Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Eusèbe Adjambri"'
Autor:
Catherine Lambert, N’ Dogomo Meité, Ibrahima Sanogo, Sébastien Lobet, Eusèbe Adjambri, Stéphane Eeckhoudt, Cedric Hermans
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background Little data is available on awareness of hemophilia carrier condition or associated bleeding risk and management in Sub-Saharan African countries. This study sought to identify hemophilia carriers in Côte d’Ivoire in order to c
Externí odkaz:
https://doaj.org/article/f62a1c54da5f4292bb9945d06ea1fed2
Autor:
MIREILLE YAYO- AYE, Adia Eusèbe Adjambri, Boidy Kouakou, Rebecca N'guessan-Blao, Louis Missa Adjé, Taïratou Kamagaté, Vincent Yapo, Duni Sawadogo
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 16, Iss 1 (2024)
Background: The lives of individuals affected by sickle cell disease are marked by painful crises sometimes accompanied by complications. Curative treatments such as bone marrow transplantation or gene therapy exist, but are not currently performed i
Externí odkaz:
https://doaj.org/article/09675179d42f49eca7840f7206f095b5
Autor:
Ibrahima Sanogo, Cedric Hermans, Eusèbe Adjambri, Sébastien Lobet, N’ Dogomo Meité, Stéphane Eeckhoudt, Catherine Lambert
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Little data is available on awareness of hemophilia carrier condition or associated bleeding risk and management in Sub-Saharan African countries. This study sought to identify hemophilia carriers in Côte d’Ivoire in order to collect da
Autor:
Marie-France Meledje, Sylvie Bouvier, Adia Eusèbe Adjambri, Mireille Yayo-Ayé, Duni Sawadogo, Missa Louis Adjé, Emma N’draman-Donou, Roseline N'guessan
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases
Mediterranean Journal of Hematology and Infectious Diseases, Vol 12, Iss 1 (2020)
Mediterranean Journal of Hematology and Infectious Diseases, Università Cattolica del Sacro Cuore, 2020, 12 (1), pp.e2020019. ⟨10.4084/MJHID.2020.019⟩
Mediterranean Journal of Hematology and Infectious Diseases, Vol 12, Iss 1 (2020)
Mediterranean Journal of Hematology and Infectious Diseases, Università Cattolica del Sacro Cuore, 2020, 12 (1), pp.e2020019. ⟨10.4084/MJHID.2020.019⟩
Aim : Type 3 von Willebrand disease (VWD) is the most severe form of VWD, characterized by a near-total absence of von Willebrand factor (vWF) leading to a huge deficiency in plasmatic factor VIII (FVIII). VWD may be confused with hemophilia A, somet
Autor:
Catherine Lambert, Stéphane Eeckhoudt, Ibrahima Sanogo, Eusèbe Adjambri, Cedric Hermans, N'Dogomo Meité, Sébastien Lobet
Publikováno v:
Haemophilia, Vol. 25, no. 2, p. 236-243 (2019)
INTRODUCTION: In sub-Saharan African countries, research on haemophilia is limited. Since 2015, a partnership has been established through the World Federation of Hemophilia (WFH)'s twinning programme between the haemophilia treatment centre (HTC) of
Publikováno v:
International Journal of Biological and Chemical Sciences. 9:2300
La drepanocytose est une maladie genetique qui constitue un probleme de sante publique en Cote d’Ivoire. Etant donne les couts onereux du traitement, les patients s’orientent vers la medecine traditionnelle avec l’utilisation de plantes, parmi
Autor:
Adia Eusèbe Adjambri, Sylvie Bouvier, Roseline N'guessan, Emma N’draman-Donou, Mireille Yayo-Ayé, Marie-France Meledje, Missa Louis Adjé, Duni Sawadogo
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 12, Iss 1 (2020)
Abstract Aim : Type 3 von Willebrand disease (VWD) is the most severe form of VWD, characterized by a near-total absence of von Willebrand factor (vWF) leading to a huge deficiency in plasmatic factor VIII (FVIII). VWD may be confused with hemophi
Externí odkaz:
https://doaj.org/article/c50764d715064f22a175e51fb14c21d3