Zobrazeno 1 - 10
of 62
pro vyhledávání: '"L, Broussine"'
Autor:
Y. Feuvrier, L Broussine, G. Blondin, A. Chergui, S. Guérin-Develay, E. Rivoal, S. Audebert, P. Vic
Publikováno v:
Archives de Pédiatrie. 11:1495-1497
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3d1cafc6855edfed10b2d0fb936e899
https://doi.org/10.1016/j.arcped.2004.09.027
https://doi.org/10.1016/j.arcped.2004.09.027
Autor:
M Bensaid, A Chabarot, L de Parscau, H. Le Guern, A Cozic, Colin A, B. Jehannin, L Broussine, Philippe Parent
Publikováno v:
Archives de Pédiatrie. 2:551-554
Resume Le syndrome de Townes-Brocks (TBS) est une entite rare se transmettant sur le mode autosomique dominant dont l'expressivite clinique marquee par des malformations ancrectales, des pavillons des oreilles et des extremites, est en fait variable.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3466275158945946f6556fc049ab4eca
https://doi.org/10.1016/0929-693x(96)81200-0
https://doi.org/10.1016/0929-693x(96)81200-0
Publikováno v:
Archives de Pédiatrie. 6:533-535
Resume Le diagnostic des dermatoses pustuleuses dans la periode neonatale est essentiellement clinique. L'erytheme toxique neonatal est la plus frequente des dermatoses neonatales benignes. Observation Trois cas d'erythemes toxiques neonatals localis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4ea343bbec0464a628c38a1dbac8de3
https://doi.org/10.1016/s0929-693x(99)80560-0
https://doi.org/10.1016/s0929-693x(99)80560-0
Autor:
S, Audebert, P, Vic, Y, Feuvrier, G, Blondin, S, Guérin-Develay, E, Rivoal, A, Chergui, L, Broussine
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 11(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a65aebfb3db36b803259fbcb2cb0244c
https://pubmed.ncbi.nlm.nih.gov/15596340
https://pubmed.ncbi.nlm.nih.gov/15596340
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 8(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e3824bd3933e346c7d8037632a34c9a
https://pubmed.ncbi.nlm.nih.gov/11484463
https://pubmed.ncbi.nlm.nih.gov/11484463
Publikováno v:
European journal of dermatology : EJD. 11(2)
Transient alterations in pigmentation are frequently observed in black neonates, but to our knowledge, have not previously been reported in Caucasian infants. In 54 Caucasian newborns, we found at least mild periungual hyperpigmentation similar to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f030044f56b133c1a14b6df898b22cb
https://pubmed.ncbi.nlm.nih.gov/11275807
https://pubmed.ncbi.nlm.nih.gov/11275807
Publikováno v:
Journal de radiologie. 81(2)
A case of small bowel volvulus due to midgut malrotation in a 4 years-old child complaining of vomiting and abdominal pain. Diagnosis was made by a Doppler ultrasound showing the volvulus and the intestinal malrotation. We are discussing the interest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd6a1a04a8ebadb90104b167fdf0fc26
https://pubmed.ncbi.nlm.nih.gov/10705146
https://pubmed.ncbi.nlm.nih.gov/10705146
Autor:
P, Vic, D, Laguette, G, Blondin, M, Blayo, S, Thirion, C, Queinnec, J, Lew, G, Mehu, L, Broussine
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 6(8)
We report our experience of the utilization of the 50% oxygen-nitrous oxide mixture (nitrous oxide 50%) in our general pediatric ward after one year of use.Between 1st April 1997 and 31st March 1998, children who had to undergo a painful procedure we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69f6d03129411fb2d65ff743597658d4
https://pubmed.ncbi.nlm.nih.gov/10472395
https://pubmed.ncbi.nlm.nih.gov/10472395
Publikováno v:
Annales de dermatologie et de venereologie. 124(5)
The Prader-Labhart-Willi syndrome was first described in 1956. Prader-Labhart-Willi syndrome is the most common genetic form of human obesity and the incidence of Prader-Labhart-Willi syndrome has been estimated to 1 in 10,000 or 25,000 live births.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2feb9c36e49c1476fcb1701fb417d628
https://pubmed.ncbi.nlm.nih.gov/9739896
https://pubmed.ncbi.nlm.nih.gov/9739896
Autor:
M, Bardainne, Y, Rolland, C, Tréguier, V, Claeyssen-Rolland, M, Dagorne, L, Broussine, H, Jouan, M, Roussey
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 3(7)
Despite post-mortem examination and autopsy, many cases of sudden infant death (SID) remain unexplained. The aim of this study was to assess usefulness of CT-scan in the Sudden Infant Death Syndrome (SIDS).Twenty-three cases of SIDS had a post-mortem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce44e4f87602d292952304cd2d118143
https://pubmed.ncbi.nlm.nih.gov/8881176
https://pubmed.ncbi.nlm.nih.gov/8881176