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                             25 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abnormal Results of Newborn Screening for SCID After Azathioprine Exposure In Utero: Benefit of TPMT Genotyping in Both Mother and Child Blom, Maartje

42 1 p. 199-202
artikel
2 A Case of Autosomal Recessive Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency with Severe COVID-19 Khanmohammadi, Shaghayegh

42 1 p. 19-24
artikel
3 A Double-Blind, Placebo-Controlled, Crossover Study of Magnesium Supplementation in Patients with XMEN Disease Chauvin, Samuel D.

42 1 p. 108-118
artikel
4 Altered Plasma Fatty Acids Associate with Gut Microbial Composition in Common Variable Immunodeficiency Skarpengland, Tonje

42 1 p. 146-157
artikel
5 An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7 Caseley, Emily A.

42 1 p. 158-170
artikel
6 BCG Disease in SCID: Three Decades of Experience in a Pediatric Transplant Center Cocchi, Nicoletta

42 1 p. 195-198
artikel
7 Bowel Histology of CVID Patients Reveals Distinct Patterns of Mucosal Inflammation van Schewick, Cornelia M.

42 1 p. 46-59
artikel
8 Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients Cifaldi, Cristina

42 1 p. 130-145
artikel
9 Comparison of Serum Total IgA Levels in Severe and Mild COVID-19 Patients and Control Group Barzegar-Amini, Maral

42 1 p. 10-18
artikel
10 Correction to: Onset and Relapse of Juvenile Dermatomyositis Following Asymptomatic SARS-CoV-2 Infection Rodero, Mathieu Paul

42 1 p. 28
artikel
11 COVID-19 in CVID: a Case Series of 17 Patients Greenmyer, Jacob R.

42 1 p. 29-31
artikel
12 Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients Amirifar, Parisa

42 1 p. 72-84
artikel
13 Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8 Tangye, Stuart G.

42 1 p. 119-129
artikel
14 Late-Onset Combined Immunodeficiency with Refractory CMV Disease due to ICOSL Deficiency Loo, Vivian G.

42 1 p. 206-209
artikel
15 Late Onset of Chronic Granulomatous Disease Revealed by Paecilomyces lilacinus Cutaneous Infection Lemaigre, Clément

42 1 p. 60-63
artikel
16 Long-Term Experience of Subcutaneous Immunoglobulin Therapy in Pediatric Primary Immunodeficient Patients with Low and Normal Body Weight Gul, Yahya

42 1 p. 64-71
artikel
17 Long-Term Immune Recovery After Hematopoietic Stem Cell Transplantation for ADA Deficiency: a Single-Center Experience Kreins, Alexandra Y.

42 1 p. 94-107
artikel
18 Multicenter Experience of Hematopoietic Stem Cell Transplantation in WHIM Syndrome Laberko, Alexandra

42 1 p. 171-182
artikel
19 Onset and Relapse of Juvenile Dermatomyositis Following Asymptomatic SARS-CoV-2 Infection Rodero, Mathieu Paul

42 1 p. 25-27
artikel
20 Partial Trisomy 9p with Clinical Symptoms Resembling Interferonopathies Inoue, Yuzaburo

42 1 p. 203-205
artikel
21 Persistent COVID-19 Infection in Wiskott-Aldrich Syndrome Cleared Following Therapeutic Vaccination: a Case Report Bradley, Rachel E.

42 1 p. 32-35
artikel
22 Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHD Arnold, Danielle E.

42 1 p. 36-45
artikel
23 Utility of Immunohistochemistry and Immunofluorescence in Determining the Pathogenic Variants of Chronic Granulomatous Disease Sekar, Aravind

42 1 p. 85-93
artikel
24 Vaccination for Patients with Inborn Errors of Immunity: a Nationwide Survey in Japan Hosaka, Sho

42 1 p. 183-194
artikel
25 X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia Abolhassani, Hassan

42 1 p. 1-9
artikel
                             25 gevonden resultaten
 
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