Authors:
Stojkovic, T
Maurage, CA
Moerman, A
Hurtevent, JF
Krivosic-Horber, R
Pellissier, JF
Vermersch, P
Citation: T. Stojkovic et al., Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibility, NEUROMUSC D, 11(6-7), 2001, pp. 538-541
Authors:
Coeslier, A
Boute-Benejean, O
Moerman, A
Fron, D
Manouvrier-Hanu, S
Citation: A. Coeslier et al., The Dyggve-Melchior-Clausen syndrome: differential diagnosis of mucopolysaccharidosis type IV or Morquio's syndrome, ARCH PED, 8(8), 2001, pp. 838-842
Authors:
Mollhoff, T
Herregods, L
Moerman, A
Blake, D
MacAdams, C
Demeyere, R
Kirno, K
Dybvik, T
Shaikh, S
Citation: T. Mollhoff et al., Comparative efficacy and safety of remifentanil and fentanyl in 'fast track' coronary artery bypass graft surgery: a randomized, double-blind study, BR J ANAEST, 87(5), 2001, pp. 718-726
Authors:
Manouvrier, S
Moerman, A
Coeslier, A
Devisme, L
Boute, O
Le Merrer, M
Citation: S. Manouvrier et al., Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: A new X-linked dominant multiple congenital anomalies syndrome?, AM J MED G, 90(5), 2000, pp. 351-355
Authors:
Walter-Nicolet, E
Coeslier, A
Joriot, S
Kacet, N
Moerman, A
Manouvrier-Hanu, S
Citation: E. Walter-nicolet et al., The Richieri-Costa and Pereira form of acrofacial dysostosis: First case in a non-Brazilian infant, AM J MED G, 87(5), 1999, pp. 430-433
Authors:
Manouvrier-Hanu, S
Amiel, J
Jacquot, S
Merienne, K
Moerman, A
Coeslier, A
Labarriere, F
Vallee, L
Croquette, MF
Hanauer, A
Citation: S. Manouvrier-hanu et al., Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome, J MED GENET, 36(10), 1999, pp. 775-778