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Virchows Archiv : an International Journal of Pathology|January 1, 1995
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophyA Malandrini, T Cavallaro, G M Fabrizi, et al.
European Neurology|January 1, 1991
Vitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case reportA Federico, C Battisti, M P Eusebi, et al.
Journal of Submicroscopic Cytology and Pathology|August 18, 2004
Mitochondrial alterations in muscle biopsies of patients on statin therapyS Gambelli, M T Dotti, A Malandrini, et al.
Muscle & Nerve|September 17, 1999
Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophyF Vitelli, M Villanova, A Malandrini, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy familyL Merlini, M Villanova, P Sabatelli, et al.
American Journal of Medical Genetics|March 1, 1994
Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome?G Guazzi, S Palmeri, A Malandrini, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1993
Optic atrophy in Marinesco-Sjögren syndrome: an additional ocular feature. Report of three cases in two familiesM T Dotti, A M Bardelli, N De Stefano, et al.
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