X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (320) 320
index medicus (244) 244
female (165) 165
male (156) 156
immunology (137) 137
child (112) 112
adolescent (94) 94
child, preschool (93) 93
hematology (72) 72
children (70) 70
adult (69) 69
infant (64) 64
abridged index medicus (63) 63
pediatrics (56) 56
research (56) 56
mutation (51) 51
infectious diseases (50) 50
animals (47) 47
neutrophils (41) 41
activation (38) 38
genetic aspects (35) 35
expression (34) 34
mice (33) 33
risk factors (32) 32
health aspects (31) 31
infection (31) 31
disease (30) 30
infant, newborn (30) 30
neutrophils - immunology (28) 28
cells, cultured (27) 27
kawasaki disease (27) 27
prospective studies (27) 27
young adult (27) 27
analysis (26) 26
magnetic resonance imaging (26) 26
middle aged (26) 26
neutrophils - metabolism (26) 26
case-control studies (25) 25
journal article (25) 25
multidisciplinary sciences (25) 25
phenotype (25) 25
research article (25) 25
cohort studies (24) 24
gene (24) 24
genetics & heredity (24) 24
immunodeficiency (24) 24
patients (24) 24
proteins (24) 24
rheumatoid-arthritis (24) 24
care and treatment (23) 23
genetics (23) 23
genotype (23) 23
infections (23) 23
article (22) 22
genes (22) 22
genetic predisposition to disease (22) 22
inflammation (22) 22
juvenile idiopathic arthritis (22) 22
arthritis (21) 21
blood (21) 21
leukocytes (21) 21
medicine & public health (21) 21
mutations (21) 21
allergy and immunology (20) 20
cell biology (20) 20
cells (20) 20
follow-up studies (20) 20
medical research (20) 20
medicine (20) 20
physiological aspects (20) 20
hiv (19) 19
hiv infections - drug therapy (19) 19
radiology, nuclear medicine & medical imaging (19) 19
rheumatology (19) 19
risk (19) 19
lymphocytes (18) 18
neutrophils - drug effects (18) 18
diagnosis (17) 17
flow cytometry (17) 17
phagocytosis (17) 17
treatment outcome (17) 17
allergy (16) 16
antiretroviral therapy (16) 16
association (16) 16
gene mutations (16) 16
retrospective studies (16) 16
science (16) 16
systemic-lupus-erythematosus (16) 16
cancer (15) 15
colony-stimulating factor (15) 15
complement (15) 15
copy number variation (15) 15
laboratories (15) 15
netherlands (15) 15
receptors (15) 15
receptors, igg - genetics (15) 15
signal transduction (15) 15
susceptibility (15) 15
biology (14) 14
chronic granulomatous disease (14) 14
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Leukocyte Biology, ISSN 0741-5400, 03/2001, Volume 69, Issue 3, pp. 467 - 473
Journal Article
Lancet Infectious Diseases, The, ISSN 1473-3099, 2014, Volume 14, Issue 11, pp. 1083 - 1089
Summary Background Group B streptococcus is the most common cause of neonatal infections. We studied the clinical and molecular epidemiology of invasive group... 
Infectious Disease | UNITED-STATES | INFECTIOUS DISEASES | ONSET NEONATAL SEPSIS | BACTERIAL-MENINGITIS | AGALACTIAE | INFANTS | PREVENTION | CLINICAL-FEATURES | ANTIBIOTIC-PROPHYLAXIS | EPIDEMIOLOGY | YOUNGER | Guidelines as Topic | Escherichia coli Infections - prevention & control | Humans | Netherlands - epidemiology | Streptococcus agalactiae - classification | Infant | Male | Streptococcal Infections - prevention & control | Infection Control - methods | Multilocus Sequence Typing | Incidence | Streptococcus agalactiae - genetics | Streptococcus agalactiae - isolation & purification | Female | Infant, Newborn | Streptococcal Infections - microbiology | Meningitis, Bacterial - microbiology | Sepsis - epidemiology | Escherichia coli Infections - microbiology | Streptococcal Infections - epidemiology | Genotype | Escherichia coli Infections - epidemiology | Epidemiological Monitoring | Molecular Epidemiology | Meningitis, Bacterial - epidemiology | Sepsis - microbiology | Infants (Newborn) | Cross infection | Genetic aspects | Nosocomial infections | Medical research | Medical examination | Escherichia coli | Medicine, Experimental | Meningitis | Epidemiology | Blood | Disease | Laboratories | Drug resistance | Patients | Risk factors | Fever | Streptococcus infections | Studies | Disease prevention | Genotype & phenotype | Surveillance | Antibiotics | E coli | Womens health | Age
Journal Article
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
PLoS ONE, ISSN 1932-6203, 2009, Volume 4, Issue 4, pp. e5234 - e5234
Journal Article
Science, ISSN 0036-8075, 7/2013, Volume 341, Issue 6142, pp. 186 - 191
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2010, Volume 107, Issue 41, pp. 17686 - 17691
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2014, Volume 10, Issue 5
  Mutations affecting the ribosome lead to several diseases known as ribosomopathies, with phenotypes that include growth defects, cytopenia, and bone marrow... 
