Suchergebnisse - "Bellissimo, Daniel B"

PubPharm (32)

1

Characterization of copy-number variants in a large cohort of patients with von Willebrand disease reveals a relationship between disrupted regions and disease type

enthalten in: Research and practice in thrombosis and haemostasis | 2023

von Sadler, B. | Christopherson, P. | Perry, C. | +8

2

Molecular pathogenesis and heterogeneity in type 3 VWD families in U.S. Zimmerman program

enthalten in: Journal of thrombosis and haemostasis : JTH | 2022

von Christopherson, P. | Haberichter, S. | Flood, V. | +54

3

Molecular pathogenesis and heterogeneity in type 3 VWD families in U.S. Zimmerman program

enthalten in: Journal of Thrombosis and Haemostasis | 2022

von Christopherson, P. | Haberichter, S. | Flood, V. | +5

4

Curated disease-causing genes for bleeding, thrombotic, and platelet disorders : Communication from the SSC of the ISTH

enthalten in: Journal of thrombosis and haemostasis : JTH | 2019

von Megy, K. | Downes, K. | Simeoni, I. | +12

5

Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders : Communication from the SSC of the ISTH

enthalten in: Journal of Thrombosis and Haemostasis | 2019

von Megy, K. | Downes, K. | Simeoni, I. | +11

6

Common VWF sequence variants associated with higher VWF and FVIII are less frequent in subjects diagnosed with type 1 VWD

enthalten in: Research and practice in thrombosis and haemostasis | 2018

von Flood, V. | Johnsen, J. | Kochelek, C. | +7

7

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

enthalten in: Blood | 2016

von Simeoni, I. | Stephens, J. | Hu, F. | +76

CommentIn: Blood. 2016 Jun 9;127(23 ):2781-2. - PMID 27282940

8

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States

enthalten in: Blood | 2016

von Flood, V. | Christopherson, P. | Gill, J. | +22

CommentIn: Blood. 2016 May 19;127(20):2373-4. - PMID 27207323

9

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States

enthalten in: Blood | 2016

von Flood, V. | Christopherson, P. | Gill, J. | +22

10

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

enthalten in: Blood | 2016

von Simeoni, I. | Stephens, J. | Hu, F. | +76