| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1034/J.1398-9995.2002.02168.X |
| P8608 | Fatcat ID | release_qeka5oimgjfd3oi753gm7yiy7y |
| P698 | PubMed publication ID | 12358995 |
| P5875 | ResearchGate publication ID | 11098593 |
| P2093 | author name string | Holland SM | |
| Belohradsky BH | |||
| Grimbacher B | |||
| P2860 | cites work | LEKTI, a novel 15-domain type of human serine proteinase inhibitor | Q22010419 |
| Isolation of a novel gene mutated in Wiskott-Aldrich syndrome | Q24317943 | ||
| Partial V(D)J recombination activity leads to Omenn syndrome | Q24336454 | ||
| Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping. | Q24539101 | ||
| Interleukin 13, a T-cell-derived cytokine that regulates human monocyte and B-cell function | Q24563054 | ||
| The Wiskott-Aldrich syndrome | Q24681854 | ||
| Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder | Q28138040 | ||
| Defective interleukin-12/interferon-gamma pathway in patients with hyperimmunoglobulinemia E syndrome | Q28144020 | ||
| Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome | Q28145552 | ||
| The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosis | Q28213469 | ||
| High-dose intravenous gamma-globulin treatment for hyperimmunoglobulinemia E syndrome | Q28236818 | ||
| Job's Syndrome. Recurrent, "cold", staphylococcal abscesses | Q28237376 | ||
| Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia | Q30195143 | ||
| Sex-linked hereditary thrombocytopenia as a variant of Wiskott-Aldrich syndrome | Q33461709 | ||
| Wiskott-Aldrich syndrome. An immunologic deficiency disease involving the afferent limb of immunity | Q33461729 | ||
| X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene | Q33489988 | ||
| A multiinstitutional survey of the Wiskott-Aldrich syndrome. | Q33491474 | ||
| IgE in asthma and atopy: cellular and molecular connections | Q33746218 | ||
| IgE myeloma: a case presentation and a review of the literature | Q33804716 | ||
| The diverse potential effector and immunoregulatory roles of mast cells in allergic disease | Q33901708 | ||
| Hyperimmunoglobulin-E syndrome with recurrent infection: a review of current opinion and treatment | Q34029021 | ||
| The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979). | Q34057440 | ||
| A revised nomenclature for allergy. An EAACI position statement from the EAACI nomenclature task force | Q34090755 | ||
| Regulation of immunoglobulin (Ig)E synthesis in the hyper-IgE syndrome | Q34251749 | ||
| Regulation of immunoglobulin production in hyperimmunoglobulin E recurrent-infection syndrome by interferon gamma | Q34326708 | ||
| The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases | Q34355151 | ||
| Genetic linkage of hyper-IgE syndrome to chromosome 4. | Q34390210 | ||
| Serum IgD and IgE concentrations in immunodeficiency diseases | Q34472498 | ||
| Immunoglobulins in the hyperimmunoglobulin E and recurrent infection (Job's) syndrome. Deficiency of anti-Staphylococcus aureus immunoglobulin A. | Q34521713 | ||
| Metabolism of immunoglobulin E in patients with markedly elevated serum immunoglobulin E levels | Q34576338 | ||
| Defective in vitro production of gamma-interferon and tumor necrosis factor-alpha by circulating T cells from patients with the hyper-immunoglobulin E syndrome | Q34580901 | ||
| Atopic eczema: role of microorganisms on the skin surface | Q35534261 | ||
| Hyperimmunoglobulin E-recurrent infection syndrome in a patient with juvenile dermatomyositis | Q35938316 | ||
| Interleukin 13 induces interleukin 4-independent IgG4 and IgE synthesis and CD23 expression by human B cells. | Q36261169 | ||
