Zobrazeno 1 - 10
of 632
pro vyhledávání: '"D. Renier"'
Autor:
DI Bhat, S Dwarkanath, PE Stieg, A Mahadevan, M Miyajima, FU Ahmed, S Ahmed, FU Ahmad, PS Chandra, RD Hayward, M Feany, S Sinha, P Barnes, KC Wang, M Dadmer, A Kahn Pierre, V Gupta, DK Gupta, NL Dorward, Y Iwasaki, JH Seatliff, H Arai, BI Devi, A Tunguria, M Hishii, K Sato, T Isu, SK Kim, A Suri, BK Cho, F Nejt, T Murakami, BS Sharma, D Agrawal, R Kamal, TK Maiti, VS Mehta, Proctor, AK Mahaptra, M Zerah, SK Kalra, D Pang, H Nakanishi, D Renier, M Yoshino, K Hida, D Gupta, A Oviedo, S Ansari, V Suri, V Tandon, H Abe, MC Sharma, MK Kasliwal, PH Champman, SK Shankar, A Srivasatava, HS Kang, P Chapman, S Yazdari, GD Satyarthee, V Naik, S Magge, KM Kim, I Koyanagi, S Sampath, A Khandelwal, M Akino, Ashok Kumar Mahapatra, AV Kulkarni, D Agarwal, K Garg, A Jindal, G Clinalli, Scott, P Garg, O Okuda
Publikováno v:
Indian Journal of Neurosurgery, Vol 01, Iss 01, Pp 004-008 (2012)
Indian Journal of Neurosurgery, Vol 1, Iss 1, Pp 4-8 (2012)
Indian Journal of Neurosurgery, Vol 1, Iss 1, Pp 4-8 (2012)
A large series of split cord malformation (SCM). Over the last 22 years, we have operated more than 1500 patients of SD, of which over 450 are (SCM), and 300 are with various lipomatus malformations. About 55% type II and 45% type I SCM. A separate s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93cb479976d8d69b2c1429e12a09c981
https://doi.org/10.4103/2277-9167.94362
https://doi.org/10.4103/2277-9167.94362
Autor:
D. Renier
Publikováno v:
EMC - Pédiatrie - Maladies infectieuses. 5:1-5
Resume Le syndrome du bebe secoue associe, chez un nourrisson, un hematome sous-dural et des hemorragies retiniennes, sans histoire de traumatisme. Il se manifeste par une apathie, une irritabilite, des vomissements ou, plus souvent, par une crise co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::555c925616777d377da6bcb1cb2f0ac9
https://doi.org/10.1016/s1637-5017(10)72457-1
https://doi.org/10.1016/s1637-5017(10)72457-1
Publikováno v:
EMC - Pediatría. 43:1-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a286d002efe6ef136a08d734f0e82901
https://doi.org/10.1016/s1245-1789(08)70229-4
https://doi.org/10.1016/s1245-1789(08)70229-4
Publikováno v:
Neurochirurgie. 52:259-263
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecf541e6a320e91c1c4a026c0a8c7973
https://doi.org/10.1016/s0028-3770(06)71220-6
https://doi.org/10.1016/s0028-3770(06)71220-6
Publikováno v:
Neurochirurgie. 52:228-237
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0414ea363f2a89a63992f849c77e3a05
https://doi.org/10.1016/s0028-3770(06)71217-6
https://doi.org/10.1016/s0028-3770(06)71217-6
Publikováno v:
Scopus-Elsevier
In patients with Apert syndrome, the hands demonstrate many disturbances of soft tissue and bony structures. These include a short thumb with radial clinodactyly, complex syndactyly with a bony fusion involving the index, long and ring fingers, symph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d495d015d8d981b97398a48564b6bee3
https://doi.org/10.1055/s-2004-817891
https://doi.org/10.1055/s-2004-817891
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 21:347-353
Objective Craniosynostosis is defined as the premature closure of the calvarial sutures. The prevalence of this heterogeneous condition is 1 in 2000 and approximately 100 different forms have been described with an established genetic transmission in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::575bde523024ef0ff33650c4f57ee08a
https://doi.org/10.1002/uog.91
https://doi.org/10.1002/uog.91
Autor:
D. Renier
Publikováno v:
Rivista di Neuroradiologia. 13:63-70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e39479cd3d9c0cc75f434f81da04bfe
https://doi.org/10.1177/19714009000130s106
https://doi.org/10.1177/19714009000130s106
Publikováno v:
Journal de Pédiatrie et de Puériculture. 11:29-38
Les traumatismes crâniens de l'enfant presentent des caracteristiques tres particulieres qui tiennent en premier lieu a certaines specificites physiologiques, ce qui implique une conduite a tenir et des mesures therapeutiques tout a fait differentes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39033ecd556b57237b10993b701b9307
https://doi.org/10.1016/s0987-7983(98)80105-9
https://doi.org/10.1016/s0987-7983(98)80105-9
Publikováno v:
Annales Françaises d'Anesthésie et de Réanimation. 16:152-164
Craniosynostosis occurs in one out of 2,000 births. It results in primary skull deformations requiring surgical repair, in infants with a body weight of less than 10 kg. Pure craniosynostosis is the most frequent situation, where the risk for cerebra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbb5e6cc673834482e7818fd47f62feb
https://doi.org/10.1016/s0750-7658(97)87196-1
https://doi.org/10.1016/s0750-7658(97)87196-1