Kostmann syndrome or infantile genetic agranulocytosis, part one: Celebrating 50 years of clinical and basic research on severe congenital neutropenia-Reference-Cited by-同舟云学术

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Kostmann syndrome or infantile genetic agranulocytosis, part one: Celebrating 50 years of clinical and basic research on severe congenital neutropenia

Published:2006-12-01 Issue:12 Volume:95 Page:1526-1532
ISSN:0803-5253
Container-title:Acta Paediatrica
language:
Short-container-title:Acta Paediatrica

Author:

Carlsson Göran,Andersson Mats,Pütsep Katrin,Garwicz Daniel,Nordenskjöld Magnus,Henter Jan-Inge,Palmblad Jan,Fadeel Bengt

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1080/08035250601087607/fullpdf

Reference30 articles.

1. [1]R Kostmann . Infantile genetic agranulocytosis. A new recessive lethal disease in man Acta Paediatr Scand, Suppl, 1956 ; 105 .

2. [5]G. Carlsson, Kostmann syndrome. A clinical and pathophysiological study . Doctoral thesis .

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Kostmann’s Neutropenia: A Case Report;Open Journal of Pediatrics;2024

2. Late-onset neutropenia induced by anti-B cell therapy with rituximab in patients with ANCA-associated systemic vasculitis;Modern Rheumatology Journal;2022-06-19

3. Kostmann disease and other forms of severe congenital neutropenia;Acta Paediatrica;2021-06-29

4. Kostmann’s disease or severe hereditary neutropenia—the man behind the syndrome;Annals of Hematology;2020-06-23

5. Icons in paediatrics: Rolf Kostmann (1909-1982);Acta Paediatrica;2017-05-08

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