scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF00999872 |
P8608 | Fatcat ID | release_6ld34sjk3vhxhgqqkzmnfswlme |
P698 | PubMed publication ID | 822903 |
P2093 | author name string | A. Girolami | |
G. Patrassi | |||
N. Borsato | |||
A. Sticchi | |||
P2860 | cites work | Quantitative immunoelectrophoresis of human serum proteins | Q72218189 |
Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies | Q72902854 | ||
[A micro-method of immuno-electrophoresis] | Q73825157 | ||
[Description of a technic simultaneously combining electrophoresis and immunological precipitation in gel: electrosyneresis] | Q79180311 | ||
Congenital abnormality of the prothrombin molecule (factor II) in four siblings: prothrombin Barcelona | Q93828278 | ||
Immunochemical quantitation of antigens by single radial immunodiffusion | Q28248574 | ||
Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant agains | Q34055947 | ||
Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin | Q34283513 | ||
The molecular basis of hereditary clotting disorders | Q39925093 | ||
An investigation of three patients with Christmas disease due to an abnormal type of factor IX. | Q41220513 | ||
Immunological characterization of anti-haemophilic factor A related antigen in haemophilia A. | Q45855041 | ||
A variant of factor 8 related antigen | Q45855059 | ||
Normal factor 8 antigen level in combined congenital deficiency of factor V and factor VIII. | Q45855064 | ||
Factor VIII immunological assay. An evaluation of several methods using whole plasma | Q45855080 | ||
The Detection of Factor-VIII-like Antigen in Haemophilic Carriers and in Patients with Raised Levels of Biologically Active Factor VIII | Q45855701 | ||
Detection of the carrier state for classic hemophilia | Q45856192 | ||
Congenital combined factor V and factor VIII deficiency in a male born from a brother-sister incest | Q45856466 | ||
The Genetic Heterogeneity of Hemophilia B | Q45858125 | ||
Combined congenital deficiency of factor V and factor VIII. Report of a further case with some considerations on the hetereditary transmission of this disorder | Q45877422 | ||
Combined deficiency of factor V and factor VIII. A report of another case | Q45878759 | ||
A new inherited coagulation disorder caused by an abnormal fibrinogen ('fibrinogen Baltimore'). | Q47717618 | ||
Crossover electrophoresis (electrosyneresis) visualization of the abnormal factor X (factor X Friuli). | Q48026725 | ||
A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred | Q53743719 | ||
Factor X Friuli: An immunological study in plasma and in serum using several methods | Q67507582 | ||
Combined hereditary deficiency of factors VII and VIII: a distinct coagulation disorder due to the 'lack' of an autosomal gene controlling factor VII and VIII activation? | Q67519235 | ||
Prothrombin padua: a "new" congenital dysprothrombinemia | Q68549962 | ||
Inherited variants of factor-VIII-related protein in von Willebrand's disease | Q69135742 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | immunology | Q101929 |
P304 | page(s) | 97-102 | |
P577 | publication date | 1976-08-01 | |
P1433 | published in | Blut | Q27709414 |
P1476 | title | An immunological investigation of factor VIII associated antigen in combined factor V and factor VIII deficiency | |
P478 | volume | 33 |
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