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Neurology|March 24, 2004
Terminology and classification of the cortical dysplasiasA Palmini, I Najm, G Avanzini, et al.The European Journal of Neuroscience|May 20, 2003
Blockade of nociceptin/orphanin FQ-NOP receptor signalling produces antidepressant-like effects: pharmacological and genetic evidences from the mouse forced swimming testE C Gavioli, G Marzola, R Guerrini, et al.Human Mutation|March 26, 2003
Mutation analysis in 16 patients with mtDNA depletionR Carrozzo, B Bornstein, S Lucioli, et al.Neurology|March 14, 2001
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR Carrozzo, A Tessa, M E Vázquez-Memije, et al.Peptides|February 21, 2012
[tBu-D-Gly5]NPS, a pure and potent antagonist of the neuropeptide S receptor: in vitro and in vivo studiesC Ruzza, A Rizzi, V Camarda, et al.Journal of Medical Genetics|January 8, 2008
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutationsH A L Tuppen, F Fattori, R Carrozzo, et al.British Journal of Pharmacology|July 26, 2012
[Dmt1]N/OFQ(1-13)-NH2: a potent nociceptin/orphanin FQ and opioid receptor universal agonistS Molinari, V Camarda, A Rizzi, et al.Journal of Neurology|July 2, 2009
Type II sialidosis: review of the clinical spectrum and identification of a new splicing defect with chitotriosidase assessment in two patientsA Caciotti, M Di Rocco, M Filocamo, et al.Neuromuscular Disorders : NMD|August 30, 2001
Respiratory chain defects in hereditary spastic paraplegiasF Piemonte, C Casali, R Carrozzo, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 24, 1998
Identification of an immunodominant IgE epitope of the Parietaria judaica major allergenP Colombo, D Kennedy, T Ramsdale, et al.Pageof 33