Phosphorylation | Genes | Cell division | Infections | Kinases | Experiments | Autophagy | Insulin | Defects | Proteins | Microscopy | Rodents | Bone marrow | Insulin resistance | Mutation
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2011, Volume 108, Issue 45, pp. 18342 - 18347
Journal Article
by Tuijnenburg, Paul and Lango Allen, Hana and Burns, Siobhan O and Burns, Siobhan and Greene, Daniel and Jansen, Machiel H and Staples, Emily and Stephens, Jonathan and Carss, Keren J and Carss, Keren and Biasci, Daniele and Baxendale, Helen and Thomas, Moira and Chandra, Anita and Kiani-Alikhan, Sorena and Longhurst, Hilary and Longhurst, Hilary J and Seneviratne, Suranjith and Seneviratne, Suranjith L and Oksenhendler, Eric and Simeoni, Ilenia and de Bree, Godelieve J and Tool, Anton T.J and van Leeuwen, Ester M.M and Ebberink, Eduard H.T.M and Meijer, Alexander B and Tuna, Salih and Whitehorn, Deborah and Brown, Matthew and Turro, Ernest and Thrasher, Adrian and Thrasher, Adrian J and Smith, Kenneth G.C and Thaventhiran, James E and Thaventhiran, James and Kuijpers, Taco W and Kuijpers, Taco and Adhya, Zoe and Alachkar, Hana and Anantharachagan, Ariharan and Antrobus, Richard and Arumugakani, Gururaj and Bacchelli, Chiara and Bethune, Claire and Bibi, Shahnaz and Boardman, Barbara and Booth, Claire and Browning, Michael and Brownlie, Mary and Clifford, Hayley and Cooper, Nichola and Davies, Sophie and Dempster, John and Devlin, Lisa and Doffinger, Rainer and Drewe, Elizabeth and Edgar, David and Egner, William and El-Shanawany, Tariq and Gaspar, Bobby and Ghurye, Rohit and Gilmour, Kimberley and Goddard, Sarah and Gordins, Pavel and Grigoriadou, Sofia and Hackett, Scott and Hague, Rosie and Harper, Lorraine and Hayman, Grant and Herwadkar, Archana and Hughes, Stephen and Huissoon, Aarnoud and Jolles, Stephen and Jones, Julie and Kelleher, Peter and Klein, Nigel and Kumararatne, Dinakantha and Laffan, James and Lear, Sara and Lorenzo, Lorena and Maimaris, Jesmeen and Manson, Ania and McDermott, Elizabeth and Millar, Hazel and Mistry, Anoop and Morrisson, Valerie and Murng, Sai and Nasir, Iman and Nejentsev, Sergey and Noorani, Sadia and Ponsford, Mark and Qasim, Waseem and Quinn, Ellen and Quinti, Isabella and Richter, Alex and Samarghitean, Crina and Sargur, Ravishankar and Savic, Sinisa and Sewall, Carrock and Shackley, Fiona and ... and NIHR BioResource-Rare Dis and NIHR BioResource–Rare Diseases Consortium
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 10/2018, Volume 142, Issue 4, pp. 1285 - 1296
Journal Article