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Alessandra Tessa

Showing results (21-30 of 116) with videos related to

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Mitochondrion|September 28, 2007
A new mtDNA-tRNA(Glu) mutation (14728T>C) presenting a late-onset mitochondrial encephalomyopathyCélia Nogueira, João Nunes, Teresinha Evangelista, et al.
Neurology. Genetics|June 3, 2026
<i>HSD17B4</i>-Related Disorder: Defining the Phenotype in Adult-Onset PatientsGrazia Maria Igea Falcone, Alessandra Tessa, Cristiano Rizzo, et al.
JIMD Reports|November 22, 2015
Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in HumansMara Doimo, Raffaele Lopreiato, Valentina Basso, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 16, 2025
A new variant in the UCHL1 gene supporting its implication in late-onset ataxia with optic atrophyValeria Gioiosa, Christian Marcotulli, Manon Degoutin, et al.
Biochemical and Biophysical Research Communications|November 22, 2011
Involvement of the mitochondrial compartment in human NCL fibroblastsFrancesco Pezzini, Floriana Gismondi, Alessandra Tessa, et al.
Journal of Neurology|February 13, 2014
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1Roberto Di Fabio, Christian Marcotulli, Alessandra Tessa, et al.
Journal of Neurology|October 22, 2013
The high prevalence of hereditary spastic paraplegia in Sardinia, insular ItalyLoretta Racis, Alessandra Tessa, Roberto Di Fabio, et al.
Bioscience Reports|May 9, 2007
Infantile mitochondrial disordersRosalba Carrozzo, Fiorella Piemonte, Alessandra Tessa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 21, 2014
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4Federica Ginanneschi, Maria A Carluccio, Andrea Mignarri, et al.
Journal of Neurology|May 3, 2002
Missense and splice site mutations in SPG4 suggest loss-of-function in dominant spastic paraplegiaClarice Patrono, Carlo Casali, Alessandra Tessa, et al.
Pageof 12

Showing results (21-30 of 116) with videos related to

Sort By:
Pageof 12
Mitochondrion|September 28, 2007
A new mtDNA-tRNA(Glu) mutation (14728T>C) presenting a late-onset mitochondrial encephalomyopathyCélia Nogueira, João Nunes, Teresinha Evangelista, et al.
Neurology. Genetics|June 3, 2026
<i>HSD17B4</i>-Related Disorder: Defining the Phenotype in Adult-Onset PatientsGrazia Maria Igea Falcone, Alessandra Tessa, Cristiano Rizzo, et al.
JIMD Reports|November 22, 2015
Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in HumansMara Doimo, Raffaele Lopreiato, Valentina Basso, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 16, 2025
A new variant in the UCHL1 gene supporting its implication in late-onset ataxia with optic atrophyValeria Gioiosa, Christian Marcotulli, Manon Degoutin, et al.
Biochemical and Biophysical Research Communications|November 22, 2011
Involvement of the mitochondrial compartment in human NCL fibroblastsFrancesco Pezzini, Floriana Gismondi, Alessandra Tessa, et al.
Journal of Neurology|February 13, 2014
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1Roberto Di Fabio, Christian Marcotulli, Alessandra Tessa, et al.
Journal of Neurology|October 22, 2013
The high prevalence of hereditary spastic paraplegia in Sardinia, insular ItalyLoretta Racis, Alessandra Tessa, Roberto Di Fabio, et al.
Bioscience Reports|May 9, 2007
Infantile mitochondrial disordersRosalba Carrozzo, Fiorella Piemonte, Alessandra Tessa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 21, 2014
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4Federica Ginanneschi, Maria A Carluccio, Andrea Mignarri, et al.
Journal of Neurology|May 3, 2002
Missense and splice site mutations in SPG4 suggest loss-of-function in dominant spastic paraplegiaClarice Patrono, Carlo Casali, Alessandra Tessa, et al.
Pageof 12