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/vufind/Search/Results?lookfor=%22Alessi%2C+Marie-Christine%22&type=Person&sort=year
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PubPharm (334)
1
Single-cell analysis of megakaryopoiesis in peripheral CD34
+
cells: insights into ETV6-related thrombocytopenia
enthalten in:
bioRxiv.org
| 2024
von
Bigot, T.
|
Gabinaud, E.
|
Hannouche, L.
| +11
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2
Association of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the Bleeding Assesment Tool - LABoratory tests substudy) : communication from the Platelet Physiology ISTH-SSC
enthalten in:
Research and practice in thrombosis and haemostasis
| 2024
von
Gresele, P.
|
Falcinelli, E.
|
Bury, L.
| +14
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3
Early Metabolic Disruption and Predictive Biomarkers of Delayed-Cerebral Ischemia in Aneurysmal Subarachnoid Hemorrhage
enthalten in:
Journal of proteome research
| 2024
von
Chikh, K.
|
Tonon, D.
|
Triglia, T.
| +8
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4
Single-cell analysis of megakaryopoiesis in peripheral CD34+ cells : insights into ETV6-related thrombocytopenia
enthalten in:
Journal of thrombosis and haemostasis : JTH
| 2023
von
Bigot, T.
|
Gabinaud, E.
|
Hannouche, L.
| +13
CommentIn: J Thromb Haemost. 2023 Sep;21(9):2367-2369. - PMID 37597896
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5
Multicenter evaluation of light transmission platelet aggregation reagents : communication from the ISTH SSC Subcommittee on Platelet Physiology
enthalten in:
Journal of thrombosis and haemostasis : JTH
| 2023
von
Alessi, M.
|
Coxon, C.
|
Ibrahim-Kosta, M.
| +33
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6
Emergency management of patients with Glanzmann thrombasthenia : consensus recommendations from the French reference center for inherited platelet disorders
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Fiore, M.
|
Giraudet, J.
|
Alessi, M.
| +17
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7
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Fiore, M.
|
Giraudet, J.
|
Alessi, M.
| +17
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8
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Fiore, M.
|
Giraudet, J.
|
Alessi, M.
| +17
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9
Early metabolic disruption and predictive biomarkers of delayed-cerebral ischemia in aneurysmal subarachnoid haemorrhage
enthalten in:
bioRxiv.org
| 2023
von
Chikh, K.
|
Tonon, D.
|
Triglia, T.
| +8
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10
APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis
enthalten in:
Haematologica
| 2023
von
Stritt, S.
|
Nurden, P.
|
Nurden, A.
| +7
CommentIn: Haematologica. 2023 Mar 01;108(3):665-667. - PMID 35638552
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Thrombosis and haemostasis
22
Blood
22
International journal of cardiology
20
Arteriosclerosis, thrombosis, and vascular biology
16
The American journal of cardiology
8
Journal of thrombosis and haemostasis : JTH
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American heart journal
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British journal of haematology
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Journal of cell science
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Orphanet journal of rare diseases
5
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105
Research Support, Non-U.S. Gov't
42
Platelet Aggregation Inhibitors
38
Clopidogrel
36
OM90ZUW7M1
36
Ticlopidine
35
A74586SNO7
26
Letter
22
Review
19
Phosphoproteins
18
Cell Adhesion Molecules
18
Microfilament Proteins
18
vasodilator-stimulated phosphoprotein
17
Purinergic P2Y Receptor Antagonists
16
Plasminogen Activator Inhibitor 1
15
Biomarkers
15
Comparative Study
15
Multicenter Study
14
Aspirin
14
G89JQ59I13
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Erscheinungszeitraum
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2020-
193
2010-2019
88
2000-2009
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