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Brain Pathology (Zurich, Switzerland)|July 21, 1998
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein geneP Montagna, P Cortelli, P Avoni, et al.Journal of Medical Genetics|July 4, 2006
The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotypeM L Valentino, P Barboni, C Rengo, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 12, 2001
Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis studyF Ferrillo, G Plazzi, L Nobili, et al.Neurology|May 24, 2006
Narcolepsy-cataplexy associated with precocious pubertyG Plazzi, A Parmeggiani, E Mignot, et al.Protoplasma|June 6, 2016
Abscisic acid-deficient sit tomato mutant responses to cadmium-induced stressGeorgia B Pompeu, Milca B Vilhena, Priscila L Gratão, et al.Oral Diseases|July 4, 2012
Analysis of the expression of heat-shock protein 27 in patients with oral lichen planusV García-García, A Bascones-Martínez, A I García-Kass, et al.Anais Da Academia Brasileira De Ciencias|December 14, 2017
Pollen morphology and viability in BromeliaceaeEverton H Souza, Fernanda V D Souza, Mônica L Rossi, et al.Minerva Ginecologica|November 25, 2005
Prenatal diagnosis of placental chorioangioma: our experienceR Napolitano, G M Maruotti, L L Mazzarelli, et al.Current Research in Microbial Sciences|March 11, 2026
Layer-dependent modulation of S. aureus biofilms by light-induced oxidative stressKate C Blanco, Paul de Figueiredo, Jace A Willis, et al.Journal of Visualized Experiments : Jove|September 3, 2019
Calvarial Model of Bone Augmentation in Rabbit for Assessment of Bone Growth and Neovascularization in Bone Substitution MaterialsLaurine Marger, Antonio Barone, Carla P Martinelli-Kläy, et al.Pageof 76