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DCEP (dexamethasone, cyclophosphamide, etoposide, and cisplatin) is an effective regimen for peripheral blood stem cell collection in multiple myeloma.
- Published in:
- Bone Marrow Transplantation, 2001, v. 28, n. 9, p. 835, doi. 10.1038/sj.bmt.1703240
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- Publication type:
- Article
The dilution of vanadyl pyrophosphate, catalyst for n-butane oxidation to maleic anhydride, with aluminum phosphate: unexpected reactivity due to the contribution of the diluting agent.
- Published in:
- Topics in Catalysis, 2006, v. 38, n. 4, p. 295, doi. 10.1007/s11244-006-0028-3
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- Publication type:
- Article
Fibrin glue from single-donation autologous plasmapheresis.
- Published in:
- 1992
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- Publication type:
- journal article
Polycythemia Vera and Essential Thrombocythemia in a General Population.
- Published in:
- Annals of Internal Medicine, 2003, v. 139, n. 6, p. I32, doi. 10.7326/0003-4819-139-6-200309160-00002
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- Publication type:
- Article
Activated protein C resistance and factor V Leiden mutation are independent risk factors for venous thromboembolism.
- Published in:
- 1999
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- Publication type:
- journal article
Hepatocellular carcinoma in hemophilia.
- Published in:
- American Journal of Hematology, 1991, v. 37, n. 4, p. 243, doi. 10.1002/ajh.2830370406
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- Publication type:
- Article
Hepatitis B vaccination of 113 hemophiliacs: Lower antibody response in anti-LAV/HTLV-III-positive patients.
- Published in:
- American Journal of Hematology, 1986, v. 23, n. 4, p. 339, doi. 10.1002/ajh.2830230406
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- Publication type:
- Article
ABO-incompatible bone marrow transplantation: a GITMO survey of current practice in Italy and comparison with the literature.
- Published in:
- Bone Marrow Transplantation, 2004, v. 34, n. 4, p. 321, doi. 10.1038/sj.bmt.1704579
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- Publication type:
- Article
Hyper-responsiveness to DDAVP for patients with type I von Willebrand's disease and normal intra-platelet von Willebrand factor.
- Published in:
- European Journal of Haematology, 1988, v. 40, n. 2, p. 163, doi. 10.1111/j.1600-0609.1988.tb00815.x
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- Publication type:
- Article
Spectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII gene.
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- Haemophilia, 2007, v. 13, n. 3, p. 311, doi. 10.1111/j.1365-2516.2007.01459.x
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- Publication type:
- Article
Laboratory issues in bleeding disorders.
- Published in:
- Haemophilia, 2006, v. 12, p. 68, doi. 10.1111/j.1365-2516.2006.01279.x
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- Publication type:
- Article
von Willebrand disease: still an intriguing disorder in the era of molecular medicine.
- Published in:
- Haemophilia, 2002, v. 8, n. 3, p. 292, doi. 10.1046/j.1365-2516.2002.00611.x
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- Publication type:
- Article
Acquired haemophilia: experience of two Italian centres with 17 new cases.
- Published in:
- Haemophilia, 1997, v. 3, n. 3, p. 183, doi. 10.1046/j.1365-2516.1997.00102.x
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- Publication type:
- Article
Desmopressin and type II B von Willebrand disease.
- Published in:
- Haemophilia, 1996, v. 2, n. 2, p. 73, doi. 10.1111/j.1365-2516.1996.tb00018.x
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- Publication type:
- Article
Survival and prognosis among 1545 patients with contemporary polycythemia vera: an international study.
- Published in:
- Leukemia (08876924), 2013, v. 27, n. 9, p. 1874, doi. 10.1038/leu.2013.163
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- Publication type:
- Article
Incidence and risk factors for bleeding in 1104 patients with essential thrombocythemia or prefibrotic myelofibrosis diagnosed according to the 2008 WHO criteria.
- Published in:
- Leukemia (08876924), 2012, v. 26, n. 4, p. 716, doi. 10.1038/leu.2011.258
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- Publication type:
- Article
Aberrant cytoplasmic expression of C-terminal-truncated NPM leukaemic mutant is dictated by tryptophans loss and a new NES motif.
- Published in:
- 2007
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- Publication type:
- Letter
‘Reply to Pitiot et al.’.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Un-mutated IgVH in chronic lymphocytic leukemia is associated with a higher risk of immune thrombocytopenia.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Identification and functional characterization of a cytoplasmic nucleophosmin leukaemic mutant generated by a novel exon-11 NPM1 mutation.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Treatment of elderly patients (=60 years) with newly diagnosed acute promyelocytic leukemia. Results of the Italian multicenter group GIMEMA with ATRA and idarubicin (AIDA) protocols.
- Published in:
- Leukemia (08876924), 2003, v. 17, n. 6, p. 1085
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- Publication type:
- Article
Recurrent Life-Threatening Epistaxis in a Child with Bernard-Soulier Syndrome Controlled by Bilateral Ligation of External Carotids and Ethmoidal Arteries.
- Published in:
- Acta Haematologica, 1987, v. 77, n. 3, p. 183, doi. 10.1159/000205988
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- Publication type:
- Article
Fatal Pulmonary Embolism and Antithrombin III Deficiency in Adult Lymphoblastic Leukaemia during L-Asparaginase Therapy.
- Published in:
- Acta Haematologica, 1983, v. 69, n. 3, p. 188, doi. 10.1159/000206887
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- Publication type:
- Article
Retrospective Analysis of Treatment of Acute Myeloblastic Leukemia in Patients More Than 55 Years Old.
