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PubPharm (6)
1
A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome
enthalten in:
Aging clinical and experimental research
| 2021
von
Ferrari, S.
|
Regazzo, D.
|
Omenetto, E.
| +4
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2
A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome
enthalten in:
Aging clinical and experimental research
| 2020
von
Ferrari, S.
|
Regazzo, D.
|
Omenetto, E.
| +4
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3
A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome
enthalten in:
Aging clinical and experimental research
| 2020
von
Ferrari, S.
|
Regazzo, D.
|
Omenetto, E.
| +4
Wird geladen...
4
Coronary microvascular dysfunction due to essential thrombocythemia and policythemia vera : the missing piece in the puzzle of their increased cardiovascular risk?
enthalten in:
American journal of hematology
| 2015
von
Vianello, F.
|
Cella, G.
|
Osto, E.
| +8
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5
Coronary microvascular dysfunction due to essential thrombocythemia and policythemia vera: The missing piece in the puzzle of their increased cardiovascular risk?
enthalten in:
American journal of hematology
| 2015
von
Vianello, F.
|
Cella, G.
|
Osto, E.
| +8
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6
Coagulation activation in children with sickle cell disease is associated with cerebral small vessel vasculopathy
enthalten in:
PloS one
| 2013
von
Colombatti, R.
|
De Bon, E.
|
Bertomoro, A.
| +14
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1
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Aging clinical and experimental research
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American journal of hematology
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Myelodysplastic syndromes
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Platelets
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Research Support, Non-U.S. Gov't
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ANKRD26
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ANKRD26 protein, human
1
Cardiovascular disease
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Core Binding Factor Alpha 2 Subunit
1
Coronary Artery Disease - etiology
1
Coronary Artery Disease - genetics
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Coronary Artery Disease - physiopathology
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EC 2.7.10.2
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EC 3.4.21.5
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Heart attacks
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Intercellular Signaling Peptides and Proteins
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