References of "Legros, Jean-Jacques"
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See detailMise en évidence de profils psychologiques différents dans un échantillon d'impuissants érectifs
Mormont, Christian ULg; Legros, Jean-Jacques ULg; Servais, J. et al

in Acta Psychiatrica Belgica (1980), 80(4), 476-486

The homogeneity of personality in patients suffering from psychogenic impotency has never been tested. In order 1. to test the homogeneity of the population and 2. to delineate putative prognostic scores ... [more ▼]

The homogeneity of personality in patients suffering from psychogenic impotency has never been tested. In order 1. to test the homogeneity of the population and 2. to delineate putative prognostic scores, the authors have applied inverse factorial analysis to MMPI and Rorschach performed in a group of 100 patient suffering from "psychogenic impotence". The results obtained evidenced an heterogeneity in the group, subgroups may differ as far as prognostic is concerned. [less ▲]

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See detailMotoneuropathie hereditaire: la forme proximale de l'adulte liee au sexe (ou maladie de Kennedy). Observations cliniques et neuroendocrinologiques.
Schoenen, Jean ULg; Delwaide, P. J.; Legros, Jean-Jacques ULg et al

in Journal of the Neurological Sciences (1979), 41(3), 343-57

Clinical, electrophysiological, histological and neuroendocrinological findings in a peculiar form of progressive spinal and bulbar muscular atrophy affecting 4 members in two different families are ... [more ▼]

Clinical, electrophysiological, histological and neuroendocrinological findings in a peculiar form of progressive spinal and bulbar muscular atrophy affecting 4 members in two different families are reported. The clinical hallmarks, which characterize this entity among the group of degenerative motor neuron diseases are: sex-linked recessive inheritance; onset in the third decade; slow progression; involvement of facial and bulbar muscles in addition to wasting of the proximal and, in some cases, the distal musculature; asymmetry of clinical signs; consistent and abundant fasciculations predominantly in the peri-oral muscles; intention tremor and a well-developed gynaecomastia, which is the first clinical sign. Electrophysiological and histological findings confirm the neurogenic origin of the muscular atrophy; in addition, muscle biopsy shows "myopathic-like" changes in one case and serum muscle enzyme levels are elevated in all neurologically affected patients. It is believed that the clinical entity corresponds to the rare type III proximal hereditary motor neuropathy (or "Kennedy's disease"), of which 25 published cases are reviewed. Neuroendocrinological data in two patients demonstrate an androgenic insufficiency of hypothalamo-hypophyseal origin and high levels of circulating oestrogens, which probably have induced gynaecomastia. Dynamic neuroendocrinological tests suggest that lesions of certain hypothalamic nuclei may exist, which should be looked for in the forthcoming anatomical studies. [less ▲]

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See detailTestostérone et sexualité chez l'homme
Legros, Jean-Jacques ULg; Mormont, Christian ULg; Servais, Jean

in Expansion Scientifique Française (1977)

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See detailLes impuissances érectives
Servais, Jean-François; Mormont, Christian ULg; Legros, Jean-Jacques ULg

in Feuillets Psychiatriques de Liège (1977), 10(1), 9-35

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See detailPerturbations neuropsychiques graves chez un jeune adolescent soumis à une thérapeutique endocrinienne
Servais, Jean-François; Mormont, Christian ULg; Bostem, F. et al

in Acta Psychiatrica Belgica (1976), 76(1), 97-106

After a treatment based on the administration of gonadotropic drugs, aimed at reduced school difficulties and caracterial difficulties by a premature onset of puberty, a young male aged 13 1/2 presents: 1 ... [more ▼]

After a treatment based on the administration of gonadotropic drugs, aimed at reduced school difficulties and caracterial difficulties by a premature onset of puberty, a young male aged 13 1/2 presents: 1 degree somatic anomalies; 2 degrees increase of intellectual, affective and behavioral troubles; 3 degrees perturbations of EEG prophiles; 4 degrees organicity tests significantly disturbed. The interruption of treatment (4 years of observation) was followed by a progressive remission, however heterogenous, of all initial troubles. The observation underlines the dangers of utilising these treatments in a pre-puberty boy. [less ▲]

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See detailL'impuissance: Aspects diagnostique et thérapeutique
Servais, J.F.; Mormont, Christian ULg; Legros, Jean-Jacques ULg

in Revue de Médecine Psychosomatique (1975), 18(3), 263-269

This study reports on 100 cases of males, aged 21 to 63 years, consulting for difficulties or inability to perform an intercourse erection with a partner of their choice. Every patient was investigated by ... [more ▼]

This study reports on 100 cases of males, aged 21 to 63 years, consulting for difficulties or inability to perform an intercourse erection with a partner of their choice. Every patient was investigated by the same psychiatrist the same psychologist and the same endocrinologist. Testosterone blood level was found insufficient (2 sigma under the mean) in 48 cases. The psychological tests emphasized an important but clinically inconspicuous psychopathology. Anxious and depressive trends were very frequent. The result of the investigations oriented the treatment, which used several methods, single or in association : brief psychotherapy, nasal stress, hormones, psychotropic drugs. After one year of follow-up, 67 men were improved or recovered and 22 unchanged. [less ▲]

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See detailSerum-gonadotrophins after oxytocin in man.
Legros, Jean-Jacques ULg; Franchimont, P.

in Lancet (1968), 2(7570), 735

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