X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (36) 36
male (26) 26
child (24) 24
index medicus (24) 24
female (23) 23
child, preschool (21) 21
immunology (19) 19
adolescent (17) 17
infant (16) 16
abridged index medicus (15) 15
allergy and immunology (15) 15
mutation (15) 15
adult (14) 14
allergy (13) 13
pediatrics (13) 13
immunodeficiency (12) 12
patients (8) 8
age (7) 7
hematology (7) 7
infections (7) 7
mutations (7) 7
pneumonia (7) 7
proteins (7) 7
article (6) 6
immunoglobulin e (6) 6
middle aged (6) 6
transplantation (6) 6
young adult (6) 6
children (5) 5
expression (5) 5
hyper-ige syndrome (5) 5
immune system (5) 5
pedigree (5) 5
analysis (4) 4
bacterial infections (4) 4
cohort studies (4) 4
deficiency (4) 4
dock8 deficiency (4) 4
health aspects (4) 4
immunologic deficiency syndromes - immunology (4) 4
infant, newborn (4) 4
job syndrome - genetics (4) 4
job syndrome - immunology (4) 4
medical colleges (4) 4
mortality (4) 4
phenotype (4) 4
retrospective studies (4) 4
risk factors (4) 4
stat3 transcription factor - genetics (4) 4
stem cells (4) 4
transplants & implants (4) 4
viral infections (4) 4
aged (3) 3
autoimmunity (3) 3
b-lymphocytes - immunology (3) 3
bacterial pneumonia (3) 3
care and treatment (3) 3
case-control studies (3) 3
cells, cultured (3) 3
chronic granulomatous disease (3) 3
common variable immunodeficiency (3) 3
cytotoxicity (3) 3
deoxyribonucleic acid--dna (3) 3
diagnosis (3) 3
diseases (3) 3
dna mutational analysis (3) 3
eczema (3) 3
flow cytometry (3) 3
genetic aspects (3) 3
genotype (3) 3
germany (3) 3
guanine nucleotide exchange factors - deficiency (3) 3
hematopoietic stem cell transplantation (3) 3
heterozygote (3) 3
hospitalization (3) 3
hospitalization - statistics & numerical data (3) 3
immunization (3) 3
immunoglobulins (3) 3
immunoglobulins, intravenous - therapeutic use (3) 3
immunologic deficiency syndromes - genetics (3) 3
immunologic deficiency syndromes - therapy (3) 3
incidence (3) 3
infection (3) 3
job syndrome - diagnosis (3) 3
logistic models (3) 3
medical research (3) 3
medicine, experimental (3) 3
siblings (3) 3
signal transduction (3) 3
t cells (3) 3
t-cells (3) 3
teenagers (3) 3
actin (2) 2
activation (2) 2
agammaglobulinemia - genetics (2) 2
age of onset (2) 2
allergies (2) 2
amelogenesis imperfecta (2) 2
amino acid substitution (2) 2
anhydrotic ectodermal dysplasia (2) 2
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, 2014, Volume 134, Issue 1, pp. 116 - 126.e11
Background Common variable immunodeficiency (CVID) is an antibody deficiency with an equal sex distribution and a high variability in clinical presentation.... 
Allergy and Immunology | patient self-reported outcomes | treatment | Common variable immunodeficiency | primary antibody deficiency | autoimmunity | enteropathy | immunoglobulin replacement | quality of life | lymphadenopathy | granulomas | INFECTIONS | PHENOTYPES | IMMUNOLOGY | DEFICIENCY | IGM | TRIAL | B-CELL | ALLERGY | HYPOGAMMAGLOBULINEMIA | INTRAVENOUS IMMUNOGLOBULIN | DISEASE | Autoimmunity | Common Variable Immunodeficiency - immunology | Common Variable Immunodeficiency - drug therapy | Humans | Child, Preschool | Lymphoproliferative Disorders - complications | Male | Lymphoproliferative Disorders - immunology | Splenomegaly - pathology | Bronchiectasis - pathology | Common Variable Immunodeficiency - mortality | Pneumonia - mortality | Pneumonia - immunology | Adult | Female | Retrospective Studies | Child | Europe | Delayed Diagnosis | Common Variable Immunodeficiency - complications | Lymphoproliferative Disorders - mortality | Pneumonia - drug therapy | Immunoglobulins, Intravenous - therapeutic use | Adolescent | Age of Onset | Survival Analysis | Pneumonia - complications | Lymphoproliferative Disorders - drug therapy | Immunological deficiency syndromes | Care and treatment | Health aspects | Respiratory tract diseases | Studies | Pneumonia | Meningitis | Lymphomas | Multivariate analysis | Patients | Age | Data bases
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 137, Issue 1, pp. 223 - 230
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2009, Volume 124, Issue 6, pp. 1311 - 1318.e7
Background Defects in the development or activation of T cells result in immunodeficiency associated with severe infections early in life. T-cell activation... 
