Found: 20
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Interleukin-36 Receptor Antagonist Deficiency (DITRA) with a Novel IL36RN Homozygous Mutation c.200G > T (P.Cys67Phe) in a Young Colombian Woman.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Successful Treatment of Sinusitis with Topical Human Milk in a Lymphoma Patient Using Rituximab.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Hemorrhagic Pneumonia as the First Manifestation of Anhidrotic Ectodermal Dysplasia with Immunodeficiency.
- Published in:
- 2019
- By:
- Publication type:
- Letter
A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Interferon-γ Receptor 1 Deficiency Corrected by Umbilical Cord Blood Transplantation.
- Published in:
- 2019
- By:
- Publication type:
- Letter
CAPS and NLRP3.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 277, doi. 10.1007/s10875-019-00638-z
- By:
- Publication type:
- Article
Successful Rituximab Treatment for Lymphoma, Secondary Immunodeficiency Causing Debilitating Sinusitis: Underlying Primary Immunodeficiency Disease, and Alternative Treatments to Improve the Quality of Life?
- Published in:
- 2019
- By:
- Publication type:
- Editorial
A Novel CARMIL2 Mutation Resulting in Combined Immunodeficiency Manifesting with Dermatitis, Fungal, and Viral Skin Infections As Well as Selective Antibody Deficiency.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Altered Peripheral Blood Leucocyte Phenotype and Responses in Healthy Individuals with Homozygous Deletion of FHR1 and FHR3 Genes.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 336, doi. 10.1007/s10875-019-00619-2
- By:
- Publication type:
- Article
RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Granule Cell Neuronopathy in a Patient with Common Variable Immunodeficiency.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Report of a Chinese Cohort with Leukocyte Adhesion Deficiency-I and Four Novel Mutations.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 309, doi. 10.1007/s10875-019-00617-4
- By:
- Publication type:
- Article
Revisiting Fatal Granulomatous Disease of Childhood Through an Autopsy: Still Lethal in the Developing World!
- Published in:
- 2019
- By:
- Publication type:
- Letter
Different Clonal T-Large Granular Lymphocyte Proliferations in SCID.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Clinical Features and HSCT Outcome for SCID in Turkey.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 316, doi. 10.1007/s10875-019-00610-x
- By:
- Publication type:
- Article
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 298, doi. 10.1007/s10875-019-00603-w
- By:
- Publication type:
- Article
Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 324, doi. 10.1007/s10875-019-00602-x
- By:
- Publication type:
- Article
EBV-Related Hodgkin Lymphoma in an ICF2 Patient: Is EBV Susceptibility a Hallmark of This ICF Subtype?
- Published in:
- 2019
- By:
- Publication type:
- Letter
Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 287, doi. 10.1007/s10875-019-0593-4
- By:
- Publication type:
- Article