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The European Respiratory Journal|August 9, 2002
Pulmonary arterial hypertension and type-I glycogen-storage disease: the serotonin hypothesisM Humbert, P Labrune, O Sitbon, et al.
Neurology|April 27, 2005
A novel mutation (G114V) in the prion protein gene in a family with inherited prion diseaseM-M Rodriguez, K Peoc'h, S Haïk, et al.
The European Respiratory Journal|March 7, 2008
Modulation of bleomycin-induced lung fibrosis by serotonin receptor antagonists in miceA Fabre, J Marchal-Sommé, S Marchand-Adam, et al.
Neuroscience|March 17, 2009
Early dysfunction of central 5-HT system in a murine model of bovine spongiform encephalopathyC Vidal, C Herzog, A M Haeberle, et al.
Cell Death & Disease|January 11, 2013
Pathogenic prions deviate PrP(C) signaling in neuronal cells and impair A-beta clearanceE Pradines, J Hernandez-Rapp, A Villa-Diaz, et al.
Circulation|June 20, 2001
Ablation of serotonin 5-HT(2B) receptors in mice leads to abnormal cardiac structure and functionC G Nebigil, P Hickel, N Messaddeq, et al.
Molecular Psychiatry|January 23, 2002
Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorderC Betancur, M Corbex, C Spielewoy, et al.
Pathologie-Biologie|December 4, 2009
[Genetic mutation databases: stakes and perspectives for orphan genetic diseases]V Humbertclaude, S Tuffery-Giraud, C Bareil, et al.
Revue Neurologique|September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe diseaseP Laforêt, K Laloui, B Granger, et al.
Translational Psychiatry|November 12, 2014
The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disordersC Pagan, R Delorme, J Callebert, et al.
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