White blood cells 1: non-malignant disorders (Q33897176)

29 July 2017

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title

White blood cells 1: non-malignant disorders (English)

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29 July 2017

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W Stock

1

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29 July 2017

R Hoffman

series ordinal

2

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29 July 2017

language of work or name

English

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publication date

1 April 2000

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29 July 2017

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29 July 2017

volume

355

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29 July 2017

issue

9212

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29 July 2017

page(s)

1351-1357

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Current concepts: immunology. Neutrophils in human diseases

29 July 2017

cites work

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Neutrophil kinetics in man

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Chronic Idiopathic Leukocytosis

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Hereditary neutrophilia.

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Comparison of agents producing a neutrophilic leukocytosis in man. Hydrocortisone, prednisone, endotoxin, and etiocholanolone

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Proposals for the classification of the myelodysplastic syndromes

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Juvenile chronic myelogenous leukemia

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The hypereosinophilic syndrome: analysis of fourteen cases with review of the literature

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Systemic vasculitis with asthma and eosinophilia: a clinical approach to the Churg-Strauss syndrome.

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Quantitative Relationships Between Circulating Leukocytes and Infection in Patients with Acute Leukemia

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Long-term safety of treatment with recombinant human granulocyte colony-stimulating factor (r-metHuG-CSF) in patients with severe congenital neutropenias

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Pathophysiology and treatment of severe chronic neutropenia

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Genetics, phenotype, and natural history of autosomal dominant cyclic hematopoiesis

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The physical and genetic map surrounding the Lyst gene on mouse chromosome 13.

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Defective CTLA-4 cycling pathway in Chediak-Higashi syndrome: a possible mechanism for deregulation of T lymphocyte activation

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1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis

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X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene

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7 January 2021

Diagnosis and management of chronic neutropenia during childhood

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7 January 2021

Drug-induced immune neutropenia.

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7 January 2021

Neutrophil Kinetics in Acute Infection*

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7 January 2021

Common variable immunodeficiency: how many diseases?

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7 January 2021

SCID: The role of adenosine deaminase deficiency

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PEG-ADA: an alternative to haploidentical bone marrow transplantation and an adjunct to gene therapy for adenosine deaminase deficiency

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Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency

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Identifiers

DOI

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29 July 2017

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