X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (15) 15
humans (14) 14
female (12) 12
immunology (11) 11
mutation (10) 10
male (9) 9
child (8) 8
adolescent (7) 7
allergy (6) 6
child, preschool (6) 6
genetic aspects (6) 6
children (5) 5
hematology (5) 5
mutations (5) 5
health aspects (4) 4
homozygote (4) 4
immunodeficiency (4) 4
infant (4) 4
patients (4) 4
thalassemia (4) 4
abridged index medicus (3) 3
adult (3) 3
allergy and immunology (3) 3
anemia (3) 3
article (3) 3
autoimmunity (3) 3
diagnosis (3) 3
disease (3) 3
genes (3) 3
genes, recessive (3) 3
hyper-ige syndrome (3) 3
infant, newborn (3) 3
internal medicine (3) 3
lymphocytes (3) 3
pediatrics (3) 3
research (3) 3
turkey (3) 3
alleles (2) 2
antigens (2) 2
bacterial infections (2) 2
bacterial infections - immunology (2) 2
beta-thalassemia (2) 2
biomedicine (2) 2
care and treatment (2) 2
chronic granulomatous disease (2) 2
complications and side effects (2) 2
consanguinity (2) 2
dedicator of cytokinesis 8 (2) 2
deferoxamine (2) 2
dna mutational analysis (2) 2
enzymes (2) 2
features (2) 2
frequency (2) 2
gene (2) 2
genome-wide association study (2) 2
genotype & phenotype (2) 2
glycosylation (2) 2
hematopoietic stem cell transplantation (2) 2
hematopoietic stem cells (2) 2
hemic and lymphatic diseases (2) 2
hemopoiesis (2) 2
identification (2) 2
immune dysregulation (2) 2
immunoglobulin e (2) 2
immunoglobulin m - blood (2) 2
infectious diseases (2) 2
iron (2) 2
job syndrome (2) 2
job syndrome - genetics (2) 2
job syndrome - immunology (2) 2
laboratories (2) 2
leukemia (2) 2
life sciences (2) 2
lymphomas (2) 2
medical microbiology (2) 2
molecular genetics (2) 2
mutation, missense (2) 2
neutropenia (2) 2
neutrophils - metabolism (2) 2
original paper (2) 2
physiological aspects (2) 2
population (2) 2
proteins (2) 2
severe combined immunodeficiency (2) 2
siblings (2) 2
signal transducer and activator of transcription 3 (2) 2
spectrum (2) 2
stat3 (2) 2
stem cell transplantation (2) 2
stem cells (2) 2
survival (2) 2
t cells (2) 2
thrombosis (2) 2
[ sdv ] life sciences [q-bio] (1) 1
[sdv.imm]life sciences [q-bio]/immunology (1) 1
[sdv]life sciences [q-bio] (1) 1
abatacept (1) 1
activation (1) 1
activation-induced cytidine deaminase gene (1) 1
acute lymphoblastic-leukemia (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


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, 2014, Volume 133, Issue 5, pp. 1410 - 1419.e13
Background Recurrent bacterial and fungal infections, eczema, and increased serum IgE levels characterize patients with the hyper-IgE syndrome (HIES). Known... 
