Disease: Intrinsic factor- congenital deficiency of
- <em>The Fibroblast Growth Factor 9 (Fgf9)</em> Participates in Palatogenesis by Promoting Palatal Growth and Elevation
- "Familial Multiple Coagulation Factor Deficiencies of FXI and FXII in an Asymptomatic Saudi Woman"
- A candidate activation pathway for coagulation factor VII
- A case of megaloblastic anemia in childhood due to congenital deficiency of intrinsic factor: review of 33 cases
- A Case Report of Severe Factor XI Deficiency during Cardiac Surgery: Less Can Be More
- A genetic polymorphism in the coding region of the gastric intrinsic factor gene (GIF) is associated with congenital intrinsic factor deficiency
- A putative inhibitory mechanism in the tenase complex responsible for loss of coagulation function in acquired haemophilia A patients with anti-C2 autoantibodies
- A Rare Case of Acquired Hemolytic Anemia and Pancytopenia Secondary to Pernicious Anemia
- A successful surgical case of atrial septal defect with congenital factor XI deficiency
- A urinary radioisotope-binding assay to diagnose Gräsbeck-Imerslund disease
- Acquired and inherited disorders of cobalamin and folate in children
- Acquired hemophilia A: a frequently overlooked autoimmune hemorrhagic disorder
- Advances and dilemmas in factor XI
- Association of combined GIF290T>C heterozygous mutation/FUT2 secretor variant with neural tube defects
- Autoimmune Gastritis
- Automated amidolytic method for evaluating the activated partial thromboplastin time compared with a conventional coagulation method
- Binding of Factor VIII to Lipid Nanodiscs Increases its Clotting Function in a Mouse Model of Hemophilia A
- CACH/VWM syndrome and leucodystrophies related to EIF2B mutations
- Captopril-induced changes on active and inactive renin in a patient with factor XII congenital deficiency
- Chromogenic substrates for activated partial thromboplastin time testing: are they worth using?
- Coagulation and fibrinolysis associated with contact phase in plasma with high molecular weight kininogen deficiency
- Coagulation factor XI as a novel target for antithrombotic treatment
- Coagulation-factor deficiencies and abnormal bleeding in Noonan's syndrome
- Combined congenital deficiencies of intrinsic factor and R binder
- Complex history of the discovery and characterization of congenital factor X deficiency
- Congenital combined deficiency of coagulation factors VII and II in a young adult
- Congenital deficiency of intrinsic factor
- Congenital deficit of intrinsic factor. Diagnostic problems apropos of 2 cases
- Congenital factor X deficiencies with a defect only or predominantly in the extrinsic or in the intrinsic system: a critical evaluation
- Congenital intrinsic factor deficiency in a Spanish patient
- Congenital intrinsic factor deficiency. Apropos of 3 cases in a sibship
- Congenital limb deficiencies with vascular etiology: Possible association with maternal thrombophilia
- Congenital macrodactyly: a clinical study
- Congenital neutrophil defects and periodontal diseases
- Corneal epithelial stem cells: deficiency and regulation
- Deficiency of the Wnt receptor Ryk causes multiple cardiac and outflow tract defects
- Emicizumab for acquired haemophilia A: A case series
- ERBIN deficiency links STAT3 and TGF-beta pathway defects with atopy in humans
- ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans
- Factor X Roma: a congenital factor X variant defective at different degrees in the intrinsic and the extrinsic activation
- Factor XI and factor XII as targets for new anticoagulants
- Factor XI-deficient mice exhibit increased bleeding after injury to the saphenous vein
- Frequency of intrinsic factor antibody in megaloblastic anaemia
- G-CSF improves murine G6PC3-deficient neutrophil function by modulating apoptosis and energy homeostasis
- Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant
- Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders
- Hereditary intrinsic factor deficiency in China caused by a novel mutation in the intrinsic factor gene-a case report
- Hereditary juvenile cobalamin deficiency due to mutations in GIF gene
- Heterozygous congenital Factor VII deficiency with the 9729del4 mutation, associated with severe spontaneous intracranial bleeding in an adolescent male
- Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in Jordan
- How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B(12) absorption?
