相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Diagnosis and classification of Graves' disease
Francesca Menconi et al.
AUTOIMMUNITY REVIEWS (2014)
Cohen syndrome is associated with major glycosylation defects
Laurence Duplomb et al.
HUMAN MOLECULAR GENETICS (2014)
Novel STAT3 Mutation Causing Hyper-IgE Syndrome: Studies of the Clinical Course and Immunopathology
Mikael Sundin et al.
JOURNAL OF CLINICAL IMMUNOLOGY (2014)
Elevated white blood cell counts in Cushing's disease: association with hypercortisolism
Hiba Masri-Iraqi et al.
PITUITARY (2014)
Etiology, clinical outcome, and laboratory features in children with neutropenia: Analysis of 104 cases
Giulia Angelino et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY (2014)
The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancy
Polina Stepensky et al.
BLOOD (2013)
Pluripotent Stem Cell Models of Shwachman-Diamond Syndrome Reveal a Common Mechanism for Pancreatic and Hematopoietic Dysfunction
Asmin Tulpule et al.
CELL STEM CELL (2013)
The relationship between bone marrow characteristics and the clinical prognosis of antithyroid drug-induced agranulocytosis
Jing Yang et al.
ENDOCRINE JOURNAL (2013)
Neutrophil mobilization via plerixafor-mediated CXCR4 inhibition arises from lung demargination and blockade of neutrophil homing to the bone marrow
Sapna Devi et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2013)
Pretherapeutic Plasma Pro- and Anti- Inflammatory Mediators Are Related to High Risk of Oral Mucositis in Pediatric Patients with Acute Leukemia: A Prospective Cohort Study
Ying Ye et al.
PLOS ONE (2013)
How to Approach Neutropenia in Childhood
Kelly Walkovich et al.
PEDIATRICS IN REVIEW (2013)
The cellular and molecular mechanisms for neutropenia in Barth syndrome
Vahagn Makaryan et al.
EUROPEAN JOURNAL OF HAEMATOLOGY (2012)
Ataxia-Telangiectasia Presenting With a Novel Immunodeficiency
Sebastien Perreault et al.
PEDIATRIC NEUROLOGY (2012)
Genetic Defects in Severe Congenital Neutropenia: Emerging Insights into Life and Death of Human Neutrophil Granulocytes
Christoph Klein
ANNUAL REVIEW OF IMMUNOLOGY, VOL 29 (2011)
Genetic etiologies of severe congenital neutropenia
Kaan Boztug et al.
CURRENT OPINION IN PEDIATRICS (2011)
Congenital neutropenia: diagnosis, molecular bases and patient management
Jean Donadieu et al.
ORPHANET JOURNAL OF RARE DISEASES (2011)
Neutrophil kinetics in health and disease
Charlotte Summers et al.
TRENDS IN IMMUNOLOGY (2010)
Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropenia
Cornelia Zeidler et al.
BRITISH JOURNAL OF HAEMATOLOGY (2009)
Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia
Jun Xia et al.
BRITISH JOURNAL OF HAEMATOLOGY (2009)
Vitamin D3 induces pro-LL-37 expression in myeloid precursors from patients with severe congenital neutropenia
Jenny Karlsson et al.
JOURNAL OF LEUKOCYTE BIOLOGY (2008)
Low plasma levels of the protein pro-LL-37 as an early indication of severe disease in patients with chronic neutropenia
Jenny Karlsson et al.
BRITISH JOURNAL OF HAEMATOLOGY (2007)
Kostmann syndrome or infantile genetic agranulocytosis, part one:: Celebrating 50 years of clinical and basic research on severe congenital neutropenia
Goran Carlsson et al.
ACTA PAEDIATRICA (2006)
Neutrophils and immunity: challenges and opportunities
C Nathan
NATURE REVIEWS IMMUNOLOGY (2006)
Mutations in SBDS are associated with Shwachman-Diamond syndrome
GRB Boocock et al.
NATURE GENETICS (2003)
Deficiency of antibacterial peptides in patients with morbus Kostmann:: an observation study
K Pütsep et al.
LANCET (2002)
Neutrophil-specific granule deficiency:: homozygous recessive inheritance of a frameshift mutation in the gene encoding transcription factor CCAAT/enhancer binding protein-ε
AF Gombart et al.
BLOOD (2001)