uu.seUppsala University Publications
Change search
ReferencesLink to record
Permanent link

Direct link
Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences. Klinisk kemi och farmakologi. (Inflammation)
Show others and affiliations
2006 (English)In: Acta Paediatrica, ISSN 0803-5253, E-ISSN 1651-2227, Vol. 95, no 12, 1526-32 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2006. Vol. 95, no 12, 1526-32 p.
Keyword [en]
Agranulocytosis/genetics/*history/physiopathology, History; 20th Century, Humans, Neutropenia/congenital/*history, Portraits as Topic, Sweden
URN: urn:nbn:se:uu:diva-17302PubMedID: 17129957OAI: oai:DiVA.org:uu-17302DiVA: diva2:45073

Publikation från annat universitet

Available from: 2008-06-19 Created: 2008-06-19 Last updated: 2015-06-18

Open Access in DiVA

No full text

Other links


Search in DiVA

By author/editor
Garwicz, Daniel
By organisation
Department of Medical Sciences
In the same journal
Acta Paediatrica

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 359 hits
ReferencesLink to record
Permanent link

Direct link