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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 | 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, 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
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2009, Volume 124, Issue 6, pp. 1289 - 1302.e4
Journal Article
Immunological Reviews, ISSN 0105-2896, 03/2015, Volume 264, Issue 1, pp. 103 - 120
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2016, Volume 113, Issue 51, pp. E8277 - E8285
Journal Article
Immunity, ISSN 1074-7613, 11/2008, Volume 29, Issue 5, pp. 746 - 757
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