Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ginette Lacroix"'
Autor:
Hubert Labelle, Mamadou Samba Boiro, Guy Grimard, Alain Moreau, Jean Ouellet, Florina Moldovan, Sacha Blain, Ginette Lacroix, Stefan Parent, Charles-Hilaire Rivard, Bouziane Azeddine, Isabelle Turgeon, Kareen Letellier, Benoit Poitras, Da Shen Wang
Publikováno v:
médecine/sciences. 23:910-916
Adolescent idiopathic scoliosis (AIS) is the most common form of scoliosis that affects a significant number of young teenagers, mainly females (0.2-6 % of the population). Historically, several hypothesis were postulated to explain the aetiology of
Autor:
Da Shan Wang, Maryam Taheri, Alain Moreau, Jean Ouellet, Stefan Parent, Benoit Poitras, Guy Grimard, Charles-Hilaire Rivard, Benoit St-Jacques, Hubert Labelle, Ginette Lacroix, Anita Franco, Isabelle Turgeon, Ginette Larouche, Marie-Yvonne Akoume
Publikováno v:
Scoliosis, Vol 5, Iss Suppl 1, p O3 (2010)
Scoliosis
Scoliosis
Purpose There are great needs for innovative pharmacotherapies in combination with clinical tests to identify asymptomatic children at risk of developing scoliosis and symptomatic ones to predict who may be at risk of scoliotic curve progression. Ear
Autor:
Kareen, Letellier, Bouziane, Azeddine, Sacha, Blain, Isabelle, Turgeon, Da Shen, Wang, Mamadou Samba, Boiro, Florina, Moldovan, Hubert, Labelle, Benoît, Poitras, Charles-Hilaire, Rivard, Guy, Grimard, Stefan, Parent, Jean, Ouellet, Ginette, Lacroix, Alain, Moreau
Publikováno v:
Medecine sciences : M/S. 23(11)
Adolescent idiopathic scoliosis (AIS) is the most common form of scoliosis that affects a significant number of young teenagers, mainly females (0.2-6 % of the population). Historically, several hypothesis were postulated to explain the aetiology of
Autor:
Ginette Larouche, Alain Moreau, Ginette Lacroix, Anita Franco, Isabelle Turgeon, Marie-Yvonne Akoume
Publikováno v:
Scoliosis
Scoliosis, Vol 5, Iss Suppl 1, p O17 (2010)
Scoliosis, Vol 5, Iss Suppl 1, p O17 (2010)
Adolescent idiopathic scoliosis (AIS) is a complex spinal deformity of unknown aetiology and extreme variability, occurring at least in genetically predisposed children. We previously demonstrated a differential dysfunction of melatonin signaling thr