• "I have been refused to be treated by three dentists": Barriers to patient care
• A Case Report of Acquired Factor X Deficiency in a Patient With Multiple Myeloma
• A case report of congenital factor X deficiency in an adult patient
• A Compound Heterozygosis of Two Novel Mutations Causes Factor X Deficiency in a Chinese Pedigree
• A Phenome-Wide Association Study Uncovers a Pathological Role of Coagulation Factor X during <em>Acinetobacter baumannii</em> Infection
• A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female
• A Rare Cause of Coagulopathy in a Patient with Rapidly Progressive Renal Failure
• A Rare Cause of Isolated Prothrombin Time Prolongation: Congenital Factor X Deficiency
• A rare presentation of homozygous factor X deficiency in a pregnant patient: A case report and review of the literature
• A review of the pharmacokinetics, efficacy and safety of high-purity factor X for the prophylactic treatment of hereditary factor X deficiency
• Acquired factor V and factor X Deficiency coexisting with acquired dysfibrinogenaemia in a patient with light chain myeloma
• Acquired factor X deficiency in a multiple myeloma without amyloidosis: a case report
• Acquired factor X deficiency in a patient with multiple myeloma: a rare case highlighting the significance of comprehensive evaluation and the need for antimyeloma therapy for bleeding diathesis
• Acquired factor X deficiency in light-chain (AL) amyloidosis is rare and associated with advanced disease
• Acquired Factor X Deficiency in Patients With Primary Light Chain Amyloidosis
• Acquired Factor X Deficiency without Amyloidosis Presenting with Massive Hematuria: A Case Report and Review of the Literature
• Acute deep vein thrombosis with concurrent new diagnosis of AL-amyloid-induced factor X deficiency
• Analysis of seven cases of multiple myeloma with initial manifestation of bleeding
• Anesthesia strategy for factor X deficiency coagulopathy: case report
• Anticoagulation in atrial fibrillation with factor X deficiency-A management dilemma
• Autoimmune Coagulation Factor X Deficiency as a Rare Acquired Hemorrhagic Disorder: A Literature Review
• Bortezomib-based treatment can improve factor X activity in immunoglobulin light-chain amyloidosis with factor X deficiency
• Cardiac Amyloidosis Presenting with Pre-Excitation Syndrome, Heart Failure, and Severe Factor X Deficiency as Part of Systemic Amyloid Light-Chain (AL) Amyloidosis - A Fatal Combination
• Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
• Clinical features and laboratory diagnostic issues of non-immune, non-amyloid related acquired factor X deficiency
• Coagulation and fibrinolytic features in AL amyloidosis with abnormal bleeding and usefulness of tranexamic acid
• Complete remission in a bleeding patient with idiopathic autoimmune factor X deficiency caused by non-neutralizing anti-factor X autoantibody
• Congenital coagulation factor X deficiency: Genetic analysis of five patients and functional characterization of mutant factor X proteins
• Congenital Factor X deficiency in women: A systematic review of the literature
• Congenital factor X deficiency: a retrospective analysis of 11 cases
• Corrigendum to "Prevalence, clinical characteristics and treatment outcome of factor X deficiency in a consecutive cohort of primary light-chain amyloidosis" Leuk. Res. 120C (2022) 106917
• Cutaneous adverse event associated with vemurafenib in a 3-year-old pediatric patient with BRAF mutation-positive metastatic melanoma and factor X deficiency
• Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency
• Direct Factor X sequestration by systemic amyloid light-chain amyloidosis
• Do Not Ignore Those Raccoon Eyes; They May Indicate Lethal AL Amyloidosis
• Evaluation of the anticoagulant effect of low-molecular-weight heparins based on the anti-Xa level during haemodialysis
• Factor X deficiency and pregnancy
• Factor X deficiency and pregnancy: case report and counselling
• Factor X Deficiency Caused by Nonsecretory Myeloma Successfully Corrected with Bortezomib: A Case Report and Review of the Literature
• Factor X Deficiency Due to a Compound Heterozygosis Between a New Mutation (Gla72Asp) in Exon 2 and an Already Known one (Gly154Arg) in Exon 5: Factor X Mar Del Plata1)
• Factor X Deficiency Management for Elective Cesarean Delivery in a Pregnant Patient
• Factor X heterozygous mutation in a patient with potential risk of bleeding: A case report
• Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report
• Fitusiran reduces bleeding in factor X-deficient mice
• Five new F10 variants in hereditary factor x deficiency detected by high-throughput sequencing
• Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID-19-A common clinical feature between a rare disorder and a new, common infection
• Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate
• Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency
• Genotypes and phenotypes characterization of 17 Iranian patients with inherited factor X deficiency: identification of a novel mutation: Leu487Phe
• Genotypic and phenotypic analysis of a case with inherited coagulation factor X deficiency
• Genotyping of five Pakistani patients with severe inherited factor X deficiency: identification of two novel mutations
