| 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 |
3 |
p. 336-345
|
artikel
|
| 2 |
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 |
3 |
p. 274-276
|
artikel
|
| 3 |
A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype
|
Rice, Laura
|
|
2019
|
39 |
3 |
p. 249-256
|
artikel
|
| 4 |
Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses
|
Siahanidou, Tania
|
|
2019
|
39 |
3 |
p. 237-240
|
artikel
|
| 5 |
CAPS and NLRP3
|
Booshehri, Laela M.
|
|
2019
|
39 |
3 |
p. 277-286
|
artikel
|
| 6 |
Clinical Features and HSCT Outcome for SCID in Turkey
|
Ikinciogullari, Aydan
|
|
2019
|
39 |
3 |
p. 316-323
|
artikel
|
| 7 |
Different Clonal T-Large Granular Lymphocyte Proliferations in SCID
|
Savaşan, Süreyya
|
|
2019
|
39 |
3 |
p. 245-248
|
artikel
|
| 8 |
EBV-Related Hodgkin Lymphoma in an ICF2 Patient: Is EBV Susceptibility a Hallmark of This ICF Subtype?
|
Licciardi, Francesco
|
|
2019
|
39 |
3 |
p. 234-236
|
artikel
|
| 9 |
Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2
|
Slade, Charlotte A.
|
|
|
39 |
3 |
p. 324-335
|
artikel
|
| 10 |
Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2
|
Slade, Charlotte A.
|
|
2019
|
39 |
3 |
p. 324-335
|
artikel
|
| 11 |
Granule Cell Neuronopathy in a Patient with Common Variable Immunodeficiency
|
McLean-Tooke, Andrew
|
|
2019
|
39 |
3 |
p. 267-269
|
artikel
|
| 12 |
Hemorrhagic Pneumonia as the First Manifestation of Anhidrotic Ectodermal Dysplasia with Immunodeficiency
|
Ichimiya, Yuko
|
|
2019
|
39 |
3 |
p. 264-266
|
artikel
|
| 13 |
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction
|
Moens, Leen
|
|
2019
|
39 |
3 |
p. 298-308
|
artikel
|
| 14 |
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction
|
Moens, Leen
|
|
|
39 |
3 |
p. 298-308
|
artikel
|
| 15 |
Interferon-γ Receptor 1 Deficiency Corrected by Umbilical Cord Blood Transplantation
|
Michniacki, Thomas F.
|
|
2019
|
39 |
3 |
p. 257-260
|
artikel
|
| 16 |
Interleukin-36 Receptor Antagonist Deficiency (DITRA) with a Novel IL36RN Homozygous Mutation c.200G > T (P.Cys67Phe) in a Young Colombian Woman
|
Zea-Vera, Andres F.
|
|
2019
|
39 |
3 |
p. 261-263
|
artikel
|
| 17 |
Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease
|
Sarrafzadeh, Shokouh Azam
|
|
2019
|
39 |
3 |
p. 287-297
|
artikel
|
| 18 |
Report of a Chinese Cohort with Leukocyte Adhesion Deficiency-I and Four Novel Mutations
|
Sun, Bijun
|
|
2019
|
39 |
3 |
p. 309-315
|
artikel
|
| 19 |
Revisiting Fatal Granulomatous Disease of Childhood Through an Autopsy: Still Lethal in the Developing World!
|
Pilania, Rakesh Kumar
|
|
2019
|
39 |
3 |
p. 241-244
|
artikel
|
| 20 |
RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency
|
Watson, Christopher M.
|
|
2019
|
39 |
3 |
p. 270-273
|
artikel
|
| 21 |
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 |
3 |
p. 229-230
|
artikel
|
| 22 |
Successful Treatment of Sinusitis with Topical Human Milk in a Lymphoma Patient Using Rituximab
|
Yamaguchi, Nise
|
|
2019
|
39 |
3 |
p. 231-233
|
artikel
|
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