Allergy and Immunology | glycosylation | Hyper-IgE syndrome | signal transducer and activator of transcription 3 | phosphoglucomutase 3 | Staphylococcus aureus | dedicator of cytokinesis 8 | DESIGN | DOCK8 | STAT3 | IMMUNOLOGY | IDENTIFICATION | DEFICIENCY | PROBES | ALLERGY | CLONING | CONGENITAL DISORDERS | MUTASE | Job Syndrome - immunology | Cell Proliferation | Job Syndrome - genetics | T-Lymphocytes - enzymology | Humans | Genetic Diseases, Inborn - genetics | Immunoglobulin E | Infant | Male | Mutation, Missense | Job Syndrome - enzymology | Adult | Female | Child | Tunisia | Genetic Linkage | Phosphoglucomutase - metabolism | Genetic Diseases, Inborn - immunology | Glycosylation | Chromosomes, Human, Pair 6 - genetics | Homozygote | Chromosomes, Human, Pair 6 - metabolism | Genetic Diseases, Inborn - enzymology | T-Lymphocytes - immunology | Phosphoglucomutase - immunology | Immunity - genetics | Phosphoglucomutase - genetics | Amino Acid Substitution | Enzymes | Polysaccharides | Molecular genetics | Stem cells | Physiological aspects | Mycoses | Genetic aspects | Cellular signal transduction | Disease susceptibility | Genetic transcription | Proteins | Signal transduction | Cell growth | Polypeptides | Disease | Values | Mutation | Tetanus | Kinases | Chromosomes | T-Lymphocytes | Genetic Diseases, Inborn | Chromosomes, Human, Pair 6 | Immunity | Phosphoglucomutase | Life Sciences | Immunology | Job Syndrome | PGM3 | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Immunologi inom det medicinska området | Immunology in the medical area
Journal Article
Heart, Lung and Circulation, ISSN 1443-9506, 2013, Volume 23, Issue 3, pp. e80 - e83
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 132, Issue 5, pp. 1156 - 1163.e5
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
International Archives of Allergy and Immunology, ISSN 1018-2438, 10/2006, Volume 141, Issue 3, pp. 213 - 216
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
by Farmer, Jocelyn R and Foldvari, Zsofia and Ujhazi, Boglarka and De Ravin, Suk See and Chen, Karin and Bleesing, Jack J.H and Schuetz, Catharina and Al-Herz, Waleed and Abraham, Roshini S and Joshi, Avni Y and Costa-Carvalho, Beatriz T and Buchbinder, David and Booth, Claire and Reiff, Andreas and Ferguson, Polly J and Aghamohammadi, Asghar and Abolhassani, Hassan and Puck, Jennifer M and Adeli, Mehdi and Cancrini, Caterina and Palma, Paolo and Bertaina, Alice and Locatelli, Franco and Di Matteo, Gigliola and Geha, Raif S and Kanariou, Maria G and Lycopoulou, Lilia and Tzanoudaki, Marianna and Sleasman, John W and Parikh, Suhag and Pinero, Gloria and Fischer, Bernard M and Dbaibo, Ghassan and Unal, Ekrem and Patiroglu, Turkan and Karakukcu, Musa and Al-Saad, Khulood Khalifa and Dilley, Meredith A and Pai, Sung-Yun and Dutmer, Cullen M and Gelfand, Erwin W and Geier, Christoph B and Eibl, Martha M and Wolf, Hermann M and Henderson, Lauren A and Hazen, Melissa M and Bonfim, Carmem and Wolska-Kuśnierz, Beata and Butte, Manish J and Hernandez, Joseph D and Nicholas, Sarah K and Stepensky, Polina and Chandrakasan, Shanmuganathan and Miano, Maurizio and Westermann-Clark, Emma and Goda, Vera and Kriván, Gergely and Holland, Steven M and Fadugba, Olajumoke and Henrickson, Sarah E and Ozen, Ahmet and Karakoc-Aydiner, Elif and Baris, Safa and Kiykim, Ayca and Bredius, Robbert and Hoeger, Birgit and Boztug, Kaan and Pashchenko, Olga and Neven, Benedicte and Moshous, Despina and Villartay, Jean-Pierre de and Bousfiha, Ahmed Aziz and Hill, Harry R and Notarangelo, Luigi D and Walter, Jolan E
The Journal of Allergy and Clinical Immunology: In Practice, ISSN 2213-2198, 07/2019, Volume 7, Issue 6, pp. 1970 - 1985.e4
Journal Article
Journal Article
Blood Cells, Molecules and Diseases, ISSN 1079-9796, 2012, Volume 48, Issue 1, pp. 53 - 61
Journal Article