| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Case of VEXAS Syndrome Complicated by Hemophagocytic Lymphohistiocytosis
|
Grey, Alice
|
|
|
41 |
7 |
p. 1648-1651
|
artikel
|
| 2 |
A Case Report of SAVI Mimicking Early-Onset ANCA Vasculitis
|
Ochfeld, Elisa
|
|
|
41 |
7 |
p. 1652-1655
|
artikel
|
| 3 |
Achromobacter xylosoxidans Pneumonia in a Young Child with Chronic Granulomatous Disease—a Case-Based Review
|
Patra, Pratap Kumar
|
|
|
41 |
7 |
p. 1686-1692
|
artikel
|
| 4 |
ALPK1 Gene Mutations Drive Autoinflammation with Ectodermal Dysplasia and Progressive Vision Loss
|
Jamilloux, Yvan
|
|
|
41 |
7 |
p. 1671-1673
|
artikel
|
| 5 |
Alternative Approach to Varicella Zoster Virus Prevention in a Child with Lymphopenia
|
Cortesi, Manuela
|
|
|
41 |
7 |
p. 1681-1682
|
artikel
|
| 6 |
Another Exciting Data—HCT Successfully Cured Patients with DADA2
|
Yamashita, Motoi
|
|
|
41 |
7 |
p. 1443-1445
|
artikel
|
| 7 |
Antibody Response to SARS-CoV-2 is Associated with Long-term Clinical Outcome in Patients with COVID-19: a Longitudinal Study
|
García-Abellán, Javier
|
|
|
41 |
7 |
p. 1490-1501
|
artikel
|
| 8 |
Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
|
Malle, Louise
|
|
|
41 |
7 |
p. 1457-1462
|
artikel
|
| 9 |
BCG Vaccine–Associated Complications in Patients with PTEN Hamartoma Tumor Syndrome
|
Taylor, Henry
|
|
|
41 |
7 |
p. 1701-1705
|
artikel
|
| 10 |
Chronically Activated T-cells Retain Their Inflammatory Properties in Common Variable Immunodeficiency
|
Berbers, Roos-Marijn
|
|
|
41 |
7 |
p. 1621-1632
|
artikel
|
| 11 |
Containment of Local COVID-19 Outbreak Among Hematopoietic Stem Cell Transplant Recipients and Healthcare Workers in a Pediatric Stem Cell Unit
|
Ouederni, Monia
|
|
|
41 |
7 |
p. 1523-1526
|
artikel
|
| 12 |
COPA Syndrome (Ala239Pro) Presenting with Isolated Follicular Bronchiolitis in Early Childhood: Case Report
|
Psarianos, Pamela
|
|
|
41 |
7 |
p. 1660-1663
|
artikel
|
| 13 |
Correction to: Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations
|
Lugo-Reyes, Saul Oswaldo
|
|
|
41 |
7 |
p. 1708
|
artikel
|
| 14 |
COVID-19 in Patients with Primary Immunodeficiency
|
Esenboga, Saliha
|
|
|
41 |
7 |
p. 1515-1522
|
artikel
|
| 15 |
COVID-19 in the Context of Inborn Errors of Immunity: a Case Series of 31 Patients from Mexico
|
Castano-Jaramillo, Lina M.
|
|
|
41 |
7 |
p. 1463-1478
|
artikel
|
| 16 |
Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation
|
Meinhardt, Andrea
|
|
|
41 |
7 |
p. 1664-1667
|
artikel
|
| 17 |
Deficiency of Adenosine Deaminase 2—a Monogenic Cause of Wunderlich Syndrome
|
Patra, Pratap Kumar
|
|
|
41 |
7 |
p. 1693-1695
|
artikel
|
| 18 |
Elevated Expression Levels of Lung Complement Anaphylatoxin, Neutrophil Chemoattractant Chemokine IL-8, and RANTES in MERS-CoV-Infected Patients: Predictive Biomarkers for Disease Severity and Mortality
|
Hamed, Maaweya E.
|
|
|
41 |
7 |
p. 1607-1620
|
artikel
|
| 19 |
Exploration of Potential Immunodeficiency Unveils Hennekam Lymphangiectasia-Lymphedema Syndrome
|
Kaut, Sara
|
|
|
41 |
7 |
p. 1674-1676
|
artikel
|
| 20 |
Haematopoietic Stem Cell Transplant for Norovirus-Induced Intestinal Failure in X-linked Agammaglobulinemia
|
Shillitoe, Ben M. J.
|
|
|
41 |
7 |
p. 1574-1581
|
artikel
|
| 21 |
Harnessing Type I IFN Immunity Against SARS-CoV-2 with Early Administration of IFN-β
|
Vinh, Donald C.
