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Refinado por: Nome da Publicação: British Journal Of Haematology remover
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1
Prevalence of HLA-H mutations in patients with premature arterial disease
Prevalence of HLA-H mutations in patients with premature arterial disease
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Prevalence of HLA-H mutations in patients with premature arterial disease

R F Franco H Ten Cate; M H Prins; J J P Kastelein; Marco Antônio Zago; P H Reitsma; Trip, M D; ISH-EHA Combined Haematology Congress (1998 Amsterdam)

British Journal of Haematology Oxford v. 102, n. 1, p. 257 res. P-1030, 1998

Oxford 1998

Item não circula. Consulte sua biblioteca.(Acessar)

2
Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease
Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease

R F Franco Marco Antônio Zago; M D Trip; H Ten Cate; A Van den Ende; M H Prins; J J P Kastelein; P H Reitsma

British Journal of Haematology Oxford v. 102, p. 1172-1175, 1998

Oxford 1998

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd E 048A p. 255 1024633 Estantes Deslizantes )(Acessar)

3
Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease
Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease

R F Franco Marco Antônio Zago; M D Trip; H Ten Cate; A Van den Ende; M H Prins; J J P Kastelein; P H Reitsma

British Journal of Haematology Oxford v. 102, p. 1172-1175, 1998

Oxford 1998

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd E 048A p. 255 1024633 Estantes Deslizantes )(Acessar)

4
The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic disease
The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic disease

Franco, R. F. ; Trip, M. D. ; Ten Cate, H. ; Van Den Ende, A. ; Prins, M. H. ; Kastelein, J. J. P. ; Reitsma, P. H.

British journal of haematology, 1999-01, Vol.104 (1), p.50-54 [Periódico revisado por pares]

Oxford, U.K. and Cambridge, USA: Blackwell Science Ltd

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5
Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease
Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease

FRANCO, R. F ; ZAGO, M. A ; TRIP, M. D ; TEN CATE, H ; VAN DEN ENDE, A ; PRINS, M. H ; KASTELEIN, J. J. P ; REITSMA, P. H

British journal of haematology, 1998-09, Vol.102 (5), p.1172-1175 [Periódico revisado por pares]

Oxford, U.K. and Cambridge, USA: Blackwell Publishers

Texto completo disponível

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6
The incidence of recurrent venous thromboembolism in carriers of factor V Leiden is related to concomitant thrombophilic disorders
The incidence of recurrent venous thromboembolism in carriers of factor V Leiden is related to concomitant thrombophilic disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

The incidence of recurrent venous thromboembolism in carriers of factor V Leiden is related to concomitant thrombophilic disorders

Meinardi, Johan R. ; Middeldorp, Saskia ; De Kam, Pieter J. ; Koopman, Maria M. W. ; Van Pampus, Elisabeth C. M. ; Hamulyák, Karly ; Prins, Martin H. ; Büller, Harry R. ; Van Der Meer, Jan

British journal of haematology, 2002-03, Vol.116 (3), p.625-631 [Periódico revisado por pares]

Oxford, UK: Blackwell Science, Ltd

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7
Risk of cardiovascular disease in double heterozygous carriers and homozygous carriers of F5 R506Q (factor V Leiden) and F2 (prothrombin) G20210A: a retrospective family cohort study
Risk of cardiovascular disease in double heterozygous carriers and homozygous carriers of F5 R506Q (factor V Leiden) and F2 (prothrombin) G20210A: a retrospective family cohort study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Risk of cardiovascular disease in double heterozygous carriers and homozygous carriers of F5 R506Q (factor V Leiden) and F2 (prothrombin) G20210A: a retrospective family cohort study

Roach, Rachel E.J. ; Roshani, Sara ; Meijer, Karina ; Hamulyák, Karly ; Lijfering, Willem M. ; Prins, Martin H. ; Büller, Harry R. ; Middeldorp, Saskia

British journal of haematology, 2011-04, Vol.153 (1), p.134-136 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
Decreased half‐life time of plasma von Willebrand factor collagen binding activity in essential thrombocythaemia: normalization after cytoreduction of the increased platelet count
Decreased half‐life time of plasma von Willebrand factor collagen binding activity in essential thrombocythaemia: normalization after cytoreduction of the increased platelet count
Material Type:
Artigo 		Adicionar ao Meu Espaço

Decreased half‐life time of plasma von Willebrand factor collagen binding activity in essential thrombocythaemia: normalization after cytoreduction of the increased platelet count

Van Genderen, Perry J. J ; Prins, Fransisco J ; Lucas, Irene S. ; Van De Moesdijk, Desiree ; Van Vliet, Huub H. D. M. ; Van Strik, Roel ; Michiels, Jan J.

British journal of haematology, 1997-12, Vol.99 (4), p.832-836 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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Deste Autor:

  1. Prins, M
  2. Trip, M
  3. Kastelein, J
  4. Zago, M
  5. Reitsma, P

Neste Assunto:

  1. Hematology
  2. Life Sciences & Biomedicine
  3. Female
  4. Male
  5. Middle Aged

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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