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N Bresolin

Showing results (131-140 of 206) with videos related to

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Clinical Genetics|April 9, 2008
First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvementL Sztriha, C Panzeri, R Kálmánchey, et al.
Journal of the Neurological Sciences|August 1, 1991
Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patientN Bresolin, P Martinelli, B Barbiroli, et al.
Journal of Neurology|March 1, 1995
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and CA Toscano, M C Fazio, G Vita, et al.
Journal of Neurology|November 1, 1990
A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyL Bet, N Bresolin, M Moggio, et al.
Federation Proceedings|October 1, 1980
The benzodiazepine receptor of mammalian brainR C Speth, R W Johnson, J Regan, et al.
Heredity|May 3, 2012
An evolutionary history of the selectin gene cluster in humansM Fumagalli, M Fracassetti, R Cagliani, et al.
Experimental Cell Research|July 20, 2001
Chemotactic factors enhance myogenic cell migration across an endothelial monolayerS Corti, S Salani, R Del Bo, et al.
Journal of Neuromuscular Diseases|December 28, 2020
A Multidisciplinary Evaluation of Patients with DMD in An Italian Tertiary Care CenterA LoMauro, S Gandossini, A Russo, et al.
Journal of Medical Genetics|August 6, 2010
The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2KC Crimella, A Tonelli, G Airoldi, et al.
Neurology Research International|December 29, 2010
IgD Multiple Myeloma Paraproteinemia as a Cause of MyositisI Colombo, M E Fruguglietti, L Napoli, et al.
Pageof 21

Showing results (131-140 of 206) with videos related to

Sort By:
Pageof 21
Clinical Genetics|April 9, 2008
First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvementL Sztriha, C Panzeri, R Kálmánchey, et al.
Journal of the Neurological Sciences|August 1, 1991
Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patientN Bresolin, P Martinelli, B Barbiroli, et al.
Journal of Neurology|March 1, 1995
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and CA Toscano, M C Fazio, G Vita, et al.
Journal of Neurology|November 1, 1990
A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyL Bet, N Bresolin, M Moggio, et al.
Federation Proceedings|October 1, 1980
The benzodiazepine receptor of mammalian brainR C Speth, R W Johnson, J Regan, et al.
Heredity|May 3, 2012
An evolutionary history of the selectin gene cluster in humansM Fumagalli, M Fracassetti, R Cagliani, et al.
Experimental Cell Research|July 20, 2001
Chemotactic factors enhance myogenic cell migration across an endothelial monolayerS Corti, S Salani, R Del Bo, et al.
Journal of Neuromuscular Diseases|December 28, 2020
A Multidisciplinary Evaluation of Patients with DMD in An Italian Tertiary Care CenterA LoMauro, S Gandossini, A Russo, et al.
Journal of Medical Genetics|August 6, 2010
The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2KC Crimella, A Tonelli, G Airoldi, et al.
Neurology Research International|December 29, 2010
IgD Multiple Myeloma Paraproteinemia as a Cause of MyositisI Colombo, M E Fruguglietti, L Napoli, et al.
Pageof 21