X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (40) 40
immunology (31) 31
index medicus (30) 30
male (28) 28
child (26) 26
female (19) 19
adolescent (17) 17
child, preschool (14) 14
infant (14) 14
immunodeficiency (12) 12
allergy (11) 11
mutation (11) 11
adult (10) 10
lymphocytes (10) 10
pediatrics (10) 10
mutations (9) 9
primary immunodeficiency (9) 9
abridged index medicus (8) 8
children (8) 8
infections (8) 8
infectious diseases (8) 8
middle aged (8) 8
diagnosis (7) 7
allergy and immunology (6) 6
article (6) 6
autoimmunity (6) 6
biomedicine (6) 6
disease (6) 6
genetic aspects (6) 6
greece (6) 6
immunoglobulins (6) 6
internal medicine (6) 6
medical microbiology (6) 6
aged (5) 5
analysis (5) 5
autoantibodies (5) 5
cd56 (5) 5
common variable immunodeficiency (5) 5
degranulation (5) 5
epidemiology (5) 5
gene (5) 5
genetics & heredity (5) 5
hematopoietic stem cell transplantation (5) 5
immunologic deficiency syndromes - immunology (5) 5
interferon-γ (5) 5
mortality (5) 5
natural killer cells (5) 5
non-homologous end joining (5) 5
phenotype (5) 5
recombinase-activating genes (5) 5
young adult (5) 5
antigens (4) 4
chemical and pharmacologic phenomena (4) 4
cytokines (4) 4
expression (4) 4
hematology (4) 4
immunologic deficiency syndromes - genetics (4) 4
immunologic deficiency syndromes - therapy (4) 4
infant, newborn (4) 4
infants (4) 4
medical colleges (4) 4
physiological aspects (4) 4
prevalence (4) 4
proteins (4) 4
registries (4) 4
risk factors (4) 4
time factors (4) 4
wiskott-aldrich syndrome (4) 4
age (3) 3
aged, 80 and over (3) 3
antibodies (3) 3
atopy (3) 3
autoimmune diseases - immunology (3) 3
b-lymphocytes - immunology (3) 3
chronic granulomatous-disease (3) 3
classification (3) 3
clinical-features (3) 3
diabetes mellitus, type 1 - complications (3) 3
diabetes mellitus, type 1 - immunology (3) 3
diseases (3) 3
dna mutational analysis (3) 3
europe (3) 3
family (3) 3
flow cytometry (3) 3
follow-up studies (3) 3
gene mutations (3) 3
gene-therapy (3) 3
genes (3) 3
genetic predisposition to disease (3) 3
genotype & phenotype (3) 3
health aspects (3) 3
immune dysregulation (3) 3
immune system (3) 3
immunoglobulin g (3) 3
immunoglobulin g - blood (3) 3
immunologic deficiency syndromes - diagnosis (3) 3
immunologic deficiency syndromes - epidemiology (3) 3
infection - immunology (3) 3
medicine, research & experimental (3) 3
multivariate analysis (3) 3
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 5, pp. 1401 - 1404.e3
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 137, Issue 1, pp. 223 - 230
Journal Article
Nature Medicine, ISSN 1078-8956, 12/2014, Volume 20, Issue 12, pp. 1410 - 1416
The protein cytotoxic T lymphocyte antigen-4 (CTLA-4) is an essential negative regulator of immune responses, and its loss causes fatal autoimmunity in mice.... 
