| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression
|
Jackson, Carolyn C.
|
|
2015
|
36 |
1 |
p. 19-27
|
artikel
|
| 2 |
Angioedema Triggered by Medication Blocking the Renin/Angiotensin System: Retrospective Study Using the French National Pharmacovigilance Database
|
Faisant, Charles
|
|
2015
|
36 |
1 |
p. 95-102
|
artikel
|
| 3 |
A Patient with CTLA-4 Haploinsufficiency Presenting Gastric Cancer
|
Hayakawa, Seiichi
|
|
2015
|
36 |
1 |
p. 28-32
|
artikel
|
| 4 |
A Successful HSCT in a Girl with Novel LRBA Mutation with Refractory Celiac Disease
|
Sari, Sinan
|
|
2015
|
36 |
1 |
p. 8-11
|
artikel
|
| 5 |
Clinical Features, Non-Infectious Manifestations and Survival Analysis of 161 Children with Primary Immunodeficiency in Mexico: A Single Center Experience Over two Decades
|
Lugo Reyes, Saul Oswaldo
|
|
2015
|
36 |
1 |
p. 56-65
|
artikel
|
| 6 |
Complement Study Versus CINH Gene Testing for the Diagnosis of Type I Hereditary Angioedema in Children
|
Pedrosa, María
|
|
2015
|
36 |
1 |
p. 16-18
|
artikel
|
| 7 |
Decreased Frequency and Secretion of CD26 Promotes Disease Progression in Indian Post Kala-azar Dermal Leishmaniasis
|
Mukherjee, Shibabrata
|
|
2015
|
36 |
1 |
p. 85-94
|
artikel
|
| 8 |
Immune Dysregulation Syndromes (IPEX, CD27 Deficiency, and Others): Always Doomed from the Start?
|
Seidel, Markus G.
|
|
2015
|
36 |
1 |
p. 6-7
|
artikel
|
| 9 |
Magnetic Resonance Imaging May Be a Valuable Radiation-Free Technique for Lung Pathologies in Patients with Primary Immunodeficiency
|
Arslan, Sevket
|
|
2015
|
36 |
1 |
p. 66-72
|
artikel
|
| 10 |
Major Histocompatibility Complex Class II Deficiency due to a Novel Mutation in RFXANK in a Child of Mexican Descent
|
Clarridge, Katherine
|
|
|
36 |
1 |
p. 4-5
|
artikel
|
| 11 |
Major Histocompatibility Complex Class II Deficiency due to a Novel Mutation in RFXANK in a Child of Mexican Descent
|
Clarridge, Katherine
|
|
2015
|
36 |
1 |
p. 4-5
|
artikel
|
| 12 |
Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine)
|
Sharapova, Svetlana O.
|
|
2015
|
36 |
1 |
p. 46-55
|
artikel
|
| 13 |
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies
|
Lougaris, Vassilios
|
|
2015
|
36 |
1 |
p. 1-3
|
artikel
|
| 14 |
Severe Mycobacterial Diseases in a Patient with GOF IκBα Mutation Without EDA
|
Lee, Alison Joanne
|
|
2015
|
36 |
1 |
p. 12-15
|
artikel
|
| 15 |
Spectrum of Phenotypes Associated with Mutations in LRBA
|
Alkhairy, Omar K.
|
|
2015
|
36 |
1 |
p. 33-45
|
artikel
|
| 16 |
The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1
|
Depner, Mark
|
|
2015
|
36 |
1 |
p. 73-84
|
artikel
|
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