| Two inhibitors of neutrophil chemotaxis are produced by hyperimmunoglobulin E recurrent infection syndrome mononuclear cells exposed to heat-killed staphylococci | Q36348382 | ||
| IgE enhances mouse mast cell Fc(epsilon)RI expression in vitro and in vivo: evidence for a novel amplification mechanism in IgE-dependent reactions | Q36376804 | ||
| Mononuclear cells from patients with the hyperimmunoglobulin E-recurrent infection syndrome produce an inhibitor of leukocyte chemotaxis | Q36983324 | ||
| Deficiency of suppressor T cells in the hyperimmunoglobulin E syndrome | Q37003505 | ||
| Immunoglobulin E anti-Staphylococcus aureus antibodies in atopic patients | Q37336747 | ||
| Interleukin 4 instructs uncommitted B lymphocytes to switch to IgG1 and IgE. | Q38535180 | ||
| A new syndrome characterised by absence of eosinophils and basophils | Q39438215 | ||
| Abnormalities in the Regulation of Human IgE Synthesis | Q39775534 | ||
| Netherton's syndrome: a syndrome of elevated IgE and characteristic skin and hair findings | Q40570245 | ||
| Regulation of the human IgE response by IL4 and IL13. | Q40620595 | ||
| Fatal histiocytic lymphoma of the brain associated with hyperimmunoglobulinemia-e and recurrent infections | Q40779568 | ||
| Complete Correction of the Wiskott-Aldrich Syndrome by Allogeneic Bone-Marrow Transplantation | Q40882151 | ||
| RAG mutations in human B cell-negative SCID. | Q41159572 | ||
| Elevated urinary histamine in the hyperimmunoglobulin E and recurrent infection (Job's) syndrome: association with eczematoid dermatitis and not with infection | Q41480480 | ||
| A unique case of trichorrhexis nodosa; bamboo hairs | Q41939868 | ||
| Cytokine-Mediated Bone Resorption in Patients with the Hyperimmunoglobulin E Syndrome | Q42480301 | ||
| Identification of the IL-6-responsive element in an acute-phase-responsive human pancreatic secretory trypsin inhibitor-encoding gene | Q42483793 | ||
| Subcutaneous immunoglobulin replacement in patients with primary antibody deficiencies: safety and costs | Q44215065 | ||
| The Buckley syndrome: recurring, severe staphylococcal infections, eczema and hyperimmunoglobulinemia E. (author's transl) | Q44264353 | ||
| Familial Neutrophil Chemotaxis Defect, Recurrent Bacterial Infections, Mucocutaneous Candidiasis, and Hyperimmunoglobulinemia E | Q44469860 | ||
| Raised serum-IgE levels and defective neutrophil chemotaxis in three children with eczema and recurrent bacterial infections | Q44806967 | ||
| Skin reactions to anti-gammaE antibody in atopic, nonatopic, and immunologically deficiency children and adults | Q46226495 | ||
| Wiskott-Aldrich syndrome protein-deficient mice reveal a role for WASP in T but not B cell activation | Q47713209 | ||
| Delayed eruption of permanent teeth in hyperimmunoglobulinemia E recurrent infection syndrome. | Q52170962 | ||
| Serum IgE levels during the first 6 years of life. | Q52979618 | ||
| IgM in cytomegalovirus mononucleosis. | Q53752195 | ||
| Craniosynostosis in hyper-IgE-syndrome. | Q54463872 | ||
| Cranial synostosis in Job's syndrome | Q56418760 | ||
| V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations | Q57173925 | ||
| Familial Reticuloendotheliosis with Eosinophilia | Q57268307 | ||
| Regulation of immunoglobulin production in hyper-IgE (Job’s) syndrome | Q57908364 | ||
| Burkitt's lymphoma developing in a 7-year-old boy with hyper-IgE syndrome1 | Q57997132 | ||
| Shifts in interleukin-4 and interferon-γ production by T cells of patients with elevated serum IgE levels and the modulatory effects of these lymphokines on spontaneous IgE synthesis | Q59358993 | ||
| Treatment of Omenn syndrome by bone marrow transplantation | Q61714702 | ||
