| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Case of Burkholderia Prostatitis in a Patient with Chronic Granulomatous Disease
|
Bahal, Sameer
|
|
|
40 |
8 |
p. 1204-1206
|
artikel
|
| 2 |
A Cry for the Development of Newborn Screening for Familial Hemophagocytic Lymphohistiocytosis
|
Hoshino, Akihiro
|
|
|
40 |
8 |
p. 1196-1198
|
artikel
|
| 3 |
Adenosine Deaminase (ADA)–Deficient Severe Combined Immune Deficiency (SCID) in the US Immunodeficiency Network (USIDNet) Registry
|
Kuo, Caroline Y.
|
|
|
40 |
8 |
p. 1124-1131
|
artikel
|
| 4 |
A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency
|
Kuehn, Hye Sun
|
|
|
40 |
8 |
p. 1093-1101
|
artikel
|
| 5 |
Case Report: Acute Thrombotic Microangiopathy in a Patient with STING-Associated Vasculopathy with Onset in Infancy (SAVI)
|
Ma, Mia
|
|
|
40 |
8 |
p. 1111-1115
|
artikel
|
| 6 |
Clinical and Immunological Characterization of Combined Immunodeficiency Due to TFRC Mutation in Eight Patients
|
Aljohani, Amal H.
|
|
|
40 |
8 |
p. 1103-1110
|
artikel
|
| 7 |
Correction: Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT
|
Marsh, Rebecca A.
|
|
|
40 |
8 |
p. 1211-1213
|
artikel
|
| 8 |
Correction to: A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency
|
Kuehn, Hye Sun
|
|
|
40 |
8 |
p. 1102
|
artikel
|
| 9 |
Disseminated Mycobacterium xenopi in an Adult with IL-12Rβ1 Deficiency
|
Palterer, Boaz
|
|
|
40 |
8 |
p. 1166-1170
|
artikel
|
| 10 |
DNA Ligase IV Deficiency Identified by Chance Following Vaccine-Derived Rubella Virus Infection
|
Matsumoto, Kazuaki
|
|
|
40 |
8 |
p. 1187-1190
|
artikel
|
| 11 |
Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia
|
Inoue, Kento
|
|
|
40 |
8 |
p. 1132-1137
|
artikel
|
| 12 |
Hematopoietic Stem Cell Transplantation in Children with Inborn Errors of Immunity: a Multi-center Experience in Colombia
|
Olaya, Manuela
|
|
|
40 |
8 |
p. 1116-1123
|
artikel
|
| 13 |
Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis
|
Partanen, Terhi
|
|
|
40 |
8 |
p. 1156-1162
|
artikel
|
| 14 |
Human STAT1 Gain-of-Function Heterozygous Mutations: Chronic Mucocutaneous Candidiasis and Type I Interferonopathy
|
Okada, Satoshi
|
|
|
40 |
8 |
p. 1065-1081
|
artikel
|
| 15 |
Immune Alterations in a Patient with SARS-CoV-2-Related Acute Respiratory Distress Syndrome
|
Bouadma, Lila
|
|
|
40 |
8 |
p. 1082-1092
|
artikel
|
| 16 |
Long-Term Survival after Progressive Multifocal Leukoencephalopathy in a Patient with Primary Immune Deficiency and NFKB1 Mutation
|
Maréchal, Emke
|
|
|
40 |
8 |
p. 1138-1143
|
artikel
|
| 17 |
Neurologic Conditions and Symptoms Reported Among Common Variable Immunodeficiency Patients in the USIDNET
|
Lee, Michael
|
|
|
40 |
8 |
p. 1181-1183
|
artikel
|
| 18 |
Nocardiosis Associated with Primary Immunodeficiencies (Nocar-DIP): an International Retrospective Study and Literature Review
|
Lafont, Emmanuel
|
|
|
40 |
8 |
p. 1144-1155
|
artikel
|
| 19 |
Non-Tuberculous Mycobacterial Infection in Hematopoietic Cell Transplant
|
Sabulski, Anthony
|
|
|
40 |
8 |
p. 1171-1175
|
artikel
|
| 20 |
Phenoidentical HLA-Related Hematopoietic Stem Cell Transplant Without Conditioning to Reconstitute a Patient with a Putative Loss-of-Function CARD11 Mutation
|
Al-Rasheed, Bashayer
|
|
|
40 |
8 |
p. 1163-1165
|
artikel
|
| 21 |
Refractory Autoimmune Cytopenia in a Young Boy with a Novel LRBA Mutation Successfully Managed with Sirolimus
|
Banday, Aaqib Zaffar
|
|
|
40 |
8 |
p. 1184-1186
|
artikel
|
| 22 |
Ruxolitinib Controls Lymphoproliferation and Diabetes in a STAT3-GOF Patient
|
Wegehaupt, Oliver
|
|
|
40 |
8 |
p. 1207-1210
|
artikel
|
| 23 |
Spontaneous Gastrointestinal Perforations in STAT3-Deficient Hyper-IgE Syndrome
|
Bhattacharya, Sumona
|
|
|
40 |
8 |
p. 1199-1203
|
artikel
|
| 24 |
Successful Hematopoietic Stem Cell Transplantation in a Patient with Complete IFN-γ Receptor 2 Deficiency: a Case Report and Literature Review
|
Tovo, Pier-Angelo
|
|
|
40 |
8 |
p. 1191-1195
|
artikel
|
| 25 |
X-Linked Thrombocytopenia and Vanishing White Matter Disease in a Child: Double Tragedy
|
Pilania, Rakesh Kumar
|
|
|
40 |
8 |
p. 1176-1180
|
artikel
|
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