Literature DB >> 13326376

Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria.

R KOSTMANN.   

Abstract

Entities:  

Keywords:  AGRANULOCYTOSIS/in infant and child; HEREDITY

Mesh:

Year:  1956        PMID: 13326376

Source DB:  PubMed          Journal:  Acta Paediatr Suppl        ISSN: 0365-5741


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  72 in total

1.  Bibliography of human genetics.

Authors:  R H POST
Journal:  Am J Hum Genet       Date:  1957-12       Impact factor: 11.025

2.  From famine to feast: sending out the clones.

Authors:  Taly Glaubach; Seth J Corey
Journal:  Blood       Date:  2012-05-31       Impact factor: 22.113

Review 3.  Neutrophil elastase, proteinase 3, and cathepsin G as therapeutic targets in human diseases.

Authors:  Brice Korkmaz; Marshall S Horwitz; Dieter E Jenne; Francis Gauthier
Journal:  Pharmacol Rev       Date:  2010-12       Impact factor: 25.468

Review 4.  Neonatal manifestations of inherited bone marrow failure syndromes.

Authors:  Payal P Khincha; Sharon A Savage
Journal:  Semin Fetal Neonatal Med       Date:  2015-12-24       Impact factor: 3.926

5.  Mutations of the ELA2 gene found in patients with severe congenital neutropenia induce the unfolded protein response and cellular apoptosis.

Authors:  David S Grenda; Mark Murakami; Jhuma Ghatak; Jun Xia; Laurence A Boxer; David Dale; Mary C Dinauer; Daniel C Link
Journal:  Blood       Date:  2007-08-30       Impact factor: 22.113

Review 6.  Genetic heterogeneity in severe congenital neutropenia: how many aberrant pathways can kill a neutrophil?

Authors:  Alejandro A Schäffer; Christoph Klein
Journal:  Curr Opin Allergy Clin Immunol       Date:  2007-12

7.  Effect of granulocyte colony-stimulating factor (G-CSF) on chemotherapy-induced oral mucositis.

Authors:  M Katano; M Nakamura; T Matsuo; A Iyama; T Hisatsugu
Journal:  Surg Today       Date:  1995       Impact factor: 2.549

8.  A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropenia.

Authors:  D C Dale; M A Bonilla; M W Davis; A M Nakanishi; W P Hammond; J Kurtzberg; W Wang; A Jakubowski; E Winton; P Lalezari
Journal:  Blood       Date:  1993-05-15       Impact factor: 22.113

Review 9.  Kostmann's Disease and HCLS1-Associated Protein X-1 (HAX1).

Authors:  Christoph Klein
Journal:  J Clin Immunol       Date:  2016-12-10       Impact factor: 8.317

Review 10.  Genetic insights into congenital neutropenia.

Authors:  Christoph Klein; Karl Welte
Journal:  Clin Rev Allergy Immunol       Date:  2010-02       Impact factor: 8.667

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