Zobrazeno 1 - 10
of 130
pro vyhledávání: '"J L, Nivelon"'
Autor:
G. Magnin, L. Larget-Piet, Charles Belon, R Moustarih, M. Vanderschueren, S. Bernasconi, J C Job, Jean-Edmond Toublanc, P. Lecomte, A Terraza, H. Chaabouni, D. Schoenberg, J M Lobaccaro, N. Bouccekine, M. Bost, Mongia Hachicha, Margherita Bozzola, P Rochiccioli, Ch. Sultan, Jean-Louis Chaussain, J M Limal, Michael B. Ranke, C. Burési, C. Moraine, J L Nivelon, G Malpuech, J Battin
Publikováno v:
Hormone Research. 37:54-59
In patients with androgen insensitivity syndrome (AIS), RFLP study of the androgen receptor gene made it possible to analyze whether deletions or mutations could be responsible for abnormalities in androgen responsiveness. We studied RFLPs of DNA fro
Publikováno v:
European Journal of Pediatrics. 156:949-951
The aim of this study was to document plasma retinol status and nocturnal vision in ten eutrophic adolescents with cystic fibrosis (CF) receiving daily retinol supplementation. Plasma retinol, alpha and beta carotenes and retinol binding protein were
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 5
Long-term effects of growth hormone (GH) treatment were studied in 59 GH deficient (GHD) children, whose treatment was started before the age of 1 year, during the period 1978-1992, under the supervision of the France-Hypophyse Association. Mean dura
Autor:
F, Huet, J L, Nivelon
Publikováno v:
Revue de pneumologie clinique. 53(2)
Aerosol therapy in cystic fibrosis is indicated in order to administer active agents directly into the diseased organ. The practical application of this technique often remains a question of personal experience rather than rigorous and validated sche
Autor:
J, Donadieu, P, Boutard, G, Tchernia, G, Oster, E C, Gordon-Smith, N, Philippe, E, Le Gall, J L, Nivelon, P, Dopfer, A, Babin-Boilletot
Publikováno v:
Nouvelle revue francaise d'hematologie. 36(6)
The present study evaluated the clinical efficacity and tolerability of the subcutaneous (SC) administration of lenograstim, a glycosylated form of rHuG-CSF identical to human G-CSF, in the treatment of congenital agranulocytosis. Assessment criteria
Autor:
A M Bertrand, P Rochiccioli, M. Bost, R. Mariani, Pierre Chatelain, R Freycon, J Battin, G Malpuech, Charles Sultan, M. David, J J Bouquier, M. Colle, G Simonin, J M Limal, P Pierron, J L Nivelon
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 83(3)
In understanding Turner's syndrome, spontaneous adult height is a prerequisite for an accurate assessment of the therapeutic efficiency of growth hormone treatment. The heights described in the literature reveal significant differences (136-147 cm).
Autor:
P, Poitrineau, G, Malpuech, J L, Nivelon, F, Huet, G, Giraud, C, François, H, Carla, Y, Loriette
Publikováno v:
Annales de pediatrie. 40(7)
The syndrome of generalized resistance to thyroid hormones is being increasingly diagnosed, albeit often belatedly. In the two families described herein the diagnosis was established when moderately elevated thyrotropin levels were found upon neonata
Autor:
J, Battin, G, Malpuech, J L, Nivelon, P, Garandeau, F, Freycon, C, Sultan, M, Bost, G, Simonin, J, Bouquier, P, Rochiccioli
Publikováno v:
Annales de pediatrie. 40(7)
A retrospective multicenter study found 58 cases of Klinefelter syndrome of which 23 (39%) were diagnosed before puberty. Although as common as Down syndrome, Klinefelter syndrome is underdiagnosed and often recognized only in adulthood. Suggestive m
Autor:
J L, Nivelon, M, Chouchane, M G, Forest, Y, Morel, F, Huet, A, Nivelon-Chevallier, C, François
Publikováno v:
Annales de pediatrie. 40(7)
Prenatal treatment based on administration of dexamethasone to the mother during pregnancy was initiated early during nine pregnancies with a high risk of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. The purpose of this treatment
Publikováno v:
Revue neurologique. 149(10)
We report 2 cases of lissencephaly and review the cardinal symptoms: microcephalia, mental retardation, pyramidal syndrome and generalized epilepsy. CT-Scan and MRI show the anatomical abnormalities of this malformation: microcephalia, smooth cortex