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 |