Allergy and Immunology | calcium channel | store-operated Ca | signal transduction | anhydrotic ectodermal dysplasia | T cells | CRAC | amelogenesis imperfecta | dental enamel | entry | STIM1 | ORAI1 | immunodeficiency | congenital myopathy | ACTIVATED CALCIUM-CHANNELS | IMMUNE-DEFICIENCY | IMMUNOLOGY | T-CELL IMMUNODEFICIENCY | MICE LACKING | SKELETAL-MUSCLE | INFLUX | ALLERGY | Ca2 | store-operated Ca2+ entry | MUTATION | PORE SUBUNIT | CRAC CHANNEL | Immunologic Deficiency Syndromes - pathology | Cell Adhesion Molecules - genetics | Frameshift Mutation | Calcium Channels - metabolism | Calcium - metabolism | Humans | Mutation, Missense | Neoplasm Proteins - metabolism | Ectodermal Dysplasia - metabolism | Transfection | Ectodermal Dysplasia - pathology | Membrane Proteins - metabolism | Neoplasm Proteins - genetics | Calcium Channels - genetics | Stromal Interaction Molecule 1 | ORAI2 Protein | Membrane Proteins - genetics | Muscular Diseases - metabolism | Stromal Interaction Molecule 2 | Muscular Diseases - pathology | Cell Adhesion Molecules - metabolism | ORAI1 Protein | Homozygote | Immunologic Deficiency Syndromes - genetics | Immunologic Deficiency Syndromes - metabolism | Ectodermal Dysplasia - genetics | Muscular Diseases - genetics | Calcium Channels - deficiency | Proteins | Cytomegalovirus | Cell growth | Plasmids | Lymphocytes | Cloning | Protein expression | Mutation | Gene expression | Patients | Age | Deoxyribonucleic acid--DNA
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 131, Issue 3, pp. 840 - 848
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2010, Volume 126, Issue 3, pp. 611 - 617.e1
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2009, Volume 124, Issue 3, pp. 536 - 543
Background Mutations in serine protease inhibitor Kazal-type 5 ( SPINK5 ), encoding the serine protease inhibitor lympho-epithelial Kazal-type 5 related... 
