Results 91 to 100 of about 28,167 (192)

Analysis of the Phenotype and Gene Mutations of Two Families With Combined Mutations of Anticoagulant Protein Genes

Molecular Genetics &Genomic Medicine, Volume 14, Issue 4, April 2026.
In these two pedigrees, we identified distinct mutations in the AT and PC genes. Individuals harboring both mutations exhibited a significantly higher incidence of venous thrombosis. ABSTRACT Background AT and PC are key components of the anticoagulant system. Mutations in their encoding genes, SERPINC1 and PROC, can lead to insufficient protein levels
Yueli Guo, Tingting Shan, Wenjieying Zheng, Chun Zhao, Wanzhong Kong, Xiaojing Zou   +5 more
wiley   +1 more source

Granulomatosis with Polyangiitis (Wegener’s Granulomatosis) Co-Existing with Antiphospholipid Syndrome – An Unusual Cutaneous Presentation

Pakistan Journal of Medicine and Dentistry
Granulomatosis with polyangiitis (GPA) is an autoimmune disease that causes inflammation of the small blood vessels and involves many organs, most commonly the upper and lower respiratory tracts and the kidneys. GPA can also affect other organs, such as
Neha Rana, Humaira Talat, Maryam Rehan, Reema Mirza, Batool ur Rehman   +4 more
doaj   +1 more source

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

Sneddon’s syndrome: case report and review of its relationship with antiphospholipid syndrome [PDF]

Einstein (São Paulo), 2012
The Sneddon’s syndrome is a rare disorder characterized by theoccurrence of cerebrovascular disease associated with livedoreticularis. The antiphospholipid syndrome is the most frequent typeof acquired thrombophilia, defined by the occurrence of ...
Livia Almeida Dutra, Pedro Braga-Neto, José Luiz Pedroso, Orlando Graziani Povoas Barsottini   +3 more
doaj  

Predictive Factors of Response and Real‐World Experience of Baricitinib on Alopecia Areata: A Single Tertiary Center Study on a 72 Patients' Cohort

International Journal of Dermatology, EarlyView.
Alonso García‐Núñez, Antonio Alcalá Ramírez Del Puerto, Roberto Daza‐García, María Teresa Monserrat‐García, Mercedes Morillo‐Andújar, Javier Jesús Domínguez‐Cruz, Román Barabash‐Neila   +6 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

Antiphospholipid Syndrome [PDF]

Journal of the Royal Society of Medicine, 2002
Sanjay C, Keswani, Naresh, Chauhan
openaire   +2 more sources

Antiphospholipid syndrome [PDF]

BMJ, 2015
Jallow, Tracy, D'Cruz, David, Lempp, Heidi   +2 more
openaire   +3 more sources

Churg–Strauss syndrome associated with antiphospholipid antibodies in a patient with recurrent myocardial and cerebral ischemia

International Medical Case Reports Journal, 2012
Marino Paroli,1 Alessandro Polidoro,1 Simone Romano,1 Daniele Accapezzato21Department of Biotechnology and Medical-Surgical Sciences, 2Department of Internal Medicine and Medical Specialties, Sapienza University of Rome, Rome, ItalyAbstract: We report on
Paroli M, Polidoro A, Romano S, Accapezzato D   +3 more
doaj  

Antiphospholipid syndrome and pregnancy-a hematologic perspective. [PDF]

Res Pract Thromb Haemost
Doyle AJ, Cox C, Breen KA.
europepmc   +1 more source