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Journal of Clinical Immunology
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1. Editorial, Journal of Clinical Immunology
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Tác giả
Jean-Laurent Casanova, Vincent Bonagura.
1. Regulatory T Cells: the Many Faces of Foxp3
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Tác giả
Peter Georgiev, Louis-Marie Charbonnier, Talal A. Chatila.
1. Prof. Dr. Beatriz Tavares Costa-Carvalho Obituary
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Tác giả
Antonio Condino-Neto.
1. Hematopoietic Stem Cell Transplantation in CARD9 Deficiency: Knight in Shining Armor?
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Tác giả
Isabelle Meyts.
1. Successful Lung Transplantation in a Patient with Chronic Granulomatous Disease
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Tác giả
Maylene Xie, Janet Lee, Maria Crespo, Merritt L. Fajt.
1. Successful Rituximab Treatment for Lymphoma, Secondary Immunodeficiency Causing Debilitating Sinusitis: Underlying Primary Immunodeficiency Disease, and Alternative Treatments to Improve the Quality of Life?
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Tác giả
Vincent R. Bonagura.
1. A Novel Recessive Mutation of Interferon-γ Receptor 1 in a Patient with Mycobacterium tuberculosis in Bone Marrow Aspirate
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Tác giả
Mahsima Shabani, Soheila Aleyasin, Sara Kashef.
1. Successful Bone Marrow Transplantation for XMEN: Hemorrhagic Risk Uncovered
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Tác giả
Dimana Dimitrova, Jeremy J. Rose, Gulbu Uzel.
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.
2. How to Identify Common Variable Immunodeficiency Patients Earlier: General Practice Patterns
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Tác giả
Frederik V. Ilkjær, Line D. Rasmussen.
2. In Memoriam: Prof. Dr. J.M.J.J. Vossen (1937–2019)
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Tác giả
Arjan Lankester, Peter Heidt, Hans Rümke, Robbert Bredius.
2. Successful Allogenic Stem Cell Transplantation in Patients with Inherited CARD9 Deficiency
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Tác giả
F. Queiroz-Telles, T. Mercier, J. Maertens, C. B. S. Sola.
2. Defining Primary Selective IgM Deficiency
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Tác giả
Sudhir Gupta, Ankmalika Gupta.
2. Successful Treatment of Sinusitis with Topical Human Milk in a Lymphoma Patient Using Rituximab
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Tác giả
Nise Yamaguchi, Patricia Palmeira, Magda Carneiro-Sampaio.
2. Compound Heterozygous Mutations of IL2-Inducible T cell Kinase in a Swedish Patient: the Importance of Early Genetic Diagnosis
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Tác giả
Mingyan Fang, Hassan Abolhassani, Qiang Pan-Hammarström.
2. MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation
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Tác giả
Maria Francisca Moraes-Fontes, Íris Caramalho, Amy P. Hsu.
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.
3. Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT
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Tác giả
Rebecca A. Marsh, Jennifer W. Leiding, Brent R. Logan.
3. WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure
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Tác giả
Lauren E. Heusinkveld, Shamik Majumdar, Ji-Liang Gao.
3. Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study
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Tác giả
Vassilios Lougaris, Annamaria Sorlini, Chiara Monfredini.
3. IKZF1 Loss-of-Function Variant Causes Autoimmunity and Severe Familial Antiphospholipid Syndrome
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Tác giả
Yannick Dieudonné, Aurélien Guffroy, Olivier Vollmer.
3. EBV-Related Hodgkin Lymphoma in an ICF2 Patient: Is EBV Susceptibility a Hallmark of This ICF Subtype?
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Tác giả
Francesco Licciardi, Marlinde van den Boogaard.
3. IFN-g:IL-10 Ratio: a Putative Predictive Biomarker to Discriminate HLH From Severe Viral Infections
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Tác giả
Snehal Shabrish, Mukesh Desai, Vinay Saxena.
3. Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence
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Tác giả
Rashmi Rikhi, Sagar Bhattad, Ankur Jindal, Biman Saikia.
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.
4. Pattern Recognition Molecules of the Lectin Pathway—Screening of Patients with Suspected Immunodeficiency
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Tác giả
Clara Mistegård Jørgensen, Lisbeth Jensen.