• Hereditary factor X deficiency in America survey: impact on quality of life and burden of disease in patients and caregivers
• Identification of non-neutralizing anti-factor X autoantibodies in three Japanese cases of autoimmune acquired factor X deficiency
• IgD multiple myeloma mimicking free light chain myeloma complicated by factor X deficiency: a case report
• Immunoglobulin Light Chain Amyloidosis with Severe Liver Dysfunction Accompanied by Factor X Deficiency
• Inherited Moderate Factor X Deficiency Presenting as Cardiac Tamponade
• Isolated coagulopathy without classic CRAB symptoms as the initial manifestation of multiple myeloma: A case report
• Liver transplantation for a patient with liver failure combined with liver amyloidosis and coagulation factor X deficiency
• Liver transplantation in a case of liver failure complicated with liver amyloidosis and coagulation factor X deficiency
• Management of a hemispherotomy for Rasmussen encephalitis in a patient with mild factor 10 deficiency and low von Willebrand factor levels
• Management of Acquired Factor X Deficiency Caused by In Vitro Non-neutralizing Anti-factor X Autoantibodies with Pre-emptive Corticosteroid Therapy
• Management of Factor X Deficiency for Vaginal Delivery in a Parturient: A Case Report
• Mechanical valve replacement without anticoagulation: a case report
• Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition
• Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family
• Multidisciplinary approach to the complex treatment for non-cirrhotic portal hypertension - case-report-based discussion
• Navigating the Challenges of Factor X Deficiency: A Case Study
• Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency
• Paving the way to factor X deficiency therapies
• Pediatric split liver transplantation for congenital factor X deficiency: first 10-year follow-up of a case with portal vein stenting
• Plasma-derived factor X concentrate compassionate use for hereditary factor X deficiency: Long-term safety and efficacy in a retrospective data-collection study
• Plasma-derived Factor X therapy for treatment of intracranial bleeding in a patient with Factor X deficiency: a case report
• Plasma-derived human factor X concentrate for the treatment of patients with hereditary factor X deficiency
• Post-COVID Factor X Deficiency: A Case Report From Pakistan
• Post-mortem diagnosis of severe factor X deficiency in a fetus with intracranial haemorrhage resulting in intrauterine death
• Posterior Fossa Hematoma Following Minor Trauma in an Infant with Rare Combined Factor V and Factor X Deficiency
• Postmortem diagnosis of severe factor X deficiency in a fetus with intracranial hemorrhage resulting in intrauterine death
• Preclinical development and characterization of a human plasma-derived high-purity factor X concentrate for therapeutic use
• Prevalence, clinical characteristics and treatment outcome of factor X deficiency in a consecutive cohort of primary light-chain amyloidosis
• Primary light chain amyloidosis onset with acquired FX deficiency: a case report and literature review
• Prophylactic treatment of bleeding episodes in children &lt;12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high-purity plasma-derived factor X (pdFX) concentrate
• Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high-purity plasma-derived factor X (pdFX) concentrate
• Response of factor X deficiency to darutumumab in the treatment of AL amyloidosis: a novel finding
• Role of individual factor X concentrate pharmacokinetic studies in perioperative management of AL amyloidosis-associated acquired factor X deficiency
• Severe Factor X Deficiency Presenting as Febrile Seizure in an Infant
• Spontaneous Neck and Upper Airway Hematoma
• Staged Surgical Palliation for HLHS in a Girl with Severe Factor X Deficiency
• Successful long-term management of ovarian bleeding and menorrhagia with prothrombin complex concentrate in a patient with congenital factor X deficiency
• Successful Treatment of Factor X Deficiency in a Patient with Lymphoplasmacytic Lymphoma with Bendamustine Plus Rituximab Regimen: A Case Report and Literature Review
• Successful Treatment of Life-threatening Bleeding Caused by Acquired Factor X Deficiency Associated with Respiratory Infection
• Supportive Care for Patients with Systemic Light Chain Amyloidosis
• Surgical excision of a pseudotumour under the coverage of the plasma-derived factor X concentrate in a patient with severe factor X deficiency: A case report
• The 13-year bleed: Exuberant amyloid angiopathies, angiodysplasias, and acquired coagulopathies of the gut
• The Disulfide Bond between Cys22 and Cys27 in the Protease Domain Modulate Clotting Activity of Coagulation Factor X
• The perils of inhibiting deficient factors
• Thromboembolism and bleeding in systemic amyloidosis: a review
• Uncovering the Challenges of Rare Diseases: Insights From a Retrospective Cross-Sectional Study in Albania (2005-2022)
• Upregulating sirtuin 6 ameliorates glycolysis, EMT and distant metastasis of pancreatic adenocarcinoma with krüppel-like factor 10 deficiency
• Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study
• Use of plasma-derived factor X concentrate in neonates and infants with congenital factor X deficiency