Current Opinion in Allergy and Clinical Immunology, ISSN 1528-4050, 12/2017, Volume 17, Issue 6, pp. 431 - 442
PURPOSE OF REVIEWOverview of neuroendocrine neoplasms in the context of their associations with primary and secondary immunodeficiency states. RECENT...
AIDS | primary immunodeficiency diseases | X-linked form of hyper-IgM syndrome | HIV | CD40Ligand gene | neuroendocrine tumors | SYSTEMIC-LUPUS-ERYTHEMATOSUS | MERKEL CELL-CARCINOMA | AUTOIMMUNE GASTRITIS | IMMUNODEFICIENCY-SYNDROME | ENETS CONSENSUS GUIDELINES | ENDOCRINE TUMORS | CHROMOGRANIN-A | IMMUNOLOGY | HYPER-IGM-SYNDROME | ORGAN TRANSPLANT RECIPIENTS | HIV-INFECTION | ALLERGY
AIDS | primary immunodeficiency diseases | X-linked form of hyper-IgM syndrome | HIV | CD40Ligand gene | neuroendocrine tumors | SYSTEMIC-LUPUS-ERYTHEMATOSUS | MERKEL CELL-CARCINOMA | AUTOIMMUNE GASTRITIS | IMMUNODEFICIENCY-SYNDROME | ENETS CONSENSUS GUIDELINES | ENDOCRINE TUMORS | CHROMOGRANIN-A | IMMUNOLOGY | HYPER-IGM-SYNDROME | ORGAN TRANSPLANT RECIPIENTS | HIV-INFECTION | ALLERGY
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 137, Issue 2, pp. AB17 - AB17
 Lung biopsy demonstrated granulomatous lymphocytic interstitial lung disease with scattered EBER+ cells; lymph node biopsy showed an atypical lymphoid...
Allergy and Immunology | Health aspects | Usage | Children | Biopsy | Lung diseases
Allergy and Immunology | Health aspects | Usage | Children | Biopsy | Lung diseases
Journal Article
Journal of Allergy and Clinical Immunology: In Practice, ISSN 2213-2198, 2015, Volume 4, Issue 1, pp. 38 - 59
 The phenotype is very broad, ranging from only bacterial infections, to progression from a CVID-like condition to severe disease similar to a combined...
Internal Medicine | Allergy and Immunology | INFLAMMATORY-BOWEL-DISEASE | NODULAR REGENERATIVE HYPERPLASIA | B-CELL | ALLERGY | CYSTIC FIBROSIS BRONCHIECTASIS | INTRAVENOUS IMMUNOGLOBULIN | IMMUNOGLOBULIN REPLACEMENT THERAPY | T-CELL-RECEPTOR | ANTIBODY-DEFICIENCY | QUALITY-OF-LIFE | IMMUNOLOGY | SELECTIVE IGA DEFICIENCY | Common Variable Immunodeficiency - immunology | Agammaglobulinemia - immunology | Diagnosis, Differential | Age Factors | Agammaglobulinemia - therapy | Humans | Agammaglobulinemia - diagnosis | Immunophenotyping | International Cooperation | Common Variable Immunodeficiency - diagnosis | Algorithms | B-Lymphocytes - immunology | Common Variable Immunodeficiency - therapy | Expert Testimony | Immunology | Bacterial infections | Laboratories | Committees | Infections | Vaccines | Patients | Age | Asthma
Internal Medicine | Allergy and Immunology | INFLAMMATORY-BOWEL-DISEASE | NODULAR REGENERATIVE HYPERPLASIA | B-CELL | ALLERGY | CYSTIC FIBROSIS BRONCHIECTASIS | INTRAVENOUS IMMUNOGLOBULIN | IMMUNOGLOBULIN REPLACEMENT THERAPY | T-CELL-RECEPTOR | ANTIBODY-DEFICIENCY | QUALITY-OF-LIFE | IMMUNOLOGY | SELECTIVE IGA DEFICIENCY | Common Variable Immunodeficiency - immunology | Agammaglobulinemia - immunology | Diagnosis, Differential | Age Factors | Agammaglobulinemia - therapy | Humans | Agammaglobulinemia - diagnosis | Immunophenotyping | International Cooperation | Common Variable Immunodeficiency - diagnosis | Algorithms | B-Lymphocytes - immunology | Common Variable Immunodeficiency - therapy | Expert Testimony | Immunology | Bacterial infections | Laboratories | Committees | Infections | Vaccines | Patients | Age | Asthma
