Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yolene Lacroix"'
Publikováno v:
The Cleft Palate-Craniofacial Journal. 52:625-628
Velopharyngeal dysfunction (VPD) can be secondary to anatomic, neurologic, or functional maldevelopment in the pediatric population. We present a case of transient VPD after the removal of a voluminous oropharyngeal hairy polyp in a newborn with an i
Publikováno v:
The Laryngoscope. 118:232-236
Objectives/Hypothesis: To determine the effectiveness of dexamethasone to reduce pain after tonsillectomy in adults by at least 13 mm on the visual analogue scale. The secondary objective was to reduce the use of narcotics by at least 20%. Study Desi
Publikováno v:
International journal of pediatric otorhinolaryngology. 79(4)
Pierre Robin sequence is not a rare condition and paediatric specialists caring for respiratory related issues are likely to encounter cases in their practice. There have been a few recent reviews on the topic, mostly focusing on the surgical interve
Publikováno v:
International journal of pediatric otorhinolaryngology. 78(4)
Foreign body (FB) aspiration is a common problem in the pediatric population. Rigid bronchoscopy is considered the treatment of choice for removal of tracheobronchial FB. This is a report of two cases of tracheobronchial foreign body aspiration that
Autor:
Yolene Lacroix, Moshe Ben-Shoshan
Publikováno v:
Archives of Disease in Childhood. 99:883-883
A 16-year-old boy presented to the emergency department with a yellowish longitudinal protrusion in the floor of his mouth (figure 1). He reported mild pain in the submandibular area postcibum without significant swelling during the last year. He did
Transplantation of Human Myoblasts in SCID Mice as a Potential Muscular Model for Myotonic Dystrophy
Autor:
Marlyne Goulet, Jacques P. Tremblay, Jack Puymirat, Jean-Pierre Bouchard, Brigitte Roy, Daniel Skuk, Jean-Thomas Vilquin, Denis Furling, Yolene Lacroix
Publikováno v:
Journal of Neuropathology and Experimental Neurology
Journal of Neuropathology and Experimental Neurology, 1999, 58 (9), pp.921-931. ⟨10.1097/00005072-199909000-00003⟩
Journal of Neuropathology and Experimental Neurology, 1999, 58 (9), pp.921-931. ⟨10.1097/00005072-199909000-00003⟩
International audience; Myotonic dystrophy (DM), the most frequent hereditary myopathy in adults, is characterized clinically by muscle weakness, myotonia, and systemic symptoms. Although the specific genetic basis for DM has been established, less i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::835b57ffe96d5ab89f7e1183db75f20e
https://hal.science/hal-03824113
https://hal.science/hal-03824113