Publications by authors named "LUBINUS H"

Alcaptonuria is a rare (incidence approx. 1:10(6)), autosomal-recessive transmitted metabolic disease. The basic defect is a lack of the enzyme homogentisic acid oxidase.

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The article reports on 20 cases of cup-plasties of the first metatarsophalangeal joint. 13 cups were done without, 7 with bone cement. The early results in both groups were promising.

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The technical procedure and results with the author's patella glide bearing total prosthesis is reported. The endoprosthesis is made of polyethylene on the patellar side and a cobalt-chrome alloy on the femoral side. It can be applied solely or in connection with intramedullary total endoprostheses and also in combination with sled-type endoprostheses.

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[The melanoma problem].

Langenbecks Arch Klin Chir Ver Dtsch Z Chir

July 2000

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