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Journal of Clinical Immunology
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Volume 39, November 2019, Issue 8, Pages 751-860
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1. Editorial, Journal of Clinical Immunology
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Tác giả
Jean-Laurent Casanova, Vincent Bonagura.
2. Survey of Infection Control Precautions for Patients with Severe Combined Immune Deficiency
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Tác giả
Brieanne A. Dergousoff, Joseph V. Vayalumkal.
3. Clinical and Molecular Features of Chronic Granulomatous Disease in Mainland China and a XL-CGD Female Infant Patient After Prenatal Diagnosis
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Tác giả
Shiyu Wang, Tao Wang, Qingqing Xiang, Min Xiao, Yao Cao.
4. Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib
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Tác giả
Tariq Al Shehri, Kimberly Gilmour, Florian Gothe.
5. Quality of Life of Patients with Wiskott Aldrich Syndrome and X-Linked Thrombocytopenia: a Study of the Primary Immune Deficiency Consortium (PIDTC), Immune Deficiency Foundation, and the Wiskott-Aldrich Foundation
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Tác giả
Ami J. Shah, Robert Sokolic, Brent Logan, Ziyan Yin.
6. A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus
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Tác giả
Ruonan Duan, Qi Liu, Jiangxia Li, Xianli Bian.
7. Provider Perceptions of Quality of Life, Neurocognition, Physical Well-being, and Psychosocial Health in Patients with Primary Immunodeficiency/Immune Dysregulation Conditions
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Tác giả
Thomas F. Michniacki, Kelly J. Walkovich, Lauren E. Merz.
8. Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
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Tác giả
Christine Anterasian, Richard Duong, Peg Gruenemeier.
9. STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman’s-Like Disease
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Tác giả
Bandar Al-Saud, Huda Alajlan, Haneen Sabar, Siddiq Anwar.
10. Autosomal Dominant Hyper-IgE Syndrome Without Significantly Elevated IgE.
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Tác giả
11. Successful Treatment of PAPA Syndrome with Dual Adalimumab and Tacrolimus Therapy
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Tác giả
Amika K. Sood, Diana B. McShane, Paul B. Googe.
12. Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease
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Tác giả
Nuria B. Zurro, Edgar B. de Oliveira Junior.
13. Abnormal Newborn Screen in a WHIM Syndrome Infant
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Tác giả
Martin O. Evans II, David H. McDermott, Philip M. Murphy.
14. Homozygous Splice ADA2 Gene Mutation Causing ADA-2 Deficiency
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Tác giả
Herberto Jose Chong-Neto, Gesmar Rodrigues Silva Segundo.
15. Management of ADA-Deficient SCID Patient on Adagen During Pregnancy
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Tác giả
Marissa Shams, Lisa Kobrynski.
16. Interstitial Lung Disease Frequently Precedes CVID Diagnosis
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Tác giả
Leif G. Hanitsch, Kirsten Wittke, Anna Barbara Stittrich.
17. Altered Monocyte Subsets in Patients with Chronic Idiopathic Neutropenia
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Tác giả
Nikoleta Bizymi, Maria Velegraki, Athina Damianaki.
18. Serum Tryptase Cannot Differentiate Vancomycin-Induced Anaphylaxis From Red Man Syndrome
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Tác giả
Satoko Noguchi, Daiki Takekawa, Junichi Saito.
19. The Value of Chromosome Analysis to Interrogate Variants in DNMT3B Causing Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome Type I (ICF1)
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Tác giả
Erinn S. Kellner, Pamela A. Rathbun, Gary S. Marshall.
20. Correction to: Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease
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Tác giả
Nuria Bengala Zurro, Edgar Borges de Oliveira Junior.