- Published in:
- Acta Haematologica, 1982, v. 67, n. 3, p. 170, doi. 10.1159/000207050
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- Publication type:
- Article
Treatment of acute lymphoblastic leukemia in adults.
- Published in:
- 1985
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- Publication type:
- journal article
Autosomal recessive von Willebrand disease associated with compound heterozygosity for a novel nonsense mutation (2908 del C) and the missense mutation C2362F: Definite evidence for the non-penetrance of the C2362F mutation.
- Published in:
- American Journal of Hematology, 2007, v. 82, n. 5, p. 376, doi. 10.1002/ajh.20803
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- Publication type:
- Article
Fifth Åland Island conference on von Willebrand disease.
- Published in:
- Haemophilia, 2018, v. 24, p. 5, doi. 10.1111/hae.13475
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- Publication type:
- Article
Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiency.
- Published in:
- Haemophilia, 2012, v. 18, n. 1, p. e6, doi. 10.1111/j.1365-2516.2011.02622.x
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- Publication type:
- Article
A comparison between two semi-quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease.
- Published in:
- Haemophilia, 2011, v. 17, n. 1, p. 165, doi. 10.1111/j.1365-2516.2010.02381.x
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- Publication type:
- Article
F8 mRNA studies in haemophilia A patients with different splice site mutations.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 786, doi. 10.1111/j.1365-2516.2010.02250.x
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- Publication type:
- Article
Severe spontaneous arterial thrombotic manifestations in patients with inherited hypo- and afibrinogenemia.
- Published in:
- Haemophilia, 2009, v. 15, n. 2, p. 533, doi. 10.1111/j.1365-2516.2009.01939.x
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- Publication type:
- Article
Relevance of quantitative assessment of bleeding in haemorrhagic disorders.
- Published in:
- Haemophilia, 2008, v. 14, p. 68, doi. 10.1111/j.1365-2516.2008.01714.x
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- Publication type:
- Article
Laboratory issues in bleeding disorders.
- Published in:
- Haemophilia, 2008, v. 14, p. 93, doi. 10.1111/j.1365-2516.2008.01716.x
- By:
- Publication type:
- Article
Bleeding scores in inherited bleeding disorders: clinical or research tools?
- Published in:
- Haemophilia, 2008, v. 14, n. 3, p. 415, doi. 10.1111/j.1365-2516.2007.01648.x
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- Publication type:
- Article
Acquired transitory factor XI inhibitor after gynaecological surgery.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bβ and γ chain mutations.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Management of menorrhagia in women with inherited bleeding disorders: general principles and use of desmopressin.
- Published in:
- Haemophilia, 2008, v. 14, p. 21, doi. 10.1111/j.1365-2516.2007.01611.x
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- Publication type:
- Article
Molecular characterization of five Italian families with inherited severe factor XIII deficiency.
- Published in:
- Haemophilia, 2008, v. 14, n. 1, p. 96, doi. 10.1111/j.1365-2516.2007.01603.x
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- Publication type:
- Article
Autosomal Recessive von Willebrand Disease Type 1 or 2 due to Homozygous or Compound Heterozygous Mutations in the von Willebrand Factor Gene.
- Published in:
- Acta Haematologica, 2009, v. 121, n. 2/3, p. 106, doi. 10.1159/000214850
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- Publication type:
- Article
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency.
- Published in:
- Human Mutation, 1996, v. 8, n. 2, p. 108, doi. 10.1002/(SICI)1098-1004(1996)8:2<108::AID-HUMU2>3.0.CO;2-7
- By:
- Publication type:
- Article
PREGNANCY IN WOMEN WITH ESSENTIAL THROMBOCYTHAEMIA.
- Published in:
- British Journal of Haematology, 1996, v. 93, n. 4, p. 977, doi. 10.1046/j.1365-2141.1996.d01-1750_93_4.x
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- Publication type:
- Article
Molecular bases of CRM<sup>+</sup> factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glul02Lys) in the second EGF-like domain.
- Published in:
- British Journal of Haematology, 1995, v. 90, n. 4, p. 910, doi. 10.1111/j.1365-2141.1995.tb05214.x
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- Publication type:
- Article
Preliminary study to identify cancer patients at high risk of venous thrombosis following major surgery.
- Published in:
- British Journal of Haematology, 1993, v. 85, n. 4, p. 745, doi. 10.1111/j.1365-2141.1993.tb03218.x
- By:
- Publication type:
- Article
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381 → Ser) in the substrate-binding pocket.
- Published in:
- British Journal of Haematology, 1993, v. 84, n. 2, p. 285, doi. 10.1111/j.1365-2141.1993.tb03066.x
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- Publication type:
- Article
Antithrombin Vicenza, Ala 384 to Pro (GCA to CCA) mutation, transforming the inhibitor into a substrate.
- Published in:
- British Journal of Haematology, 1991, v. 77, n. 1, p. 87, doi. 10.1111/j.1365-2141.1991.tb07953.x
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- Publication type:
- Article
Immunoelectrophoretic evidence of a thrombin-induced abnormality in a new variant of hereditary dysfunctional antithrombin III (AT III 'Vicenza').
- Published in:
- British Journal of Haematology, 1983, v. 54, n. 4, p. 561, doi. 10.1111/j.1365-2141.1983.00509.x-i1
- By:
- Publication type:
- Article
Subunits A and S Inheritance in Four Families with Congenital Factor XIII Deficiency.
- Published in:
- British Journal of Haematology, 1978, v. 38, n. 2, p. 267, doi. 10.1111/j.1365-2141.1978.tb01042.x
- By:
- Publication type:
- Article