Journal Article
Journal of Pediatrics, ISSN 0022-3476, 05/2012, Volume 160, Issue 5, p. 756
Journal Article
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 | Immunology | Multicenter Study | Immunology and Allergy | Journal Article | Observational Study | 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) | 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
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 | Immunology | Multicenter Study | Immunology and Allergy | Journal Article | Observational Study | 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) | 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
The Journal of Pediatrics, ISSN 0022-3476, 05/2012, Volume 160, Issue 5, pp. 756 - 756
Journal Article
Journal of Allergy and Clinical Immunology: In Practice, ISSN 2213-2198, 2016, Volume 4, Issue 6, pp. 1023 - 1036
The primary immunodeficiency (PID) diseases comprise a heterogeneous group of inherited disorders of immune function. Technical advancements in whole-genome,...
Internal Medicine | Allergy and Immunology | Hyper-IgM syndrome | Class switch recombination defects | XHIGM | HIGM | CD40 LIGAND DEFICIENCY | 3-KINASE DELTA SYNDROME | IMMUNOGLOBULIN CLASS-SWITCH | NIJMEGEN BREAKAGE SYNDROME | BONE-MARROW-TRANSPLANTATION | IMMUNOLOGY | ALLERGY | X-LINKED IMMUNODEFICIENCY | CHRONIC LYMPHOCYTIC-LEUKEMIA | CLASS-SWITCH RECOMBINATION | STEM-CELL TRANSPLANTATION | AUTOSOMAL RECESSIVE FORM | Hyper-IgM Immunodeficiency Syndrome - genetics | Phenotype | Immunoglobulin G - immunology | Immunoglobulin Class Switching | Humans | Hyper-IgM Immunodeficiency Syndrome - immunology | Disease | Laboratories | Microcephaly | Defects | Copyright | Genotype & phenotype | Immunology | Ataxia | Accreditation | Chronic obstructive pulmonary disease | Deoxyribonucleic acid--DNA | Gastroesophageal reflux | Antigens | Cytomegalovirus | Immunoglobulins | Bacterial infections | Staphylococcus infections | Health education | Allergies | Asthma | Studies | Inflammatory bowel disease | Algorithms | Ulcers | Genetic testing
Internal Medicine | Allergy and Immunology | Hyper-IgM syndrome | Class switch recombination defects | XHIGM | HIGM | CD40 LIGAND DEFICIENCY | 3-KINASE DELTA SYNDROME | IMMUNOGLOBULIN CLASS-SWITCH | NIJMEGEN BREAKAGE SYNDROME | BONE-MARROW-TRANSPLANTATION | IMMUNOLOGY | ALLERGY | X-LINKED IMMUNODEFICIENCY | CHRONIC LYMPHOCYTIC-LEUKEMIA | CLASS-SWITCH RECOMBINATION | STEM-CELL TRANSPLANTATION | AUTOSOMAL RECESSIVE FORM | Hyper-IgM Immunodeficiency Syndrome - genetics | Phenotype | Immunoglobulin G - immunology | Immunoglobulin Class Switching | Humans | Hyper-IgM Immunodeficiency Syndrome - immunology | Disease | Laboratories | Microcephaly | Defects | Copyright | Genotype & phenotype | Immunology | Ataxia | Accreditation | Chronic obstructive pulmonary disease | Deoxyribonucleic acid--DNA | Gastroesophageal reflux | Antigens | Cytomegalovirus | Immunoglobulins | Bacterial infections | Staphylococcus infections | Health education | Allergies | Asthma | Studies | Inflammatory bowel disease | Algorithms | Ulcers | Genetic testing
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 138, Issue 4, pp. 1142 - 1151.e2
Background Primary immunodeficiency diseases (PIDDs) are inherited disorders of the immune system. The most severe form, severe combined immunodeficiency...
