Results 121 to 130 of about 388 (169)

[Drepanocytosis and navigation personnel].

Bulletin de la Societe de pathologie exotique et de ses filiales, 1977
In West and Central Africa one adult in 4 or 5 carries AS trait. This haemoglobin abnormality therefore underlines the question of aptitude of navigation personnel in national or international air-lines. Among these personnel one should separate commercial navigation personnel (CNP) and technical navigation personnel (TNP), if the aptitude in flight of
M, Gentilini, P, Fourn, D, Richard-Lenoble, P, Ducosson   +3 more
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[Genetic polymorphism of drepanocytosis].

Annales de genetique, 1985
The pathophysiological mechanism of sickle cell anemia has been thoroughly studied and is now well understood, in contrast to the extreme clinical heterogeneity of the disease. A possible genetic explanation for this diversity arose from the discovery of an HpaI restriction polymorphism 3' to the beta globin gene, in linkage disequilibrium with the Hb ...
J, Pagnier, H, Wajcman, V, Baudin, D, Labie   +3 more
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[Major drepanocytosis and fertility].

Journal de gynecologie, obstetrique et biologie de la reproduction, 1987
The authors report on 4 observations they have made in cases of full-blown sickle-cell disease who became pregnant, to demonstrate that: fertility is normal in women with sickle-cell disease, it is important to screen systematically for haemoglobinopathies in populations at risk, that the condition is relatively rare, and very high-risk pregnancies do ...
M, Mounanga, A, Awassi-Ndouono, R D, Zinsou   +2 more
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[Respiratory distress and drepanocytosis].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2000
Acute chest syndrome (ACS) is characterized by chest pain with dyspnea and recent radiologic abnormalities, and is an acute lung complication whose problem is one of etiology. Alveolar hypoventilation linked to infarcts of the thoracic ribs, thoracoabdominal trauma, subdiaphragmatic pain, the administration of analgesics causing respiratory depression,
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Thalassemia (Microkarterocytosis) and Drepanocytosis their Forms and Genetics

Acta geneticae medicae et gemellologiae, 1952
SummaryThalassemia, that I propose to call Microkarterocytosis, can be divided into three forms to be distinguished under the names of minima (healthy carriers), minor (Rietti and Greppi's disease), major (Cooley disease).It can be inferred that Thalassemia is a mutation developped in a mediterranean superior paleolitic race that showed also the ...
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[Drepanocytosis].

Gazette medicale de France, 1998
P, GIRAUD, A, ORSINI, J, COIGNET
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[Recurrent macroscopic hematuria and heterozygote drepanocytosis].

Annales de medecine interne, 1987
The sickle cell trait may result in recurrent macroscopic haematuria which can cause severe anaemia. Despite normal intravenous urography and CAT, the haemorrhage probably occurs in the renal medulla due to the operative physiopathogenic conditions. A proliferative mesangial glomerulonephritis with IgG, IgA, IgM and complement deposits, which has a ...
G, Nedelec, F, Didelot, C P, Giudicelli, S, Perrot, T, Debord, R, Brouard, Y, Rougier   +6 more
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Drepanocytosis and surgery

Journal of Pediatric Surgery, 1980
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[Drepanocytosis].

La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris, 1970
P, Seringe, P, Despres, C, Allaneau
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