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Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2009, Volume 124, Issue 6, pp. 1289 - 1302.e4
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 136, Issue 2, pp. 402 - 412
Background Mutations in dedicator of cytokinesis 8 (DOCK8) cause a combined immunodeficiency (CID) also classified as autosomal recessive (AR) hyper-IgE... 
Allergy and Immunology | Primary combined immunodeficiency | autosomal recessive hyper-IgE syndrome | signal transducer and activator of transcription 3 | Molluscum contagiosum | hyper-IgE syndrome | dedicator of cytokinesis 8 | SURVIVAL | BONE-MARROW-TRANSPLANTATION | STAT3 | GLYCOSYLATION | IMMUNOLOGY | ALLERGY | DOCK8 DEFICIENCY | DISORDER | MUTATIONS | STEM-CELL TRANSPLANTATION | IMMUNODEFICIENCY | Job Syndrome - genetics | Job Syndrome - mortality | Humans | Middle Aged | Child, Preschool | Male | Support Vector Machine | Virus Diseases - complications | Eosinophils - immunology | Immunoglobulin E - blood | CD4-Positive T-Lymphocytes - immunology | Bacterial Infections - genetics | Eosinophils - pathology | Virus Diseases - genetics | Child | Guanine Nucleotide Exchange Factors - deficiency | STAT3 Transcription Factor - genetics | Skin Diseases - mortality | Immunoglobulin M - genetics | Guanine Nucleotide Exchange Factors - genetics | Virus Diseases - immunology | Skin Diseases - immunology | Antigens, Viral - immunology | Phenotype | Skin Diseases - complications | Job Syndrome - complications | Adolescent | Survival Analysis | Virus Diseases - mortality | Mutation | STAT3 Transcription Factor - immunology | CD8-Positive T-Lymphocytes - immunology | Bacterial Infections - mortality | Job Syndrome - immunology | CD8-Positive T-Lymphocytes - pathology | Skin Diseases - genetics | Antigens, Bacterial - immunology | Infant | Antigens, Bacterial - blood | CD4-Positive T-Lymphocytes - pathology | Antigens, Viral - blood | Bacterial Infections - complications | Immunoglobulin E - genetics | Bacterial Infections - immunology | Adult | Female | Immunoglobulin M - blood | Guanine Nucleotide Exchange Factors - immunology | Lymphocyte Count | Genotype & phenotype | Immunoglobulins | Laboratories | Lymphocytes | Families & family life | Lymphomas | Viral infections | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus | Immunoglobulin M | Immunoglobulin E | CD8-Positive T-Lymphocytes | Life Sciences | Antigens, Viral | Bacterial Infections | Job Syndrome | CD4-Positive T-Lymphocytes | Virus Diseases | Skin Diseases | Antigens, Bacterial | Guanine Nucleotide Exchange Factors | STAT3 Transcription Factor | Eosinophils
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 137, Issue 3, pp. 889 - 898.e6
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 134, Issue 1, pp. 135 - 144.e7
Background Individuals with genetic defects in CD40 ligand (CD40L) or B-cell antigen receptor coreceptor molecules CD19 and CD81 suffer from an antibody... 
Allergy and Immunology | CD40L | autoreactivity | somatic hypermutation | selection | immunoglobulin | CD19 | REPERTOIRE | CYTIDINE DEAMINASE AID | HUMAN B-CELLS | IMMUNOLOGY | ALLERGY | CLASS-SWITCH RECOMBINATION | MICE | MUTATIONS | DNA-POLYMERASE-ETA | GENE HYPERMUTATION | Immunologic Deficiency Syndromes - pathology | Cytidine Deaminase - immunology | Humans | Middle Aged | Immunoglobulin A - genetics | Child, Preschool | Infant | Male | Antigens, CD19 - genetics | CD40 Ligand - immunology | Flow Cytometry | Immunoglobulin G - immunology | Adult | B-Lymphocyte Subsets - immunology | Female | Immunologic Deficiency Syndromes - immunology | Child | Immunoglobulin Class Switching | Antigens, CD19 - immunology | B-Lymphocyte Subsets - pathology | CD40 Ligand - deficiency | Signal Transduction | Lymphocyte Activation | Cytidine Deaminase - genetics | Gene Expression Regulation | Immunophenotyping | Immunoglobulin G - genetics | Uracil-DNA Glycosidase - immunology | B-Lymphocyte Subsets - metabolism | CD40 Ligand - genetics | Immunoglobulin A - immunology | DNA Repair - immunology | Immunologic Deficiency Syndromes - genetics | Lymphocyte Count | Immunologic Memory | Mutation | Uracil-DNA Glycosidase - genetics | Viral antibodies | Antibodies | Children | B cells | Health aspects | Antigens | Immunoglobulins | Immune system | Index Medicus | Abridged Index Medicus
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 136, Issue 1, pp. 140 - 150.e7
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 138, Issue 5, pp. 1384 - 1394.e2
Background The autosomal recessive hyper-IgE syndrome (HIES) caused by dedicator of cytokinesis 8 (DOCK8) deficiency shares clinical features with autosomal... 