4. Respiratory Complications in Patients with Hyper IgM Syndrome
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Tác giả
Bobak Moazzami, Reza Yazdani, Gholamreza Azizi.
4. Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome
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Tác giả
Stefano Volpi, Antonella Insalaco, Roberta Caorsi.
4. Recurrent Salmonella typhi Infection and Autoimmunity in a Young Boy with Complete IL-12 Receptor β1 Deficiency
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Tác giả
Ankur Kumar Jindal, Deepti Suri, Sandesh Guleria.
4. Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses
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Tác giả
Tania Siahanidou, Eirini Nikaina, Christina Kontogiorgou.
4. Auto-inflammation in a Patient with a Novel Homozygous OTULIN Mutation
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Tác giả
Mohammad Nabavi, Mohammad Shahrooei, Hassan Rokni-Zadeh.
4. A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis
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Tác giả
Samin Sharafian, Vahid Ziaee, Mohammad Shahrooei.
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.
5. 30-Year Review of Pediatric- and Adult-Onset CVID: Clinical Correlates and Prognostic Indicators
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Tác giả
Carolyn Baloh, Anupama Reddy, Michele Henson.
5. Cellular Defects in CVID Patients with Chronic Lung Disease in the USIDNET Registry
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Tác giả
Erinn S. Kellner, Ramsay Fuleihan.
5. iPLA2 Activation Mediates Granular Exocytosis and Corrects Microbicidal Defects in ROS-Deficient and CGD Human Neutrophils
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Tác giả
Issam Harfi, Stéphanie D’Hondt, Eric Sariban.
5. Fifteen Years of the J Project
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Tác giả
László Maródi.
5. Revisiting Fatal Granulomatous Disease of Childhood Through an Autopsy: Still Lethal in the Developing World!
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Tác giả
Rakesh Kumar Pilania, Ashwini Prithvi.
5. In Memoriam: Fernando Aiuti, MD (June 8, 1935–January 9, 2019)
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Tác giả
Alessandro Aiuti, Isabella Quinti.
5. Two Prenatal Cases of Hyper-IgE Syndrome
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Tác giả
Makiko Egawa, Kohsuke Imai, Yoko Taketani, Tomohiro Morio.
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.
6. Predicting the Occurrence of Variants in RAG1 and RAG2
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Tác giả
Dylan Lawless, Hana Lango Allen, James Thaventhiran.
6. Diagnostic Yield of Next Generation Sequencing in Genetically Undiagnosed Patients with Primary Immunodeficiencies: a Systematic Review
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Tác giả
Hemmo A. F. Yska, Kim Elsink, Taco W. Kuijpers.
6. Chronic Granulomatous Disorder–Associated Colitis Can Be Accurately Evaluated with MRI Scans and Fecal Calprotectin Level
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Tác giả
David M. Lowe, Philip J. Smith, Fernando Moreira.
6. Variable Responses to Tocilizumab in Four Patients with Schnitzler Syndrome
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Tác giả
Jonas Claus, Steven Vanderschueren.
6. Different Clonal T-Large Granular Lymphocyte Proliferations in SCID
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Tác giả
Süreyya Savaşan, Erin Wakeling, Tristan Knight.
6. A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency
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Tác giả
Sinem Firtina, Funda Cipe, Yuk Yin Ng, Ayca Kiykim.
6. Successful Treatment with SCIG of a Child with Refractory Chronic ITP
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Tác giả
Anna Karastaneva, Daniela S. Klobassa, Milen Minkov.
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.
7. A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency
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Tác giả
Hélène Coignard-Biehler, Nizar Mahlaoui, Benoit Pilmis.
7. Compound Heterozygous DOCK8 Mutations in a Patient with B Lymphoblastic Leukemia and EBV-Associated Diffuse Large B Cell Lymphoma
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Tác giả
David Buchbinder, Ivan Kirov, Jeffrey Danielson.
7. Use of TCR α+β+/CD19+–Depleted Haploidentical Hematopoietic Stem Cell Transplant Is a Viable Option in Patients With Primary Immune Deficiency Without Matched Sibling Donor
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Tác giả
Tim Brettig, Joanne Smart, Sharon Choo.
