|
🦁
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Clinical features and survival of patients with indolent systemic mastocytosis defined by the updated WHO classification
43 auth.
J. Trizuljak,
W. Sperr,
L. Nekvindová,
Hanneke N G Oude Elberink,
K. Gleixner,
A. Górska,
M. Lange,
K. Hartmann,
A. Illerhaus,
M. Bonifacio,
C. Perkins,
C. Elena,
L. Malcovati,
A. Belloni Fortina,
K. Shoumariyeh,
...
M. Jawhar,
R. Zanotti,
P. Bonadonna,
F. Caroppo,
A. Zink,
M. Triggiani,
R. Parente,
N. von Bubnoff,
Akif Selim Yavuz,
H. Hägglund,
M. Mattsson,
J. Panse,
N. Jäkel,
Alex Kilbertus,
O. Hermine,
M. Arock,
D. Fuchs,
V. Sabato,
K. Brockow,
A. Bretterklieber,
M. Niedoszytko,
B. van Anrooij,
A. Reiter,
J. Gotlib,
H. Kluin-Nelemans,
J. Mayer,
M. Doubek,
P. Valent
|
5 |
2020 |
5
🦁
|
|
🐜
|
Ofatumumab added to dexamethasone in patients with relapsed or refractory chronic lymphocytic leukemia: Results from a phase II study
22 auth.
M. Doubek,
Y. Brychtova,
A. Panovska,
Ludmila Šebejová,
O. Stehlikova,
J. Chovancová,
J. Malcikova,
J. Šmardová,
K. Plevová,
P. Volfová,
...
M. Trbušek,
M. Mraz,
Denisa Bakešová,
J. Trizuljak,
M. Hadrabová,
P. Obrtlíková,
J. Karban,
L. Smolej,
A. Oltová,
E. Jelínková,
Š. Pospíšilová,
J. Mayer
|
4 |
2015 |
4
🐜
|
|
🐜
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A novel germline mutation of the SFTPA1 gene in familial interstitial pneumonia
12 auth.
M. Doubková,
K. Staňo Kozubík,
L. Radová,
M. Pešová,
J. Trizuljak,
K. Pal,
...
Klára Svobodová,
K. Réblová,
H. Svozilová,
Z. Vrzalova,
Š. Pospíšilová,
M. Doubek
|
4 |
2019 |
4
🐜
|
|
🦁
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A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome
13 auth.
J. Trizuljak,
K. S. Kozubík,
L. Radová,
M. Pešová,
K. Pal,
K. Réblová,
O. Stehlikova,
P. Smejkal,
J. Zavřelová,
Milan Pacejka,
...
J. Mayer,
Š. Pospíšilová,
M. Doubek
|
3 |
2018 |
3
🦁
|
|
🐜
|
Novel genetic variant of HPS1 gene in Hermansky-Pudlak syndrome with fulminant progression of pulmonary fibrosis: a case report
8 auth.
M. Doubková,
J. Trizuljak,
Z. Vrzalova,
A. Hrazdirová,
I. Blaháková,
L. Radová,
...
Š. Pospíšilová,
M. Doubek
|
3 |
2019 |
3
🐜
|
|
🐜
|
C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies
13 auth.
K. Staňo Kozubík,
L. Radová,
M. Pešová,
K. Réblová,
J. Trizuljak,
K. Plevová,
V. Fiamoli,
J. Gumulec,
H. Urbankova,
T. Szotkowski,
...
J. Mayer,
Š. Pospíšilová,
M. Doubek
|
3 |
2018 |
3
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|
