| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Large Cohort of RAG1/2-Deficient SCID Patients—Clinical, Immunological, and Prognostic Analysis
|
Greenberg-Kushnir, Noa
|
|
|
40 |
1 |
p. 211-222
|
artikel
|
| 2 |
A New Patient with Inherited TYK2 Deficiency
|
Sarrafzadeh, Shokouh Azam
|
|
|
40 |
1 |
p. 232-235
|
artikel
|
| 3 |
BCG Moreau Vaccine Safety Profile and NK Cells—Double Protection Against Disseminated BCG Infection in Retrospective Study of BCG Vaccination in 52 Polish Children with Severe Combined Immunodeficiency
|
Bernatowska, Ewa
|
|
|
40 |
1 |
p. 138-146
|
artikel
|
| 4 |
2019 Clinical Immunology Society Compensation Survey
|
Williams, Kelli W.
|
|
|
40 |
1 |
p. 251-253
|
artikel
|
| 5 |
Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions
|
Ittiwut, Chupong
|
|
|
40 |
1 |
p. 227-231
|
artikel
|
| 6 |
Conversations with Founders of the Field of Human Inborn Errors of Immunity
|
Buckley, Rebecca H.
|
|
|
40 |
1 |
p. 1-8
|
artikel
|
| 7 |
Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
|
Tangye, Stuart G.
|
|
|
40 |
1 |
p. 65
|
artikel
|
| 8 |
Defining Polysaccharide Antibody Deficiency: Measurement of Anti-Pneumococcal Antibodies and Anti-Salmonella typhi Antibodies in a Cohort of Patients with Recurrent Infections
|
Bucciol, Giorgia
|
|
|
40 |
1 |
p. 105-113
|
artikel
|
| 9 |
Extended Follow-up After Hematopoietic Cell Transplantation for IκBα Deficiency with Disseminated Mycobacterium avium Infection
|
Seghezzo, Sara P.
|
|
|
40 |
1 |
p. 248-250
|
artikel
|
| 10 |
Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families
|
Ben-Ali, Meriem
|
|
|
40 |
1 |
p. 96-104
|
artikel
|
| 11 |
How I Manage Natural Killer Cell Deficiency
|
Orange, Jordan S.
|
|
|
40 |
1 |
p. 13-23
|
artikel
|
| 12 |
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification
|
Bousfiha, Aziz
|
|
|
40 |
1 |
p. 66-81
|
artikel
|
| 13 |
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
|
Tangye, Stuart G.
|
|
|
40 |
1 |
p. 24-64
|
artikel
|
| 14 |
Immune Dysregulation in the Tonsillar Microenvironment of Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA) Syndrome
|
Luu, Irene
|
|
|
40 |
1 |
p. 179-190
|
artikel
|
| 15 |
Lazy Leukocyte Syndrome—an Enigma Finally Solved?
|
Etzioni, Amos
|
|
|
40 |
1 |
p. 9-12
|
artikel
|
| 16 |
Low-Dose Pioglitazone does not Increase ROS Production in Chronic Granulomatous Disease Patients with Severe Infection
|
Hui, Xiaoying
|
|
|
40 |
1 |
p. 131-137
|
artikel
|
| 17 |
MiR-608 Exerts Anti-inflammatory Effects by Targeting ELANE in Monocytes
|
Gu, Wei
|
|
|
40 |
1 |
p. 147-157
|
artikel
|
| 18 |
Molecular and Phenotypic Characterization of Nine Patients with STAT1 GOF Mutations in China
|
Chen, Xuemei
|
|
|
40 |
1 |
p. 82-95
|
artikel
|
| 19 |
Mutual alteration of NOD2-associated Blau syndrome and IFNγR1 deficiency
|
Parackova, Zuzana
|
|
|
40 |
1 |
p. 165-178
|
artikel
|
| 20 |
NAPDH Oxidase-Specific Flow Cytometry Allows for Rapid Genetic Triage and Classification of Novel Variants in Chronic Granulomatous Disease
|
Sacco, Keith A.
|
|
|
40 |
1 |
p. 191-202
|
artikel
|
| 21 |
Novel Missense Mutation inSP110Associated with Combined Immunodeficiency and Advanced Liver Disease Without VOD
|
Delmonte, Ottavia M.
|
|
|
40 |
1 |
p. 236-239
|
artikel
|
| 22 |
Prophylactic Antibiotics Versus Immunoglobulin Replacement in Specific Antibody Deficiency
|
Joud Hajjar,
|
|
|
40 |
1 |
p. 158-164
|
artikel
|
| 23 |
Should MASP-2 Deficiency Be Considered a Primary Immunodeficiency? Relevance of the Lectin Pathway
|
García-Laorden, M. Isabel
|
|
|
40 |
1 |
p. 203-210
|
artikel
|
| 24 |
STING-Associated Vasculopathy with Onset in Infancy in Three Children with New Clinical Aspect and Unsatisfactory Therapeutic Responses to Tofacitinib
|
Tang, Xiaolei
|
|
|
40 |
1 |
p. 114-122
|
artikel
|
| 25 |
Successful Treatment of a Patient with Chronic Systemic Capillary Leak Syndrome, Neutropenia and Thymoma
|
Ghurye, Rohit R.
|
|
|
40 |
1 |
p. 240-244
|
artikel
|
| 26 |
The Broad Clinical Spectrum and Transplant Results of PNP Deficiency
|
Schejter, Yael Dinur
|
|
|
40 |
1 |
p. 123-130
|
artikel
|
| 27 |
TTC7A Variants Previously Described to Cause Enteropathy Are Observed on a Single Haplotype and Appear Non-pathogenic in Pediatric Inflammatory Bowel Disease Patients
|
Ashton, James J.
|
|
|
40 |
1 |
p. 245-247
|
artikel
|
| 28 |
Unreported Missense Mutation in the Dimerization Domain of ADA2 Leads to ADA2 Deficiency Associated with Severe Oral Ulcers and Neutropenia in a Female Somalian Patient—Addendum to the Genotype-Phenotype Puzzle
|
Göschl, Lisa
|
|
|
40 |
1 |
p. 223-226
|
artikel
|
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