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E Bertini

Showing results (21-30 of 205) with videos related to

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Developmental Neuroscience|January 1, 1991
Experience on therapy of adrenoleukodystrophy and adrenomyeloneuropathyG Uziel, E Bertini, P Bardelli, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|November 15, 1978
[Laterality of the electrocephalographic changes induced by electroshock]M Scuderi, E Bertini, A Bianchi, et al.
Minerva Pediatrica|March 1, 1991
[Diet therapy with erucic acid in patients with X-linked adrenoleukodystrophy]G Uziel, E Bertini, P Bardelli, et al.
American Journal of Obstetrics and Gynecology|July 1, 1985
Immune complexes in preeclampsia and normal pregnancyM Massobrio, C Benedetto, E Bertini, et al.
Spine|April 29, 1998
An unusual cause of lumbar discitisS D Gertzbein, M Hollopeter, J E Bertini, et al.
European Journal of Pediatrics|May 1, 1990
A new therapeutic approach for X-linked adrenoleukodystrophyM Cappa, E Bertini, M Di Capua, et al.
Human Mutation|June 22, 2000
A novel nonsense mutation (Q509X) in three Italian late-infantile neuronal ceroid-lipofuscinosis childrenA Tessa, A Simonati, A Tavoni, et al.
American Journal of Human Genetics|July 1, 1996
A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2qG T Fouad, S Servidei, S Durcan, et al.
Neuromuscular Disorders : NMD|March 16, 2013
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathiesA D'Amico, F Fattori, E Bellacchio, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|July 1, 1981
[Neonatal myoclonic encephalopathy. Contribution of a case with suspected dysmetabolic etiology]F Vigevano, P Cincinnati, E Bertini, et al.
Pageof 21

Showing results (21-30 of 205) with videos related to

Sort By:
Pageof 21
Developmental Neuroscience|January 1, 1991
Experience on therapy of adrenoleukodystrophy and adrenomyeloneuropathyG Uziel, E Bertini, P Bardelli, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|November 15, 1978
[Laterality of the electrocephalographic changes induced by electroshock]M Scuderi, E Bertini, A Bianchi, et al.
Minerva Pediatrica|March 1, 1991
[Diet therapy with erucic acid in patients with X-linked adrenoleukodystrophy]G Uziel, E Bertini, P Bardelli, et al.
American Journal of Obstetrics and Gynecology|July 1, 1985
Immune complexes in preeclampsia and normal pregnancyM Massobrio, C Benedetto, E Bertini, et al.
Spine|April 29, 1998
An unusual cause of lumbar discitisS D Gertzbein, M Hollopeter, J E Bertini, et al.
European Journal of Pediatrics|May 1, 1990
A new therapeutic approach for X-linked adrenoleukodystrophyM Cappa, E Bertini, M Di Capua, et al.
Human Mutation|June 22, 2000
A novel nonsense mutation (Q509X) in three Italian late-infantile neuronal ceroid-lipofuscinosis childrenA Tessa, A Simonati, A Tavoni, et al.
American Journal of Human Genetics|July 1, 1996
A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2qG T Fouad, S Servidei, S Durcan, et al.
Neuromuscular Disorders : NMD|March 16, 2013
A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathiesA D'Amico, F Fattori, E Bellacchio, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|July 1, 1981
[Neonatal myoclonic encephalopathy. Contribution of a case with suspected dysmetabolic etiology]F Vigevano, P Cincinnati, E Bertini, et al.
Pageof 21