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Enza Maria Valente

Showing results (71-80 of 335) with videos related to

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Annals of Neurology|April 27, 2005
Pallidal stimulation improves pantothenate kinase-associated neurodegenerationPierre Castelnau, Laura Cif, Enza Maria Valente, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystoniaFrancesco Brancati, Giovanni Defazio, Viviana Caputo, et al.
Neurogenetics|June 30, 2025
Complete commissural agenesis in a child with Noonan-like syndrome with loose anagen hair 2Simone Gana, Luisa Piccinni, Elisa Rognone, et al.
American Journal of Medical Genetics. Part A|November 11, 2022
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC geneJessica Galli, Enza Maria Valente, Joseph Dewulf, et al.
Journal of Autism and Developmental Disorders|May 3, 2024
Feasibility and Efficacy of a Virtual Reality Social Prediction Training in Children and Young Adults with Congenital Cerebellar MalformationsNiccolò Butti, Emilia Biffi, Romina Romaniello, et al.
Cells|February 25, 2022
PINK1 Protects against Staurosporine-Induced Apoptosis by Interacting with Beclin1 and Impairing Its Pro-Apoptotic CleavageFrancesco Brunelli, Liliana Torosantucci, Vania Gelmetti, et al.
Movement Disorders Clinical Practice|February 5, 2019
Genetic Paradoxes in an Italian Family with <i>PARK2</i> Multiexon DuplicationSimona Petrucci, Gina Ferrazzano, Monia Ginevrino, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 22, 2021
Profiling the Biochemical Signature of GBA-Related Parkinson's Disease in Peripheral Blood Mononuclear CellsMicol Avenali, Silvia Cerri, Gerardo Ongari, et al.
European Journal of Human Genetics : EJHG|April 15, 2004
Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian familyAntonio Novelli, Enza Maria Valente, Laura Bernardini, et al.
Parkinsonism & Related Disorders|August 22, 2020
KCTD17-related myoclonus-dystonia syndrome: clinical and electrophysiological findings of a patient with atypical late onsetMassimiliano Todisco, Simone Gana, Giuseppe Cosentino, et al.
Pageof 34

Showing results (71-80 of 335) with videos related to

Sort By:
Pageof 34
Annals of Neurology|April 27, 2005
Pallidal stimulation improves pantothenate kinase-associated neurodegenerationPierre Castelnau, Laura Cif, Enza Maria Valente, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystoniaFrancesco Brancati, Giovanni Defazio, Viviana Caputo, et al.
Neurogenetics|June 30, 2025
Complete commissural agenesis in a child with Noonan-like syndrome with loose anagen hair 2Simone Gana, Luisa Piccinni, Elisa Rognone, et al.
American Journal of Medical Genetics. Part A|November 11, 2022
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC geneJessica Galli, Enza Maria Valente, Joseph Dewulf, et al.
Journal of Autism and Developmental Disorders|May 3, 2024
Feasibility and Efficacy of a Virtual Reality Social Prediction Training in Children and Young Adults with Congenital Cerebellar MalformationsNiccolò Butti, Emilia Biffi, Romina Romaniello, et al.
Cells|February 25, 2022
PINK1 Protects against Staurosporine-Induced Apoptosis by Interacting with Beclin1 and Impairing Its Pro-Apoptotic CleavageFrancesco Brunelli, Liliana Torosantucci, Vania Gelmetti, et al.
Movement Disorders Clinical Practice|February 5, 2019
Genetic Paradoxes in an Italian Family with <i>PARK2</i> Multiexon DuplicationSimona Petrucci, Gina Ferrazzano, Monia Ginevrino, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 22, 2021
Profiling the Biochemical Signature of GBA-Related Parkinson's Disease in Peripheral Blood Mononuclear CellsMicol Avenali, Silvia Cerri, Gerardo Ongari, et al.
European Journal of Human Genetics : EJHG|April 15, 2004
Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian familyAntonio Novelli, Enza Maria Valente, Laura Bernardini, et al.
Parkinsonism & Related Disorders|August 22, 2020
KCTD17-related myoclonus-dystonia syndrome: clinical and electrophysiological findings of a patient with atypical late onsetMassimiliano Todisco, Simone Gana, Giuseppe Cosentino, et al.
Pageof 34