Allergy and Immunology | immune deficiency | NK-cell cytotoxicity | Comèl-Netherton syndrome | bamboo hair | SPINK5 | LEKTI | IVIG | selective antibody deficiency | ichthyosis | atopic diathesis | WISKOTT-ALDRICH-SYNDROME | IGM SYNDROME | ERYTHRODERMA | PERIPHERAL-BLOOD | IMMUNOLOGY | MEMORY B-CELLS | NK CELLS | ALLERGY | Comel-Netherton syndrome | MUTATIONS | ANTIBODY-RESPONSES | EXPRESSION | T-Lymphocytes, Regulatory - metabolism | Humans | Proteinase Inhibitory Proteins, Secretory - genetics | Proteinase Inhibitory Proteins, Secretory - metabolism | Child, Preschool | Male | Serine Peptidase Inhibitor Kazal-Type 5 | Proteinase Inhibitory Proteins, Secretory - biosynthesis | T-Lymphocytes, Regulatory - immunology | Staphylococcal Skin Infections - drug therapy | Natural Killer T-Cells - metabolism | Staphylococcal Skin Infections - immunology | Female | Immunologic Deficiency Syndromes - immunology | Child | B-Lymphocytes - metabolism | Staphylococcus aureus | Cytokines - blood | B-Lymphocytes - immunology | Immunoglobulins, Intravenous - therapeutic use | Immunologic Deficiency Syndromes - genetics | Immunologic Deficiency Syndromes - drug therapy | Mutation | Immunologic Factors - therapeutic use | Natural Killer T-Cells - immunology | Staphylococcal Skin Infections - genetics | Medical colleges | Immunoglobulins | Genetic disorders | Protease inhibitors | Immunodeficiency | Fluorescein | Thrombin | T cells | Food allergies | Pneumonia | Cytokines | Cytotoxicity | Patients | Allergies | Asthma | Lymphocytes | Eczema | Age | Deoxyribonucleic acid--DNA | Immune system | Food | Comèl-Netherton Syndrome | NK cell cytotoxicity
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2017, Volume 141, Issue 1, pp. 322 - 328.e10
Abstract Background Rare DNA breakage-repair disorders predispose to infection and lympho-reticular malignancies. Hematopoietic cell transplantation (HCT) is... 
Allergy and Immunology | Ataxia-Telangiectasia | DNA Ligase 4 deficiency | Nijmegen Breakage syndrome | DNA repair disorders | Hematopoietic stem cell transplantation | Cernunnos-XLF deficiency
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 139, Issue 1, pp. 212 - 219.e3
Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymatic disorder of red blood cells in human subjects, causing hemolytic... 
Allergy and Immunology | Glucose-6-phosphate dehydrogenase deficiency | NADPH | immunodeficiency | innate immunity | neutrophil extracellular trap formation | chronic granulomatous disease | NADPH OXIDASE | CHRONIC NONSPHEROCYTIC ANEMIA | G6PD DEFICIENCY | CHRONIC GRANULOMATOUS-DISEASE | GRANULOCYTE DYSFUNCTION | IMMUNOLOGY | neutrophil extracellular trap forma-tion | HEMOLYTIC-ANEMIA | NEUTROPHIL EXTRACELLULAR TRAPS | DEHYDROGENASE-DEFICIENCY | BACTERICIDAL ACTIVITY | ALLERGY | LEUKOCYTE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE | Leukocyte Elastase - metabolism | Disease Susceptibility | Reactive Oxygen Species - metabolism | Extracellular Traps - metabolism | Humans | Infant | Male | Glucosephosphate Dehydrogenase Deficiency - diagnosis | Bacterial Infections | Erythrocytes - metabolism | Glucosephosphate Dehydrogenase - metabolism | Glucosephosphate Dehydrogenase Deficiency - metabolism | Glucosephosphate Dehydrogenase - genetics | Granulocytes - metabolism | NADP - metabolism | Child | Glucosephosphate Dehydrogenase Deficiency - genetics | Phosphates | Niacinamide | Purines | Enzymes | Anemia | Communicable diseases | Disease susceptibility | Glucose | Health aspects | Dextrose | Oxidases | Analysis | Pneumonia | Dehydrogenases | Neutrophils | African Americans | Staphylococcus infections | Patients | Defects | Streptococcus infections | Proteins | Tonsillitis | Antibiotics | Sepsis | Age | Viral infections
Journal Article
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2008, Volume 122, Issue 1, pp. 181 - 187
Background Hyper-IgE syndrome (HIES) is a rare, autosomal-dominant immunodeficiency characterized by eczema, Staphylococcus aureus skin abscesses, pneumonia... 
Allergy and Immunology
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2012, Volume 130, Issue 6, pp. 1426 - 1428
  To confirm STAT3-HIES, sequencing of the gene STAT3 was performed by using the Sanger technique with genomic DNA (gDNA) extracted from peripheral blood, as... 
Allergy and Immunology | GERM-LINE MOSAICISM | MUTATIONS | IMMUNOLOGY | ALLERGY | Job Syndrome - genetics | Job Syndrome - diagnosis | Humans | Cells, Cultured