Suchergebnisse - "Lombardi, Anna Maria"

PubPharm (90)

1

Multi-segment rupture of the 2016 Amatrice-Visso-Norcia seismic sequence (central Italy) constrained by the first high-quality catalog of Early Aftershocks

enthalten in: Scientific reports | 2019

von Improta, L. | Latorre, D. | Margheriti, L. | +47

2

Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels : An indication for splenectomy?

enthalten in: Hematology reports | 2019

von Lombardi, A. | Pasquale, I. | Businaro, M. | +4

3

Collaboration between human and veterinary medicine as a tool to solve public health problems

enthalten in: The Lancet. Planetary health | 2019

von De Giusti, M. | Barbato, D. | Lia, L. | +5

CommentIn: Lancet Planet Health. 2019 May;3(5):e210. - PMID 31128765

4

Link between von Willebrand factor multimers, relapses and coronary microcirculation in patients with thrombotic thrombocytopenic purpura in remission

enthalten in: Thrombosis research | 2019

von Di Pasquale, I. | Budde, U. | Tona, F. | +7

5

A structure-function analysis in patients with prekallikrein deficiency

enthalten in: Hematology (Amsterdam, Netherlands) | 2018

von Girolami, A. | Ferrari, S. | Cosi, E. | +1

6

Two novel missense mutations in EPOR gene causes erythrocytosis in two unrelated patients

enthalten in: British journal of haematology | 2018

von Peroni, E. | Bertozzi, I. | Gherlinzoni, F. | +5

7

Congenital prothrombin defects : they are not only associated with bleeding but also with thrombosis: a new classification is needed

enthalten in: Hematology (Amsterdam, Netherlands) | 2018

von Girolami, A. | Ferrari, S. | Cosi, E. | +2

8

Factor X Friuli Coagulation Disorder : Almost 50 Years Later

enthalten in: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis | 2018

von Girolami, A. | Cosi, E. | Santarossa, C. | +3

9

Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study

enthalten in: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 2017

von Girolami, A. | Santarossa, C. | Cosi, E. | +3

10

Spectrum of 5'UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia : c.-140C>G mutation is more frequent than expected

enthalten in: Platelets | 2017

von Ferrari, S. | Lombardi, A. | Putti, M. | +5

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