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Icons in paediatrics: Rolf Kostmann (1909-1982)
Region Östergötland, Center of Paediatrics and Gynaecology and Obstetrics, Department of Paediatrics in Norrköping.
Linköping University, Department of Clinical and Experimental Medicine, Division of Children's and Women's health. Linköping University, Faculty of Medicine and Health Sciences. Region Östergötland, Center of Paediatrics and Gynaecology and Obstetrics, Department of Paediatrics in Norrköping.
Region Östergötland, Center of Paediatrics and Gynaecology and Obstetrics, Department of Paediatrics in Norrköping.
2017 (English)In: Acta Paediatrica, ISSN 0803-5253, E-ISSN 1651-2227, Vol. 106, no 7, p. 1070-1072Article in journal, Editorial material (Other academic) Published
Abstract [en]

In the medical literature, diseases and syndromes are sometimes named after the first person to publish a report on, or describe, a condition. This is, of course, a great honour, both for the physician and his or her country and only a handful of Swedish medical researchers have achieved this. Swedish paediatrician Rolf Kostmann (Fig. 1) joined this elite group following his report on what he called infantile hereditary agranulocytosis (agranulocytosis infantilis hereditaria), which was first published 1950 in Swedish (1), and his dissertation in 1956 (2), He was the first to describe severe chronic neutropenia as an inherited disease. This article is protected by copyright.

Place, publisher, year, edition, pages
WILEY , 2017. Vol. 106, no 7, p. 1070-1072
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Clinical Medicine
Identifiers
URN: urn:nbn:se:liu:diva-139607DOI: 10.1111/apa.13871ISI: 000405216700017PubMedID: 28403560OAI: oai:DiVA.org:liu-139607DiVA, id: diva2:1133765
Available from: 2017-08-16 Created: 2017-08-16 Last updated: 2018-04-03

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