| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal Newborn Screen in a WHIM Syndrome Infant
|
Evans, Martin O.
|
|
|
39 |
8 |
p. 839-841
|
artikel
|
| 2 |
A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus
|
Duan, Ruonan
|
|
|
39 |
8 |
p. 795-804
|
artikel
|
| 3 |
A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus
|
Duan, Ruonan
|
|
|
39 |
8 |
p. 795-804
|
artikel
|
| 4 |
Altered Monocyte Subsets in Patients with Chronic Idiopathic Neutropenia
|
Bizymi, Nikoleta
|
|
|
39 |
8 |
p. 852-854
|
artikel
|
| 5 |
Autosomal Dominant Hyper-IgE Syndrome Without Significantly Elevated IgE
|
Larsen, Carsten S.
|
|
|
39 |
8 |
p. 827-831
|
artikel
|
| 6 |
Clinical and Molecular Features of Chronic Granulomatous Disease in Mainland China and a XL-CGD Female Infant Patient After Prenatal Diagnosis
|
Wang, Shiyu
|
|
|
39 |
8 |
p. 762-775
|
artikel
|
| 7 |
Correction to: Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease
|
Zurro, Nuria Bengala
|
|
|
39 |
8 |
p. 860
|
artikel
|
| 8 |
Editorial, Journal of Clinical Immunology
|
Casanova, Jean-Laurent
|
|
|
39 |
8 |
p. 751-752
|
artikel
|
| 9 |
Homozygous Splice ADA2 Gene Mutation Causing ADA-2 Deficiency
|
Chong-Neto, Herberto Jose
|
|
|
39 |
8 |
p. 842-845
|
artikel
|
| 10 |
Interstitial Lung Disease Frequently Precedes CVID Diagnosis
|
Hanitsch, Leif G.
|
|
|
39 |
8 |
p. 849-851
|
artikel
|
| 11 |
Management of ADA-Deficient SCID Patient on Adagen During Pregnancy
|
Shams, Marissa
|
|
|
39 |
8 |
p. 846-848
|
artikel
|
| 12 |
Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib
|
Shehri, Tariq Al
|
|
|
39 |
8 |
p. 776-785
|
artikel
|
| 13 |
Provider Perceptions of Quality of Life, Neurocognition, Physical Well-being, and Psychosocial Health in Patients with Primary Immunodeficiency/Immune Dysregulation Conditions
|
Michniacki, Thomas F.
|
|
|
39 |
8 |
p. 805-813
|
artikel
|
| 14 |
Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
|
Anterasian, Christine
|
|
|
39 |
8 |
p. 814-822
|
artikel
|
| 15 |
Quality of Life of Patients with Wiskott Aldrich Syndrome and X-Linked Thrombocytopenia: a Study of the Primary Immune Deficiency Consortium (PIDTC), Immune Deficiency Foundation, and the Wiskott-Aldrich Foundation
|
Shah, Ami J.
|
|
|
39 |
8 |
p. 786-794
|
artikel
|
| 16 |
Serum Tryptase Cannot Differentiate Vancomycin-Induced Anaphylaxis From Red Man Syndrome
|
Noguchi, Satoko
|
|
|
39 |
8 |
p. 855-856
|
artikel
|
| 17 |
STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman’s-Like Disease
|
Al-Saud, Bandar
|
|
|
39 |
8 |
p. 823-826
|
artikel
|
| 18 |
Successful Treatment of PAPA Syndrome with Dual Adalimumab and Tacrolimus Therapy
|
Sood, Amika K.
|
|
|
39 |
8 |
p. 832-835
|
artikel
|
| 19 |
Survey of Infection Control Precautions for Patients with Severe Combined Immune Deficiency
|
Dergousoff, Brieanne A.
|
|
|
39 |
8 |
p. 753-761
|
artikel
|
| 20 |
The Value of Chromosome Analysis to Interrogate Variants in DNMT3B Causing Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome Type I (ICF1)
|
Kellner, Erinn S.
|
|
|
39 |
8 |
p. 857-859
|
artikel
|
| 21 |
Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease
|
Zurro, Nuria B.
|
|
|
39 |
8 |
p. 836-838
|
artikel
|
| 22 |
Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease
|
Zurro, Nuria B.
|
|
|
39 |
8 |
p. 836-838
|
artikel
|
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