Search Results - "Boulyjenkov, V."

Impact, diagnosis and treatment of von Willebrand disease by Sadler, J E, Mannucci, P M, Berntorp, E, Bochkov, N, Boulyjenkov, V, Ginsburg, D, Meyer, D, Peake, I, Rodeghiero, F, Srivastava, A

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Prevention and control of haemoglobinopathies by ANGASTINIOTIS, M, MODELL, B, ENGLEZOS, P, BOULYJENKOV, V

“…In many developing countries the haemoglobinopathies (thalassaemias and sickle-cell disorder) are so common that they provide a convenient model for working…”
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Modern treatment of haemophilia by BERNTORP, E, BOULYJENKOV, V, SEREMETIS, S, BRETTLER, D, CHANDY, M, JONES, P, LEE, C, LUSHER, J, MANNUCCI, P, PEAK, I, RICKARD, K

“…Many rapid advances have been made in the diagnosis and therapy of haemophilia. Nevertheless, the condition still poses problems and challenges (e.g., joint…”
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Haemophilia: strategies for carrier detection and prenatal diagnosis by PEAKE, I. R, LILLICRAP, D. P, TUDDENHAM, E. G. D, BOULYJENKOV, V, BRIET, E, CHAN, V, GINTER, E. K, KRAUS, E. M, LJUNG, R, MANNUCCI, P. M, NICOLAIDES, K

“…In 1977 WHO published in the Bulletin a Memorandum on Methods for the Detection of Haemophilia Carriers. This was produced following a WHO/WFH (World…”
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Report of a joint WHO/WFH meeting on the control of haemophilia: carrier detection and prenatal diagnosis by Peake, I R, Lillicrap, D P, Boulyjenkov, V, Briët, E, Chan, V, Ginter, E K, Kraus, E M, Ljung, R, Mannucci, P M, Nicolaides, K

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New possibilities for population control of cystic fibrosis by DODGE, J. A, BOULYJENKOV, V

“…Cystic fibrosis (CF), which is caused exclusively by mutation of a single gene, is inherited in autosomal recessive fashion and is the commonest such disorder…”
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Inherited thrombophilia: Part 1 by Lane, D A, Mannucci, P M, Bauer, K A, Bertina, R M, Bochkov, N P, Boulyjenkov, V, Chandy, M, Dahlbäck, B, Ginter, E K, Miletich, J P, Rosendaal, F R, Seligsohn, U

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Inherited thrombophilia: Part 2 by Lane, D A, Mannucci, P M, Bauer, K A, Bertina, R M, Bochkov, N P, Boulyjenkov, V, Chandy, M, Dahlbäck, B, Ginter, E K, Miletich, J P, Rosendaal, F R, Seligsohn, U

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The role of the World Health Organization in promoting medical genetics in Latin America by Boulyjenkov, Victor

“…The Human Genetics Program of the World Health Organization (WHO) has analyzed the needs for genetic services worldwide and the promotion of genetic approaches…”
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Inherited thrombophilia: memorandum from a joint WHO/International Society on Thrombosis and Haemostasis meeting

“…Inherited thrombophilias are common disorders with a worldwide distribution, including antithrombin, protein C, and protein S deficiencies as well as…”
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Introduction by Jones, P. M., Boulyjenkov, V.

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Introduction by Jones, P. M., Boulyjenkov, V.

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Introduction by Jones, P. M., Boulyjenkov, V.

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Les nouvelles possibilités de lutte contre la mucoviscidose en population by Dodge, J.A., Boulyjenkov, V.

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Implementation of cystic fibrosis services in developing countries: memorandum from a Joint WHO/ICF(M)A meeting

“…A Joint WHO/ICF(M)A meeting defined strategies for the implementation and development of cystic fibrosis (CF) services in countries where CF is thought to be…”
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Les nouvelles possibilités de lutte contre la mucoviscidose en population by DODGE, J. A, BOULYJENKOV, V

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Noninvasive screening for prenatal genetic diagnosis by SIMPSON, J. L

“…During the last two decades a number of methods of prenatal diagnosis have become available and have been used either in laboratory research or in routine…”
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Haemophilia : strategies for carrier detection and prenatal diagnosis by Peake, I R, Lillicrap, D P, Boulyjenkov, V, Briet, E, Chan, V, Ginter, E K, Kraus, E M, Ljung, R, Mannucci, P M, Nicolaides, K

“…In 1977 WHO published in the Bulletin a Memorandum on Methods for the Detection of Haemophilia Carriers. This was produced following a WHO/WFH (World…”
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