| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Altered Peripheral Blood Leucocyte Phenotype and Responses in Healthy Individuals with Homozygous Deletion of FHR1 and FHR3 Genes
|
Bhasym, Angika
|
|
2019
|
39 |
Suppl 1 |
p. 336-345
|
artikel
|
| 2 |
Alternative Splicing Rescues Loss of Common Gamma Chain Function and Results in IL-21R-like Deficiency
|
Illig, David
|
|
2019
|
39 |
Suppl 1 |
p. 207-215
|
artikel
|
| 3 |
A Novel CARMIL2 Mutation Resulting in Combined Immunodeficiency Manifesting with Dermatitis, Fungal, and Viral Skin Infections As Well as Selective Antibody Deficiency
|
Atschekzei, Faranaz
|
|
2019
|
39 |
Suppl 1 |
p. 274-276
|
artikel
|
| 4 |
A Novel Recessive Mutation of Interferon-γ Receptor 1 in a Patient with Mycobacterium tuberculosis in Bone Marrow Aspirate
|
Shabani, Mahsima
|
|
2019
|
39 |
Suppl 1 |
p. 127-130
|
artikel
|
| 5 |
A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects
|
Cagdas, Deniz
|
|
2019
|
39 |
Suppl 1 |
p. 726-738
|
artikel
|
| 6 |
A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant
|
Kurolap, Alina
|
|
2019
|
39 |
Suppl 1 |
p. 430-439
|
artikel
|
| 7 |
A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency
|
Coignard-Biehler, Hélène
|
|
2019
|
39 |
Suppl 1 |
p. 702-712
|
artikel
|
| 8 |
A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency
|
Coignard-Biehler, Hélène
|
|
|
39 |
Suppl 1 |
p. 702-712
|
artikel
|
| 9 |
CAPS and NLRP3
|
Booshehri, Laela M.
|
|
2019
|
39 |
Suppl 1 |
p. 277-286
|
artikel
|
| 10 |
Cellular Defects in CVID Patients with Chronic Lung Disease in the USIDNET Registry
|
Kellner, Erinn S.
|
|
2019
|
39 |
Suppl 1 |
p. 569-576
|
artikel
|
| 11 |
Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT
|
Marsh, Rebecca A.
|
|
2019
|
39 |
Suppl 1 |
p. 653-667
|
artikel
|
| 12 |
Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT
|
Marsh, Rebecca A.
|
|
|
39 |
Suppl 1 |
p. 653-667
|
artikel
|
| 13 |
Chronic Granulomatous Disorder–Associated Colitis Can Be Accurately Evaluated with MRI Scans and Fecal Calprotectin Level
|
Lowe, David M.
|
|
2019
|
39 |
Suppl 1 |
p. 494-504
|
artikel
|
| 14 |
Correction to: Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease
|
Zurro, Nuria Bengala
|
|
|
39 |
Suppl 1 |
p. 860
|
artikel
|
| 15 |
Current Status of the Management of Mendelian Susceptibility to Mycobacterial Disease in Mainland China
|
Ying, Wenjing
|
|
2019
|
39 |
Suppl 1 |
p. 600-610
|
artikel
|
| 16 |
DDX58 and Classic Singleton-Merten Syndrome
|
Ferreira, Carlos R.
|
|
2018
|
39 |
Suppl 1 |
p. 75-80
|
artikel
|
| 17 |
Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immune Deficiency Disorders in Children: Challenges and Outcome from a Tertiary Care Center in South India
|
Uppuluri, Ramya
|
|
2019
|
39 |
Suppl 1 |
p. 182-187
|
artikel
|
| 18 |
Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immune Deficiency Disorders in Children: Challenges and Outcome from a Tertiary Care Center in South India
|
Uppuluri, Ramya
|
|
|
39 |
Suppl 1 |
p. 182-187
|
artikel
|
| 19 |
Hematopoietic Stem Cell Transplantation in CARD9 Deficiency: Knight in Shining Armor?
|
Meyts, Isabelle
|
|
2019
|
39 |
Suppl 1 |
p. 459-461
|
artikel
|
| 20 |
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
|
Kiykim, Ayca
|
|
2018
|
39 |
Suppl 1 |
p. 37-44
|
artikel
|
| 21 |
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
|
Kiykim, Ayca
|
|
|
39 |
Suppl 1 |
p. 37-44
|
artikel
|
| 22 |
How to Identify Common Variable Immunodeficiency Patients Earlier: General Practice Patterns
|
Ilkjær, Frederik V.
