Zobrazeno 1 - 10
of 25
pro vyhledávání: '"I. Tiran-Rajaofera"'
Autor:
J.L. Alessandri, S. Samperiz, Stéphanie Robin, L. Dupuy, H Pilorget, I. Tiran-Rajaofera, T. Attali, Duksha Ramful, C Brayer
Publikováno v:
Archives de Pédiatrie. 14:903-907
Resume Le syndrome de Fryns est un syndrome de transmission recessive autosomique habituellement letal associant une hernie diaphragmatique congenitale (HDC), une hypoplasie pulmonaire, une dysmorphie crânio-faciale avec facies grossier, fente labio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3b577402ed7593f08f8faa6eb77f02b
https://doi.org/10.1016/j.arcped.2007.03.015
https://doi.org/10.1016/j.arcped.2007.03.015
Autor:
J.L. Alessandri, I. Tiran-Rajaofera, D Graber, S. De Napoli-Cocci, S. Samperiz, H Pilorget, T. Attali, A Montbrun
Publikováno v:
Archives de Pédiatrie. 7:637-640
Resume Le syndrome de Feingold associe de facon variable des anomalies des mains (mesobrachyphalangie) et des pieds (syndactylie des orteils), une microcephalie, une atresie œsophagienne et/ou duodenale, une dysmorphie faciale mineure et un retard m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dff4fede5fad1bf8f0bbf0f122125a60
https://doi.org/10.1016/s0929-693x(00)80132-3
https://doi.org/10.1016/s0929-693x(00)80132-3
Autor:
A S, Pellot, J L, Alessandri, S, Robin, S, Sampériz, T, Attali, C, Brayer, M, Pasquet, M C, Jaffar-Bandjee, L S, Benhamou, I, Tiran-Rajaofera, D, Ramful
Publikováno v:
Medecine tropicale : revue du Corps de sante colonial.
In 2005-2006, an unexpected, massive outbreak of chikungunya occurred on Reunion Island, a French overseas territory in the Indian Ocean. This arboviral infection transmitted by a mosquito of the Aedes genus is usually benign. A surprising feature of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2372c9c1f1082df33a79abea6c595e09
https://pubmed.ncbi.nlm.nih.gov/22693937
https://pubmed.ncbi.nlm.nih.gov/22693937
Autor:
J-L, Alessandri, T, Attali, C, Brayer, L, Dupuy, H, Pilorget, D, Ramful, S, Samperiz, I, Tiran-Rajaofera, S, Robin
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 14(7)
Fryns syndrome is a lethal autosomal recessive syndrome which includes congenital diaphragmatic hernia (CDH), pulmonary hypoplasia, cranio-facial manifestations including a coarse face, a cleft palate / lip and cloudy corneae, distal limb hypoplasia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0bc0b05ddab1f5a2f06a5f825d4f7aec
https://pubmed.ncbi.nlm.nih.gov/17442547
https://pubmed.ncbi.nlm.nih.gov/17442547
Publikováno v:
Genetic counseling (Geneva, Switzerland). 16(4)
Fryns syndrome is an autosomal recessive multiple congenital anomaly syndrome characterized by coarse facies, diaphragmatic hernia, distal limb hypoplasia and malformations of the cardiovascular, gastrointestinal, genitourinary and central nervous sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70dcfd4f19111458736173695449b5e2
https://pubmed.ncbi.nlm.nih.gov/16440878
https://pubmed.ncbi.nlm.nih.gov/16440878
Autor:
H, Pilorget, A, Montbrun, T, Attali, I, Tiran-Rajaofera, C, Bony, C, Brayer, S, Sampériz, J-L, Alessandri
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 10(9)
Pertussis remains in France the first cause of bacterial, infectious death in infant aged 10 days to 2 months. It is especially in this age group that malignant pertussis occurs.A 40-day-old infant was admitted in the intensive care unit with symptom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c962368b3895d54d518eb158f1de36a0
https://pubmed.ncbi.nlm.nih.gov/12972206
https://pubmed.ncbi.nlm.nih.gov/12972206
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 9(7)
We report a case of warfarin embryopathy. This disease affects more than 6% of fetuses exposed in utero to a vitamin K antagonist.A child whose mother was treated with acenocoumarol because of a mechanical heart valve presented with signs of warfarin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::40691ad92e9ea103a30e9241b7278fae
https://pubmed.ncbi.nlm.nih.gov/12162160
https://pubmed.ncbi.nlm.nih.gov/12162160
Autor:
I, Tiran-Rajaofera, S, Sampériz, C, Trouilloud, H, Pilorget, A, Montbrun, T, Attali, J L, Alessandri
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 8(8)
Percutaneous central venous catheterization for parenteral feeding is a permanent problem in the management of very low birth weight neonates. Usually, 23-gauge catheters (diameter: 0.6 mm) are used. In our unit, we have started to use 27-gauge cathe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::756fc5316d7ce4eaffb4675f1875f2d6
https://pubmed.ncbi.nlm.nih.gov/11524911
https://pubmed.ncbi.nlm.nih.gov/11524911
Autor:
J L, Alessandri, D, Graber, I, Tiran-Rajaofera, A, Montbrun, H, Pilorget, S, Samperiz, T, Attali, S, de Napoli-Cocci
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 7(6)
Feingold syndrome is a combination of hand and foot anomalies, microcephaly, tracheo-esophageal fistula, esophageal/duodenal atresia, short palpebral fissures and developmental delay. The most frequent physical findings are clinodactyly of the second
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1487009eaf478947533d702e45558ef8
https://pubmed.ncbi.nlm.nih.gov/10911531
https://pubmed.ncbi.nlm.nih.gov/10911531
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