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A Tessa

Showing results (1-10 of 61) with videos related to

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American Heart Journal|January 3, 2001
The emerging concept of mitochondrial cardiomyopathiesF M Santorelli, A Tessa, G D'amati, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
MtDNA-related idiopathic dilated cardiomyopathyA Tessa, L Vilarinho, C Casali, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2015
Ataxia with oculomotor apraxia type 2: not always an easy diagnosisA Mignarri, A Tessa, A Federico, et al.
Neurology|June 9, 2004
Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin geneA D'Amico, A Tessa, A Sabino, et al.
Clinical Genetics|August 31, 1999
Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitationG Siciliano, A Tessa, M Renna, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2016
Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56M Masciullo, A Tessa, S Perazza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathiesG Siciliano, M Mancuso, L Pasquali, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Maternally inherited deafness associated with a T1095C mutation in the mDNAA Tessa, A Giannotti, L Tieri, et al.
The Journal of Organic Chemistry|July 16, 2005
Disulfide exchange in hydrogen-bonded cyclic assemblies: stereochemical self-selection by double dynamic chemistryA Tessa ten Cate, Patricia Y W Dankers, Rint P Sijbesma, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
American Heart Journal|January 3, 2001
The emerging concept of mitochondrial cardiomyopathiesF M Santorelli, A Tessa, G D'amati, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
MtDNA-related idiopathic dilated cardiomyopathyA Tessa, L Vilarinho, C Casali, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2015
Ataxia with oculomotor apraxia type 2: not always an easy diagnosisA Mignarri, A Tessa, A Federico, et al.
Neurology|June 9, 2004
Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin geneA D'Amico, A Tessa, A Sabino, et al.
Clinical Genetics|August 31, 1999
Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitationG Siciliano, A Tessa, M Renna, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2016
Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56M Masciullo, A Tessa, S Perazza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathiesG Siciliano, M Mancuso, L Pasquali, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Maternally inherited deafness associated with a T1095C mutation in the mDNAA Tessa, A Giannotti, L Tieri, et al.
The Journal of Organic Chemistry|July 16, 2005
Disulfide exchange in hydrogen-bonded cyclic assemblies: stereochemical self-selection by double dynamic chemistryA Tessa ten Cate, Patricia Y W Dankers, Rint P Sijbesma, et al.
Pageof 7