Zobrazeno 1 - 10
of 42
pro vyhledávání: '"F, Dalla Vale"'
Autor:
L. Ichay, J. Tenenbaum, F. Dalla Vale, A. Douillard, Denis Morin, N. Nagot, M. Golay, Marc Fila
Publikováno v:
Archives de Pédiatrie. 24:1096-1102
Resume Objectifs Plus de la moitie des enfants presentant un syndrome nephrotique idiopathique (SNI) sont cortico-dependants et necessitent un traitement en complement de la corticotherapie. Il est important de pouvoir identifier ces patients afin d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d5240eeddfc0310c43f766ee3f460c2
https://doi.org/10.1016/j.arcped.2017.08.013
https://doi.org/10.1016/j.arcped.2017.08.013
Publikováno v:
Archives de Pédiatrie. 22:241-246
Since 1st January 2000, the PEDIAB-LR registry has listed new cases of diabetes in children under 16 years of age in the Languedoc-Roussillon region of France, in order to assess the incidence and epidemiological characteristics of children affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be56c70d171f34beb8dada6eedba9d2d
https://doi.org/10.1016/j.arcped.2014.12.009
https://doi.org/10.1016/j.arcped.2014.12.009
Autor:
A.-L. Adra, C. Milesi, L. Ichay, F. Dalla-Vale, J.-F. Mouba, Denis Morin, J. Tenenbaum, C. Amouroux
Publikováno v:
Archives de Pédiatrie. 19:150-155
Resume Les cas de syndromes hemolytiques et uremiques (SHU) postdiarrheiques avec atteinte neurologique severe posent encore un probleme de prise en charge. Nous rapportons l’observation de 2 enfants âges de 2 ans et demi qui avaient presente un S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c8ab84b1d0e0766cdfb53083b281c1b
https://doi.org/10.1016/j.arcped.2011.11.015
https://doi.org/10.1016/j.arcped.2011.11.015
Autor:
A.-L. Adra, F. Dalla-Vale, M. Averous, J.-F. Mouba, C. Lopez, M. Trellu, Denis Morin, R.-B. Galifer, L. Ichay
Publikováno v:
Archives de Pédiatrie. 16:417-425
Resume Les valves de l’uretre posterieur (VUP) peuvent constituer, en presence de signes antenatals de gravite, un motif d’interruption medicale de grossesse (IMG). Le but de cette etude etait d’evaluer le retentissement du diagnostic prenatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5972efc206ba810418ae65040981d0c
https://doi.org/10.1016/j.arcped.2009.02.006
https://doi.org/10.1016/j.arcped.2009.02.006
Publikováno v:
Archives de Pédiatrie
Archives de Pédiatrie, Elsevier, 2015, 22 (3), pp.241-246. ⟨10.1016/j.arcped.2014.12.009⟩
Archives de Pédiatrie, Elsevier, 2015, 22 (3), pp.241-246. ⟨10.1016/j.arcped.2014.12.009⟩
International audience; Since 1st January 2000, the PEDIAB-LR registry has listed new cases of diabetes in children under 16 years of age in the Languedoc-Roussillon region of France, in order to assess the incidence and epidemiological characteristi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::090db809a53cc78662c44970afa07950
https://hal.umontpellier.fr/hal-02124376
https://hal.umontpellier.fr/hal-02124376
Autor:
P.O. Kotzki, M. F. Durand, F. Dalla Vale, Denis Morin, C. Lopez, J. Astruc, C. Veyrac, R. Dumas
Publikováno v:
Pediatric Nephrology. 13:219-222
The strategy for morphological investigations in children with acute pyelonephritis (APN) remains debatable. We studied 70 children (median age 2.0 years) admitted with a first episode of pyelonephritis using a high-resolution ultrasound technique (R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50c31e8b520bb4728661e20503b82d33
https://doi.org/10.1007/s004670050596
https://doi.org/10.1007/s004670050596
Publikováno v:
Archives de Pédiatrie. 6:182-185
Resume Les manifestations uronephrologiques sont parfois revelatrices d'une hyperparathyroie primaire chez I'enfant. Observation. Un garcon de 10 ans a ete pris en charge pour ('exploration d'une hematurie macroscopique rattachee a one lithiase renal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::369ea3110af09f3185df0b8cdd9a9f63
https://doi.org/10.1016/s0929-693x(99)80207-3
https://doi.org/10.1016/s0929-693x(99)80207-3
Autor:
C, Amouroux, A-L, Adra, J-F, Mouba, J, Tenenbaum, L, Ichay, F, Dalla-Vale, C, Milesi, D, Morin
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 19(2)
The management of diarrhea-associated hemolytic and uremic syndrome (D(+) HUS) with severe acute neurological involvement continues to be debated. We report on 2 cases and discuss the treatment. CASE REPORT 1: A 2.5-year-old girl presented with gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a542cf401f37717a3a4313656d740651
https://pubmed.ncbi.nlm.nih.gov/22245485
https://pubmed.ncbi.nlm.nih.gov/22245485
Autor:
M, Trellu, A-L, Adra, J-F, Mouba, C, Lopez, M, Averous, R-B, Galifer, F, Dalla-Vale, L, Ichay, D, Morin
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 16(5)
To evaluate the impact of prenatal diagnosis on the epidemiology and outcome of children with posterior urethral valves (PUV), considering that today termination of pregnancy may be proposed in the most severe cases.Forty-three cases of patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5e4d8550384e84908b52eb802833e4c
https://pubmed.ncbi.nlm.nih.gov/19339163
https://pubmed.ncbi.nlm.nih.gov/19339163
Publikováno v:
Annales de dermatologie et de venereologie. 132(2)
Ito hypomelanosis-type pigmentary mosaicism is characterized by congenital pigmentation disorders along Blaschko's lines. We report a case of Ito-type pigmentary mosaicism associated with a congenital growth hormone deficiency having revealed trisomy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5dfcccd847744e556a312f2f0382fe1
https://pubmed.ncbi.nlm.nih.gov/15798568
https://pubmed.ncbi.nlm.nih.gov/15798568