Results 51 to 60 of about 128 (89)

[Results of a systematic study of drepanocytosis in 1,500 Gabonese using hemoglobin electrophoresis].

, 1980
International audienceHemoglobin electrophoresis realised as a routine screening test on 1 500 gabonese individuals revealed the existence of a sickle cell abnormality n 24.40% cases (22.27% were AS heterozygotous and 2.1% were SS homozygotous). Bapounov
Toublanc, J. E., Kombila, M., Carme, Bernard, Zinsou, R. D., Richard-Lenoble, D.   +4 more
core   +1 more source

23rd Congress of the European Hematology Association Stockholm, Sweden, June 14‐17, 2018

, 2018
HemaSphere, Volume 2, Issue S1, Page 1-1113, June 2018.
wiley   +1 more source

Lésions osseuses et drépanocytose en pays africains

, 1976
Summary. The drepanocytosis, genetics disease, affects the skeleton of young child especially at the extremity of members. In adolescent the long bones are affected.
Bourrel, P., Chippaux, Claude
core   +1 more source

UEG Week 2014 Poster Presentations

, 2014
United European Gastroenterology Journal, Volume 2, Issue S1, Page A132-A605, October 2014.
wiley   +1 more source

Blood cells diseases and thrombosis

Haematologica, 2001
BACKGROUND AND OBJECTIVES: In recent years knowledge about thrombophilia and the mechanisms underlying the pathogenesis of thrombosis has increased greatly.
G Leone, S Sica, P Chiusolo, L Teofili, V De Stefano   +4 more
doaj  

Aportes al estudio de la drepanocitosis: Análisis clínico y hematológico en los primeros 5 años de la vida Contributions to the study of drepanocytosis: Clinical and hematological analysis in the first 5 years of life

Revista Cubana de Hematología, Inmunología y Hemoterapia, 1999
Se estudiaron 104 pacientes menores de 6 años de edad. En el 93,1 % el diagnóstico se hizo antes del primer año de la vida y en el 47,6 % fue prenatal. La mediana de seguimiento fue de 31 meses (1-108).
Tania García Peralta, Ileana Nordet Carrera, Sergio Machín García, Alejandro González Otero, Adriana Muñiz Fernández, Gisela Martínez Antuña, Maura Wade Mateo, Eva Svarch   +7 more
doaj  

Identification of Inhibitors for the Lutheran Blood Group Glycoprotein - Laminin 511/521 Interaction by Molecular Modelling and Simulation Techniques

, 2018
International audienceBackground: Drepanocytosis is a genetic blood disorder characterized by red blood cells that assume an abnormal, rigid, sickle shape.
Madeleine, Noelly, Gardebien, Fabrice
core   +1 more source

Anemie chronique severe et anomalies endocrines chez l'enfant. [Severe chronic anemia and endocrine disorders in children]

, 2007
Hemolytic anemias can induce various anomalies of the endocrine glands which can already be observed in children. Endocrine dysfunction is also found in the course of therapy for aplastic anemias, usually as undesirable side effects.
Theintz, G., Hauschild, M.
core  

Oral Status and Clinical Problems of Toothless Patients of Older Age Suffering from Blood Dyscrasias - Prosthodontic Treatment Modalities?

, 2021
Objectives of investigation: Clinical signs of blood dyscrasias’ in the mouths vary. Methods used: Inspection with additional specific and nonspecific laboratory tests.
Poštić, Srđan
core   +1 more source

Crisis drepanocítica y tratamiento del dolor

, 2015
Drepanocytosis includes a group of genetically inherited disorders in which low oxygen saturation rigid polymers aggregation deoxygenated hemoglobin S occurs, giving the red cell sickling and damaging the vascular endothelium through multiple mechanisms,
Vidal, M.A., Arroyo, F., Torres Morera, Luis Miguel, Rojas Martínez, Augusto, García Hernández, Rafael, Calderón Seoane, Enrique   +5 more
core