Allergy and Immunology
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2009, Volume 124, Issue 2, pp. 342 - 348.e5
Background The hyper IgE syndrome (HIES) is characterized by abscesses, eczema, recurrent infections, skeletal and connective tissue abnormalities, elevated... 
Allergy and Immunology
Journal Article
World Allergy Organization Journal, ISSN 1939-4551, Volume 4, Issue 11, pp. 170 - 178
Background Allergy is associated with considerable morbidity.Objective The aim of this multicenter study was to provide insight into allergy knowledge and... 
Journal Article
Journal of Medical Sciences(Faisalabad), ISSN 1682-4474, 05/2003, Volume 3, Issue 5, pp. 411 - 417
Journal Article
Nature Immunology, ISSN 1529-2908, 06/2012, Volume 13, Issue 6, pp. 612 - 620
Journal Article
by Scott, Eric M and Halees, Anason and Itan, Yuval and Spencer, Emily G and He, Yupeng and Azab, Mostafa Abdellateef and Gabriel, Stacey B and Belkadi, Aziz and Boisson, Bertrand and Abel, Laurent and Clark, Andrew G and Rahim, Sohair Abdel and Alkuraya, Fowzan S and Casanova, Jean-Laurent and Gleeson, Joseph G and Abdou, Mohammed and Abhytankar, Avinash and Adimi, Parisa and Ahmad, Jamil and Akcakus, Mustafa and Aksu, Guside and Al Hajjar, Sami and Al Juamaah, Suliman and Al Muhsen, Saleh and Al Sannaa, Nouriya and Al Tameni, Salem and Al-Aama, Jumana and Al-Allawi, Nasir and Al-Baradie, Raidah and Al-Gazali, Lihadh and Al-Hashem, Amal and Al-Herz, Waleed and Al-Jeaid, Deema and Al-Tawari, Asma and Alangari, Abdullah and Alcais, Alexandre and AlFawaz, Tariq S and Alsum, Zobaida and Ammar-Khodja, Aomar and Amouian, Sepideh and Arikan, Cigdem and Aryani, Omid and Aslanger, Ayca and Aydogmus, Cigdem and Aytekin, Caner and Azam, Matloob and Bansagi, Boglarka and Barbouche, Mohamed-Rhida and Bastaki, Laila and Ben-Omran, Tawfeg and Bindu, Parayil Sankaran and Blancas, Lizbeth and Boisson-Dupuis, Stéphanie and Bonnet, Damien and Stambouli, Omar Boudghene and Bousfiha, Aziz and Boussafara, Lobna and Boutros, Jeannette and Bustamante, Jacinta and Caksen, Huseyin and Camcioglu, Yildiz and Catherinot, Emilie and Celik, Fatma C and Ciancanelli, Michael and Cipe, Funda E and Clark, Gary and Cobat, Aurélie and Comu, Sinan and Condie, Angela and Condino-Neto, Antonio and Desai, Mukesh and Dobyns, William and Dogu, Figen and Domaia, Mohamed and Dorum, Meltem and Egritas, Odul and El Azbaoui, Safa and El Baghdadi, Jamila and El Ruby, Mona and El-Harouni, Ashraf and Elfeky, Reem A and Elghazali, Gehad and Faqeih, Eissa and Fenerci, Elif and Fieschi, Claire and Funda, Cipe and Gamal, Iman and Gelik, Umit and Genel, Fetah and Gezdirici, Alper and Girisha, Katta M and Goldstein, Amy and Grattan-Smith, Padraic and Gupta, Neerja and Hahn, Jin and Hatipoglu, Nevin and Hennekam, Raoul and Houshmand, Massoud and Ichai, Philippe and Ikinciogullari, Aydan and ... and Greater Middle East Variome Consortium
Nature Genetics, ISSN 1061-4036, 09/2016, Volume 48, Issue 9, pp. 1071 - 1079
Journal Article