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M T Dotti

Showing results (21-30 of 144) with videos related to

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Acta Neurologica|December 1, 1989
Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two familiesM T Dotti, A Federico, S Palmeri, et al.
Pharmacological Research Communications|February 1, 1980
Plasma ACTH and cortisol levels in benzodiazepine treated ratsG Bruni, P Dal Pra, M T Dotti, et al.
Current Molecular Medicine|October 18, 2014
Adult-Onset Genetic Leukoencephalopathies. Focus on the More Recently Defined FormsI Di Donato, S Banchi, A Federico, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2004
Normalisation of serum cholestanol concentration in a patient with cerebrotendinous xanthomatosis by combined treatment with chenodeoxycholic acid, simvastatin and LDL apheresisM T Dotti, D Lütjohann, K von Bergmann, et al.
Brain & Development|March 1, 1994
Association of myopathy with multiple exostoses and mental retardation: a case reportN De Stefano, M T Dotti, A Malandrini, et al.
Pharmacological Research Communications|April 1, 1980
Effect of various antiinflammatory drugs on plasma ACTH and cortisol levels in ratsG Bruni, P Dal Pra, M T Dotti, et al.
American Journal of Medical Genetics|January 1, 1989
Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generationsL Mangano, S Palmeri, M T Dotti, et al.
Journal of the Neurological Sciences|September 28, 2001
Cerebrotendinous xanthomatosis: 11-year treatment with chenodeoxycholic acid in five patients. An electrophysiological studyM Mondelli, F Sicurelli, C Scarpini, et al.
Archives of Neurology|May 1, 1992
Evoked potentials in cerebrotendinous xanthomatosis and effect induced by chenodeoxycholic acidM Mondelli, A Rossi, C Scarpini, et al.
Acta Neurologica Scandinavica|October 1, 1991
Leber's optic atrophy: VEP and BAEP changes in 16 asymptomatic subjectsM Mondelli, A Rossi, C Scarpini, et al.
Pageof 15

Showing results (21-30 of 144) with videos related to

Sort By:
Pageof 15
Acta Neurologica|December 1, 1989
Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two familiesM T Dotti, A Federico, S Palmeri, et al.
Pharmacological Research Communications|February 1, 1980
Plasma ACTH and cortisol levels in benzodiazepine treated ratsG Bruni, P Dal Pra, M T Dotti, et al.
Current Molecular Medicine|October 18, 2014
Adult-Onset Genetic Leukoencephalopathies. Focus on the More Recently Defined FormsI Di Donato, S Banchi, A Federico, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2004
Normalisation of serum cholestanol concentration in a patient with cerebrotendinous xanthomatosis by combined treatment with chenodeoxycholic acid, simvastatin and LDL apheresisM T Dotti, D Lütjohann, K von Bergmann, et al.
Brain & Development|March 1, 1994
Association of myopathy with multiple exostoses and mental retardation: a case reportN De Stefano, M T Dotti, A Malandrini, et al.
Pharmacological Research Communications|April 1, 1980
Effect of various antiinflammatory drugs on plasma ACTH and cortisol levels in ratsG Bruni, P Dal Pra, M T Dotti, et al.
American Journal of Medical Genetics|January 1, 1989
Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generationsL Mangano, S Palmeri, M T Dotti, et al.
Journal of the Neurological Sciences|September 28, 2001
Cerebrotendinous xanthomatosis: 11-year treatment with chenodeoxycholic acid in five patients. An electrophysiological studyM Mondelli, F Sicurelli, C Scarpini, et al.
Archives of Neurology|May 1, 1992
Evoked potentials in cerebrotendinous xanthomatosis and effect induced by chenodeoxycholic acidM Mondelli, A Rossi, C Scarpini, et al.
Acta Neurologica Scandinavica|October 1, 1991
Leber's optic atrophy: VEP and BAEP changes in 16 asymptomatic subjectsM Mondelli, A Rossi, C Scarpini, et al.
Pageof 15