Published in Immunol Lett on November 24, 2009
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Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome. J Allergy Clin Immunol (2008) 2.50
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Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen. Pediatr Hematol Oncol (2012) 1.65
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The genotype of the original Wiskott phenotype. N Engl J Med (2006) 1.57
The burden of varicella complications before the introduction of routine varicella vaccination in Germany. Pediatr Infect Dis J (2008) 1.52
Regulatory T-cell impairment in cystic fibrosis patients with chronic pseudomonas infection. Am J Respir Crit Care Med (2015) 1.51
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Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol (2013) 1.31
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Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22. Eur J Hum Genet (2002) 1.24
Modified Foxp3 mRNA protects against asthma through an IL-10-dependent mechanism. J Clin Invest (2013) 1.12
ICOS deficiency in patients with common variable immunodeficiency. Clin Immunol (2004) 1.11
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Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis. J Allergy Clin Immunol (2010) 1.03
Rates of postoperative complications among human immunodeficiency virus-infected women who have undergone obstetric and gynecologic surgical procedures. Clin Infect Dis (2002) 1.01
Clinical and molecular analysis of patients with defects in micro heavy chain gene. J Clin Invest (2002) 1.00
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Neurologic varicella complications before routine immunization in Germany. Pediatr Neurol (2010) 0.98
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Clinical score for nonbacterial osteitis in children and adults. Arthritis Rheum (2009) 0.96
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Notch signaling in embryonic and adult myelopoiesis. Cells Tissues Organs (2008) 0.94
Acellular pertussis booster in adolescents induces Th1 and memory CD8+ T cell immune response. PLoS One (2011) 0.93
The chitinase-like protein YKL-40 modulates cystic fibrosis lung disease. PLoS One (2011) 0.92
Impaired suppression of synovial fluid CD4+CD25- T cells from patients with juvenile idiopathic arthritis by CD4+CD25+ Treg cells. Arthritis Rheum (2011) 0.92
Dysregulation of innate immune receptors on neutrophils in chronic granulomatous disease. J Allergy Clin Immunol (2007) 0.91
The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events. Hum Mutat (2010) 0.90
Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease. J Allergy Clin Immunol (2010) 0.90
Differences of humoral and cellular immune response to an acellular pertussis booster in adolescents with a whole cell or acellular primary vaccination. Vaccine (2008) 0.90
Granulocytic myeloid derived suppressor cells expand in human pregnancy and modulate T-cell responses. Eur J Immunol (2014) 0.90
Neutrophils express distinct RNA receptors in a non-canonical way. J Biol Chem (2012) 0.88
Comèl-Netherton syndrome defined as primary immunodeficiency. J Allergy Clin Immunol (2009) 0.88
Immunocompetent children account for the majority of complications in childhood herpes zoster. J Infect Dis (2007) 0.87
The risk of respiratory syncytial virus-related hospitalizations in preterm infants of 29 to 35 weeks' gestational age. Pediatr Infect Dis J (2006) 0.87
A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy. J Clin Immunol (2013) 0.86
Celiac disease and pulmonary hemosiderosis in a patient with chronic granulomatous disease. Pediatr Pulmonol (2004) 0.84
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A new low-penetrance TNFRSF1A mutation causing atypical periodic fever. Pediatr Int (2006) 0.81
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease. Eur Respir J (2011) 0.81
A novel CIAS1 mutation and plasma/cerebrospinal fluid cytokine profile in a German patient with neonatal-onset multisystem inflammatory disease responsive to methotrexate therapy. Pediatrics (2004) 0.81
Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome. J Clin Immunol (2013) 0.81
Severe variant of x-linked dyskeratosis congenita (Hoyeraal-Hreidarsson Syndrome) causes significant enterocolitis in early infancy. J Pediatr Gastroenterol Nutr (2009) 0.80
Heterozygous signal transducer and activator of transcription 3 mutations in hyper-IgE syndrome result in altered B-cell maturation. J Allergy Clin Immunol (2011) 0.79
Successful antifungal combination therapy with voriconazole and caspofungin. Pediatr Blood Cancer (2005) 0.79
Induction of Myeloid-Derived Suppressor Cells in Cryopyrin-Associated Periodic Syndromes. J Innate Immun (2016) 0.79
Lack of serologic immunity against vaccine-preventable diseases in children after thoracic transplantation. Transpl Int (2009) 0.79
Rituximab-induced long-term remission in two children with SLE. Eur J Pediatr (2006) 0.78
Reactogenicity of tetanus, diphtheria, 5-component acellular pertussis vaccine administered as a sixth consecutive acellular pertussis vaccine dose to adolescents. Pediatr Infect Dis J (2010) 0.78
A donor splice site mutation in intron 1 of CYBA, leading to chronic granulomatous disease. Blood Cells Mol Dis (2005) 0.78
Novel mutation in Hermansky-Pudlak syndrome type 2 with mild immunological phenotype. Platelets (2012) 0.78
Immune response, diagnosis and treatment of allergic bronchopulmonary aspergillosis in cystic fibrosis lung disease. Curr Pharm Des (2013) 0.77
Challenges of genetic counseling in patients with autosomal dominant diseases, such as the hyper-IgE syndrome (STAT3-HIES). J Allergy Clin Immunol (2012) 0.77
Expression and regulation of interferon-related development regulator-1 in cystic fibrosis neutrophils. Am J Respir Cell Mol Biol (2012) 0.77
Two new families with X-linked inhibitor of apoptosis deficiency and a review of all 26 published cases. J Allergy Clin Immunol (2011) 0.76
Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutation. Eur J Hum Genet (2005) 0.75
Reactive arthritis associated with prolonged cryptosporidial infection. J Infect (2003) 0.75
Impaired cellular immune response to diphtheria and tetanus vaccines in children after thoracic transplantation. Pediatr Transplant (2011) 0.75