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Clinical Dysmorphology
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March 29, 2019
A novel pathogenic frameshift variant of KAT6B identified by clinical exome sequencing in a newborn with the Say-Barber-Biesecker-Young-Simpson syndrome
Rodrigo Mendez, Marisol Delea, Liliana Dain, et al.
IEEE ... International Conference on Rehabilitation Robotics : [Proceedings]
|
July 11, 2025
Design of an Active Sling-Suspension Robot for Adaptive Gravity Compensation of the Upper Limbs
Rodrigo Mendez, Aine Grady, Peter Snow, et al.
Bioengineering (Basel, Switzerland)
|
May 27, 2026
Robot-Assisted Gravity Compensation for Upper Limb Motor Rehabilitation: A Systematic Review
Rodrigo Mendez, Claudia Simon Rueda, Rui C V Loureiro
IEEE ... International Conference on Rehabilitation Robotics : [Proceedings]
|
July 11, 2025
Design of a Low-Cost VR-Based Robotic Pedal System with Dynamic Resistance and Muscle Activity Feedback
Claudia Simon Rueda, Peter Snow, Rodrigo Mendez, et al.
Journal of Experimental Botany
|
October 15, 2013
How do leaf veins influence the worldwide leaf economic spectrum? Review and synthesis
Lawren Sack, Christine Scoffoni, Grace P John, et al.
Journal of Experimental Botany
|
August 14, 2014
Leaf mass per area is independent of vein length per area: avoiding pitfalls when modelling phenotypic integration (reply to Blonder et al. 2014)
Lawren Sack, Christine Scoffoni, Grace P John, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Ensilication preserves high-molecular weight native DNA for clinical long-read sequencing
Alexis Ferrasse, Rodrigo Mendez, John E Gorzynski, et al.
Genome Biology
|
June 16, 2026
Ensilication preserves high-molecular weight native DNA for clinical long-read sequencing
Alexis Ferrasse, Rodrigo Mendez, John E Gorzynski, et al.
Ophthalmic Genetics
|
February 18, 2021
Oculocutaneous albinism type 1B associated with a functionally significant tyrosinase gene polymorphism detected with Whole Exome Sequencing
Rodrigo Mendez, Sumaiya Iqbal, Sebastián Vishnopolska, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 5, 2025
Biallelic variants in <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorder
Daniel Greene, Rodrigo Mendez, Jon Lees, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Clinical Dysmorphology
|
March 29, 2019
A novel pathogenic frameshift variant of KAT6B identified by clinical exome sequencing in a newborn with the Say-Barber-Biesecker-Young-Simpson syndrome
Rodrigo Mendez, Marisol Delea, Liliana Dain, et al.
IEEE ... International Conference on Rehabilitation Robotics : [Proceedings]
|
July 11, 2025
Design of an Active Sling-Suspension Robot for Adaptive Gravity Compensation of the Upper Limbs
Rodrigo Mendez, Aine Grady, Peter Snow, et al.
Bioengineering (Basel, Switzerland)
|
May 27, 2026
Robot-Assisted Gravity Compensation for Upper Limb Motor Rehabilitation: A Systematic Review
Rodrigo Mendez, Claudia Simon Rueda, Rui C V Loureiro
IEEE ... International Conference on Rehabilitation Robotics : [Proceedings]
|
July 11, 2025
Design of a Low-Cost VR-Based Robotic Pedal System with Dynamic Resistance and Muscle Activity Feedback
Claudia Simon Rueda, Peter Snow, Rodrigo Mendez, et al.
Journal of Experimental Botany
|
October 15, 2013
How do leaf veins influence the worldwide leaf economic spectrum? Review and synthesis
Lawren Sack, Christine Scoffoni, Grace P John, et al.
Journal of Experimental Botany
|
August 14, 2014
Leaf mass per area is independent of vein length per area: avoiding pitfalls when modelling phenotypic integration (reply to Blonder et al. 2014)
Lawren Sack, Christine Scoffoni, Grace P John, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Ensilication preserves high-molecular weight native DNA for clinical long-read sequencing
Alexis Ferrasse, Rodrigo Mendez, John E Gorzynski, et al.
Genome Biology
|
June 16, 2026
Ensilication preserves high-molecular weight native DNA for clinical long-read sequencing
Alexis Ferrasse, Rodrigo Mendez, John E Gorzynski, et al.
Ophthalmic Genetics
|
February 18, 2021
Oculocutaneous albinism type 1B associated with a functionally significant tyrosinase gene polymorphism detected with Whole Exome Sequencing
Rodrigo Mendez, Sumaiya Iqbal, Sebastián Vishnopolska, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 5, 2025
Biallelic variants in <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorder
Daniel Greene, Rodrigo Mendez, Jon Lees, et al.
Page
of 3