| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Distinct Feature of T Cell Subpopulations in a Patient with CHARGE Syndrome and Omenn Syndrome
|
Uchiyama, Toru
|
|
|
41 |
1 |
p. 233-237
|
artikel
|
| 2 |
A Novel Case of Complement Factor B Deficiency
|
Gauthier, Amélie
|
|
|
41 |
1 |
p. 277-279
|
artikel
|
| 3 |
A Novel CYBB Variant Causing X-Linked Chronic Granulomatous Disease in a Patient with Empyema
|
Kitcharoensakkul, Maleewan
|
|
|
41 |
1 |
p. 266-269
|
artikel
|
| 4 |
Anti-IFN-γ Immunodeficiency Syndrome Presenting as Blurred Vision and Salmonellosis
|
Peng, Shu-Yu
|
|
|
41 |
1 |
p. 274-276
|
artikel
|
| 5 |
A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells
|
Sefer, Asena Pınar
|
|
|
41 |
1 |
p. 251-255
|
artikel
|
| 6 |
Bacillus Calmette–Guerin (BCG) Vaccine-associated Complications in Immunodeficient Patients Following Stem Cell Transplantation
|
NaserEddin, Adeeb
|
|
|
41 |
1 |
p. 147-162
|
artikel
|
| 7 |
CADINS in an Adult with Chronic Sinusitis and Atopic Disease
|
Izadi, Neema
|
|
|
41 |
1 |
p. 256-258
|
artikel
|
| 8 |
Circulating Levels of Interleukin-6 and Interleukin-10, But Not Tumor Necrosis Factor-Alpha, as Potential Biomarkers of Severity and Mortality for COVID-19: Systematic Review with Meta-analysis
|
Udomsinprasert, Wanvisa
|
|
|
41 |
1 |
p. 11-22
|
artikel
|
| 9 |
Clinical Spectrum of Ras-Associated Autoimmune Leukoproliferative Disorder (RALD)
|
Neven, Quentin
|
|
|
41 |
1 |
p. 51-58
|
artikel
|
| 10 |
Common Variable Immunodeficiency with the Concomitant Diagnosis of an Inflammatory Myofibroblastic Tumor
|
Sewell, Craig
|
|
|
41 |
1 |
p. 230-232
|
artikel
|
| 11 |
Correction to: IFN-α2a Therapy in Two Patients with Inborn Errors of TLR3 and IRF3 Infected with SARS-CoV-2
|
Lévy, Romain
|
|
|
41 |
1 |
p. 28
|
artikel
|
| 12 |
Cytomegalovirus Laryngitis in Primary Combined Immunodeficiency Diseases
|
Inoue, Maiko
|
|
|
41 |
1 |
p. 243-247
|
artikel
|
| 13 |
Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?
|
Germenis, Anastasios E.
|
|
|
41 |
1 |
p. 248-250
|
artikel
|
| 14 |
Deforming Polyarthritis in a North Indian Family—Clinical Expansion of STING-Associated Vasculopathy with Onset in Infancy (SAVI)
|
Anjani, Gummadi
|
|
|
41 |
1 |
p. 209-211
|
artikel
|
| 15 |
Developmental Adaptive Immune Defects Associated with STAT5B Deficiency in Three Young Siblings
|
Foley, Corinne L.
|
|
|
41 |
1 |
p. 136-146
|
artikel
|
| 16 |
Expanding the Clinical Phenotype of Chronic Granulomatous Disease: a Female Patient with a De Novo Mutation in CYBB
|
Wu, Eveline Y.
|
|
|
41 |
1 |
p. 224-226
|
artikel
|
| 17 |
Experience with a Reduced Toxicity Allogeneic Transplant Regimen for Non-CGD Primary Immune Deficiencies Requiring Myeloablation
|
Chandra, Sharat
|
|
|
41 |
1 |
p. 89-98
|
artikel
|
| 18 |
Haematopoietic Stem Cell Transplantation for DNA Ligase 1 Deficiency
|
Silva, Juliana M. F.
|
|
|
41 |
1 |
p. 238-242
|
artikel
|
| 19 |
Haemolytic Uremic Syndrome Associated with Citrobacter freundii in a Young Boy with X-Linked Agammaglobulinemia
|
Sudhakar, Murugan
|
|
|
41 |
1 |
p. 227-229
|
artikel
|
| 20 |
Hereditary Angioedema with and Without C1-Inhibitor Deficiency in Postmenopausal Women
|
Billebeau, Aurore
|
|
|
41 |
1 |
p. 163-170
|
artikel
|
| 21 |
IFN-α2a Therapy in Two Patients with Inborn Errors of TLR3 and IRF3 Infected with SARS-CoV-2
|
Lévy, Romain
|
|
|
41 |
1 |
p. 26-27
|
artikel
|
| 22 |
IKAROS-Associated Diseases in 2020: Genotypes, Phenotypes, and Outcomes in Primary Immune Deficiency/Inborn Errors of Immunity
|
Kuehn, Hye Sun
|
|
|
41 |
1 |
p. 1-10
|
artikel
|
| 23 |
Immunodeficiency Disease Spectrum in HIV-Negative Individuals with Talaromycosis
|
Qiu, Ye
|
|
|
41 |
1 |
p. 221-223
|
artikel
|
| 24 |
Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers
|
Dorsey, Morna J.