|
|
|
41 |
7 |
p. 1425-1442
|
artikel
|
| 22 |
Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients
|
Hashem, Hasan
|
|
|
41 |
7 |
p. 1633-1647
|
artikel
|
| 23 |
Hematopoietic Stem Cell Transplantation Successfully Treats CD40LG Duplication
|
Sun, Di
|
|
|
41 |
7 |
p. 1668-1670
|
artikel
|
| 24 |
Hemophagocytic Lymphohistiocytosis in Activated PI3K Delta Syndrome: an Illustrative Case Report
|
Zhou, Zijun
|
|
|
41 |
7 |
p. 1656-1659
|
artikel
|
| 25 |
Human Disease Phenotypes Associated with Loss and Gain of Function Mutations in STAT2: Viral Susceptibility and Type I Interferonopathy
|
Duncan, Christopher James Arthur
|
|
|
41 |
7 |
p. 1446-1456
|
artikel
|
| 26 |
Killing Two Birds with One Stone: the Therapeutic Role of Ibrutinib in Schnitzler Syndrome
|
Wang, Chen
|
|
|
41 |
7 |
p. 1706-1707
|
artikel
|
| 27 |
Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency
|
Raedler, Johannes
|
|
|
41 |
7 |
p. 1536-1548
|
artikel
|
| 28 |
Listeria Monocytogenes Meningoencephalitis Due to IRAK4 Deficiency
|
Liu, Ding
|
|
|
41 |
7 |
p. 1677-1680
|
artikel
|
| 29 |
Macrophage Activation Syndrome in a Patient with Prolidase Deficiency: a Rare Genetic Disorder Associated with Elevated IgE and Lupus-Like Syndrome
|
Chidambaram, Aakash Chandran
|
|
|
41 |
7 |
p. 1696-1700
|
artikel
|
| 30 |
Myelodysplastic Syndrome in a Patient with IPEX Syndrome
|
Toyama, Daisuke
|
|
|
41 |
7 |
p. 1683-1685
|
artikel
|
| 31 |
Neutralizing Anti-interferon-γ Autoantibodies: an Ameliorating Factor in COVID-19 Infection?
|
Kacar, Mark
|
|
|
41 |
7 |
p. 1531-1535
|
artikel
|
| 32 |
Normal IgH Repertoire Diversity in an Infant with ADA Deficiency After Gene Therapy
|
Baloh, Carolyn H.
|
|
|
41 |
7 |
p. 1597-1606
|
artikel
|
| 33 |
Outcome of SARS-CoV-2 Infection in 121 Patients with Inborn Errors of Immunity: A Cross-Sectional Study
|
Goudouris, Ekaterini Simões
|
|
|
41 |
7 |
p. 1479-1489
|
artikel
|
| 34 |
Pulmonary Hypertension in Patients with Common Variable Immunodeficiency
|
Thoré, Pierre
|
|
|
41 |
7 |
p. 1549-1562
|
artikel
|
| 35 |
Safety of COVID-19 Vaccination in Immune-Deficient Patients Receiving Supplemental Immunoglobulin Therapies
|
Squire, Jacqueline D.
|
|
|
41 |
7 |
p. 1527-1530
|
artikel
|
| 36 |
SARS-CoV-2 infection in a pediatrics STAT1 GOF patient under Ruxolitinib therapy-a matter of balance?
|
Guisado Hernández, Paloma
|
|
|
41 |
7 |
p. 1502-1506
|
artikel
|
| 37 |
SARS-CoV-2 infection inducing severe flare up of Deficiency of Interleukin Thirty-six (IL-36) Receptor Antagonist (DITRA) resulting from a mutation invalidating the activating cleavage site of the IL-36 receptor antagonist
|
Bozonnat, Alizée
|
|
|
41 |
7 |
p. 1511-1514
|
artikel
|
| 38 |
SARS-CoV-2–Related Acute Respiratory Distress Syndrome Uncovers a Patient with Severe Combined Immunodeficiency Disease
|
Al-Saud, Bandar
|
|
|
41 |
7 |
p. 1507-1510
|
artikel
|
| 39 |
Single-Center Study of 72 Patients with Severe Combined Immunodeficiency: Clinical and Laboratory Features and Outcomes
|
Bayram, Ozlem
|
|
|
41 |
7 |
p. 1563-1573
|
artikel
|
| 40 |
T Cell-Epstein-Barr Virus–Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non-Asians and Is Associated with a T Cell Activation State that Is Comparable to Primary HLH
|
Shamriz, Oded
|
|
|
41 |
7 |
p. 1582-1596
|
artikel
|
Tijdschrift beschrijving