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Neurology|March 24, 2004
Terminology and classification of the cortical dysplasiasA Palmini, I Najm, G Avanzini, 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.
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.
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.
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