Introduction: Continuing insights into the healthy and diseased immune system through human genetic investigation.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 5, doi. 10.1111/imr.12730
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Works matching IS 01052896 AND DT 2019 AND VI 287 AND IP 1
Results: 19
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Newborn screening for severe combined immunodeficiency and T‐cell lymphopenia.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 241, doi. 10.1111/imr.12729
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3
Common variable immune deficiency: Dissection of the variable.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 145, doi. 10.1111/imr.12728
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4
The clinical and mechanistic intersection of primary atopic disorders and inborn errors of growth and metabolism.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 135, doi. 10.1111/imr.12727
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5
Early‐onset inflammatory bowel disease as a model disease to identify key regulators of immune homeostasis mechanisms.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 162, doi. 10.1111/imr.12726
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6
Emerging insights into human health and NK cell biology from the study of NK cell deficiencies.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 202, doi. 10.1111/imr.12725
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7
Primary immunodeficiencies reveal the essential role of tissue neutrophils in periodontitis.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 226, doi. 10.1111/imr.12724
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8
Insights into immunity from clinical and basic science studies of DOCK8 immunodeficiency syndrome.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 9, doi. 10.1111/imr.12723
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9
Human adenosine deaminase 2 deficiency: A multi‐faceted inborn error of immunity.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 62, doi. 10.1111/imr.12722
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10
What did we learn from CTLA‐4 insufficiency on the human immune system?
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- Immunological Reviews, 2019, v. 287, n. 1, p. 33, doi. 10.1111/imr.12721
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11
FAS and RAS related Apoptosis defects: From autoimmunity to leukemia.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 50, doi. 10.1111/imr.12720
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12
WHIM syndrome: Immunopathogenesis, treatment and cure strategies.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 91, doi. 10.1111/imr.12719
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13
Zero tolerance! A perspective on monogenic disorders with defective regulatory T cells and IBD‐like disease.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 236, doi. 10.1111/imr.12717
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14
Primary immunodeficiencies caused by mutations in actin regulatory proteins.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 121, doi. 10.1111/imr.12716
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15
CHAPLE syndrome uncovers the primary role of complement in a familial form of Waldmann's disease.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 20, doi. 10.1111/imr.12715
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16
Lessons from primary immunodeficiencies: Autoimmune regulator and autoimmune polyendocrinopathy‐candidiasis‐ectodermal dystrophy.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 103, doi. 10.1111/imr.12714
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17
RAG gene defects at the verge of immunodeficiency and immune dysregulation.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 73, doi. 10.1111/imr.12713
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18
Chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.
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- Immunological Reviews, 2019, v. 287, n. 1, p. 186, doi. 10.1111/imr.12701
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19
Issue Information.
- Published in:
- Immunological Reviews, 2019, v. 287, n. 1, p. 1, doi. 10.1111/imr.12673
- Publication type:
- Article