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European Journal of Pediatrics|November 2, 2004
Delta1-pyrroline-5-carboxylate synthase deficiency: neurodegeneration, cataracts and connective tissue manifestations combined with hyperammonaemia and reduced ornithine, citrulline, arginine and prolineMatthias R Baumgartner, Daniel Rabier, Marie-Cécile Nassogne, et al.Gerontology|August 10, 2002
Age-related modifications of circadian rhythm of serum leptin in healthy menZi-Yan Zhao, Yue-Rong Fu, Xin-Hua Li, et al.Chronobiology International|May 3, 2019
Twenty-four-hour pattern of operations-related injury occurrence and severity of off-site/on-call volunteer French firefightersMarc Riedel, Michael H Smolensky, Alain Reinberg, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|August 30, 2012
Asymptomatic atrophy of the temporal median raphe of the retina associated with cerebral vasculopathy in homozygous sickle cell diseaseMatthieu P Robert, Isabelle Ingster-Moati, Olivier Roche, et al.European Journal of Clinical Pharmacology|July 2, 2005
Population pharmacokinetics of tacrolimus in full liver transplant patients: modelling of the post-operative clearanceMarie Antignac, Jean Sebastien Hulot, Emmanuel Boleslawski, et al.Indian Journal of Experimental Biology|May 24, 2014
Twenty-four-hour pattern in French firemen of lag time response to out-of-hospital cardiac arrest and work-related injuryYvan Touitou, Alain Reinberg, Michael H Smolensky, et al.Chronobiology International|April 2, 2011
24-hour pattern in lag time of response by firemen to calls for urgent medical aidEric Brousse, Coralie Forget, Marc Riedel, et al.Human Mutation|November 25, 2003
NDP gene mutations in 14 French families with Norrie diseaseGhislaine Royer, Sylvain Hanein, Valérie Raclin, et al.Chronobiology International|April 19, 2002
Marker rhythms of circadian system function: a study of patients with metastatic colorectal cancer and good performance statusMarie-Christine Mormont, Anne Marie Langouët, Bruno Claustrat, et al.American Journal of Human Genetics|August 24, 2004
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosisIsabelle Perrault, Sylvain Hanein, Sylvie Gerber, et al.Pageof 14