleroses, Cerebral,Pseudosclerosis, Cerebral,Storage Disease, Copper,Storage Diseases, Copper,Syndrome, Hepatolenticular Degeneration,Syndromes, Hepatolenticular Degeneration,Westphal Strumpell Syndrome,Westphal-Strumpell Syndromes,Wilson Disease, Hepato-Neurologic,Wilson Diseases, Hepato-Neurologic,Wilsons Disease

Related Publications

H TSCHABITSCHER, and H SCHINKO
December 1958, Munchener medizinische Wochenschrift (1950),
H TSCHABITSCHER, and H SCHINKO
September 1962, Revue medicale de Liege,
H TSCHABITSCHER, and H SCHINKO
February 1952, Folha medica,
H TSCHABITSCHER, and H SCHINKO
March 1960, Chinese medical journal (Peking, China : 1932),
H TSCHABITSCHER, and H SCHINKO
August 1954, Revista clinica espanola,
H TSCHABITSCHER, and H SCHINKO
February 1968, Revue de l'infirmiere et de l'assistante sociale,
H TSCHABITSCHER, and H SCHINKO
January 1974, Vojnosanitetski pregled,
H TSCHABITSCHER, and H SCHINKO
March 1955, Prensa medica argentina,
H TSCHABITSCHER, and H SCHINKO
January 1990, Neurologija,
H TSCHABITSCHER, and H SCHINKO
October 1971, Prensa medica argentina,
Copied contents to your clipboard!