Results 71 to 80 of about 22,070 (144)

Classification of Platelet‐Activating Anti‐Platelet Factor 4 Disorders

International Journal of Laboratory Hematology, Volume 48, Issue 2, Page 259-271, April 2026.
ABSTRACT Introduction The prototypic anti‐platelet factor 4 (PF4) disorder—heparin‐induced thrombocytopenia and thrombosis (HITT)—features immunoglobulin G (IgG) class antibodies that activate platelets, monocytes, and neutrophils in a mainly heparin‐dependent fashion via Fcγ receptor‐dependent cellular activation.
Theodore E. Warkentin
wiley   +1 more source

A case of propylthiouracil induced antineutrophil cytoplasmic antibody associated vasculopathy

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Nikhil Dwivedi, Jessica Witherspoon, Sarath Bodapati   +2 more
wiley   +1 more source

A 17-Year-Old Female with Systemic Lupus Presents with Complex Movement Disorder: Possible Relationship with Antiribosomal P Antibodies

Case Reports in Neurological Medicine, 2013
Complex movement disorder is a relatively rare presentation of neurolupus. Antiphospholipid antibodies are associated with movement disorders likely via aberrant neuronal stimulation.
Muhammed Emin Özcan, Meriç Adil Altınöz, Hasan Hüseyin Karadeli, Talip Asil, Abdulkadir Koçer   +4 more
doaj   +1 more source

Lingual Dyskinesia as the Presenting Feature of Acquired Demyelinating Syndrome: A Case Report and Review of Differential Diagnoses

Journal of Paediatrics and Child Health, EarlyView.
Briana Davis, Ahmed Kaki, Eppie M. Yiu, Emma Macdonald‐Laurs   +3 more
wiley   +1 more source

Protean Manifestations of Systemic Lupus Erythematosus With Antiphospholipid Syndrome: A Case Report of a Rare Variant of Libman‐Sack's Endocarditis and Optic Perineuritis

ACR Open Rheumatology, Volume 8, Issue 4, April 2026.
Mikako Harata, Anne Abel, Ying Jin
wiley   +1 more source

Serum markers thrombophilia in pregnant women with Systemic Lupus Erythematosus

Revista Brasileira de Saúde Materno Infantil
Objectives: to determine the frequency of serum markers for hereditary and acquired thrombophilia and their association with pregnancy in women with Systemic Lupus Erythematosus (SLE).
Vanessa Marcon de Oliveira, Ernesto Antonio Figueiró-Filho, Cristiane Munaretto Ferreira, Erica Freire de Vasconcelos Pereira   +3 more
doaj   +1 more source

Antiphospholipid Syndrome and the Kidney

Kidney International Reports
Antiphospholipid syndrome (APS) is a rare autoimmune disorder characterized by the persistent positivity of antiphospholipid antibodies (aPLs) along with thrombotic manifestations, obstetrical complications, or nonthrombotic manifestations. The kidney is
Maxime Taghavi, Lucas Jacobs, Dario Roccatello, Savino Sciascia   +3 more
doaj   +1 more source

Neurovascular complications of antiphospholipid syndrome: a narrative review

Arquivos de Neuro-Psiquiatria
Background Antiphospholipid syndrome (APS) is a systemic autoimmune disorder characterized by thrombosis, pregnancy complications, and other nonthrombotic manifestations in the presence of antiphospholipid antibodies.
George Nilton Nunes Mendes, Alessandra Braga Cruz Guedes de Morais, Laura Catherine Gioia, Grégory Jacquin, Alexandre Y. Poppe, Felipe Hideki Soga, João Brainer Clares de Andrade   +6 more
doaj   +1 more source

Antiphospholipid antibody-positive Takayasu arteritis： a case report and literature review

Linchuang shenzangbing zazhi
ObjectiveTo investigate the clinical features of antiphospholipid antibody-positive Takayasu arteritis and to enhance the awareness of its diagnosis and treatment.MethodsThe clinical features and imaging data of one patient with antiphospholipid antibody-
Wang Ding-ding, Wu Hao-wen, Sun Miao-xin, Chai Wen-xiu, Li Yun-xia, Zhao Xin-cheng, Li Zi-wei, Duan Li-ping   +7 more
doaj   +1 more source

Effects of antiphospholipid antibodies in the severity and outcome of COVID-19. [PDF]

BMC Infect Dis
Zamani B, Najafizadeh M, Jokar A, Rahimi H, Motedayyen H.   +4 more
europepmc   +1 more source