| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Defective Oxidative Burst and Impaired Antigen Presentation are Hallmarks of Human Visceral Leishmaniasis
|
Roy, Susmita
|
|
2014
|
35 |
1 |
p. 56-67
|
artikel
|
| 2 |
Dramatic Improvement in the Multifocal Positron Emission Tomography Findings of a Young Adult with Chronic Granulomatous Disease Following Allogeneic Hematopoietic Stem Cell Transplantation
|
Shigemura, Tomonari
|
|
2014
|
35 |
1 |
p. 84-86
|
artikel
|
| 3 |
Epidemiology of Primary Immunodeficiency in Iceland
|
Ludviksson, Bjorn R.
|
|
2014
|
35 |
1 |
p. 75-79
|
artikel
|
| 4 |
Gain of Function Mutations of PIK3CD as a Cause of Primary Sclerosing Cholangitis
|
Hartman, Heather N.
|
|
2014
|
35 |
1 |
p. 11-14
|
artikel
|
| 5 |
Germline CARD11 Mutation in a Patient with Severe Congenital B Cell Lymphocytosis
|
Brohl, Andrew S.
|
|
2014
|
35 |
1 |
p. 32-46
|
artikel
|
| 6 |
Hematopoietic Stem Cell Transplantation for X-Linked Thrombocytopenia With Mutations in the WAS gene
|
Oshima, Koichi
|
|
2014
|
35 |
1 |
p. 15-21
|
artikel
|
| 7 |
Interaction of Pattern Recognition Receptors with Mycobacterium Tuberculosis
|
Mortaz, Esmaeil
|
|
2014
|
35 |
1 |
p. 1-10
|
artikel
|
| 8 |
Invariant Natural Killer T Cells are Reduced in Hereditary Hemochromatosis Patients
|
Maia, M. L.
|
|
2014
|
35 |
1 |
p. 68-74
|
artikel
|
| 9 |
Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia
|
Esmaeilzadeh, Hossein
|
|
2014
|
35 |
1 |
p. 22-25
|
artikel
|
| 10 |
Orf Infection in a Patient with Stat1 Gain-of-Function
|
Kilic, Sara Sebnem
|
|
|
35 |
1 |
p. 80-83
|
artikel
|
| 11 |
Orf Infection in a Patient with Stat1 Gain-of-Function
|
Kilic, Sara Sebnem
|
|
2014
|
35 |
1 |
p. 80-83
|
artikel
|
| 12 |
Relationships Between Clinico-Epidemiological Patterns of Invasive Meningococcal Infections and Complement Deficiencies in French South Pacific Islands (New Caledonia)
|
Daures, Maguy
|
|
2014
|
35 |
1 |
p. 47-55
|
artikel
|
| 13 |
Reversal of Immunoglobulin A Deficiency in Children
|
Lim, Che Kang
|
|
2014
|
35 |
1 |
p. 87-91
|
artikel
|
| 14 |
Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A Gene
|
Tóth, B.
|
|
2014
|
35 |
1 |
p. 26-31
|
artikel
|
| 15 |
Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal Leukoencephalopathy
|
Day-Williams, Aaron G.
|
|
2014
|
35 |
1 |
p. 92-96
|
artikel
|
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