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Plant Physiology and Biochemistry : PPB
|
March 22, 2024
Unravelling the combined impacts of drought and Cu in barley plants - double trouble?
Maria Martins, Licínio Oliveira, Bruno Sousa, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
July 11, 2018
Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT
Caterina Toma, Giulio Ruberto, Federico Marzi, et al.
Journal of Plant Physiology
|
December 18, 2025
Dissecting the physiology of wild tomatoes under abiotic stress: Dynamic photosynthesis and metabolic adaptations to combined drought and salinity
Sofia Spormann, João Neves, Cláudia Pereira, et al.
Human Mutation
|
August 10, 2005
Novel EXT1 and EXT2 mutations identified by DHPLC in Italian patients with multiple osteochondromas
Elena Pedrini, Alessandro De Luca, Enza Maria Valente, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 25, 2023
Impaired Mitochondrial Respiration in REM-Sleep Behavior Disorder: A Biomarker of Parkinson's Disease?
Gerardo Ongari, Cristina Ghezzi, Deborah Di Martino, et al.
Journal of Hazardous Materials
|
June 7, 2025
Acid mine drainage and waste dispersion in legacy mining sites: An integrated approach using UAV photogrammetry and geospatial analysis
Ana Barroso, Renato Henriques, Ângela Cerqueira, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 1, 2008
Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study
Vania Gelmetti, Alessandro Ferraris, Livia Brusa, et al.
Advances in Therapy
|
July 17, 2020
Electroretinographic Assessment in Joubert Syndrome: A Suggested Objective Method to Evaluate the Effectiveness of Future Targeted Treatment
Giulio Ruberto, Vincenzo Parisi, Chiara Bertone, et al.
Neurology. Genetics
|
April 24, 2023
Neurologic, Neuropsychologic, and Neuroradiologic Features of <i>EBF3</i>-Related Syndrome
Claudia Ciaccio, Chiara Pantaleoni, Marco Moscatelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 23, 2003
Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene
Giovanni Defazio, Francesco Brancati, Enza Maria Valente, et al.
Page
of 36
Search research articles
Search
Showing results (111-120 of 358) with videos related to
Sort By:
Page
of 36
Plant Physiology and Biochemistry : PPB
|
March 22, 2024
Unravelling the combined impacts of drought and Cu in barley plants - double trouble?
Maria Martins, Licínio Oliveira, Bruno Sousa, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
July 11, 2018
Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT
Caterina Toma, Giulio Ruberto, Federico Marzi, et al.
Journal of Plant Physiology
|
December 18, 2025
Dissecting the physiology of wild tomatoes under abiotic stress: Dynamic photosynthesis and metabolic adaptations to combined drought and salinity
Sofia Spormann, João Neves, Cláudia Pereira, et al.
Human Mutation
|
August 10, 2005
Novel EXT1 and EXT2 mutations identified by DHPLC in Italian patients with multiple osteochondromas
Elena Pedrini, Alessandro De Luca, Enza Maria Valente, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 25, 2023
Impaired Mitochondrial Respiration in REM-Sleep Behavior Disorder: A Biomarker of Parkinson's Disease?
Gerardo Ongari, Cristina Ghezzi, Deborah Di Martino, et al.
Journal of Hazardous Materials
|
June 7, 2025
Acid mine drainage and waste dispersion in legacy mining sites: An integrated approach using UAV photogrammetry and geospatial analysis
Ana Barroso, Renato Henriques, Ângela Cerqueira, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 1, 2008
Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study
Vania Gelmetti, Alessandro Ferraris, Livia Brusa, et al.
Advances in Therapy
|
July 17, 2020
Electroretinographic Assessment in Joubert Syndrome: A Suggested Objective Method to Evaluate the Effectiveness of Future Targeted Treatment
Giulio Ruberto, Vincenzo Parisi, Chiara Bertone, et al.
Neurology. Genetics
|
April 24, 2023
Neurologic, Neuropsychologic, and Neuroradiologic Features of <i>EBF3</i>-Related Syndrome
Claudia Ciaccio, Chiara Pantaleoni, Marco Moscatelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 23, 2003
Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene
Giovanni Defazio, Francesco Brancati, Enza Maria Valente, et al.
Page
of 36