• A Case of Hemophagocytic Lymphohistiocytosis (HLH) Secondary to T Cell Lymphoma and Cytomegalovirus (CMV) Infection and Complicated by Tumor Lysis Syndrome (TLS)
• A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene
• A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene
• A case report of patient with severe acute cholangitis with tigecycline treatment causing coagulopathy and hypofibrinogenemia
• A Chinese family with congenital Dysfibrinogenemia carries a heterozygous missense mutation in FGA: Concerning the genetic abnormality and clinical treatment
• A Family with Congenital Dysfibrinogenemia and Blood Transfusion
• A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family
• A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family
• A low-dose therapy of fibrinogen supplement during perioperative period of total knee arthroplasty in an asymptomatic man with congenital dysfibrinogenemia: A case report
• A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec
• A novel fibrinogen gamma-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese family
• A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the gamma165Cys-Bbeta227Cys disulfide bond and ultimately leads to hypofibrinogenemia
• A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the γ165Cys-Bβ227Cys disulfide bond and ultimately leads to hypofibrinogenemia
• A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report
• A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese family
• A novel heterozygous mutation (gammaIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family
• A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family
• A novel mutation in exon 2 of FGB caused by c.221G>T () substitution, predicting the replacement of the native Arginine at position 74 with a Leucine (p.Arg74Leu () ) in a proband from a Kurdish family with dysfibrinogenaemia and familial venous and ar
• A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family
• A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review
• A Rare Cause of Pancytopenia in an Exclusively Breastfed Infant
• A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family
• An <em>FGA</em> Frameshift Variant Associated with Afibrinogenemia in Dachshunds
• An FGA Frameshift Variant Associated with Afibrinogenemia in Dachshunds
• Analysis of a family with congenital hypodysfibrinogenemia presented with thrombosis
• Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene
• Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T&gt;A variant of the FGB gene
• Can the phenotype of inherited fibrinogen disorders be predicted?
• Case reports of envenomation and venom composition differences between two Arizona populations of the Southwestern Speckled Rattlesnake, Crotalus pyrrhus (Cope, 1867)
• Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population
• Clinical phenotype and laboratory characteristics of 93 patients with congenital fibrinogen disorders from unrelated 36 families
• Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia
• Clinical, Biochemical, Molecular, and Outcome Features of Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency in 10 Chinese Patients
• Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria
• Clinicopathological features of hepatic fibrinogen storage disease in children
• Combined Congenital Hypodysfibrinogemia and Factor XI Deficiency in a Chinese Family
• Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia
• Congenital Afibrinogenemia With Facial Haematoma
• Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management
• Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region
• Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BbetaAla68Thr) manifesting as superior sagittal sinus thrombosis
• Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BβAla68Thr) manifesting as superior sagittal sinus thrombosis
• Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literature
• Congenital Fibrinogen Deficiency Caused by Novel FGG Gene Mutation
• Congenital hypodysfibrinogenemia associated with a novel deletion of three residues (γAla289_Asp291del) in fibrinogen
• Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report
• Cortical venous thrombosis, multiple cortical infarctions, and vaginal bleeding in a Chinese family with hypofibrinogenemia caused by the FGG mutation c.1019C&gt;T: a case report
• Cortical venous thrombosis, multiple cortical infarctions, and vaginal bleeding in a Chinese family with hypofibrinogenemia caused by the FGG mutation c.1019C>T: a case report
• Diagnosis of congenital fibrinogen disorders
• Dysfibrinogenemia-Potential Impact of Genotype on Thrombosis or Bleeding
• Extension of the Human Fibrinogen Database with Detailed Clinical Information-The αC-Connector Segment
• Familial hemophagocytic lymphohistiocytosis in a neonate: Case report and literature review
• Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases
• Familial hemophagocytic lymphohistiocytosis type 5 in a Chinese Tibetan patient caused by a novel compound heterozygous mutation in STXBP2
• Familial hemophagocytic lymphohistiocytosis: from autopsy to prenatal diagnosis. Report of a case
• Fibrinogen BOE II: Intracerebral hemorrhage associated with a novel compound mutation in a Chinese family with dysfibrinogenemia
• Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia
• First case of very late-onset FHL2 in Spain with two variants in the PRF1 gene
• Genetic Analysis of A Case of Congenital Dysfibrinogenemia Caused by Arg16His Mutation in Exon 2 of FGA
• Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene
• Genetics of Primary Hemophagocytic Lymphohistiocytosis
• Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation
• Germline Compound Heterozygous Variants Identified in the <em>STXBP2</em> Gene Leading to a Familial Hemophagocytic Lymphohistiocytosis Type 5: A Case Report
• Germline Compound Heterozygous Variants Identified in the STXBP2 Gene Leading to a Familial Hemophagocytic Lymphohistiocytosis Type 5: A Case Report
• Guideline for diagnosis and management of congenital dysfibrinogenemia
• Hemizygous FGG p.Ala108Gly in a hypofibrinogenemic patient with a heterozygous 14.8 Mb deletion encompassing the entire fibrinogen gene cluster
• Hemophagocytic lymphohistiocytosis in a child with human immunodeficiency virus infection - a case report
• Hemophagocytic Lymphohistiocytosis in Children
• Hemophagocytic lymphohistiocytosis responding to withdrawal of gluten: a case report
• Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis
• Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis
• Hiding in plain sight: Diagnosing congenital dysfibrinogenemia in a child presenting with acute myeloid leukemia
• Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications
• Hypofibrinogenaemia associated with novel Aalpha126ValAsp mutation in the fibrinogen coiled coil
• Hypofibrinogenaemia associated with novel Aα126Val→Asp mutation in the fibrinogen coiled coil
• Identification of a novel mutation in congenital afibrinogenemia in Iranian patients
• Identification of Two Novel Fibrinogen Bbeta Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders
• Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders
• Management of congenital dysfibrinogenemia in pregnancy: A challenging patient case
• Management of congenital quantitative fibrinogen disorders: a Delphi consensus
• Management of dysfibrinogenemia in pregnancy: A case report
• Mild Bleeders: Diagnosis is Elusive in Large Number of Patients
• Misdiagnosis of a patient with congenital dysfibrinogenemia: A case report and literature review
• Mutation analysis of a FGG gene causing hereditary abnormal fibrinogen
• Mutations in inherited fibrinogen disorders correlated with clinical features in the Chinese population
• Neonatal Haemophagocytic Lymphohistiocytosis Associated with Maternal Adult-Onset Still's Disease
• Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report
• Perioperative management of pregnant women combined with congenital fibrinogen deficiency: four cases report and literature review
• Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency
• Rare clotting factor deficiency among Sudanese children
• Rethinking fibrinogen storage disease of the liver: ground glass and globular inclusions do not represent a congenital metabolic disorder but acquired collective retention of proteins
• Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders
• Role of Fibrinogen in Trauma-Induced Coagulopathy
• Severe Wound Healing Impairment in a Patient with Dysfibrinogenaemia
• Similar but not the same: Differential diagnosis of HLH and sepsis
• The Bioflavonoids Rutin and Rutin Succinate Neutralize the Toxins of <em>B. jararaca</em> Venom and Inhibit its Lethality
• Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His
• Tocilizumab in COVID-19: a study of adverse drug events reported in the WHO database
• Two Novel Heterozygous Mutations (p.gammaPhe230Val and p.AalphaAsn839Thr) Cause Hereditary Hypodysfibrinogenemia in Two Chinese Independent Families
• Two Novel Heterozygous Mutations (p.γPhe230Val and p.AαAsn839Thr) Cause Hereditary Hypodysfibrinogenemia in Two Chinese Independent Families