| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acquired Hemophilia A in Wiskott–Aldrich Syndrome
|
He, Tingyan
|
|
|
41 |
5 |
p. 1119-1122
|
artikel
|
| 2 |
Adenosine Deaminase Deficient SCID with Myocardial Hypertrophy
|
Flinn, Aisling M.
|
|
|
41 |
5 |
p. 1128-1130
|
artikel
|
| 3 |
A novel 333 bp deletion of IL10RA in Chinese patients with neonatal-onset inflammatory bowel disease
|
Peng, Xiaomin
|
|
|
41 |
5 |
p. 1095-1098
|
artikel
|
| 4 |
A Patient with X-Linked Agammaglobulinemia and COVID-19 Infection Treated with Remdesivir and Convalescent Plasma
|
Iaboni, Aled
|
|
|
41 |
5 |
p. 923-925
|
artikel
|
| 5 |
Care of Children with DiGeorge Before and After Cultured Thymus Tissue Implantation
|
Gupton, Stephanie E.
|
|
|
41 |
5 |
p. 896-905
|
artikel
|
| 6 |
Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience
|
Akar, Halil Tuna
|
|
|
41 |
5 |
p. 992-1003
|
artikel
|
| 7 |
Congenital Athymia: Genetic Etiologies, Clinical Manifestations, Diagnosis, and Treatment
|
Collins, Cathleen
|
|
|
41 |
5 |
p. 881-895
|
artikel
|
| 8 |
Correction to: Gene Editing Rescues in Vitro T Cell Development of RAG2-Deficient Induced Pluripotent Stem Cells in an Artificial Thymic Organoid System
|
Gardner, Cameron L.
|
|
|
41 |
5 |
p. 863
|
artikel
|
| 9 |
Correction to: Resolution of Persistent COVID-19 After Convalescent Plasma in a Patient with B Cell Aplasia
|
McKemey, Emily
|
|
|
41 |
5 |
p. 930
|
artikel
|
| 10 |
EDA-ID: a Severe Clinical Presentation Associated with a New IKBKG Mutation
|
Bret Puvilland, Coline
|
|
|
41 |
5 |
p. 1099-1102
|
artikel
|
| 11 |
Gene Editing Rescues In vitro T Cell Development of RAG2-Deficient Induced Pluripotent Stem Cells in an Artificial Thymic Organoid System
|
Gardner, Cameron L.
|
|
|
41 |
5 |
p. 852-862
|
artikel
|
| 12 |
Hematopoietic Cell Transplantation with Reduced Intensity Conditioning Using Fludarabine/Busulfan or Fludarabine/Melphalan for Primary Immunodeficiency Diseases
|
Nishimura, Akira
|
|
|
41 |
5 |
p. 944-957
|
artikel
|
| 13 |
Hematopoietic Stem Cell Transplantation Resolves the Immune Deficit Associated with STAT3-Dominant-Negative Hyper-IgE Syndrome
|
Harrison, Stephanie C.
|
|
|
41 |
5 |
p. 934-943
|
artikel
|
| 14 |
Immune Reconstitution after Hematopoietic Stem Cell Transplantation in Immunodeficiency–Centromeric Instability–Facial Anomalies Syndrome Type 1
|
Kraft, Monica T.
