Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Alice Lageron"'
Niemann Pick c or storage by excessive blood cell destruction: a case presenting a diagnosis problem
Publikováno v:
Acta histochemica. 92(1)
A case of storage disease followed up during 12 a was studied by morphological, histochemical, immunological, and biochemical techniques. Data were analysed in an attempt to differentiate an acquired storage by excessive cell degradation from a stora
Storage by excessive blood cell destruction or due to Niemann-Pick disease type C: an ambiguous case
Publikováno v:
Journal of inherited metabolic disease. 15(2)
Autor:
Louis Rosensztajn, Darnis F, Paul Prudhomme de Saint-Maur, Thierry Gombeau, Alice Lageron, Raoul Poupon
Publikováno v:
Digestion. 20:145-150
In order to assess the prevalence and characteristics of perhexiline maleate (PM)-associated hepatic injury, we have conducted a study in 46 patients on PM therapy (100-400 mg/day) for angina pectoris
Autor:
Monique Saffroy, Jean-Robert Rapin, Monique Leponcin-Lafitte, Claudette Bulach, Alice Lageron
Publikováno v:
Acta Histochemica. 65:184-190
Resume La thrombose cerebrale par microspheres de 35 ,µm marquees a 1’125I chez le rat provoque des lesions d'infaretus reperables grâce au marquage de la microsphere. A, leur niveau les NADH diaphorase, succino-deshydrogenase, mono-amino-oxydase
Publikováno v:
Acta Histochemica. 65:8-14
Resume Les modifications histologiques et histoenzymologiques des foies de sujets lithiasiques traites par ACDC sont analysees par rapport a ces memes foies avant traitement. Le profil histologique de ces foies est peu modifie a part une augmentation
Autor:
Monique Le Poncin, Jean Luc Moretti, Jean Claude Saccavini, Alice Lageron, Jean René Rapin, André Bardy
Publikováno v:
International Journal of Nuclear Medicine and Biology. 11:275-279
Using DMSA labeled with 117 m Sn, 14 C, 95 m Tc and 99 m Tc the renal kinetic and receptor identification by autoradiography and subcellular studies was performed. The half-life was found to be 6.5 days in the kidney. The binding receptors of the Tc-
Publikováno v:
Journal of Inherited Metabolic Disease. 12:375-378
Glycosphingolipid storage due to α-galactosidase deficiency (EC 3.2.1.22) characterizes the X-linked inherited Fabry’s disease (McKusick 30150). Accurate sugar moiety visualization obtained in kidney patients by lectin binding (Faraggiana et al.,
Autor:
Jacques Polonovski, Alice Lageron
Publikováno v:
Acta Histochemica. 57:157-164
Spleen of adult-type Gaucher's disease has been investigated by histochemical technics. As usually, an overload of cerebroside (revealed by the PAS reaction for glycolipids) with beta-glucosidase deficiency has been demonstrated. But many particulari
Publikováno v:
Acta Histochemica. 65:1-7
Resume 46 foies de sujets lithiasiques ont ete etudies par rapport a un groupe temion en histologie et histoenzymologie. Les lesions les plus frequemment rencontrees sont l'inflammation et la fibrose periportale,la plus caracteristique etant la conge
Autor:
Jacques Emerit, Françise Calman, Nicole Hinglais, Alice Lageron, Jean Brière, Monique Saffroy
Publikováno v:
Acta Histochemica. 59:106-121
Resume Les auteurs confrontant les donnees cliniques, biologiques, histologiques, histochimiques, ultrastructurales et biochimiques a propos d'une observation complexe d'une patiente atteinte de Niemann-Pick dont l'evolution est suivie de l'enfance a