Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Alexis Elira, Dokekias"'
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:
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:
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
Autor:
Lydie Ocini Ngolet, Simo Josué Luokdom, Alexis Fortuné Bolenga Liboko, Firmine Olivia Galiba Atipo Tsiba, Alexis Elira Dokekias
Publikováno v:
Open Journal of Blood Diseases. 12:1-9
Autor:
Presley Jeanel Msengui, Alexis Elira Dokekias, Henri Germain Monabeka, Tatiana Doukaga Makouka, Gilbert NDziessi, Emile Godefroy Ngakeni, Michel Gbala Sapoulou, Regis Ondzé, Guy Emergence Poaty, Pascal Ibata, René Soussa Gadoua, Lambert Kitembo, Jethro Massala Peya, Henriette Poaty
Publikováno v:
African Health Sciences; Vol. 21 No. 3 (2021); 1100-1106
Background: The global pandemic Coronavirus Disease 2019 (COVID-19) due to the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is reported to be potentially severe in patients with morbid conditions. One common reported comorbidities is
Autor:
Alexis Elira, Dokekias, Josué Simo, Louokdom, Letso Thibaut Ocko, Gokaba, Firmine Olivia Galiba Atipo Tsiba, Gokaba, Jayne Chelsea, Bango, Lydie Ngolet, Ocini, Clatere, Itoua, James, Taylor
Publikováno v:
Journal of neonatal biology. 11(3)
Sickle-cell disease, a genetic condition with a high prevalence in sub-Saharan Africa, is transmitted in an autosomal recessive mode. Its screening during pregnancy makes it possible to identify carriers of the S gene which constitute a risk for the
Autor:
Donatien Moukassa, Ange Antoine Abena, Chaldam Jespère Mbani, Alexis Elira Dokekias, Serge Oscar Mokono, Fabien Roch Niama, Etienne Mokondjimobe, Olivia Galiba Atipo-Tsiba, Edwige Paola Louanga Nanitelamio
Publikováno v:
Open Journal of Blood Diseases. 11:57-65
Introduction: Sickle cell disease is a public health problem in the Republic of Congo where the prevalence of sickle cell trait is estimated at 1.25%. The objective of this study is to describe the variations of hematological and biochemical paramete
Autor:
Laure Flora Josiane Kibangou, Rachel Moyen, Nanikaly Moyen, Innocent Kocko, Lydie Ngolet, Ettienne Nguimbi, Alexis Elira Dokekias
Publikováno v:
Open Journal of Blood Diseases. 11:140-149