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ACS Omega
|
February 9, 2026
Anti-<i>Campylobacter</i> Activity of Ternary Copper(II) Complexes with Imine Ligands and 4'-(4-Methylphenyl)-2,2':6',2″-Terpyridine
Micaela G Takeuchi, Ana Laura M Ferreira, Luana M S Ramos, et al.
Analytical Chemistry
|
March 27, 2025
Advanced Computational Techniques for Plasmonic Metasurfaces in the Detection of Neglected Infectious Diseases
Felipe M F Teixeira, Ary V R Portes, Talles E M Marques, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients
Marie Le Roux, Magalie Barth, Sophie Gueden, et al.
Current Medicinal Chemistry
|
May 5, 2026
Antiviral Potential of 3,4-Dimethoxychalcone Against SARS-CoV-2: A Promising Candidate
Washington Kleber Rodrigues Lima, Glaucio Monteiro Ferreira, Claudia Zeneida Gomes Parente Alves Lima, et al.
Plos Neglected Tropical Diseases
|
June 9, 2020
The relationship between clinics and the venom of the causative Amazon pit viper (Bothrops atrox)
Ana Maria Moura-da-Silva, Jorge Carlos Contreras-Bernal, Sarah Natalie Cirilo Gimenes, et al.
Annals of Neurology
|
April 10, 2018
The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant
Nicolas Chatron, Rikke S Møller, Neena L Champaigne, et al.
Human Mutation
|
June 5, 2010
Type I hyperprolinemia: genotype/phenotype correlations
Audrey Guilmatre, Solenn Legallic, Gary Steel, et al.
Molecular Autism
|
October 26, 2019
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism
Hyung-Goo Kim, Jill A Rosenfeld, Daryl A Scott, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
European Journal of Human Genetics : EJHG
|
December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Page
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Search research articles
Search
Showing results (631-640 of 669) with videos related to
Sort By:
Page
of 67
ACS Omega
|
February 9, 2026
Anti-<i>Campylobacter</i> Activity of Ternary Copper(II) Complexes with Imine Ligands and 4'-(4-Methylphenyl)-2,2':6',2″-Terpyridine
Micaela G Takeuchi, Ana Laura M Ferreira, Luana M S Ramos, et al.
Analytical Chemistry
|
March 27, 2025
Advanced Computational Techniques for Plasmonic Metasurfaces in the Detection of Neglected Infectious Diseases
Felipe M F Teixeira, Ary V R Portes, Talles E M Marques, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients
Marie Le Roux, Magalie Barth, Sophie Gueden, et al.
Current Medicinal Chemistry
|
May 5, 2026
Antiviral Potential of 3,4-Dimethoxychalcone Against SARS-CoV-2: A Promising Candidate
Washington Kleber Rodrigues Lima, Glaucio Monteiro Ferreira, Claudia Zeneida Gomes Parente Alves Lima, et al.
Plos Neglected Tropical Diseases
|
June 9, 2020
The relationship between clinics and the venom of the causative Amazon pit viper (Bothrops atrox)
Ana Maria Moura-da-Silva, Jorge Carlos Contreras-Bernal, Sarah Natalie Cirilo Gimenes, et al.
Annals of Neurology
|
April 10, 2018
The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant
Nicolas Chatron, Rikke S Møller, Neena L Champaigne, et al.
Human Mutation
|
June 5, 2010
Type I hyperprolinemia: genotype/phenotype correlations
Audrey Guilmatre, Solenn Legallic, Gary Steel, et al.
Molecular Autism
|
October 26, 2019
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism
Hyung-Goo Kim, Jill A Rosenfeld, Daryl A Scott, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
European Journal of Human Genetics : EJHG
|
December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Page
of 67