Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia-Reference-Cited by-同舟云学术

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Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia

Published:2007-05-24 Issue:6 Volume:96 Page:813-819
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:

Author:

Carlsson Göran,Melin Malin,Dahl Niklas,Ramme Kim Göransdotter,Nordenskjöld Magnus,Palmblad Jan,Henter Jan-Inge,Fadeel Bengt

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2007.00274.x/fullpdf

Reference48 articles.

1. Infantile genetic agranulocytosis. A new recessive lethal disease in man;Kostmann;Acta Paediatr,1956

2. Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia;Carlsson;Acta Paediatr,2006

3. Hereditär reticulos - en ny systemsjukdom;Kostmann;Sv Läkartidningen [Swedish],1950

4. Infantile genetic agranulocytosis. A review with presentation of ten new cases;Kostmann;Acta Paediatr,1975

5. Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis;Horwitz;Nat Genet,1999

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

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5. A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia;Journal of Pediatric Hematology/Oncology;2021-02-03

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