P
Pierre Boivin
Researcher at University of Paris
Publications - 19
Citations - 373
Pierre Boivin is an academic researcher from University of Paris. The author has contributed to research in topics: Superoxide dismutase & Pyruvate kinase. The author has an hindex of 10, co-authored 19 publications receiving 370 citations. Previous affiliations of Pierre Boivin include French Institute of Health and Medical Research & University of Grenoble.
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Journal ArticleDOI
Blood polymorphonuclear dysfunction in patients with alcoholic cirrhosis.
Evarist Feliu,Marie-Anne Gougerot,Jacques Hakim,Elisabeth M. Cramer,Christian Auclair,Bernard Rueff,Pierre Boivin +6 more
TL;DR: Polymorphonuclear leucocyte abnormalities are frequent in cirrhosis and may account in part for increased susceptibility to infection in that disease.
Journal ArticleDOI
Acquired erythroenzymopathies in blood disorders: study of 200 cases.
TL;DR: Enzyme abnormalities are frequently found in the red cells of patients with various acquired blood disorders and changes in enzyme activity are usually characterized by the coexistence of deficiency of some enzymes and an increased activity of others.
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Pyruvate kinase isozymes in man. I. M type isozymes in adult and foetal tissues, electrofocusing and immunological studies.
TL;DR: This paper showed that pyruvate kinase from all the other tissues on the other hand were inhibited by anti-M2 and not at all by anti L serum, and the latter group represent the M type pyruve kinase isozymes.
Journal ArticleDOI
Molecular mechanism of erythrocyte pyruvate kinase deficiency
Axel Kahn,Axel Kahn,Joelle Marie,Joelle Marie,Colette Galand,Colette Galand,Pierre Boivin,Pierre Boivin +7 more
TL;DR: The heterogeneity of the molecular mechanisms of the deficiency on the one hand, and the abnormalities of electrofocusing patterns on the other hand seem to indicate that erythrocyte PK deficiency is due to the synthesis by muted structural genes of various abnormal PK molecules.
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Metabolic activity of phagocytosing granulocytes in chronic granulocytic leukemia: ultrastructural observation of a degranulation defect
Elisabeth M. Cramer,Christian Auclair,Jacques Hakim,Evarist Feliu,Jeannie Boucherot,Huguette Troube,Jean-François Bernard,Eugénie Bergogne,Pierre Boivin +8 more
TL;DR: The functional capacities of granulocytes in patients with chronic granulocytic leukemia are still a subject of controversy, probably due to the heterogeneity of the abnormalities observed from patient to patient, but a degranulation defect which was observed ultrastructurally in the only patient studied among these six.