- Human gastric intrinsic factor: characterization of cDNA and genomic clones and localization to human chromosome 11
- Hypothesis: a new role for the Renin-Angiotensin system in ureteric bud branching
- ICON: the early diagnosis of congenital immunodeficiencies
- Imerslund disease
- Imerslund-Gräsbeck syndrome in an African patient
- Immunocytochemical analysis of dystrophin in congenital muscular dystrophy
- Intrinsic coagulation pathway in end-stage renal disease associated with spinal cord injury treated with hemodialysis
- Intrinsic susceptibility to misfolding of a hot-spot for Hirschsprung disease mutations in the ectodomain of RET
- Is factor XII deficiency related to recurrent miscarriage?
- Isolated Prolongation of Activated Partial Thromboplastin Time: Not Just Bleeding Risk!
- Linkage analysis of a large inbred family with congenital megaloblastic anemia
- Malabsorption and the nervous system
- Missense mutations of dual oxidase 2 (DUOX2) implicated in congenital hypothyroidism have impaired trafficking in cells reconstituted with DUOX2 maturation factor
- Molecular analysis of factor XII gene in Thai patients with factor XII deficiency
- Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X "Vorarlberg")
- Monitoring prothrombin activation in plasma through loss of Förster resonance energy transfer
- Multimodal imaging reveals a role for Akt1 in fetal cardiac development
- No developmental failure of cultured tooth germs from osteopetrotic (op/op) mice
- Nontuberculous mycobacterial infections
- Novel CUBN Mutation in a Young Child With Megaloblastic Anemia
- Novel Majeed Syndrome-Causing LPIN2 Mutations Link Bone Inflammation to Inflammatory M2 Macrophages and Accelerated Osteoclastogenesis
- One-step chromogenic equivalent of activated partial thromboplastin time evaluated for clinical application
- Paradoxical hyperfibrinolysis is associated with a more intensely haemorrhagic phenotype in severe congenital haemophilia
- Pernicious anemia associated with cryptogenic cirrhosis: Two case reports and a literature review
- Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era
- Phosphatase Wip1 negatively regulates neutrophil development through p38 MAPK-STAT1
- Plasma Kallikrein Contributes to Coagulation in the Absence of Factor XI by Activating Factor IX
- Prenatal radiation-induced limb defects mediated by Trp53-dependent apoptosis in mice
- Primary immunodeficiencies associated with pneumococcal disease
- Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors
- Recent developments in the understanding of the pathophysiology of osteopetrosis
- Reduced neuronal innervation in the distal end of the proximal esophageal atretic segment in cases of esophageal atresia with distal tracheoesophageal fistula
- Report 2 cases of congenital factor XII deficiency: a rare coagulation disorder
- Selective vitamin B 12 malabsorption in a 19-year-old patient
- Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence
- Studies on a circulating anticoagulant inhibiting factor XI in a patient with congenital deficiency and carcinoma of the prostate
- Surgical management in the patient with congenital factor XII deficiency. Report of a case
- Terbium chelation, a specific fluorescent tagging of human transferrin. Optimization of conditions in view of its application to the HPLC analysis of carbohydrate-deficient transferrin (CDT)
- The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain
- The clinical findings and prophylactic treatment in children with factor X deficiency
- The Fibroblast Growth Factor 9 (Fgf9) Participates in Palatogenesis by Promoting Palatal Growth and Elevation
- The intrinsic pathway of coagulation: a target for treating thromboembolic disease?
- The relationship between major intrinsic protein genes and cataract
- The routine determination of the endogenous thrombin potential, first results in different forms of hyper- and hypocoagulability
- The sample that would not clot
- The Standard Point-of-Care Hemochron Jr. ACT+ Test in Monitoring Heparin Administration for Cardiopulmonary Bypass in Severe Factor XII Deficiency
- Thromboelastometry as an Ancillary Tool for Evaluation of Coagulation Status after rFVIIa Therapy in a Pregnant Woman with Severe Hypoproconvertinemia-A Case Series and Review of the Literature
- Vitamin B12 in health and disease: part I--inherited disorders of function, absorption, and transport
- Von Willebrand factor--cleaving protease activity in congenital thrombotic thrombocytopenic purpura