A Lageron

Medicine · Health Sciences

12h-index448citations104works0.02yr avg
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Research Topics

Lysosomal Storage Disorders Research(15), Liver Disease Diagnosis and Treatment(9), Metabolism and Genetic Disorders(9), Carbohydrate Chemistry and Synthesis(8), Drug-Induced Hepatotoxicity and Protection(6)

Publications101 total

[ENZYMOLOGIC MODIFICATIONS OF THE VAGINA AND UTERUS OF THE RAT IN NORMAL STATES AND UNDER THE EFFECT OF FOLLICULIN AND PROGESTERONE].
PubMed·1996
[ENZYMATIC VARIATIONS DURING THE ESTROUS CYCLE AND AFTER HORMONAL TREATMENT IN THE OVARY OF THE ALBINO RAT].
PubMed·1996· 2 cited
EARLY ALTERATIONS OF ACTIN IN CULTURED HUMAN KERATINOCYTES AND FIBROBLASTS EXPOSED TO LONG‐WAVELENGTH RADIATIONS. POSSIBLE INVOLVEMENT IN THE UVA‐INDUCED PERTURBATIONS OF ENDOCYTOTIC PROCESSES
Photochemistry and Photobiology·1994· 26 cited
Storage by excessive blood cell destruction or due to Niemann‐Pick disease type C: An ambiguous case
Journal of Inherited Metabolic Disease·1992
[Severe hepatic steatosis: a cause of sudden death in the alcoholic patient].
PubMed·1992· 11 cited
Niemann Pick c or storage by excessive blood cell destruction: A case presenting a diagnosis problem
Acta Histochemica·1992· 1 cited
An Atypical Ultrastructural Pattern in Fabry's Disease: A Study on Its Nature and Incidence in 7 Cases
Ultrastructural Pathology·1990· 13 cited
Visualization of the Sugar Moiety in Lymphoid Cell Lines from Fabry's Disease by Lectin Binding
Journal of Inherited Metabolic Disease·1989· 1 cited
Diffuse storage of vegetal wax hydrocarbons of dietary origin. Pathologic and chemical findings in a case.
PubMed·1989· 3 cited
Visualization of the Sugar Moiety in Lymphoid Cell Lines from Fabry’s Disease by Lectin Binding
1989
[Hepatic lipid overload in 2 cases of cholestasis associated with parenteral feeding].
PubMed·1988· 6 cited
Histochemical abnormalities in liver and jejunal biopsies from a case of cholesterol ester storage disease
Journal of Inherited Metabolic Disease·1988· 3 cited
A new human pathology with visceral accumulation of long-chain n-alkanes; tissue distribution of the stored compounds and pathophysiological hypotheses
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism·1988· 27 cited
Increase in Sterol Synthesis and Decrease in Cholesterol Efflux in Niemann-Pick Disease Type C Fibroblasts
1988· 1 cited
The effects of perhexiline maleate on low density lipoprotein processing and cholesterol metabolism in cultured human fibroblasts
European Journal of Clinical Pharmacology·1988· 3 cited
Alkane Storage Disease (Very Long Chain N-Alkanes): An Original Type of Lipid Storage of Dietary Origin from Plant Wax Hydrocarbons
1988· 1 cited
Histoenzymological Study of One Case of Fabry Disease Before and After Transplantation
1988
Histochemical Abnormalities in Liver and Jejunal Biopsies from a Case of Cholesterol Ester Storage Disease
1988
Abnormaln-nonacosane storage in humans: Detection by gas chromatography/mass spectrometry of tissue extracts
Journal of Mass Spectrometry·1987· 6 cited
Characterization by lectin binding of the sugar moiety of glycocompounds stored in inherited diseases
The Histochemical Journal·1987· 14 cited
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Frequent Co-authors

J Caroli(5), Monique Saffroy(5), F. Rocchiccioli(4), C Duboucher(4), Cécile Mazière(4), P Hadchouel(4), Robert Salvayre(3), Anne Nègre(3), J. Polonovski(3), F Darnis(3), Liliana Mora(3), Michel Beaugrand(3), P Callard(3), D Lecomte(3), R Wegmann(3), J Scotto(3), J. R. Rapin(3), Victor-Georges Lévy(3), J Polonovski(3), Paul Prudhomme de Saint-Maur(2)