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Sullivan, Kathleen
One or more keywords matched the following items that are connected to Sullivan, Kathleen
Item TypeName
Academic Article Lack of Clinical Hypersensitivity to Penicillin Antibiotics in Common Variable Immunodeficiency.
Concept Allergy and Immunology
Concept Drug Hypersensitivity
Concept Food Hypersensitivity
Concept Hypersensitivity
Concept Hypersensitivity, Immediate
Academic Article The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.
Academic Article Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
Academic Article X-linked lymphoproliferative syndrome: an X-cellent question.
Academic Article DiGeorge syndrome/velocardiofacial syndrome: the chromosome 22q11.2 deletion syndrome.
Academic Article Allogeneic hematopoietic cell transplantation for primary immune deficiency diseases: current status and critical needs.
Academic Article Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
Academic Article Pediatric common variable immunodeficiency: immunologic and phenotypic associations with switched memory B cells.
Academic Article Myeloid differentiation primary response gene 88 (MyD88) deficiency in a large kindred.
Academic Article Genome-wide association identifies diverse causes of common variable immunodeficiency.
Academic Article Novel mutation in STXBP2 prevents IL-2-induced natural killer cell cytotoxicity.
Academic Article Primary Immune Deficiency Treatment Consortium (PIDTC) report.
Academic Article The diverse clinical features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome).
Academic Article Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency.
Academic Article Multicenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency.
Academic Article Rare variants at 16p11.2 are associated with common variable immunodeficiency.
Academic Article Health care utilization by patients with common variable immune deficiency defined by International Classification of Diseases, Ninth Revision code 279.06.
Academic Article The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies.
Academic Article Enteroviruses in X-Linked Agammaglobulinemia: Update on Epidemiology and Therapy.
Academic Article Rubella persistence in epidermal keratinocytes and granuloma M2 macrophages in patients with primary immunodeficiencies.
Academic Article Successful unrelated cord blood transplant for complete IFN-? receptor 2 deficiency.
Academic Article C3 nephritic factors: A?changing landscape.
Academic Article Frequency of untreated hypogammaglobulinemia in bronchiectasis.
Academic Article Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations.
Academic Article Inflammatory Bowel Disease in Primary Immunodeficiencies.
Academic Article T-cell lymphopenia in 22q11.2 deletion syndrome: Relationship to cardiac disease.
Academic Article The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
Academic Article International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity.
Academic Article EMSY is increased and activates TSLP & CCL5 expression in eosinophilic esophagitis.
Academic Article Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responses.
Academic Article Cancer in primary immunodeficiency diseases: Cancer incidence in the United States Immune Deficiency Network Registry.
Academic Article Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry.
Academic Article Mevalonate kinase deficiency presenting as recurrent rectal abscesses and perianal fistulae.
Academic Article Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects.
Academic Article Very early-onset inflammatory bowel disease: an integrated approach.
Academic Article Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease.
Academic Article American Academy of Allergy, Asthma and Immunology response to the EAACI/GA2 LEN/EDF/WAO guideline for the definition, classification, diagnosis, and management of Urticaria 2017 revision.
Academic Article Allogeneic hematopoietic stem cell transplantation in adolescent patients with chronic granulomatous disease.
Academic Article Chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.
Academic Article Toll-like receptor 2 stimulation augments esophageal barrier integrity.
Academic Article Immune Biomarkers of Autoimmunity in Chromosome 22q11.2 Deletion Syndrome.
Academic Article Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A?working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology.
Academic Article Neutropenia as a sign of immunodeficiency.
Academic Article Early-Onset Inflammatory Bowel Disease.
Academic Article Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study.
Academic Article X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world.
Academic Article Common variable immunodeficiency-associated endotoxemia promotes early commitment to the T follicular lineage.
Academic Article Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.
Academic Article The scary world of variants of uncertain significance (VUS): A?hitchhiker's guide to interpretation.
Academic Article Coronavirus disease 2019 in patients with inborn errors of immunity: An international study.
Academic Article Rubella virus-associated chronic inflammation in primary immunodeficiency diseases.
Academic Article Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management.
Academic Article Immune Dysregulation in Human ITCH Deficiency Successfully Treated with Hematopoietic Cell Transplantation.
Academic Article Therapeutic options for CTLA-4 insufficiency.
Academic Article Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases.
Academic Article The relevance of primary immunodeficiency registries on a global perspective.
Academic Article ?????: Power, life force, and purpose in mentoring.
Academic Article The diagnosis of severe combined immunodeficiency: Implementation of the PIDTC 2022 Definitions.
Academic Article Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.
Academic Article Ocular Manifestations in Primary Immunodeficiency Disorders: A Report From the United States Immunodeficiency Network (USIDNET) Registry.
Academic Article The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity.
Academic Article Chronic Granulomatous Disease With Inflammatory Bowel Disease: Clinical Presentation, Treatment, and Outcomes From the USIDNET Registry.
Academic Article Risk Factors of Pneumonia in Primary Antibody Deficiency Patients Receiving Immunoglobulin Therapy: Data from the US Immunodeficiency Network (USIDNET).
Academic Article The lung in inborn errors of immunity: From clinical disease patterns to molecular pathogenesis.
Academic Article Morbidity, Mortality, and Therapeutics in Combined Immunodeficiency: Data From the USIDNET Registry.
Academic Article Outcomes among racial and ethnic minority groups with X-linked agammaglobulinemia from the USIDNET registry.
Academic Article Delayed post-COVID-19 hemophagocytic lymphohistiocytosis in patient with XIAP deficiency.
Academic Article Difficult Cases in Primary Immunodeficiency.
Academic Article Surveillance for rubella virus in samples obtained from non-immunodeficient individuals.
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