Suchergebnisse - "Cosi, Elisabetta"

PubPharm (56)

1

Coexistence of Multiple Gene Variants in Some Patients with Erythrocytoses

enthalten in: Mediterranean journal of hematology and infectious diseases | 2024

von Benetti, A. | Bertozzi, I. | Ceolotto, G. | +5

2

A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding

enthalten in: Journal of thrombosis and thrombolysis | 2021

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

3

A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding

enthalten in: Journal of thrombosis and thrombolysis | 2020

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

4

A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding

enthalten in: Journal of thrombosis and thrombolysis | 2020

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

5

A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding

enthalten in: Journal of thrombosis and thrombolysis | 2020

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

6

Prevalence and Causes of Anemia in Hospitalized Patients : Impact on Diseases Outcome

enthalten in: Journal of clinical medicine | 2020

von Randi, M. | Bertozzi, I. | Santarossa, C. | +5

7

African and African-American Contribution to the Knowledge of the FVII Padua (Arg304Gln) Defect

enthalten in: Journal of the National Medical Association | 2020

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

8

Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States

enthalten in: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis | 2020

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

9

Systemic Mastocytosis and Essential Thrombocythemia : Case Report and Literature Overview

enthalten in: Medicina (Kaunas, Lithuania) | 2019

von Cancian, M. | Cosi, E. | Pizzi, M. | +4

10

Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations

enthalten in: British journal of haematology | 2019

von Gurnari, C. | Lombardi, A. | Cosi, E. | +11

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