Thrombotic Thrombocytopenic Purpura (ADAMTS13 [a Disintegrin and Metalloproteinase With a Thrombospondin Type 1 Motif, Member 13] Deficiency) as Cause of Recurrent Multiterritory Ischemic Strokes-Reference-Cited by-同舟云学术

Thrombotic Thrombocytopenic Purpura (ADAMTS13 [a Disintegrin and Metalloproteinase With a Thrombospondin Type 1 Motif, Member 13] Deficiency) as Cause of Recurrent Multiterritory Ischemic Strokes

Published:2022-06 Issue:6 Volume:53 Page:
ISSN:0039-2499
Container-title:Stroke
language:en
Short-container-title:Stroke

Author:

Albo Zimbul¹²^ORCID,Mathew Carol³⁴^ORCID,Catton Raymond¹^ORCID,Silver Brian¹^ORCID,Moonis Majaz¹^ORCID

Affiliation:

1. Department of Neurology (Z.A., R.C., B.S., M.M.), University of Massachusetts Medical School, Worcester.

2. Now with: Department of Neurology, Tufts University Medical School, MA (Z.A.).

3. Hematology and Oncology (C.M.), University of Massachusetts Medical School, Worcester.

4. Now with: Hematology and Oncology, University of Florida, Gainesville (C.M.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

Reference10 articles.

1. Hereditary Thrombotic Thrombocytopenic Purpura

2. Reduced ADAMTS13 activity during TTP remission is associated with stroke in TTP survivors

3. Thrombotic Thrombocytopenic Purpura: A Thrombotic Disorder Caused by ADAMTS13 Deficiency

4. Emerging roles of adjunct therapies in acquired thrombotic thrombocytopenia purpura

5. Targeting von Willebrand Factor in Ischaemic Stroke: Focus on Clinical Evidence

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