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Postoperative complications of laparoscopic cholecystectomy in children with homozygous sickle cell disease: experience of a French pediatric hospital
Triki, Z, Nghe, M C, Shaffii, A, Nivoche, Y
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TIRET, L, NIVOCHE, Y, HATTON, F, DESMONTS, J. M, VOURC'H, G
Published in British journal of anaesthesia : BJA (01.09.1988)
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Nivoche, Y, Lucas, M-M, Souhayl, D, Léculée, R, Wodey, E, Courrèges, P
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Postoperative Pain Management in Children and Infants: An Update
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Multicentre evaluation of in vitro contracture testing with bolus administration of 4-chloro-m-cresol for diagnosis of malignant hyperthermia susceptibility
Wappler, F, Anetseder, M, Baur, C P, Censier, K, Doetsch, S, Felleiter, P, Fiege, M, Fricker, R, Halsall, P J, Hartung, E, Heffron, J J A, Heytens, L, Hopkins, P M, Klingler, W, Lehmann-Horn, F, Nivoche, Y, Tegazzin, V, Tzanova, I, Urwyler, A, Weisshorn, R, Schulte am Esch, J
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Opioid-sparing effect of ketamine during tonsillectomy in children
Abback, P-S, Ben Sallah, T, Hilly, J, Skhiri, A, Silins, V, Brasher, C, François, M, Van Den Abeele, T, Wood, C, Nivoche, Y, Dahmani, S
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An individual scoring system for the prediction of postpartum anaemia
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Published in Annales françaises d'anesthésie et de réanimation (01.01.2013)
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Postoperative decrease in plasma sodium concentration after infusion of hypotonic intravenous solutions in neonatal surgery††This article is accompanied by Editorial III
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Published in British journal of anaesthesia : BJA (01.03.2014)
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Published in Anesthesiology (Philadelphia) (01.11.2002)
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Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor
MONNIER, Nicole, ROMERO, Norma Beatriz, LERALE, Joëlle, LANDRIEU, Pierre, NIVOCHE, Yves, FARDEAU, Michel, LUNARDI, Joël
Published in Human molecular genetics (15.10.2001)
Published in Human molecular genetics (15.10.2001)
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A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene
Ferreiro, Ana, Monnier, Nicole, Romero, Norma B., Leroy, Jean-Paul, Bönnemann, Carsten, Haenggeli, Charles-Antoine, Straub, Volker, Voss, Wolfgang D., Nivoche, Yves, Jungbluth, Heinz, Lemainque, Arnaud, Voit, Thomas, Lunardi, Joël, Fardeau, Michel, Guicheney, Pascale
Published in Annals of neurology (01.06.2002)
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Correlations between genotype and pharmacological, histological, functional, and clinical phenotypes in malignant hyperthermia susceptibility
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Published in Human mutation (01.11.2005)
Published in Human mutation (01.11.2005)
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An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor
MONNIER, Nicole, ROMERO, Norma Beatriz, LERALE, Joëlle, NIVOCHE, Yves, DONG QI, MACLENNAN, David H, FARDEAU, Michel, LUNARDI, Joël
Published in Human molecular genetics (01.11.2000)
Published in Human molecular genetics (01.11.2000)
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