Allergy and Immunology | molecular diagnostics | severe combined immunodeficiency newborn screening | Severe combined immunodeficiency | next-generation sequencing | DEFECTS | INFECTIONS | OMENN SYNDROME | IMMUNOLOGY | ALLERGY | DISEASE | ARTEMIS | EXPERIENCE | TBX1 HAPLOINSUFFICIENCY | MUTATIONS | THYMUS TRANSPLANTATION | DELETIONS | Genetic Variation | Pathology, Molecular - trends | Severe Combined Immunodeficiency - genetics | Severe Combined Immunodeficiency - diagnosis | Humans | Adolescent | Female | Male | Pathology, Molecular - standards | Child | Sequence Analysis, DNA | Allergy | Medical colleges | Immunodeficiency | Medical genetics | B cells | T cells | Allergic reaction | Analysis | Genes | Genomics | Mortality | T cell receptors | Mutation | Genetic testing | Kinases | Medical screening | Deoxyribonucleic acid--DNA | Defects
Allergy and Immunology | molecular diagnostics | severe combined immunodeficiency newborn screening | Severe combined immunodeficiency | next-generation sequencing | DEFECTS | INFECTIONS | OMENN SYNDROME | IMMUNOLOGY | ALLERGY | DISEASE | ARTEMIS | EXPERIENCE | TBX1 HAPLOINSUFFICIENCY | MUTATIONS | THYMUS TRANSPLANTATION | DELETIONS | Genetic Variation | Pathology, Molecular - trends | Severe Combined Immunodeficiency - genetics | Severe Combined Immunodeficiency - diagnosis | Humans | Adolescent | Female | Male | Pathology, Molecular - standards | Child | Sequence Analysis, DNA | Allergy | Medical colleges | Immunodeficiency | Medical genetics | B cells | T cells | Allergic reaction | Analysis | Genes | Genomics | Mortality | T cell receptors | Mutation | Genetic testing | Kinases | Medical screening | Deoxyribonucleic acid--DNA | Defects
Journal Article
Journal of Pediatrics, The, ISSN 0022-3476, 2012, Volume 160, Issue 5, pp. 756 - 756
Journal Article
Blood, ISSN 0006-4971, 09/2017, Volume 130, Issue 13, pp. 1553 - 1564
NF-kappa B signaling through its NFKB1-dependent canonical and NFKB2-dependent non-canonical pathways plays distinctive roles in a diverse range of immune...
IMMUNE DYSREGULATION | RESPONSES | TRANSCRIPTIONAL ACTIVITY | ACTIVATION | SIGNALING PATHWAY | NF-KAPPA-B2 | GERMLINE MUTATIONS | STAT1 MUTATIONS | HEMATOLOGY | NF-KAPPA-B | DEFICIENCY | Severe Combined Immunodeficiency - genetics | Phenotype | NF-kappa B p52 Subunit - genetics | Adrenal Insufficiency - genetics | Humans | HEK293 Cells | Common Variable Immunodeficiency - genetics | Ectodermal Dysplasia - genetics | Codon, Nonsense | Mutation, Missense | Growth Hormone - deficiency | 100 | Immunobiology
IMMUNE DYSREGULATION | RESPONSES | TRANSCRIPTIONAL ACTIVITY | ACTIVATION | SIGNALING PATHWAY | NF-KAPPA-B2 | GERMLINE MUTATIONS | STAT1 MUTATIONS | HEMATOLOGY | NF-KAPPA-B | DEFICIENCY | Severe Combined Immunodeficiency - genetics | Phenotype | NF-kappa B p52 Subunit - genetics | Adrenal Insufficiency - genetics | Humans | HEK293 Cells | Common Variable Immunodeficiency - genetics | Ectodermal Dysplasia - genetics | Codon, Nonsense | Mutation, Missense | Growth Hormone - deficiency | 100 | Immunobiology
Journal Article