Biomedical subjects
M Reboul
Publications and source records attributed to M Reboul.
[Retroperitoneal fibrosis. Clinical remarks apropos of a case with cavography].
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[Osteology and cephalometry].
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[Photography in the orthodontic study of the face].
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[Osteology and tridimensional teleradiography].
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[A chart for transcription of panoramic radiographies].
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[Dental balance in orthodontics].
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[The relationship between dentist and child].
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[Osteology and cephalometry].
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[A new simplified head holder for the teleradiography of the cranium in profile].
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Anti-MHC immunity detected prior to intentional alloimmunization. IV. Natural monoclonal H-2-specific antibodies.
Naturally occurring H-2-specific antibodies can be detected rather frequently in sera of non-alloimmunized mice by sufficiently sensitive techniques (Cerny-Provaznik et al., 1985a; Cerny-Provaznik & Ivanyi, 1985). In this report, we summarize our experiences with the preparation of monoclonal anit-H-2 antibodies obtained from hybridization experiments from non-alloimmunized mice. From a total of 30 spleen cell hybridization experiments, we could isolate only four anti-H-2 monoclonal antibodies (mAB). Two of the mAB are described in this report. Monoclonal antibody By-2 is anti-Kf and mAB By-3 is anti-Db, Ds. We investigated which conditions favour the isolation of monoclonal H-2-specific antibodies from non-alloimmunized mice. The presence of naturally occurring serum antibodies, the age of the spleen donor mouse or non-specific B cell stimulation were not critical for the isolation of natural anti-H-2 mAB. We hypothesise that the 'natural' H-2-specific antibodies represent compartments of the B cell repertoire which were triggered by modified or aberrant self-MHC expression.
[Migrating and recurrent superficial phlebitis and Takayasu's disease (apropos of a case)].
This case of recurrent migratory superficial phlebitis is reported because of the highly unusual nature of the lesion observed. The picture was dominated by periphlebitis with inflammatory granuloma, giant cells and elastophagia. When the condition had been present for sixteen months, an aortic arch syndrome developed in an inflammatory context. In this light, various auto-immunological etiologies were considered, among them Takayashu's arteritis of which, in the author's opinion, this would be the first case to be combined with venopathy.
[Heart failure in hemochromatosis. Apropos of a case].
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[Importance of early diagnosis in idiopathic retroperitoneal fibrosis. Role of cavography].
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