Factor XI deficiency in Ashkenazi Jews in Israel.

High incidence of myeloproliferative disorders in Ashkenazi Jews in northern Israel.

Prostatectomy in factor XI deficiency.

A common Lithuanian mutation causing familial hypercholesterolemia in Ashkenazi Jews.

Factor XI-related thrombosis and the role of concentrate treatment in factor XI deficiency.

Factor XI Double Knockout Mice.

Factor XI deficiency acquired by liver transplantation.

Genetic contribution to multiple sclerosis risk among Ashkenazi Jews.

Transurethral prostatectomy in severe factor XI deficiency without bleeding complications.

Factor XI (plasma thromboplastin antecedent) deficiency in cattle.

Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.

Why factor XI deficiency is a clinical concern.

Factor XI deficiency diagnosed following use of adalimumab.

Cerebellar haemorrhage, factor XI deficiency and concomitant risk factors.

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.

Anaesthesia Management of a Patient with Factor XI Deficiency.

Factor XI deficiency: incidental diagnosis post coronary artery bypass graft.

Factor XI: a review of its biochemistry and deficiency.

Acquired factor XI deficiency: a rare complication after liver transplantation.

Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance.

Genetic variants associated with susceptibility of Ashkenazi Jews to West Nile virus infection.

High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews.

A genetic contribution from the Far East into Ashkenazi Jews via the ancient Silk Road.

No evidence from genome-wide data of a Khazar origin for the Ashkenazi Jews.

Lung cancer histology in Jews and Arabs in Israel, 1962-1982.

Suggest Documents

High incidence of myeloproliferative disorders in Ashkenazi Jews in northern Israel.

Prostatectomy in factor XI deficiency.

A common Lithuanian mutation causing familial hypercholesterolemia in Ashkenazi Jews.

Factor XI-related thrombosis and the role of concentrate treatment in factor XI deficiency.

Factor XI Double Knockout Mice.

Factor XI deficiency acquired by liver transplantation.

Genetic contribution to multiple sclerosis risk among Ashkenazi Jews.

Transurethral prostatectomy in severe factor XI deficiency without bleeding complications.

Factor XI (plasma thromboplastin antecedent) deficiency in cattle.

Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.

Why factor XI deficiency is a clinical concern.

Factor XI deficiency diagnosed following use of adalimumab.

Cerebellar haemorrhage, factor XI deficiency and concomitant risk factors.

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.

Anaesthesia Management of a Patient with Factor XI Deficiency.

Factor XI deficiency: incidental diagnosis post coronary artery bypass graft.

Factor XI: a review of its biochemistry and deficiency.

Acquired factor XI deficiency: a rare complication after liver transplantation.

Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance.

Genetic variants associated with susceptibility of Ashkenazi Jews to West Nile virus infection.

High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews.

A genetic contribution from the Far East into Ashkenazi Jews via the ancient Silk Road.

No evidence from genome-wide data of a Khazar origin for the Ashkenazi Jews.

Lung cancer histology in Jews and Arabs in Israel, 1962-1982.

Factor XI deficiency in Ashkenazi Jews in Israel.

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