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Alessandra Tessa

Showing results (31-40 of 116) with videos related to

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Frontiers in Neurology|September 8, 2022
Cardiac magnetic resonance findings in neuronal ceroid lipofuscinosis: A case reportGiancarlo Todiere, Stefania Della Vecchia, Maria Aurora Morales, et al.
Pediatric Nephrology (Berlin, Germany)|December 31, 2005
"Bartter-like" phenotype in Kearns-Sayre syndromeFrancesco Emma, Carla Pizzini, Alessandra Tessa, et al.
Biochemical and Biophysical Research Communications|February 3, 2007
Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathyCristina Pereira, Celia Nogueira, Clara Barbot, et al.
Journal of Neurology|May 11, 2015
Acute optic neuropathy associated with a novel MFN2 mutationLuca Leonardi, Christian Marcotulli, Eugenia Storti, et al.
Journal of Clinical Medicine|April 27, 2024
Primary Coenzyme Q10 Deficiency-Related AtaxiasPiervito Lopriore, Marco Vista, Alessandra Tessa, et al.
Archives of Neurology|February 18, 2004
Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotypeMariarosa A B Melone, Alessandra Tessa, Stefania Petrini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 24, 2018
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotypeGiulia Iapadre, Giovanni Morana, Maria Stella Vari, et al.
Journal of Neurology|June 18, 2014
Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the diseaseLuca Leonardi, Christian Marcotulli, Karen N McFarland, et al.
Functional Neurology|August 13, 2003
The relationship between anaerobic lactate threshold and plasma catecholamines during incremental exercise in hereditary spastic paraplegiaGabriele Siciliano, Livia Pasquali, Maria Laura Manca, et al.
Journal of Affective Disorders|June 26, 2007
Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a familyMichelangelo Mancuso, Giulia Ricci, Anna Choub, et al.
Pageof 12

Showing results (31-40 of 116) with videos related to

Sort By:
Pageof 12
Frontiers in Neurology|September 8, 2022
Cardiac magnetic resonance findings in neuronal ceroid lipofuscinosis: A case reportGiancarlo Todiere, Stefania Della Vecchia, Maria Aurora Morales, et al.
Pediatric Nephrology (Berlin, Germany)|December 31, 2005
"Bartter-like" phenotype in Kearns-Sayre syndromeFrancesco Emma, Carla Pizzini, Alessandra Tessa, et al.
Biochemical and Biophysical Research Communications|February 3, 2007
Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathyCristina Pereira, Celia Nogueira, Clara Barbot, et al.
Journal of Neurology|May 11, 2015
Acute optic neuropathy associated with a novel MFN2 mutationLuca Leonardi, Christian Marcotulli, Eugenia Storti, et al.
Journal of Clinical Medicine|April 27, 2024
Primary Coenzyme Q10 Deficiency-Related AtaxiasPiervito Lopriore, Marco Vista, Alessandra Tessa, et al.
Archives of Neurology|February 18, 2004
Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotypeMariarosa A B Melone, Alessandra Tessa, Stefania Petrini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 24, 2018
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotypeGiulia Iapadre, Giovanni Morana, Maria Stella Vari, et al.
Journal of Neurology|June 18, 2014
Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the diseaseLuca Leonardi, Christian Marcotulli, Karen N McFarland, et al.
Functional Neurology|August 13, 2003
The relationship between anaerobic lactate threshold and plasma catecholamines during incremental exercise in hereditary spastic paraplegiaGabriele Siciliano, Livia Pasquali, Maria Laura Manca, et al.
Journal of Affective Disorders|June 26, 2007
Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a familyMichelangelo Mancuso, Giulia Ricci, Anna Choub, et al.
Pageof 12