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E Bertini

Showing results (81-90 of 205) with videos related to

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Epilepsia|November 1, 1989
Hemimegalencephaly and intractable epilepsy: benefits of hemispherectomyF Vigevano, E Bertini, R Boldrini, et al.
Acta Neuropathologica|January 1, 1994
Autosomal recessive hypermyelinating neuropathyM Sabatelli, T Mignogna, G Lippi, et al.
Neurology|November 11, 2009
Congenital muscular dystrophy with defective alpha-dystroglycan, cerebellar hypoplasia, and epilepsyS Messina, G Tortorella, D Concolino, et al.
Neuropediatrics|August 26, 2004
Severe abnormalities of the pons in two infants with goldenhar syndromeM Pane, G Baranello, D Battaglia, et al.
Scandinavian Journal of Immunology|July 18, 2002
Restriction in T-cell receptor repertoire in a patient affected by trichothiodystrophy and CD4+ lymphopeniaC Cancrini, M L Romiti, S Di Cesare, et al.
Human Mutation|September 12, 2000
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutationsM G Lira, M Mottes, P F Pignatti, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1993
Myopathy and hypertrophic cardiomyopathy with selective lysis of thick filamentsE Bertini, C Bosman, G Salviati, et al.
The Journal of Pediatrics|May 1, 1991
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyC Dionisi Vici, A B Burlina, E Bertini, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
Neuromuscular Disorders : NMD|September 27, 2008
Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; report of three expert workshops: TREAT-NMD/ENMC workshop on outcome measures, 12th--13th May 2007, Naarden, The Netherlands; TREAT-NMD workshop on outcome measures in experimental trials for DMD, 30th June--1st July 2007, Naarden, The Netherlands; conjoint Institute of Myology TREAT-NMD meeting on physical activity monitoring in neuromuscular disorders, 11th July 2007, Paris, FranceE Mercuri, A Mayhew, F Muntoni, et al.
Pageof 21

Showing results (81-90 of 205) with videos related to

Sort By:
Pageof 21
Epilepsia|November 1, 1989
Hemimegalencephaly and intractable epilepsy: benefits of hemispherectomyF Vigevano, E Bertini, R Boldrini, et al.
Acta Neuropathologica|January 1, 1994
Autosomal recessive hypermyelinating neuropathyM Sabatelli, T Mignogna, G Lippi, et al.
Neurology|November 11, 2009
Congenital muscular dystrophy with defective alpha-dystroglycan, cerebellar hypoplasia, and epilepsyS Messina, G Tortorella, D Concolino, et al.
Neuropediatrics|August 26, 2004
Severe abnormalities of the pons in two infants with goldenhar syndromeM Pane, G Baranello, D Battaglia, et al.
Scandinavian Journal of Immunology|July 18, 2002
Restriction in T-cell receptor repertoire in a patient affected by trichothiodystrophy and CD4+ lymphopeniaC Cancrini, M L Romiti, S Di Cesare, et al.
Human Mutation|September 12, 2000
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutationsM G Lira, M Mottes, P F Pignatti, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1993
Myopathy and hypertrophic cardiomyopathy with selective lysis of thick filamentsE Bertini, C Bosman, G Salviati, et al.
The Journal of Pediatrics|May 1, 1991
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyC Dionisi Vici, A B Burlina, E Bertini, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
Neuromuscular Disorders : NMD|September 27, 2008
Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; report of three expert workshops: TREAT-NMD/ENMC workshop on outcome measures, 12th--13th May 2007, Naarden, The Netherlands; TREAT-NMD workshop on outcome measures in experimental trials for DMD, 30th June--1st July 2007, Naarden, The Netherlands; conjoint Institute of Myology TREAT-NMD meeting on physical activity monitoring in neuromuscular disorders, 11th July 2007, Paris, FranceE Mercuri, A Mayhew, F Muntoni, et al.
Pageof 21