Pages that link to "Q40980369"
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The following pages link to Congenital SPCA deficiency: a hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum fractions (Q40980369):
Displaying 50 items.
- Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state (Q30448554) (← links)
- Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency (Q30448556) (← links)
- Inherited bleeding disorders (Q33382672) (← links)
- Application of continuous flow electrophoresis to the study of the blood coagulation proteins and the fibrinolytic enzyme system. I. Normal human materials (Q33709012) (← links)
- The Laboratory of Coagulation A review of present laboratory techniques (Q33801938) (← links)
- History of tissue factor (Q34022469) (← links)
- Disappearance rate of concentrated proconvertin extracts in congenital and acquired hypoproconvertinemia (Q34104078) (← links)
- Factor VII deficiency and the FVII mutation database (Q34119225) (← links)
- Management of Pregnancy in a Chilean Patient with Congenital Deficiency of Factor VII and Glanzmann's Thrombasthenia Variant (Q34705279) (← links)
- Congenital factor VII deficiency; a review with a report of a case in an Indian infant (Q35237888) (← links)
- A brief historical review of the waterfall/cascade of blood coagulation (Q35564946) (← links)
- Clinical implications of plasma fractionation (Q35649708) (← links)
- Hereditary heterozygous factor VII deficiency in patients undergoing surgery : Clinical relevance (Q36120702) (← links)
- Genetics of coagulation: considerations for cardiac surgery (Q36697910) (← links)
- Familial haemophilia and factor VII deficiency (Q36702457) (← links)
- Theories of blood coagulation (Q36809566) (← links)
- Haemophilia and related conditions (Q36818622) (← links)
- The two-stage prothrombin assay in study of bleeding and clotting disorders (Q37016309) (← links)
- Congenital bleeding disorders of the vitamin K-dependent clotting factors (Q37122121) (← links)
- Historical perspective and future direction of coagulation research (Q37903961) (← links)
- Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) (Q38091658) (← links)
- Transporters for the Intestinal Absorption of Cholesterol, Vitamin E, and Vitamin K. (Q38768787) (← links)
- Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region. (Q38905795) (← links)
- Coagulopathies (Q39624434) (← links)
- Congenital "Hypoprothrombinemias": Deficiency of Factors II, VII, and X (Q39912823) (← links)
- Benjamin Alexander (1909 – 1978) (Q40939298) (← links)
- Factor VII Deficiency: A Rare Case Report (Q41158160) (← links)
- NPC1L1 is a key regulator of intestinal vitamin K absorption and a modulator of warfarin therapy (Q41390942) (← links)
- The coagulation of human blood (Q41427004) (← links)
- Intracranial hemorrhage in congenital factor VII deficiency (Q41454784) (← links)
- The measurement of prothrombin in plasma; a case of prothrombin deficiency (Q41786648) (← links)
- Anesthesia and factor VII deficiency (Q42151651) (← links)
- Haemorrhagic diathesis due to deficiency of factor VII (Q42576073) (← links)
- Inhibition of tissue factor-activated platelets by low-molecular-weight heparins and glycoprotein IIb/IIIa receptor antagonist (Q43588770) (← links)
- Factor VII activity and antigen in a patient with abnormal factor VII (Q44017614) (← links)
- Development of a subdural vein thrombosis following aggressive factor VII replacement for postnatal intracranial haemorrhage in a homozygous factor VII-deficient infant (Q45855336) (← links)
- Surgical management in hemophilia and the hemophilioid diseases (Q45866652) (← links)
- Tissue factor and biotechnology. (Q47788839) (← links)
- Further studies on factor VII Padua defect: the report of the fourth homozygous patient from the same valley (Q48938698) (← links)
- Isolated factor VII deficiency diagnosed after a life-threatening brain haemorrhage (Q49013359) (← links)
- Pediatric cardiac intervention in a case of congenital factor VII deficiency: a challenge to overcome. (Q49338090) (← links)
- Analysis of the gene in a hereditary coagulation factor Ⅶ deficiency pedigree (Q49968785) (← links)
- Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period (Q50905261) (← links)
- The hereditary haemorrhagic diseases: their classification and diagnosis. (Q55479066) (← links)
- Congenital factor VII deficiency. A report of four new cases (Q67466934) (← links)
- Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7) (Q68214111) (← links)
- Hemophilia (Q69269986) (← links)
- Congenital factor VII deficiency. A case report (Q69593810) (← links)
- Clinical studies of familial hereditary factor VII deficiency (author's transl) (Q70788285) (← links)
- Congenital factor VII deficiency in a patient with an abdominal aortic aneurysm (Q71381532) (← links)