| Recurrent severe staphylococcal infections, eczematoid rash, extreme elevations of IgE, eosinophilia, and divergent chemotactic responses in two generations | Q67550690 | ||
| Cryptococcosis of the colon resembling Crohn's disease in a patient with the hyperimmunoglobulinemia E-recurrent infection (Job's) syndrome | Q68257416 | ||
| Combined immunodeficiency and reticuloendotheliosis with eosinophilia | Q68860209 | ||
| [Highly malignant non-Hodgkin's lymphoma in hyper-IgE syndrome] | Q68873207 | ||
| Evolution of the hyperimmunoglobulin E and recurrent infection (HIE, JOB's) syndrome in a young girl | Q69448593 | ||
| Circulating IgG autoantibodies to IgE in atopic syndromes | Q70032119 | ||
| Wiskott-Aldrich syndrome. A study of 6 cases with determination of the immunoglobulins A, D, G, M and ND | Q70101323 | ||
| T helper type 2-like cells and therapeutic effects of interferon-gamma in combined immunodeficiency with hypereosinophilia (Omenn's syndrome) | Q70527043 | ||
| CD30 cell expression and abnormal soluble CD30 serum accumulation in Omenn's syndrome: evidence for a T helper 2-mediated condition | Q71047892 | ||
| Primary immunodeficiency syndrome in Japan. I. Overview of a nationwide survey on primary immunodeficiency syndrome | Q71085313 | ||
| Multiple defects of the hair shaft in Netherton's disease. Association with ichthyosis linearis circumflexa | Q71260439 | ||
| Case of the season. Job's syndrome with superimposed lymphoma | Q71734617 | ||
| Multiple antigens are altered on T and B lymphocytes from peripheral blood and spleen of patients with Wiskott-Aldrich syndrome | Q71778729 | ||
| Systemic lupus erythematosus complicating hyper IgE syndrome | Q73303860 | ||
| In vitro cell death of activated lymphocytes in Omenn's syndrome | Q73933702 | ||
| NETHERTON'S DISEASE; TRICHORRHEXIS INVAGINATA (BAMBOO HAIR), CONGENITAL ICHTHYOSIFORM ERYTHRODERMA AND THE ATOPIC DIATHESIS. A HISTOPATHOLOGIC STUDY | Q76582535 | ||
| The face of Job | Q77112855 | ||
| Discordance for systemic lupus erythematosus and hyper IgE syndrome in a pair of monozygotic twins | Q77134354 | ||
| Altered lamellar body secretion and stratum corneum membrane structure in Netherton syndrome: differentiation from other infantile erythrodermas and pathogenic implications | Q78015171 | ||
| Effects of allogeneic peripheral stem cell transplantation in a patient with job syndrome of hyperimmunoglobulinemia E and recurrent infections | Q93911703 | ||
| P433 | issue | 11 | |
| P304 | page(s) | 995-1007 | |
| P577 | publication date | 2002-11-01 | |
| P1433 | published in | Allergy | Q2699825 |
| P1476 | title | Immunoglobulin E in primary immunodeficiency diseases | |
| P478 | volume | 57 |
| Q34289747 | Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity |
| Q44687424 | Critical aneurysmal dilatation of the thoracic aorta in young adolescents with variant hyperimmunoglobulin E syndrome |
| Q99579097 | Diffuse Large B-Cell Lymphoma and Job's Syndrome: A Case Report |
| Q40098119 | Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome |
| Q37152148 | Evaluation and clinical interpretation of hypergammaglobulinemia E: differentiating atopy from immunodeficiency |
| Q36015053 | Hyper-IgE syndromes |
| Q33660776 | Hyperimmunoglobulin E syndrome: Genetics, immunopathogenesis, clinical findings, and treatment modalities |
| Q46491813 | Lung function in hyper IgE syndrome |
| Q56333390 | Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome |
| Q21202861 | The hyperimmunoglobulin E syndrome--clinical manifestation diversity in primary immune deficiency |
| Q92239402 | When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura |
| Q88318558 | [Unexpected outcome in entropion lower eyelid repair] |
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