Results 61 to 70 of about 43,474 (218)
Primary Cerebral Venous Thrombosis in a Patient with Immune Thrombocytopenic Purpura
Case Reports in Neurological Medicine, 2022 Introduction. Immune thrombocytopenic purpura is an autoimmune hematological disorder characterized by low platelet level due to its destruction through autoimmune antibodies.
M. Taher Farfouti +3 more
doaj +1 more source
ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis [PDF]
, 2005 Members of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family are known to influence development, angiogenesis, coagulation and progression of arthritis.
Jones, GC, Riley, GP
core +2 more sources
Utility and Safety of Romiplostim as an Alternative to Platelet Transfusion for Neonates
Pediatric Blood &Cancer, Volume 72, Issue 7, July 2025.ABSTRACT Thrombocytopenia is a common challenge in the neonatal intensive care unit, traditionally managed with platelet transfusions. However, transfusions are associated with significant risks, including increased mortality and neurodevelopmental impairment.
Rachel N. Zeno, Sara Awad, Harry Lesmana
wiley +1 more source
Rare Presentation of Refractory Thrombotic Thrombocytopenic Purpura: Jejunal Stricture
International Journal of Hematology-Oncology and Stem Cell Research, 2017 Thrombotic thrombocytopenic purpura is a rare thrombotic disease characterized by episodes of thrombocytopenia and microangiopathic hemolytic anemia due to disseminated microvascular thrombosis.
Prabath K. Abeysundara +5 more
doaj
Intracranial Hemorrhage Due to Secondary Hypertension from Intracranial Large Vessel Occlusion [PDF]
, 2020 Simultaneous hemorrhagic and ischemic strokes have been previously reported in the literature. Typically, these occur in patients secondary to dialysis, cerebral amyloid angiopathy, or thrombotic thrombocytopenic purpura.1,2,3 However, this is the unique
Khan, Asif A. +3 more
core
Idiopathic thrombocytopenic purpura: current concepts in pathophysiology and management. [PDF]
, 2008 Idiopathic thrombocytopenic purpura (ITP) is characterized by a low platelet count, which is the result of both increased pla- telet destruction and insufficient platelet production.
Amadori, S +5 more
core +1 more source
Clinical Physiology and Functional Imaging, Volume 45, Issue 4, July 2025.Abstract Introduction It remains to be established whether it provides any clinical or diagnostic benefits to perform ventilation/perfusion (V/Q) scintigraphy as a single photon emission computed tomography in children. Here, we report our experience with this modality, evaluate its impact on clinical decision‐making and assess its interrater agreement.
Lise Borgwardt +6 more
wiley +1 more source
Idiopathic thrombocytopenic purpura
Japanese Journal of Thrombosis and Hemostasis, 2008 Point（1）診断は血小板減少をきたす他の疾患の除外を基本とする．（2）血小板数と出血症状の程度，背景因子やライフスタイルに基づいて治療適応を決める．（3）治療はまずステロイド療法,次いで摘脾を行う．（4）ITPと診断されればまずH. pyloriを検索し，陽性であれば除菌療法を優先する．
openaire +3 more sources
Applied Research, Volume 4, Issue 3, June 2025.The development of a nanobody for Nogo‐A, a potent neurite outgrowth inhibitor crucial in multiple sclerosis, is reported using a rational design approach. The nanobody targets the Nogo‐A ectodomain at the S1PR2 receptor‐binding region with submicromolar KD.
Vaidehi Roy Chowdhury +9 more
wiley +1 more source
Immune Thrombocytopenia as a Consequence of Rocky Mountain Spotted Fever
Case Reports in Oncology, 2017 Primary immune thrombocytopenia (ITP) – also called idiopathic thrombocytopenic purpura or immune thrombocytopenic purpura – is an acquired thrombocytopenia caused by autoantibodies against platelet antigens.
Cherisse Baldeo +2 more
doaj +1 more source