Haemophilia

Rare inherited disorders of fibrinogen
pp. 1151-1158(8)
Authors: ACHARYA, S. S.; DIMICHELE, D. M.

Abnormalities of prothrombin: a review of the pathophysiology, diagnosis, and treatment
pp. 1159-1163(5)
Authors: MEEKS, S. L.; ABSHIRE, T. C.

Factor V deficiency: a concise review
pp. 1164-1169(6)
Authors: HUANG, J. N.; KOERPER, M. A.

Factor VII deficiency: defining the clinical picture and optimizing therapeutic options
pp. 1170-1175(6)
Authors: LAPECORELLA, M.; MARIANI, G.

Diagnosis and treatment of inherited factor X deficiency
pp. 1176-1182(7)
Authors: BROWN, D. L.; KOUIDES, P. A.

Factor XI deficiency
pp. 1183-1189(7)
Authors: GOMEZ, K.; BOLTON-MAGGS, P.

Factor XIII deficiency
pp. 1190-1200(11)
Authors: HSIEH, L.; NUGENT, D.

Combined FV and FVIII deficiency
pp. 1201-1208(8)
Authors: SPREAFICO, M.; PEYVANDI, F.

Familial deficiency of vitamin K-dependent clotting factors
pp. 1209-1213(5)
Authors: WESTON, B. W.; MONAHAN, P. E.

Protein C deficiency
pp. 1214-1221(8)
Authors: GOLDENBERG, N. A.; MANCO-JOHNSON, M. J.

Protein S deficiency: a clinical perspective
pp. 1222-1228(7)
Authors: TEN KATE, M. K.; VAN DER MEER, J.

Inherited antithrombin deficiency: a review
pp. 1229-1239(11)
Authors: PATNAIK, M. M.; MOLL, S.

Platelet function defects
pp. 1240-1249(10)
Authors: SIMON, D.; KUNICKI, T.; NUGENT, D.

α₂-Antiplasmin and its deficiency: fibrinolysis out of balance
pp. 1250-1254(5)
Authors: CARPENTER, S. L.; MATHEW, P.

Plasminogen activator inhibitor type 1 deficiency
pp. 1255-1260(6)
Authors: MEHTA, R.; SHAPIRO, A. D.

Plasminogen deficiency
pp. 1261-1268(8)
Authors: MEHTA, R.; SHAPIRO, A. D.

Hereditary haemorrhagic telangiectasia
pp. 1269-1280(12)
Authors: SHARATHKUMAR, A. A.; SHAPIRO, A.