Results 31 to 40 of about 8,625 (250)

Neurological, Neurodevelopmental and Treatment Outcomes in Patients With Pyruvate Dehydrogenase Complex Deficiency

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The aim of this study was to characterize intellectual and motor function, neurological features including epilepsy, treatment response, and adaptive behavior in patients with pyruvate dehydrogenase complex deficiency (PDCD) in Sweden.
Antri Savvidou, Colin Reilly, Kalliopi Sofou, Sofia Ygberg, Erik A. Eklund, Karin Naess, Niklas Darin   +6 more
wiley   +1 more source

Assessing the Sensitivity and the Clinical Impact of the 2023 American College of Rheumatology/EULAR Classification Criteria in Obstetric Antiphospholid Syndrome: Findings From a Multicenter Italian Cohort With a Long‐Term Follow‐Up

Arthritis Care &Research, EarlyView.
Objective The aim of this study was to evaluate the sensitivity of the 2023 American College of Rheumatology (ACR)/EULAR classification criteria for antiphospholipid syndrome (APS) in a real‐world cohort of women diagnosed with primary obstetric APS (oAPS) and to assess their ability to identify patients at risk of future pregnancy complications ...
Francesca Ruffilli, Cecilia Nalli, Francesca Crisafulli, Carlo Garaffoni, Marcello Govoni, Giulia Voltarel, Alba C. Pozzi, Beatrice Maranini, Ettore Silvagni, Alessandra Bortoluzzi, Angela Tincani   +10 more
wiley   +1 more source

Assessment of Nutritional Status among Adult Hemophilia Patients in Gaza Strip

Proceedings, 2023
Congenital Hemophilia is an X-linked bleeding disorder caused by a deficiency of coagulation factor VII (in hemophilia A) or factor IX (in hemophilia B). The deficiency is the result of mutations of respective clotting factor genes.
Ibrahim M. Ashour
doaj   +1 more source

Safe Neuraxial Anesthesia in a Pregnant Patient with Congenital Factor VII Deficiency: A Case Report

Journal of Obstetric Anaesthesia and Critical Care
Congenital factor VII deficiency is a rare autosomal recessive bleeding disorder with a variable clinical phenotype, ranging from asymptomatic individuals to those with severe hemorrhage.
Keith Asselborn, Manuel Alexander Winninger, Alex Farr, Johannes Gratz   +3 more
doaj   +1 more source

A Case Report of Severe Factor XI Deficiency during Cardiac Surgery: Less Can Be More

Journal of Cardiovascular Development and Disease, 2022
Severe congenital Factor XI (FXI) deficiency (
Toshinobu Kazui, Vance G. Nielsen, Spencer D. Audie, Rajagopalan M. Venkataramani, John T. Bryant, Kristin Swenson, Paul M. Ford   +6 more
doaj   +1 more source

Incidence, Risk Factors and Management of Adverse Events in Contemporary Real‐World Care of Children with Juvenile Idiopathic Arthritis

Arthritis Care &Research, Accepted Article.
Objective We describe the frequency, risk factors, severity, and management of actionable and serious adverse events (AAE and SAE) in children with newly diagnosed Juvenile Idiopathic Arthritis (JIA) in Canada. Methods We enrolled patients within 3 months of JIA diagnosis in the Canadian Alliance of Pediatric Rheumatology Investigators (CAPRI) Registry,
Bashayer Alnuaimi, Roberta A. Berard, Jean‐Philippe Proulx‐Gauthier, Heinrike Schmeling, Michelle Batthish, Gilles Boire, Adam M. Huber, Dax G. Rumsey, Jaime Guzman, Gaëlle Chédeville, The CAPRI registry Investigators   +10 more
wiley   +1 more source

Biochemical, molecular and clinical aspects of coagulation factor VII and its role in hemostasis and thrombosis

Haematologica, 2021
Activated factor VII (FVIIa), the first protease of clotting, expresses its physiological procoagulant potential only after complexing with tissue factor (TF) exposed to blood.
Francesco Bernardi, Guglielmo Mariani
doaj   +1 more source

Intrasplenic Thymus Organogenesis from Injectable Tissue Fragments Restores Functional T‐Cell Immunity

Advanced Science, EarlyView.
Clinical intramuscular thymus transplantation yields only short‐lived efficacy and marginal therapeutic benefits. Benefiting from the spleen's intrinsic strengths—rapid vascular perfusion, abundant developmental factors, and resident progenitors—the intrasplenic thymic grafts achieve robust thymic regeneration and substantial T‐cell reconstitution ...
Shaocong Wang, Zijian Zhang, Fulin Dai, Zhijie Yin, Zhen Xing, Yurong Li, Haochong Lei, Junfeng Zhang, Chunyan Liu, Yan Li, Lei Dong   +10 more
wiley   +1 more source

Late diagnosed factor VII deficiency – a rare but significant haemorrhagic diathesis

Pediatria Polska
Factor VII (FVII) deficiency is a rare but significant inherited autosomal recessive coagulation disorder, occurring with a frequency of 1 in 300,000-500,000 people.
Karolina Małgorzata Różycka, Beata Kuczyńska, Kinga Podsiadło, Małgorzata Mitura-Lesiuk, Irena Woźnica- Karczmarz   +4 more
doaj   +1 more source

A child with congenital factor VII deficiency

Sri Lanka Journal of Child Health, 2009
Sri Lanka Journal of Child Health, 2003; 32: 113-4(Key words: congenital factor VII deficiency, child) doi: 10.4038/sljch.v32i4 ...
M Ranjan, H K Welgama
openaire   +2 more sources