|
|
|
41 |
5 |
p. 1089-1094
|
artikel
|
| 15 |
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
|
Imanaka, Yusuke
|
|
|
41 |
5 |
p. 975-986
|
artikel
|
| 16 |
Interferon-β Therapy in a Patient with Incontinentia Pigmenti and Autoantibodies against Type I IFNs Infected with SARS-CoV-2
|
Bastard, Paul
|
|
|
41 |
5 |
p. 931-933
|
artikel
|
| 17 |
Lymphopenia with Low T and NK Cells in a Patient with USB1 Mutation, Rare Findings in Clericuzio-Type Poikiloderma with Neutropenia
|
Bilgic Eltan, Sevgi
|
|
|
41 |
5 |
p. 1106-1111
|
artikel
|
| 18 |
Neutralizing Autoantibodies to Type I IFNs in >10% of Patients with Severe COVID-19 Pneumonia Hospitalized in Madrid, Spain
|
Troya, Jesús
|
|
|
41 |
5 |
p. 914-922
|
artikel
|
| 19 |
Novel Case of Tripeptidyl Peptidase 2 Deficiency Associated with Mild Clinical Phenotype
|
Stockdale, Claire
|
|
|
41 |
5 |
p. 1123-1127
|
artikel
|
| 20 |
Novel CD3Z and CD3E Deficiency in Two Unrelated Females
|
Setia, Priyanka
|
|
|
41 |
5 |
p. 1116-1118
|
artikel
|
| 21 |
Novel ORAI1 Mutation Disrupts Channel Trafficking Resulting in Combined Immunodeficiency
|
Yu, Fang
|
|
|
41 |
5 |
p. 1004-1015
|
artikel
|
| 22 |
Phenotypical and Functional Characterization of Neutrophils in Two Pyrin-Associated Auto-inflammatory Diseases
|
Malengier-Devlies, Bert
|
|
|
41 |
5 |
p. 1072-1084
|
artikel
|
| 23 |
Pulmonary Follow-Up Imaging in Cartilage-Hair Hypoplasia: a Prospective Cohort Study
|
Vakkilainen, Svetlana
|
|
|
41 |
5 |
p. 1064-1071
|
artikel
|
| 24 |
Rare Pathogenic Variants in Mitochondrial and Inflammation-Associated Genes May Lead to Inflammatory Cardiomyopathy in Chagas Disease
|
Ouarhache, Maryem
|
|
|
41 |
5 |
p. 1048-1063
|
artikel
|
| 25 |
Recurrent Chronic HEV in Severe Combined Immunodeficiency
|
Moodley, Prebashan
|
|
|
41 |
5 |
p. 1103-1105
|
artikel
|
| 26 |
Resolution of Persistent COVID-19 After Convalescent Plasma in a Patient with B Cell Aplasia
|
McKemey, Emily
|
|
|
41 |
5 |
p. 926-929
|
artikel
|
| 27 |
Serologic Cross-Reactivity of SARS-CoV-2 with Endemic and Seasonal Betacoronaviruses
|
Hicks, Jennifer
|
|
|
41 |
5 |
p. 906-913
|
artikel
|
| 28 |
Serum IgG Profiling of Toddlers Reveals a Subgroup with Elevated Seropositive Antibodies to Viruses Correlating with Increased Vaccine and Autoantigen Responses
|
Pichilingue-Reto, Patricia
|
|
|
41 |
5 |
p. 1031-1047
|
artikel
|
| 29 |
Severe Liver Disorder Following Liver Transplantation in STING-Associated Vasculopathy with Onset in Infancy
|
Ishikawa, Takashi
|
|
|
41 |
5 |
p. 967-974
|
artikel
|
| 30 |
STAT3 Hyper-IgE Syndrome—an Update and Unanswered Questions
|
Tsilifis, Christo
|
|
|
41 |
5 |
p. 864-880
|
artikel
|
| 31 |
Systemic and Nodular Hyperinflammation in a Patient with Refractory Familial Hemophagocytic Lymphohistiocytosis 2
|
Segal, Julia E.
|
|
|
41 |
5 |
p. 987-991
|
artikel
|
| 32 |
The “Editors” Take to RAG: Promise of CRISPR/Cas9/rAAV6-Based Gene Therapy for RAG2 Deficiency
|
Béziat, Vivien
|
|
|
41 |
5 |
p. 849-851
|
artikel
|
| 33 |
Thymopoiesis, Alterations in Dendritic Cells and Tregs, and Reduced T Cell Activation in Successful Extracorporeal Photopheresis Treatment of GVHD
|
Flinn, Aisling M.
|
|
|
41 |
5 |
p. 1016-1030
|
artikel
|
| 34 |
Treatment of Immune Dysregulation Due to a PTEN Variant with Sirolimus
|
Emerson, Jonathan S.
|
|
|
41 |
5 |
p. 1085-1088
|
artikel
|
| 35 |
Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations
|
Fusaro, Mathieu
|
|
|
41 |
5 |
p. 958-966
|
artikel
|
| 36 |
Upfront Enzyme Replacement via Erythrocyte Transfusions for PNP Deficiency
|
Eichinger, Anna
|
|
|
41 |
5 |
p. 1112-1115
|
artikel
|
Tijdschrift beschrijving