Biomedical subjects
A Propst
Publications and source records attributed to A Propst.
[Feyrter's granular neuroma. Electron-optic study].
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[Morphological methods in routine diagnostics. Round-table discussion at the occasion of the 4th Symposium of the German Section of the International Academy for Pathology in Hamburg, June 26-27, 1970. Rapid section technics].
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[Purpura fulminans].
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[Concentrically laminated nuclear inclusions in a human adrenal adenoma].
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[Clinical picture and morphology of leprosy].
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[On the pathology of the adrenal gland].
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[Thymus tumor with extreme lymphopenia and atrophy of the lymphatic tissue with normal plasma cell count and with occurrence of a monoclonal IGM(lambda) increase].
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[Oncolysis of malignant tumors through the M 55 clostridium strain. II].
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[Oncolysis of malignant tumors by Clostridium strain M 55].
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[Metastatic angioblastomatosis of the uterus (so-called stromaendometriosis)].
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[The effect of non-pathogenic Clostridia on malignant tumors].
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[The zones of the adrenal cortex of the rat. Electron microscopic study].
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[Sporulation and germination in Clostridium butyricum M 55. Electron microscopic studies].
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[Electron microscopic investigation of the germination of the Clostridium strain M 55].
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Spasms of the hepatic artery following percutaneous transluminal angioplasty and tolazoline administration in a liver transplant patient.
Vascular complications after liver transplantation include occlusion or stenosis near the sites of anastomosis in the hepatic artery, portal vein, and vena cava. Balloon angioplasty of these stenoses carries little risk and is a useful procedure for the treatment of these problems. Here we describe the case of a liver transplant patient who underwent balloon angioplasty for stenosis of the hepatic artery and who developed spasms of the hepatic artery which were aggravated following intraarterial administration of Tolazoline.
Alpha-1-antitrypsin deficiency and liver disease.
Alpha-1-antitrypsin deficiency is a common autosomal recessive disorder associated with premature development of emphysema, liver cirrhosis and hepatocellular carcinoma. This article reviews the existing literature on alpha-1-antitrypsin deficiency, with an emphasis on recent developments. A description of the protein, gene structure and function of alpha-1-antitrypsin as well as clinical aspects are presented. Treatment issues are addressed and a framework for the diagnostic workup and management of patients with alpha-1-antitrypsin deficiency and chronic liver disease is provided.