The Clinical, Immunohematological, and Molecular Study of Iranian Patients with Severe Congenital Neutropenia-Reference-Cited by-同舟云学术

The Clinical, Immunohematological, and Molecular Study of Iranian Patients with Severe Congenital Neutropenia

Published:2007-06-21 Issue:5 Volume:27 Page:525-533
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Rezaei Nima,Moin Mostafa,Pourpak Zahra,Ramyar Asghar,Izadyar Mina,Chavoshzadeh Zahra,Sherkat Roya,Aghamohammadi Asghar,Yeganeh Mehdi,Mahmoudi Maryam,Mahjoub Fatemeh,Germeshausen Manuela,Grudzien Magda,Horwitz Marshall S.,Klein Christoph,Farhoudi Abolhassan

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://link.springer.com/content/pdf/10.1007/s10875-007-9106-y.pdf

Reference24 articles.

1. Welte K, Zeidler C, Dale DC. Severe congenital neutropenia. Semin Hematol 2006;43:189–95.

2. Rezaei N, Farhoudi A, Ramyar A, Pourpak Z, Aghamohammadi A, Mohammadpour B, et al. Congenital neutropenia and primary immunodeficiency disorders: a survey of 26 Iranian patients. J Pediatr Hematol Oncol 2005;27:351–6.

3. Zeidler C, Welte K. Kostmann syndrome and severe congenital neutropenia. Semin Hematol 2002;39:82–8.

4. Zeidler C, Schwinzer B, Welte K. Congenital neutropenias. Rev Clin Exp Hematol 2003;7:72–83.

5. Kostmann R. Infantile genetic agranulocytosis: a new recessive lethal disease in man. Acta Paediatr Scand 1956;45:1–78.

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