Sandra L Haberichter
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Explore the profile of Sandra L Haberichter including associated specialties, affiliations and a list of published articles.
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54
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1055
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Recent Articles
1.
Perry C, Christopherson P, Agostini T, Haberichter S, Montgomery R, Flood V
Blood Adv
. 2024 Aug;
8(19):5051-5061.
PMID: 39088757
von Willebrand disease (VWD) is an inherited bleeding disorder caused by quantitative or qualitative defects in the von Willebrand factor (VWF) protein. Type 3 VWD has a severe bleeding phenotype...
2.
Cuker A, Kunkle R, Bercovitz R, Byrne M, Djulbegovic B, Haberichter S, et al.
Blood Adv
. 2024 Apr;
8(11):2960-2963.
PMID: 38593461
The American Society of Hematology (ASH) develops a variety of resources that provide guidance to clinicians on the diagnosis and management of blood diseases. These resources include clinical practice guidelines...
3.
Sadler B, Christopherson P, Perry C, Bellissimo D, Haberichter S, Haller G, et al.
Res Pract Thromb Haemost
. 2023 Dec;
7(7):102232.
PMID: 38077814
Background: Genetic analysis for von Willebrand disease (VWD) commonly utilizes DNA sequencing to identify variants in the von Willebrand factor () gene; however, this technique cannot always detect copy-number variants...
4.
Christopherson P, Tijet N, Haberichter S, Flood V, Ross J, Notley C, et al.
J Thromb Haemost
. 2023 Dec;
22(3):666-675.
PMID: 38040335
Background: As knowledge of the human genome has advanced, so too has the recognition that interpretation of the pathogenic nature of sequence variants can be challenging. The von Willebrand factor...
5.
Lavin M, Luceros A, Kouides P, Abdul-Kadir R, ODonnell J, Baker R, et al.
J Thromb Haemost
. 2023 Feb;
21(4):1068.
PMID: 36828770
No abstract available.
6.
Christopherson P, Haberichter S, Flood V, Sicking U, Abshire T, Montgomery R
Res Pract Thromb Haemost
. 2022 Nov;
6(7):e12807.
PMID: 36381287
Background: Von Willebrand disease (VWD) is a common inherited bleeding disorder, however the diagnosis can be complicated by a subjective bleeding history and issues with some current von Willebrand factor...
7.
Parker E, Haberichter S, Lollar P
ACS Omega
. 2022 Sep;
7(35):31183-31196.
PMID: 36092565
Von Willebrand factor (VWF) is a plasma glycoprotein that participates in platelet adhesion and aggregation and serves as a carrier for blood coagulation factor VIII (fVIII). Plasma VWF consists of...
8.
Lavin M, Christopherson P, Grabell J, Abshire T, Flood V, Haberichter S, et al.
J Thromb Haemost
. 2022 Jul;
20(10):2246-2254.
PMID: 35780487
Background: Assessment of bleeding phenotype is critically important in the diagnosis of von Willebrand disease (VWD). Despite advances in bleeding assessment tools (BATs), standardized tools to evaluate bleeding following diagnosis...
9.
Doherty D, Lavin M, Byrne M, Nolan M, OSullivan J, Ryan K, et al.
Blood Adv
. 2022 May;
7(3):302-308.
PMID: 35523118
Increased von Willebrand factor (VWF) clearance plays a key role in the pathogenesis of type 1 and type 2 von Willebrand disease (VWD). However, the pathological mechanisms involved in patients...
10.
Christopherson P, Haberichter S, Flood V, Perry C, Sadler B, Bellissimo D, et al.
J Thromb Haemost
. 2022 Mar;
20(7):1576-1588.
PMID: 35343054
Background: Type 3 von Willebrand Disease (VWD) is a rare and severe form of VWD characterized by the absence of von Willebrand factor (VWF). Objectives: As part of the Zimmerman...