S. Allford

发表

A case of cerebral arteriovenous malformation in pregnancy associated with MALT lymphoma

J. Macaulay, S. Sen, S. Allford, 2010, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Guidelines on the diagnosis and management of the thrombotic microangiopathic haemolytic anaemias

B. Hunt, S. Machin, P. Rose, 2003, British journal of haematology.

Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency.

L. P. Van den Heuvel, L. Monnens, K. Assink, 2003, Kidney international.

Thrombotic Thrombocytopenic Purpura Following Stem Cell Transplantation

D. Marks, J. Bird, S. Allford, 2002, Leukemia & lymphoma.

Levels of von Willebrand factor‐cleaving protease are normal in methylene blue‐treated fresh‐frozen PLASMA

R. Cardigan, L. Williamson, S. Allford, 2002, British journal of haematology.

More on: endoplasmic reticulum loop VKORC1 substitutions cause warfarin resistance but do not diminish gamma‐carboxylation of the vitamin K‐dependent coagulation factors

M. Shearer, A. Mumford, S. Allford, 2011, Journal of thrombosis and haemostasis : JTH.

Chronic relapsing thrombotic thrombocytopenic purpura due to a deficiency of von Willebrand factor‐cleaving protease activity

J. Hanley, J. Wallis, S. Allford, 2002, British journal of haematology.

von Willebrand factor‐cleaving protease activity in congenital thrombotic thrombocytopenic purpura

R. Liesner, I. Mackie, S. Machin, 2000, British journal of haematology.

Identification of the t(15;17) in AML FAB types other than M3: evaluation of the role of molecular screening for the PML/RARα rearrangement in newly diagnosed AML

B. Bain, P. Freemont, S. Langabeer, 1999 .

Identification of the t(15;17) in AML FAB types other than M3: evaluation of the role of molecular screening for the PML/RARalpha rearrangement in newly diagnosed AML. The Medical Research Council (MRC) Adult Leukaemia Working Party.

B. Bain, P. Freemont, P. Freemont, 1999, British journal of haematology.

Severe prekallikrein deficiency associated with homozygosity for an Arg94Stop nonsense mutation

D. Bowden, G. Hawkins, K. Burdon, 2004, British journal of haematology.

Successful treatment of congenital thrombotic thrombocytopenic purpura using the intermediate purity factor VIII concentrate BPL 8Y

S. Machin, S. Allford, W. Lester, 2002, British journal of haematology.