7. Enterovirus-Associated HLH: Addition of Anakinra to IVIG and Corticosteroids
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Tác giả
Simon Jonathan Hardman, Gidado Tukur, Catherine Waruiru.
7. A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype
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Tác giả
Laura Rice, Claire Stockdale, Ian Berry, Sean O’Riordan.
7. Immune Dysregulation and Disease Pathogenesis due to Activating Mutations in PIK3CD—the Goldilocks’ Effect
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Tác giả
Stuart G. Tangye, Julia Bier, Anthony Lau, Tina Nguyen.
7. Damaging BTK Variant Demonstrated by Carrier, Allele-Specific BTK Expression in B Cells and Monocytes
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Tác giả
Mary T. Bausch-Jurken, Mary Hintermeyer, Jeffrey Woodliff.
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.
8. The Phytopathogenic Fungus Pallidocercospora crystallina-Caused Localized Subcutaneous Phaeohyphomycosis in a Patient with a Homozygous Missense CARD9 Mutation
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Tác giả
Yanyang Guo, Zhenlai Zhu, Jixin Gao, Chen Zhang.
8. Chronic Mucocutaneous Candidiasis in an Adolescent Boy Due to a Novel Mutation in TRAF3IP2
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Tác giả
Sagar Bhattad, Chitra Dinakar, Haneesha Pinnamaraju.
8. Juvenile-Onset Immunodeficiency Secondary to Anti-Interferon-Gamma Autoantibodies
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Tác giả
Woei-Kang Liew, Koh-Cheng Thoon, Chia-Yin Chong.
8. Life-Threatening Infections Due to Live-Attenuated Vaccines: Early Manifestations of Inborn Errors of Immunity
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Tác giả
Laura Pöyhönen, Jacinta Bustamante, Jean-Laurent Casanova.
8. Interferon-γ Receptor 1 Deficiency Corrected by Umbilical Cord Blood Transplantation
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Tác giả
Thomas F. Michniacki, Kelly J. Walkovich, David G. Frame.
8. Health-Related Quality of Life in Patients with CVID Under Different Schedules of Immunoglobulin Administration: Prospective Multicenter Study
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Tác giả
Federica Pulvirenti, Francesco Cinetto, Antonio Pecoraro.
8. Childhood Hodgkin Lymphoma: Think DADA2
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Tác giả
Fahad Alabbas, Ghaleb Elyamany, Omar Alsharif.
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.
9. A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects
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Tác giả
Deniz Cagdas, Sevil Oskay Halaçlı, Çağman Tan, Bernice Lo.
9. Current Status of the Management of Mendelian Susceptibility to Mycobacterial Disease in Mainland China
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Tác giả
Wenjing Ying, Danru Liu, Xiaolong Dong, Wenjie Wang.
9. Autoinflammation Masquerading as Autoimmunity in an Adult with Heterozygous p.E250K PSTPIP1 Mutation
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Tác giả
Pei Dai, Tim Furlong, Gary Gracie, Min Li Huang, Tao Yang.
9. Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells
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Tác giả
Ahmet Eken, Murat Cansever, Ido Somekh, Yoko Mizoguchi.
9. Interleukin-36 Receptor Antagonist Deficiency (DITRA) with a Novel IL36RN Homozygous Mutation c.200G > T (P.Cys67Phe) in a Young Colombian Woman
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Tác giả
Andres F. Zea-Vera, Felipe E. Estupiñan-Lopez.
9. Neurological Involvement in Childhood Evans Syndrome
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Tác giả
Thomas Pincez, Bénédicte Neven, Hubert Ducou Le Pointe.
9. Autoimmunity and Inflammation in CVID: a Possible Crosstalk between Immune Activation, Gut Microbiota, and Epigenetic Modifications
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Tác giả
Silje F. Jørgensen, Børre Fevang, Pål Aukrust.
10. Autosomal Dominant Hyper-IgE Syndrome Without Significantly Elevated IgE.
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Tác giả
10. LINE-1-Mediated AluYa5 Insertion Underlying Complete Autosomal Recessive IFN-γR1 Deficiency
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Tác giả
Jérémie Rosain, Caroline Deswarte, Gonca Hancioglu.
10. Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect
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Tác giả
Pandiarajan Vignesh, Madhubala Sharma.
10. Different Phenotypic Presentations of X-Linked Lymphoproliferative Disease in Siblings with Identical Mutations
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Tác giả
Zohreh Nademi, Nesrine Radwan, Kanchan Rao.
10. Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor Repertoire
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Tác giả
Shirly Frizinsky, Erez Rechavi, Ortal Barel.
10. Hemorrhagic Pneumonia as the First Manifestation of Anhidrotic Ectodermal Dysplasia with Immunodeficiency
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Tác giả
Yuko Ichimiya, Motoshi Sonoda, Masataka Ishimura.
10. Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immune Deficiency Disorders in Children: Challenges and Outcome from a Tertiary Care Center in South India
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Tác giả
Ramya Uppuluri, Meena Sivasankaran, Shivani Patel.
10. Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
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Tác giả
Ayca Kiykim, Louis Marie Charbonnier, Arzu Akcay.
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.
11. Disseminated Mycobacterial Disease in a Patient with 22q11.2 Deletion Syndrome: Case Report and Review of the Literature
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Tác giả
Rodrigo Hoyos-Bachiloglu, Silvanna Gallo, Cecilia Vizcaya.
11. Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency
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Tác giả
Jessica R. Saunders, Anna Lehman, Stuart E. Turvey.
11. Correction to: Life-Threatening Infections Due to Live-Attenuated Vaccines: Early Manifestations of Inborn Errors of Immunity
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Tác giả
Laura Pöyhönen, Jacinta Bustamante, Jean-Laurent Casanova.
11. Graft Versus Host Disease Following HLA-Matched Sibling Donor Compared with Matched Related Donor for Hematopoietic Stem Cell Transplantation for the Treatment of Severe Combined Immunodeficiency Disease
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Tác giả
Bandar Al-Saud, Alhanouf Al-Saleem, Bashayer Al Rasheed.
11. Granule Cell Neuronopathy in a Patient with Common Variable Immunodeficiency
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Tác giả
Andrew McLean-Tooke, Constantine Chris Phatouros.
11. Novel Heterogeneous Mutation of TNFAIP3 in a Chinese Patient with Behçet-Like Phenotype and Persistent EBV Viremia
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Tác giả
Xiaolong Dong, Luyao Liu, Ying Wang, Xiaotao Yang.
11. Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
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Tác giả
Katharina Schütz, Diana Alecsandru, Bodo Grimbacher.
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.
12. Autoimmune Lymphoproliferative Syndrome with Cryptococcus Infection
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Tác giả
Kai Mu, Jing Zhang, Yan Gu, Hongjuan Li, Hongmei Wang.
12. RNASEH2B Related Adult-Onset Interferonopathy
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Tác giả
Tracy A. Briggs, Anindita Paul, Gillian Rice.
12. Ficolin-3 Deficiency Is Associated with Disease and an Increased Risk of Systemic Lupus Erythematosus
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Tác giả
Anne Troldborg, Rudi Steffensen, Marten Trendelenburg.
12. RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency
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Tác giả
Christopher M. Watson, Claire Stockdale, Ian Berry.
12. Health-Related Quality of Life and Emotional Health in X-Linked Carriers of Chronic Granulomatous Disease in the United Kingdom
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Tác giả
Alexandra C. Battersby, Helen Braggins, Mark S. Pearce.
12. Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies
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Tác giả
Jérôme Hadjadj, Aurélien Guffroy, Christophe Delavaud.
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.
13. A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant
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Tác giả
Alina Kurolap, Orly Eshach Adiv, Liza Konnikova.
13. A Novel CARMIL2 Mutation Resulting in Combined Immunodeficiency Manifesting with Dermatitis, Fungal, and Viral Skin Infections As Well as Selective Antibody Deficiency
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Tác giả
Faranaz Atschekzei, Roland Jacobs, Martin Wetzke.
13. Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic Neutropenia
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Tác giả
Julie Seguier, Vincent Barlogis, Laure Croisille.
13. Lymphocyte Apoptosis and FAS Expression in Patients with 22q11.2 Deletion Syndrome
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Tác giả
Dina M. Aresvik, Torstein Øverland, Kari Lima.