|
|
|
41 |
1 |
p. 38-50
|
artikel
|
| 25 |
Infections in Patients with Chronic Granulomatous Disease Treated with Tumor Necrosis Factor Alpha Blockers for Inflammatory Complications
|
Conrad, Anne
|
|
|
41 |
1 |
p. 185-193
|
artikel
|
| 26 |
IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation
|
Nishimura, Shiho
|
|
|
41 |
1 |
p. 125-135
|
artikel
|
| 27 |
JAK Inhibition in a Patient with X-Linked Reticulate Pigmentary Disorder
|
Légeret, Corinne
|
|
|
41 |
1 |
p. 212-216
|
artikel
|
| 28 |
MSMD in a 3-Generation Multiplex Kindred Due to Autosomal Dominant STAT1 Deficiency
|
Bhattad, Sagar
|
|
|
41 |
1 |
p. 259-261
|
artikel
|
| 29 |
Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis
|
Yucel, Esra
|
|
|
41 |
1 |
p. 59-65
|
artikel
|
| 30 |
Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary Immunodeficiency
|
Lum, Su Han
|
|
|
41 |
1 |
p. 171-184
|
artikel
|
| 31 |
Parents’ Perspectives and Societal Acceptance of Implementation of Newborn Screening for SCID in the Netherlands
|
Blom, Maartje
|
|
|
41 |
1 |
p. 99-108
|
artikel
|
| 32 |
Pathogenic TLR3 Variant in a Patient with Recurrent Herpes Simplex Virus 1–Triggered Erythema Multiforme
|
Bucciol, Giorgia
|
|
|
41 |
1 |
p. 280-282
|
artikel
|
| 33 |
Persistent Unexplained Transaminitis in COPA Syndrome
|
Thaivalappil, Silpa S.
|
|
|
41 |
1 |
p. 205-208
|
artikel
|
| 34 |
POLD1 Deficiency Reveals a Role for POLD1 in DNA Repair and T and B Cell Development
|
Nichols-Vinueza, Diana X.
|
|
|
41 |
1 |
p. 270-273
|
artikel
|
| 35 |
Recovery from COVID-19 in a Child with Chronic Granulomatous Disease and T Cell Lymphopenia
|
Mantravadi, Vasudha
|
|
|
41 |
1 |
p. 23-25
|
artikel
|
| 36 |
Relationship Between Severity of T Cell Lymphopenia and Immune Dysregulation in Patients with DiGeorge Syndrome (22q11.2 Deletions and/or Related TBX1 Mutations): a USIDNET Study
|
Deshpande, Deepti R.
|
|
|
41 |
1 |
p. 29-37
|
artikel
|
| 37 |
Safety and Tolerability of Manual Push Administration of Subcutaneous IgPro20 at High Infusion Rates in Patients with Primary Immunodeficiency: Findings from the Manual Push Administration Cohort of the HILO Study
|
Cowan, Juthaporn
|
|
|
41 |
1 |
p. 66-75
|
artikel
|
| 38 |
Seasonal Influenza Vaccine: Uptake, Attitude, and Knowledge Among Patients Receiving Immunoglobulin Replacement Therapy
|
Cox, Fionnuala
|
|
|
41 |
1 |
p. 194-204
|
artikel
|
| 39 |
STK4 Deficiency Impairs Innate Immunity and Interferon Production Through Negative Regulation of TBK1-IRF3 Signaling
|
Jørgensen, Sofie E.
|
|
|
41 |
1 |
p. 109-124
|
artikel
|
| 40 |
The J Daughter Siberia Project
|
Tuzankina, Irina
|
|
|
41 |
1 |
p. 262-265
|
artikel
|
| 41 |
Unusual Prominent Pulmonary Involvement in a Homozygous PRF1 Gene Variant in a Female Patient
|
Alsohime, Fahad
|
|
|
41 |
1 |
p. 217-220
|
artikel
|
| 42 |
Variable Abnormalities in T and B Cell Subsets in Ataxia Telangiectasia
|
Moeini Shad, Tannaz
|
|
|
41 |
1 |
p. 76-88
|
artikel
|
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