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8 in total

1. Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism.

Authors: K Wieland; D S Millar; C B Grundy; R S Mibashan; V V Kakkar; D N Cooper
Journal: Hum Genet Date: 1991-01 Impact factor: 4.132

2. Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period.

Authors: Antonio Girolami; Silvia Ferrari; Elisabetta Cosi; Bruno Girolami; Maria Luigia Randi
Journal: J Thromb Thrombolysis Date: 2019-04 Impact factor: 2.300

3. Symptomatic combined homozygous factor XII deficiency and heterozygous factor V Leiden. luscaber@tin.it.

Authors: A Girolami; P Simioni; L Scarano; B Girolami; P Zerbinati
Journal: J Thromb Thrombolysis Date: 2000-04 Impact factor: 2.300

Review 4. Laboratory evaluation of a bleeding patient.

Authors: R O Wallerstein
Journal: West J Med Date: 1989-01

Review 5. The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literature.

Authors: A Girolami; M L Randi; S Gavasso; A M Lombardi; F Spiezia
Journal: J Thromb Thrombolysis Date: 2004-04 Impact factor: 2.300

Rarer quantitative and qualitative abnormalities of coagulation.

1. Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism.

2. Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period.

3. Symptomatic combined homozygous factor XII deficiency and heterozygous factor V Leiden. luscaber@tin.it.

Review 4. Laboratory evaluation of a bleeding patient.

Review 5. The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literature.

Review 6. Bone Density Status in Bleeding Disorders: Where Are We and What Needs to Be Done?

7. Clinical Phenotype and Genetic Analysis of Twins With Congenital Coagulation Factor V Deficiency.

8. Report of a rare co-incidence of congenital factor V deficiency and thalassemia intermedia in a family.