PATHWAYS | MEDICINE, RESEARCH & EXPERIMENTAL | CLINICAL-PICTURE | HOMEOSTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | AUTOIMMUNITY | REGULATORY T-CELLS | GERMLINE MUTATIONS | MICE | BLOCKADE | IMMUNODEFICIENCY | ABATACEPT | Recurrence | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Purpura, Thrombocytopenic, Idiopathic - genetics | Exons | Immune System Diseases - genetics | Humans | Middle Aged | Male | Anemia, Hemolytic, Autoimmune - genetics | Mutation, Missense | Respiratory Tract Infections - genetics | T-Lymphocytes, Regulatory - immunology | Autoimmune Diseases - genetics | Young Adult | Purpura, Thrombocytopenic, Idiopathic - immunology | Adult | Female | Endocytosis - genetics | Polyendocrinopathies, Autoimmune - genetics | Child | Endocytosis - immunology | Granuloma - genetics | Autoimmune Diseases - immunology | CTLA-4 Antigen - genetics | B7-1 Antigen - metabolism | Codon, Nonsense | CTLA-4 Antigen - immunology | Syndrome | Polyendocrinopathies, Autoimmune - immunology | Lung Diseases, Interstitial - immunology | Animals | B-Lymphocytes - immunology | Lung Diseases, Interstitial - genetics | Pedigree | Anemia, Hemolytic, Autoimmune - immunology | Adolescent | Respiratory Tract Infections - immunology | Granuloma - immunology | Heterozygote | Mice | Antigens | Gene mutations | Physiological aspects | Genetic aspects | Immunologic diseases | Research | Risk factors | Proteins | Homeostasis | Cytotoxicity | Ligands | T cell receptors | Mutation | Immune system
Journal Article
by de la Morena, M. Teresa, MD and Leonard, David, PhD and Torgerson, Troy R., MD, PhD and Cabral-Marques, Otavio, PhD and Slatter, Mary, MD and Aghamohammadi, Asghar, MD and Chandra, Sharat, MD and Murguia-Favela, Luis, MD and Bonilla, Francisco A., MD, PhD and Kanariou, Maria, MD and Damrongwatanasuk, Rongras, MD and Kuo, Caroline Y., MD and Dvorak, Christopher C., MD and Meyts, Isabelle, MD and Chen, Karin, MD and Kobrynski, Lisa, MD, MPH and Kapoor, Neena, MD and Richter, Darko, MD and DiGiovanni, Daniela, MD and Dhalla, Fatima, MD and Farmaki, Evangelia, MD and Speckmann, Carsten, MD and Español, Teresa, MD and Shcherbina, Anna, MD and Hanson, Imelda Celine, MD and Litzman, Jiri, MD and Routes, John M., MD and Wong, Melanie, MD, PhD and Fuleihan, Ramsay, MD and Seneviratne, Suranjith L., MD and Small, Trudy N., MD and Janda, Ales, MD and Bezrodnik, Liliana, MD and Seger, Reinhard, MD and Raccio, Andrea Gomez, MD and Edgar, J. David M., MD and Chou, Janet, MD and Abbott, Jordan K., MD and van Montfrans, Joris, MD and González-Granado, Luis Ignacio, MD and Bunin, Nancy, MD and Kutukculer, Necil, MD and Gray, Paul, MD and Seminario, Gisela, MD and Pasic, Srdjan, MD and Aquino, Victor, MD and Wysocki, Christian, MD, PhD and Abolhassani, Hassan, MD and Dorsey, Morna, MD and Cunningham-Rundles, Charlotte, MD, PhD and Knutsen, Alan P., MD and Sleasman, John, MD and Costa Carvalho, Beatriz Tavares, MD and Condino-Neto, Antonio, MD and Grunebaum, Eyal, MD and Chapel, Helen, MD and Ochs, Hans D., MD, PhD and Filipovich, Alexandra, MD and Cowan, Mort, MD and Gennery, Andrew, MD and Cant, Andrew, MD and Notarangelo, Luigi D., MD and Roifman, Chaim M., MD
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 139, Issue 4, pp. 1282 - 1292
Background X-linked hyper-IgM syndrome (XHIGM) is a primary immunodeficiency with high morbidity and mortality compared with those seen in healthy subjects.... 
