| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activated PI3 Kinase Delta Syndrome Revealed by Vasculitis and Disseminated Toxoplasmosis
|
Larrauffie, Aurore
|
|
|
42 |
3 |
p. 688-690
|
artikel
|
| 2 |
A De Novo Cause of PGM3 Deficiency Treated with Hematopoietic Stem Cell Transplantation
|
Winslow, Andrew
|
|
|
42 |
3 |
p. 691-694
|
artikel
|
| 3 |
A Multi‑Center, Open‑Label, Single‑Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency
|
Santamaria, Manuel
|
|
|
42 |
3 |
p. 500-511
|
artikel
|
| 4 |
Antiviral T-Cell Frequencies in a Healthy Population: Reference Values for Evaluating Antiviral Immune Cell Profiles in Immunocompromised Patients
|
Schulze Lammers, Friederike C.
|
|
|
42 |
3 |
p. 546-558
|
artikel
|
| 5 |
A Pitfall of Whole Exome Sequencing: Variants in the 5′UTR Splice Site of BTK Causing XLA
|
Takada, Sanami
|
|
|
42 |
3 |
p. 709-712
|
artikel
|
| 6 |
Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital
|
Chauvineau-Grenier, Angélique
|
|
|
42 |
3 |
p. 459-470
|
artikel
|
| 7 |
CD40 Ligand Deficiency in Latin America: Clinical, Immunological, and Genetic Characteristics
|
França, Tábata Takahashi
|
|
|
42 |
3 |
p. 514-526
|
artikel
|
| 8 |
Clinical Outcome and Underlying Genetic Cause of Functional Terminal Complement Pathway Deficiencies in a Multicenter UK Cohort
|
Shears, Annalie
|
|
|
42 |
3 |
p. 665-671
|
artikel
|
| 9 |
Clinicopathological Manifestations and Immune Phenotypes in Adult-Onset Immunodeficiency with Anti-interferon-γ Autoantibodies
|
Chen, Yi-Chun
|
|
|
42 |
3 |
p. 672-683
|
artikel
|
| 10 |
Cocktails of KLK5 Protease Inhibitors and Anti-TNFα Therapeutics: an Effective Treatment for Netherton Syndrome
|
Zingkou, Eleni
|
|
|
42 |
3 |
p. 597-605
|
artikel
|
| 11 |
Comprehensive Assessment of Skin Disorders in Patients with Common Variable Immunodeficiency (CVID)
|
Zarezadeh Mehrabadi, Ali
|
|
|
42 |
3 |
p. 653-664
|
artikel
|
| 12 |
Correction to: A Multi-center, Open-Label, Single-Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency
|
Santamaria, Manuel
|
|
|
42 |
3 |
p. 512-513
|
artikel
|
| 13 |
Correction to: CD40 Ligand Deficiency in Latin America: Clinical, Immunological, and Genetic Characteristics
|
França, Tábata Takahashi
|
|
|
42 |
3 |
p. 527-528
|
artikel
|
| 14 |
Correction to: The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity
|
Seidel, Markus G.
|
|
|
42 |
3 |
p. 499
|
artikel
|
| 15 |
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency
|
Sefer, Asena Pinar
|
|
|
42 |
3 |
p. 634-652
|
artikel
|
| 16 |
First Identified Case of Fatal Fulminant Necrotizing Eosinophilic Myocarditis Following the Initial Dose of the Pfizer-BioNTech mRNA COVID-19 Vaccine (BNT162b2, Comirnaty): an Extremely Rare Idiosyncratic Hypersensitivity Reaction
|
Ameratunga, Rohan
|
|
|
42 |
3 |
p. 441-447
|
artikel
|
| 17 |
Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985–2016
|
Miyamoto, Satoshi
|
|
|
42 |
3 |
p. 529-545
|
artikel
|
| 18 |
Hematopoietic Cell Transplant for CD40 Ligand Deficiency—Comparing Busulfan Versus Treosulfan
|
Carruthers, Vicky-Anne
|
|
|
42 |
3 |
p. 703-705
|
artikel
|
| 19 |
Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence
|
Sbihi, Zineb
|
|
|
42 |
3 |
p. 559-571
|
artikel
|
| 20 |
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome
|
Abolhassani, Hassan
|
|
|
42 |
3 |
p. 471-483
|
artikel
|
| 21 |
In memoriam: Stephen J Seligman, MD
|
Casanova, Jean-Laurent
|
|
|
42 |
3 |
p. 437-440
|
artikel
|
| 22 |
Life-Threatening Enterovirus 71 Encephalitis in Unrelated Children with Autosomal Dominant TLR3 Deficiency
|
Kuo, Chen-Yen
|
|
|
42 |
3 |
p. 606-617
|
artikel
|
| 23 |
Long-Term Follow-Up of Newborns with 22q11 Deletion Syndrome and Low TRECs
|
Framme, Jenny Lingman
|
|
|
42 |
3 |
p. 618-633
|
artikel
|
| 24 |
Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency
|
Surucu Yilmaz, Naz
|
|
|
42 |
3 |
p. 582-596
|
artikel
|
| 25 |
Malignancy in STAT3 Deficient Hyper IgE Syndrome
|
Urban, Amanda
|
|
|
42 |
3 |
p. 699-702
|
artikel
|
| 26 |
Predictive Factors for and Complications of Bronchiectasis in Common Variable Immunodeficiency Disorders
|
Sperlich, Johannes M.
|
|
|
42 |
3 |
p. 572-581
|
artikel
|
| 27 |
Psychological Symptoms in Primary Immunodeficiencies: a Common Comorbidity?
|
Manusama, Olivia R.
|
|
|
42 |
3 |
p. 695-698
|
artikel
|
| 28 |
Seasonal Betacoronavirus Antibodies’ Expansion Post-BNT161b2 Vaccination Associates with Reduced SARS-CoV-2 VoC Neutralization
|
Dispinseri, Stefania
|
|
|
42 |
3 |
p. 448-458
|
artikel
|
| 29 |
The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity
|
Seidel, Markus G.
|
|
|
42 |
3 |
p. 484-498
|
artikel
|
| 30 |
To the Editor: “Complete Resolution of Multiple Warts after a First Dose of the Receptor Interleukin-5 Inhibitor”
|
Guevara-Hoyer, Kissy
|
|
|
42 |
3 |
p. 684-687
|
artikel
|
| 31 |
Vanishing Lymphocytes in a Case of Vanishing Bone Disease
|
Iyengar, Vaishnavi V.
|
|
|
42 |
3 |
p. 706-708
|
artikel
|
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