Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
|
|
6.
|
|
|
7.
|
|
|
8.
|
|
|
9.
|
|
|
10.
|
TLR4 single nucleotide polymorphisms and thrombosis risk in patients with myeloproliferative disorders. [electronic resource] by
- Speletas, M
- Liadaki, K
- Kalala, F
- Daiou, C
- Katodritou, E
- Mandala, E
- Korantzis, I
- Ritis, K
- Zintzaras, E
- Germenis, A E
Producer: 20080811
In:
Thrombosis research vol. 122
Availability: No items available.
|
|
11.
|
|
|
12.
|
International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency. [electronic resource] by
- Farkas, H
- Martinez-Saguer, I
- Bork, K
- Bowen, T
- Craig, T
- Frank, M
- Germenis, A E
- Grumach, A S
- Luczay, A
- Varga, L
- Zanichelli, A
Producer: 20171207
In:
Allergy vol. 72
Availability: No items available.
|
|
13.
|
F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema. [electronic resource] by
- Speletas, M
- Szilágyi, Á
- Csuka, D
- Koutsostathis, N
- Psarros, F
- Moldovan, D
- Magerl, M
- Kompoti, M
- Varga, L
- Maurer, M
- Farkas, H
- Germenis, A E
Producer: 20161109
In:
Allergy vol. 70
Availability: No items available.
|
|
14.
|
On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema. [electronic resource] by
- Germenis, A E
- Loules, G
- Zamanakou, M
- Psarros, F
- González-Quevedo, T
- Speletas, M
- Bork, K
- Wulff, K
- Steinmüller-Magin, L
- Braenne, I
- Staubach-Renz, P
- Witzke, G
- Hardt, J
Producer: 20190415
In:
Allergy vol. 73
Availability: No items available.
|