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Journal of Assisted Reproduction and Genetics
|
March 30, 2022
Biallelic mutations in PSMC3IP are associated with secondary amenorrhea: expanding the spectrum of premature ovarian insufficiency
Fabio Sirchia, Elisa Giorgio, Laura Cucinella, et al.
Disability and Rehabilitation
|
April 25, 2007
Computerized gait analysis of botulinum toxin treatment in children with cerebral palsy
Manuela Galli, Veronica Cimolin, Enza Maria Valente, et al.
Brain & Development
|
May 17, 2021
WITHDRAWN: Schuurs-Hoeijmakers syndrome: Severe expression of the recurrent PACS1 c.607C>T mutation
Simone Gana, Federica Morelli, Massimo Plumari, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 24, 2022
Simultaneous Labeling of Adipogenic and Osteogenic Differentiating Stem Cells for Live Confocal Analysis
Patrizia Vaghi, Amanda Oldani, Paola Fulghieri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 15, 2008
Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp
Vasiliki Koukouni, Enza Maria Valente, Carla Cordivari, et al.
BMC Neurology
|
January 13, 2021
Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report
Marina Picillo, Sara Scannapieco, Alessandro Iavarone, et al.
European Journal of Neurology
|
January 20, 2025
Mitochondrial DNA (mtDNA) as fluid biomarker in neurodegenerative disorders: A systematic review
Barbara Risi, Alberto Imarisio, Giada Cuconato, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 30, 2009
GIGYF2 variants are not associated with Parkinson's disease in Italy
Monica Bonetti, Alessandro Ferraris, Martina Petracca, et al.
American Journal of Medical Genetics. Part A
|
June 26, 2024
ACOX1 gain-of-function variation in a 10-years-old patient responsive to immunomodulating therapy
Corinna Filippi, Sara Brunetti, Massimo Plumari, et al.
Movement Disorders Clinical Practice
|
June 5, 2026
Tracking Genetic Parkinson's Disease with Molecular Imaging: A Systematic Review
Chiara Meneghini, Luca Gallo, Arianna Sala, et al.
Page
of 34
Search research articles
Search
Showing results (41-50 of 335) with videos related to
Sort By:
Page
of 34
Journal of Assisted Reproduction and Genetics
|
March 30, 2022
Biallelic mutations in PSMC3IP are associated with secondary amenorrhea: expanding the spectrum of premature ovarian insufficiency
Fabio Sirchia, Elisa Giorgio, Laura Cucinella, et al.
Disability and Rehabilitation
|
April 25, 2007
Computerized gait analysis of botulinum toxin treatment in children with cerebral palsy
Manuela Galli, Veronica Cimolin, Enza Maria Valente, et al.
Brain & Development
|
May 17, 2021
WITHDRAWN: Schuurs-Hoeijmakers syndrome: Severe expression of the recurrent PACS1 c.607C>T mutation
Simone Gana, Federica Morelli, Massimo Plumari, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 24, 2022
Simultaneous Labeling of Adipogenic and Osteogenic Differentiating Stem Cells for Live Confocal Analysis
Patrizia Vaghi, Amanda Oldani, Paola Fulghieri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 15, 2008
Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp
Vasiliki Koukouni, Enza Maria Valente, Carla Cordivari, et al.
BMC Neurology
|
January 13, 2021
Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report
Marina Picillo, Sara Scannapieco, Alessandro Iavarone, et al.
European Journal of Neurology
|
January 20, 2025
Mitochondrial DNA (mtDNA) as fluid biomarker in neurodegenerative disorders: A systematic review
Barbara Risi, Alberto Imarisio, Giada Cuconato, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 30, 2009
GIGYF2 variants are not associated with Parkinson's disease in Italy
Monica Bonetti, Alessandro Ferraris, Martina Petracca, et al.
American Journal of Medical Genetics. Part A
|
June 26, 2024
ACOX1 gain-of-function variation in a 10-years-old patient responsive to immunomodulating therapy
Corinna Filippi, Sara Brunetti, Massimo Plumari, et al.
Movement Disorders Clinical Practice
|
June 5, 2026
Tracking Genetic Parkinson's Disease with Molecular Imaging: A Systematic Review
Chiara Meneghini, Luca Gallo, Arianna Sala, et al.
Page
of 34