14. Homozygous Splice ADA2 Gene Mutation Causing ADA-2 Deficiency
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Tác giả
Herberto Jose Chong-Neto, Gesmar Rodrigues Silva Segundo.
14. Factors Beyond Lack of Antibody Govern Pulmonary Complications in Primary Antibody Deficiency
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Tác giả
Tamar Weinberger, Ramsay Fuleihan.
14. CAPS and NLRP3
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Tác giả
Laela M. Booshehri, Hal M. Hoffman.
14. Alternative Splicing Rescues Loss of Common Gamma Chain Function and Results in IL-21R-like Deficiency
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Tác giả
David Illig, Marta Navratil, Jadranka Kelečić.
14. DDX58 and Classic Singleton-Merten Syndrome
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Tác giả
Carlos R. Ferreira, Yanick J. Crow, William A. Gahl.
15. Management of ADA-Deficient SCID Patient on Adagen During Pregnancy
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Tác giả
Marissa Shams, Lisa Kobrynski.
15. Role of Allogeneic Hematopoietic Stem Cell Transplant for Chronic Granulomatous Disease (CGD): a Report of the United States Immunodeficiency Network
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Tác giả
Jennifer R. Yonkof, Ashish Gupta, Pingfu Fu.
15. Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease
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Tác giả
Shokouh Azam Sarrafzadeh, Maryam Nourizadeh.
15. Nasal Nitric Oxide in Primary Immunodeficiency and Primary Ciliary Dyskinesia: Helping to Distinguish Between Clinically Similar Diseases
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Tác giả
Zofia N. Zysman-Colman, Kimberley R. Kaspy.
15. Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders
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Tác giả
David Buchbinder, Fabian Hauck, Michael H. Albert.
16. Interstitial Lung Disease Frequently Precedes CVID Diagnosis
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Tác giả
Leif G. Hanitsch, Kirsten Wittke, Anna Barbara Stittrich.
16. Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction
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Tác giả
Leen Moens, Mieke Gouwy, Barbara Bosch.
16. Correction to: Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
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Tác giả
Katharina Schütz, Diana Alecsandru, Bodo Grimbacher.
16. Differing Performance of the Warning Signs for Immunodeficiency in the Diagnosis of Pediatric Versus Adult Patients in a Two-Center Tertiary Referral Population
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Tác giả
Jaclyn A. Bjelac, Jennifer R. Yonkof, James Fernandez.
17. Altered Monocyte Subsets in Patients with Chronic Idiopathic Neutropenia
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Tác giả
Nikoleta Bizymi, Maria Velegraki, Athina Damianaki.
17. Report of a Chinese Cohort with Leukocyte Adhesion Deficiency-I and Four Novel Mutations
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Tác giả
Bijun Sun, Qiuyu Chen, Xiaolong Dong, Danru Liu, Jia Hou.
17. A Novel Missense LIG4 Mutation in a Patient With a Phenotype Mimicking Behçet’s Disease
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Tác giả
Ekim Z. Taskiran, Hafize E. Sonmez, Can Kosukcu.
18. Serum Tryptase Cannot Differentiate Vancomycin-Induced Anaphylaxis From Red Man Syndrome
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Tác giả
Satoko Noguchi, Daiki Takekawa, Junichi Saito.
18. Clinical Features and HSCT Outcome for SCID in Turkey
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Tác giả
Aydan Ikinciogullari, Deniz Cagdas, Figen Dogu.
18. Mosaicism of an ELANE Mutation in an Asymptomatic Mother.
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Tác giả
Tomonari Shigemura, Norimoto Kobayashi, Kazunaga Agematsu.
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.
19. Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2
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Tác giả
Charlotte A. Slade, Catriona McLean, Thomas Scerri.
19. Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma
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Tác giả
Ludmila Perelygina, David Buchbinder, Morna J. Dorsey.
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.
20. Altered Peripheral Blood Leucocyte Phenotype and Responses in Healthy Individuals with Homozygous Deletion of FHR1 and FHR3 Genes
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Tác giả
Angika Bhasym, Bahadur Singh Gurjar, Savit Prabhu.
20. TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia
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Tác giả
C. Paradis, M. Cadieux-Dion, C. Meloche, M. Gravel.