|
|
2019
|
39 |
Suppl 1 |
p. 641-652
|
artikel
|
| 23 |
Interferon-γ Receptor 1 Deficiency Corrected by Umbilical Cord Blood Transplantation
|
Michniacki, Thomas F.
|
|
2019
|
39 |
Suppl 1 |
p. 257-260
|
artikel
|
| 24 |
Juvenile-Onset Immunodeficiency Secondary to Anti-Interferon-Gamma Autoantibodies
|
Liew, Woei-Kang
|
|
|
39 |
Suppl 1 |
p. 512-518
|
artikel
|
| 25 |
Juvenile-Onset Immunodeficiency Secondary to Anti-Interferon-Gamma Autoantibodies
|
Liew, Woei-Kang
|
|
2019
|
39 |
Suppl 1 |
p. 512-518
|
artikel
|
| 26 |
LINE-1-Mediated AluYa5 Insertion Underlying Complete Autosomal Recessive IFN-γR1 Deficiency
|
Rosain, Jérémie
|
|
2019
|
39 |
Suppl 1 |
p. 739-742
|
artikel
|
| 27 |
Mosaicism of an ELANE Mutation in an Asymptomatic Mother
|
Shigemura, Tomonari
|
|
2019
|
39 |
Suppl 1 |
p. 106-111
|
artikel
|
| 28 |
Nasal Nitric Oxide in Primary Immunodeficiency and Primary Ciliary Dyskinesia: Helping to Distinguish Between Clinically Similar Diseases
|
Zysman-Colman, Zofia N.
|
|
2019
|
39 |
Suppl 1 |
p. 216-224
|
artikel
|
| 29 |
Neurological Involvement in Childhood Evans Syndrome
|
Pincez, Thomas
|
|
2019
|
39 |
Suppl 1 |
p. 171-181
|
artikel
|
| 30 |
Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor Repertoire
|
Frizinsky, Shirly
|
|
2019
|
39 |
Suppl 1 |
p. 401-413
|
artikel
|
| 31 |
Pattern Recognition Molecules of the Lectin Pathway—Screening of Patients with Suspected Immunodeficiency
|
Jørgensen, Clara Mistegård
|
|
2019
|
39 |
Suppl 1 |
p. 668-677
|
artikel
|
| 32 |
Predicting the Occurrence of Variants in RAG1 and RAG2
|
Lawless, Dylan
|
|
2019
|
39 |
Suppl 1 |
p. 688-701
|
artikel
|
| 33 |
Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies
|
Hadjadj, Jérôme
|
|
2018
|
39 |
Suppl 1 |
p. 55-64
|
artikel
|
| 34 |
Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
|
Anterasian, Christine
|
|
|
39 |
Suppl 1 |
p. 814-822
|
artikel
|
| 35 |
Recurrent Salmonella typhi Infection and Autoimmunity in a Young Boy with Complete IL-12 Receptor β1 Deficiency
|
Jindal, Ankur Kumar
|
|
2019
|
39 |
Suppl 1 |
p. 358-362
|
artikel
|
| 36 |
Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders
|
Buchbinder, David
|
|
2019
|
39 |
Suppl 1 |
p. 81-89
|
artikel
|
| 37 |
Successful Rituximab Treatment for Lymphoma, Secondary Immunodeficiency Causing Debilitating Sinusitis: Underlying Primary Immunodeficiency Disease, and Alternative Treatments to Improve the Quality of Life?
|
Bonagura, Vincent R.
|
|
2019
|
39 |
Suppl 1 |
p. 229-230
|
artikel
|
| 38 |
TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia
|
Paradis, C.
|
|
2019
|
39 |
Suppl 1 |
p. 118-125
|
artikel
|
| 39 |
Variable Responses to Tocilizumab in Four Patients with Schnitzler Syndrome
|
Claus, Jonas
|
|
2019
|
39 |
Suppl 1 |
p. 370-372
|
artikel
|
| 40 |
WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure
|
Heusinkveld, Lauren E.
|
|
2019
|
39 |
Suppl 1 |
p. 532-556
|
artikel
|
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