Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Elira Dokekias, A."'
Autor:
Firmine Olivia Galiba Atipo-Tsiba, Earl Quincy Gayaba Mouyabi, Brunel Monic Angounda, Serge Oscar Mokono, Lethso Thibaut Ocko Gokaba, Alexis Elira Dokekias
Publikováno v:
Anemia, Vol 2023 (2023)
Introduction. Blood donation is not without risk to the donor. It results in a substantial loss of iron and decreased hemoglobin. In our country, no predonation assessment is carried out and the selection of blood donors is only clinical. Objectives.
Externí odkaz:
https://doaj.org/article/dd824a2ae5374d01b174b902c7bd4403
Autor:
Firmine Olivia Galiba Atipo Tsiba, Clément Pacha Mikia, Jennifer Armandine Elira Samba, Jade Vanessa Nziengui Mboumba, Félix Malanda, Clausina Mikolele Ahoui, Alexis Elira Dokekias
Publikováno v:
Anemia, Vol 2023 (2023)
Introduction. Chronic hemolysis predisposes sickle cell patients to the development of gallstones. Their frequency increases with age, but they may appear early in young children. In the absence of management, they expose the patient to complications
Externí odkaz:
https://doaj.org/article/fd1032add8634dbb8f4f8af3d6d55631
Autor:
Galiba Atipo Tsiba FO, Ngolet OL, Ngakengni NY, Ollandzobo Ikobo LC, Nziengui-Mboumba JV, Elira Dokekias A
Publikováno v:
The Journal of Haemophilia Practice, Vol 7, Iss 1, Pp 53-58 (2020)
Haemophilia is a rare hereditary haemorrhagic disease caused by coagulation factor VIII (haemophilia A) or IX (haemophilia B) deficiency. Very few data exist on this disease in Congo. This survey aims to describe the epidemiological and clinical aspe
Externí odkaz:
https://doaj.org/article/7d8ac2e9356f4a9d84b8dfdc1b4a2445
Autor:
Alexis Elira Dokekias, Lethso Thibaut Ocko Gokaba, Josué Simo Louokdom, Lydie Ngolet Ocini, Firmine Olivia Galiba Atipo Tsiba, Coreillia Irène Ondzotto Ibatta, Quentin Ngoma Kouandzi, Serge Talomg Tamekue, Jayne Chelsea Bango, Jade Vanessa Nziengui Mboumba, Simon Charles Kobawila
Publikováno v:
Anemia, Vol 2022 (2022)
Introduction. Sickle cell disease is an autosomal recessive inherited disorder due to the mutation of a gene coding for the globin beta chain. The aim of this study is to update the epidemiological data on hemoglobinoses, in particular sickle cell di
Externí odkaz:
https://doaj.org/article/622b0e656f394510b353ff2eff1b4f10
Autor:
ATIPO-TSIBA GALIBA F., ITOUA C., EHOUROSSIKA C., NGAKEGNI N., BUAMBO G., POTOKOUE MPIA S., ELIRA DOKEKIAS A.
Publikováno v:
HemaSphere, Vol 6, Pp 35-36 (2022)
Externí odkaz:
https://doaj.org/article/77ae410e310441bea50ec620cf2824d7
Autor:
F. O. Galiba Atipo-Tsiba, A. Bilongo-Bouyou, J. C. Bango, J. A. Elira Samba, B. M. Gatsongui, F. Malanda, L. O. Ngolet, A. Elira Dokekias
Publikováno v:
International Blood Research & Reviews. 14:1-7
Introduction: The avascular osteonecrosis of the femoral head (AOFH) is a common complication of sickle cell disease (SCD). It exposes to lameness and sometimes to a very debilitating handicap. It is a source of desocialization, particularly in devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eccb37734e0eace90917f4a9a146716
https://doi.org/10.9734/ibrr/2023/v14i4311
https://doi.org/10.9734/ibrr/2023/v14i4311
Autor:
P.E. GANDZALI, L. Ngolet Ocini, A.D.R. Bitoumbou, J.B. Ikapi, L.T. Oko Gokaba, R. Loumingou, A. Elira Dokekias
Publikováno v:
Kidney International Reports, Vol 6, Iss 4, Pp S135-S136 (2021)
Externí odkaz:
https://doaj.org/article/54e9461df94942098b95e63cac0620da
Autor:
F. O. Galiba Atipo Tsiba, C. Itoua, C. Ehourossika, N. Y. Ngakegni, G. Buambo, N. S. B. Potokoue Mpia, A. Elira Dokekias
Publikováno v:
Anemia, Vol 2020 (2020)
Introduction. Sickle cell disease (SCD) is one of the most common genetic diseases in the world. It combines, in its homozygous form, chronic hemolytic anemia, vasoocclusive complications, and susceptibility to infections. It is well known that the c
Externí odkaz:
https://doaj.org/article/c8727b7ac7f34b1aa3579aac2abe38cf
Autor:
Lethso Thibaut Ocko Gokaba, Olivia Firmine Atipo Galiba, Géril Sekangue Obili, Lydie Ocini Ngolet, Alexis Elira Dokekias
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 1, Pp XD01-XD02 (2020)
The association between Chronic Myeloid Leukaemia (CML)-Filariasis is rare. Moreover, finding microfilariae in the bone marrow is uncommon. We reported the case of 47-year-old patient living in a rural area who was admitted in the haematology ward in
Externí odkaz:
https://doaj.org/article/346d6fc666694c84ba5a48f08346bd6e
Autor:
Josué Simo Louokdom, Innocent Kocko, Thibaut Lethso Ocko Gokaba, Félix Malanda, Olivia Firmine Galiba Atipo, Serge Léopold Talomg Tamekue, Maryline Seuko Njopwouo, Lydie Ngolet Ocini, Alexis Elira Dokekias
Publikováno v:
PAMJ Clinical Medicine, Vol 2, Iss 16 (2020)
It is a Congolese male child living with homozygous sickle cell disease who has a false thrombocytosis at 988 000/μL and a regenerative hypochromic normocytic anemia with automated hemogram. Peripheral blood smear examination revealed spherical, spe
Externí odkaz:
https://doaj.org/article/436c527cc3f24dceba2683f9ab9b5577