|
🐜
|
Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation.
12 auth.
K. Huck,
O. Feyen,
T. Niehues,
F. Rüschendorf,
N. Hübner,
H. Laws,
...
T. Telieps,
S. Knapp,
H. Wacker,
A. Meindl,
H. Jumaa,
A. Borkhardt
|
8 |
2009 |
8
🐜
|
|
🐜
|
An immunodeficiency disease with RAG mutations and granulomas.
17 auth.
C. Schuetz,
K. Huck,
S. Gudowius,
M. Megahed,
O. Feyen,
B. Hubner,
D. Schneider,
B. Manfras,
U. Pannicke,
R. Willemze,
...
R. Knüchel,
U. Göbel,
A. Schulz,
A. Borkhardt,
W. Friedrich,
K. Schwarz,
T. Niehues
|
7 |
2008 |
7
🐜
|
|
🐜
|
The BH3-only member Noxa causes apoptosis in melanoma cells by multiple pathways
9 auth.
Mohamed Hassan,
A. Alaoui,
O. Feyen,
A. Mirmohammadsadegh,
F. Essmann,
A. Tannapfel,
...
Erich Gulbins,
K. Schulze-Osthoff,
Ulrich R. Hengge
|
6 |
2008 |
6
🐜
|
|
🐜
|
A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells
15 auth.
M. Grimm,
S. Schmitt,
P. Teriete,
T. Biegner,
A. Stenzl,
J. Hennenlotter,
H. Muhs,
A. Munz,
Tatjana Nadtotschi,
K. König,
...
J. Sänger,
O. Feyen,
H. Hofmann,
S. Reinert,
J. Coy
|
5 |
2013 |
5
🐜
|
|
🐜
|
Primary necrotizing lymphocytic central nervous system vasculitis due to perforin deficiency in a four-year-old girl.
10 auth.
D. Moshous,
O. Feyen,
P. Lankisch,
K. Schwarz,
J. Schaper,
Marion Schneider,
...
D. Dilloo,
H. Laws,
B. Schwahn,
T. Niehues
|
5 |
2007 |
5
🐜
|
|
🐬
|
Memory B-cells in healthy and antibody-deficient children.
K. Huck,
O. Feyen,
Sujal Ghosh,
K. Beltz,
Sven Bellert,
T. Niehues
|
5 |
2009 |
5
🐬
|
|
🐜
|
iNKT Cell Frequency in Peripheral Blood of Caucasian Children and Adolescent: The Absolute iNKT Cell Count is Stable from Birth to Adulthood
10 auth.
K. Bienemann,
K. Iouannidou,
K. Schoenberg,
F. Krux,
S. Reuther,
O. Feyen,
...
F. Schuster,
M. Uhrberg,
H. Laws,
A. Borkhardt
|
5 |
2011 |
5
🐜
|
|
🐬
|
Description of the mutations in 15 subjects with variant forms of maple syrup urine disease
N. Flaschker,
O. Feyen,
S. Fend,
E. Simon,
P. Schadewaldt,
U. Wendel
|
5 |
2007 |
5
🐬
|
|
🐜
|
Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be tested.
13 auth.
C. Schuetz,
U. Pannicke,
Eva Jacobsen,
S. Burggraf,
M. Albert,
M. Hönig,
T. Niehues,
O. Feyen,
S. Ehl,
K. Debatin,
...
W. Friedrich,
A. Schulz,
K. Schwarz
|
5 |
2014 |
5
🐜
|