Allergy and Immunology | hematopoietic cell transplantation | CD40 ligand | primary immunodeficiency | defects in class-switch recombination | long-term outcomes | X-linked hyper-IgM syndrome | Karnofsky/Lansky scores | CD40 LIGAND DEFICIENCY | BONE-MARROW-TRANSPLANTATION | CHRONIC GRANULOMATOUS-DISEASE | WISKOTT-ALDRICH-SYNDROME | CLINICAL-FEATURES | IMMUNOLOGY | CHILDREN | DEFECTIVE EXPRESSION | PRIMARY IMMUNODEFICIENCY DISEASES | ALLERGY | EUROPEAN EXPERIENCE | T-CELLS | Hyper-IgM Immunodeficiency Syndrome - therapy | Follow-Up Studies | Humans | Middle Aged | Kaplan-Meier Estimate | Proportional Hazards Models | Child, Preschool | Infant | Male | Time | Hematopoietic Stem Cell Transplantation - mortality | Young Adult | Hyper-IgM Immunodeficiency Syndrome - mortality | Adolescent | Adult | Female | Retrospective Studies | Child | Cohort Studies | Transplantation | Hematopoietic stem cells | Analysis | Therapy | Disease | Liver | Central nervous system | Nervous system | Antiinfectives and antibacterials | Blood | Risk factors | Antibody response | Neurodegeneration | Bone marrow | Genetics | Diagnosis | Conditioning | Neutropenia | Binding | Wiskott-Aldrich syndrome | Immunoglobulins | Liver diseases | Mortality | Agammaglobulinemia | BCG | Cholangitis | Hazards | Regression analysis | Survival | Bile duct | Studies | Stem cells | Accident prevention | Ligands | Mutation | Protocol (computers) | Bile | Immunoglobulin M | Pneumonia | Transplants & implants | Physicians | Immunoglobulin G | Medical services | Prophylaxis | Infections | Malignancy | Defects | Respiratory tract | Allografts | Bacteria | Children | Age | Medical personnel | Bacterial infections | Complications | Blood cells | Hypersensitivity | Switching | Morbidity | Computer programs | Lymphocytes B | Aplasia | Collaboration | Medical prognosis | Health hazards | Cancer | Lansky scores | Karnofsky
Journal Article
by Gathmann, B and Binder, N and Ehl, S and Kindle, G and Mahlaoui, Nizar and Devergnes, Nathalie and Brosselin, Pauline and Sanal, Özden and Yegin, Olcay and Kütükcüler, Necil and Kilic, Sara Sebnem and Barlan, Isil B and Reisli, Ismail and Caracseghi, Fabiola and Santos, Juan Luis and Llobet, Pilar and Carbone, Javier and Gonzalez, Luis Ignacio Granado and Sanchez-Ramon, Silvia and Tricas, Lourdes and Matamoros, Nuria and Exley, Andrew and Kumararatne, Dinakantha and Allwood, Zoe and Grimbacher, Bodo and Longhurst, Hilary and Knerr, Viviane and Bangs, Catherine and Boardman, Barbara and Tierney, Patricia and Chapel, Helen and Notarangelo, Luigi D and Plebani, Alessandro and Pignata, Claudio and Nickel, Renate and Schauer, Uwe and Späth, Brigitta and Kaiser, Petra and Roesler, Joachim and Bienemann, Kirsten and Linde, Richard and Schubert, Ralf and El-Helou, Sabine and Ritterbusch, Henrike and Goldacker, Sigune and Schaefer, Marzena and Baumann, Ulrich and Witte, Torsten and Dückers, Gregor and Fabhauer, Maria and Borte, Michael and Notheis, Gundula and Belohradsky, Bernd H and Sollinger, Franz and Classen, Carl Friedrich and Apel, Katrin and Steinmann, Sandra and Müglich, Carmen and Szaflarska, Anna and Bernatowska, Ewa and Heropolitanska, Edyta and Kuijpers, Taco W and van Beem, Rachel and Galal, Nermeen Mouftah and Reda, Shereen and Farber, Claire-Michele and Meyts, Isabelle and Velbri, Sirje and Kanariou, Maria and Farmaki, Evangelia and Papadopoulou-Alataki, Efimia and Trachana, Maria and Richter, Darko and Blaziene, Audra and Seidel, Markus and Marques, Laura and Feighery, Conleth and Cucuruz, Maria and Konoplyannikova, Julia and Paschenko, Olga and Shcherbina, Anna and Berglöf, Anna and Jardefors, Helene and Wagström, Per and Brodszki, Nicholas and Cantoni, Nathan and Duppenthaler, Andrea and Fahrni, Gaby and Hoernes, Miriam and Sahrbacher, Ulrike and Pasic, Srdjan and Ciznar, Peter and Jeverica, Anja Koren and Litzman, Jiri and Hlavackova, Eva and Savchak, Ihor and Farkas, Henriette and Marodi, Laszlo and ESID Registry Working Party
Clinical and Experimental Immunology, ISSN 0009-9104, 03/2012, Volume 167, Issue 3, pp. 479 - 491
Journal Article
Nature Immunology, ISSN 1529-2908, 06/2012, Volume 13, Issue 6, pp. 612 - 620
Journal Article
Journal Article
Molecular Genetics and Metabolism Reports, ISSN 2214-4269, 09/2019, Volume 20, p. 100477
Lysosomal Storage Diseases (LSDs) are rare genetic diseases, the majority of which are caused by specific lysosomal enzyme deficiencies and all are... 
Autoimmunity | Niemann pick type C disease | Immunoglobulins | Gaucher disease | Sanfilippo B syndrome
Journal Article