| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activity, Severity and Impact of Respiratory Disease in Primary Antibody Deficiency Syndromes
|
Hurst, John R.
|
|
2013
|
34 |
1 |
p. 68-75
|
artikel
|
| 2 |
Allogeneic Bone Marrow Transplantation Appears to Ameliorate IgA Nephropathy in a Patient with X-linked Thrombocytopenia
|
Hoshino, Akihiro
|
|
2013
|
34 |
1 |
p. 53-57
|
artikel
|
| 3 |
Attending to Warning Signs of Primary Immunodeficiency Diseases Across the Range of Clinical Practice
|
Costa-Carvalho, Beatriz Tavares
|
|
2013
|
34 |
1 |
p. 10-22
|
artikel
|
| 4 |
Chronic Granulomatous Disease: Two Decades of Experience From a Tertiary Care Centre in North West India
|
Rawat, Amit
|
|
2013
|
34 |
1 |
p. 58-67
|
artikel
|
| 5 |
Clinical and Genetic Profile of Children with Periodic Fever Syndromes from a Single Medical Center in South East Michigan
|
Chandrakasan, Shanmuganathan
|
|
2013
|
34 |
1 |
p. 104-113
|
artikel
|
| 6 |
Compound Heterozygous RAG2 Mutations Mimicking Hyper IgM Syndrome
|
Riccetto, A. G. L.
|
|
2013
|
34 |
1 |
p. 7-9
|
artikel
|
| 7 |
Increased Circulating Th17 Cell Populations and Elevated CSF Osteopontin and IL-17 Concentrations in Patients with Guillain-Barré Syndrome
|
Han, Rong kun
|
|
2013
|
34 |
1 |
p. 94-103
|
artikel
|
| 8 |
In Memoriam
|
Cunningham Rundles, Charlotte
|
|
2013
|
34 |
1 |
p. 1-2
|
artikel
|
| 9 |
Intact IFN-γR1 Expression and Function Distinguishes Langerhans Cell Histiocytosis From Mendelian Susceptibility to Mycobacterial Disease
|
Quispel, Willemijn T.
|
|
2013
|
34 |
1 |
p. 84-93
|
artikel
|
| 10 |
Intermittent Neutropenia as an Early Feature of Mild Mevalonate Kinase Deficiency
|
Parvaneh, Nima
|
|
2013
|
34 |
1 |
p. 123-126
|
artikel
|
| 11 |
Measurement of Pneumococcal Polysaccharide Vaccine Responses for Immunodeficiency Diagnostics: Combined IgG Responses Compared to Serotype Specific IgG Responses
|
Janssen, Willemijn J. M.
|
|
2013
|
34 |
1 |
p. 3-6
|
artikel
|
| 12 |
Novel SMARCAL1 Bi-allelic Mutations Associated with a Chromosomal Breakage Phenotype in a Severe SIOD Patient
|
Simon, Amos J.
|
|
2013
|
34 |
1 |
p. 76-83
|
artikel
|
| 13 |
Ocular Involvement in Primary Immunodeficiency Diseases
|
Hosseinverdi, Sima
|
|
2013
|
34 |
1 |
p. 23-38
|
artikel
|
| 14 |
Ocular Involvement in Primary Immunodeficiency Diseases
|
Hosseinverdi, Sima
|
|
|
34 |
1 |
p. 23-38
|
artikel
|
| 15 |
Phenotypic Variations of Cartilage Hair Hypoplasia: Granulomatous Skin Inflammation and Severe T Cell Immunodeficiency as Initial Clinical Presentation in Otherwise Well Child with Short Stature
|
McCann, Liza J.
|
|
2013
|
34 |
1 |
p. 42-48
|
artikel
|
| 16 |
Phenotypic Variations of Cartilage Hair Hypoplasia: Granulomatous Skin Inflammation and Severe T Cell Immunodeficiency as Initial Clinical Presentation in Otherwise Well Child with Short Stature
|
McCann, Liza J.
|
|
|
34 |
1 |
p. 42-48
|
artikel
|
| 17 |
Psychrobacter immobilis Septicemia in a Boy with X-linked Chronic Granulomatous Disease and Fulminant Hepatic Failure
|
Sriaroon, Panida
|
|
2013
|
34 |
1 |
p. 39-41
|
artikel
|
| 18 |
Renal Amyloidosis in a Patient with X-linked Agammaglobulinemia (Bruton’s Disease) and Bronchiectasis
|
Gonzalo-Garijo, M. A.
|
|
2013
|
34 |
1 |
p. 119-122
|
artikel
|
| 19 |
Sporothrix schenckii Lymphadentitis in a Male with X-linked Chronic Granulomatous Disease
|
Trotter, Jessica R.
|
|
2013
|
34 |
1 |
p. 49-52
|
artikel
|
| 20 |
Terminal Deletion of 11q with Significant Late-Onset Combined Immune Deficiency
|
Seppänen, Mikko
|
|
2013
|
34 |
1 |
p. 114-118
|
artikel
|
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