Haemophilia
TABLE OF CONTENTS
Volume 14 Issue 6, Pages 1151 - 1280 (November 2008)
Original Articles

Rare inherited disorders of fibrinogen (p 1151-1158)
S. S. ACHARYA, D. M. DIMICHELE

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

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

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

Diagnosis and treatment of inherited factor X deficiency (p 1176-1182)
D. L. BROWN, P. A. KOUIDES

Factor XI deficiency (p 1183-1189)
K. GOMEZ, P. BOLTON-MAGGS

Factor XIII deficiency (p 1190-1200)
L. HSIEH, D. NUGENT

Combined FV and FVIII deficiency (p 1201-1208)
M. SPREAFICO, F. PEYVANDI

Familial deficiency of vitamin K-dependent clotting factors (p 1209-1213)
B. W. WESTON, P. E. MONAHAN

Protein C deficiency (p 1214-1221)
N. A. GOLDENBERG, M. J. MANCO-JOHNSON
Published Online: Oct 30 2008 9:21PM

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

Inherited antithrombin deficiency: a review (p 1229-1239)
M. M. PATNAIK, S. MOLL

Platelet function defects (p 1240-1249)
D. SIMON, T. KUNICKI, D. NUGENT

A2-Antiplasmin and its deficiency: fibrinolysis out of balance (p 1250-1254)
S. L. CARPENTER, P. MATHEW

Plasminogen activator inhibitor type 1 deficiency (p 1255-1260)
R. MEHTA, A. D. SHAPIRO

Plasminogen deficiency (p 1261-1268)
R. MEHTA, A. D. SHAPIRO

Hereditary haemorrhagic telangiectasia (p 1269-1280)
A. A. SHARATHKUMAR, A. SHAPIRO