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American Journal of Preventive Medicine
|
September 21, 2012
Physical activity implementation in schools: a 4-year follow-up
Louise C Mâsse, Heather McKay, Maria Valente, et al.
Msphere
|
August 18, 2017
Structural Characterization of Acidic M17 Leucine Aminopeptidases from the TriTryps and Evaluation of Their Role in Nutrient Starvation in <i>Trypanosoma brucei</i>
Jennifer Timm, Maria Valente, Daniel García-Caballero, 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.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
November 5, 2013
Ameloblastic carcinoma in a young patient
Davide Sozzi, Valeria Morganti, Gabriella Maria Valente, et al.
Arthritis Research & Therapy
|
August 14, 2020
Relationship between radiological severity and physical and mental health in elderly individuals with knee osteoarthritis
Isadora Cristina Ribeiro, Arlete Maria Valente Coimbra, Beatriz Lavras Costallat, 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WITHDRAWN: Schuurs-Hoeijmakers syndrome: Severe expression of the recurrent PACS1 c.607C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.
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.
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.
Page
of 36
Search research articles
Search
Showing results (41-50 of 358) with videos related to
Sort By:
Page
of 36
American Journal of Preventive Medicine
|
September 21, 2012
Physical activity implementation in schools: a 4-year follow-up
Louise C Mâsse, Heather McKay, Maria Valente, et al.
Msphere
|
August 18, 2017
Structural Characterization of Acidic M17 Leucine Aminopeptidases from the TriTryps and Evaluation of Their Role in Nutrient Starvation in <i>Trypanosoma brucei</i>
Jennifer Timm, Maria Valente, Daniel García-Caballero, 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.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
November 5, 2013
Ameloblastic carcinoma in a young patient
Davide Sozzi, Valeria Morganti, Gabriella Maria Valente, et al.
Arthritis Research & Therapy
|
August 14, 2020
Relationship between radiological severity and physical and mental health in elderly individuals with knee osteoarthritis
Isadora Cristina Ribeiro, Arlete Maria Valente Coimbra, Beatriz Lavras Costallat, 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.
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.
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.
Page
of 36