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American Journal of Human Genetics|May 1, 1994
Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiencyS Tsujino, S Servidei, P Tonin, et al.
Neuropathology and Applied Neurobiology|February 13, 2003
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseasesM Filosto, P Tonin, G Vattemi, et al.
Journal of Neuroimmunology|November 7, 2000
T-cell anti-apoptotic mechanisms in inflammatory myopathiesG Vattemi, P Tonin, M Filosto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 4, 2001
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case reportM Filosto, P Tonin, G Vattemi, et al.
Rivista Di Patologia Nervosa E Mentale|November 1, 1980
Regional cerebral blood flow compared to angiography in ischemic cerebrovascular diseasesG Meneghetti, P Tonin, L De Zanche, et al.
Neurology|January 17, 2007
The role of muscle biopsy in investigating isolated muscle painM Filosto, P Tonin, G Vattemi, et al.
Journal of Medical Genetics|October 1, 1996
Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sitesF Durocher, P Tonin, D Shattuck-Eidens, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|July 9, 2013
[A case of acute renal failure secondary to late-onset McArdle's disease]V Cosentini, A Cosaro, L Gammaro, et al.
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