Search research articles
Contact Us
Filters
Showing results (1031-1040 of 1,073) with videos related to
Page
of 108
Sort By:
Brain : a Journal of Neurology
|
October 21, 2017
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy
Steffen Syrbe, Frederike L Harms, Elena Parrini, et al.
The Lancet. Digital Health
|
December 26, 2024
The potential of Generative Pre-trained Transformer 4 (GPT-4) to analyse medical notes in three different languages: a retrospective model-evaluation study
Maria Clara Saad Menezes, Alexander F Hoffmann, Amelia L M Tan, et al.
Journal of Extracellular Vesicles
|
January 5, 2023
Special considerations for studies of extracellular vesicles from parasitic helminths: A community-led roadmap to increase rigour and reproducibility
Ruby White, Javier Sotillo, María Eugenia Ancarola, et al.
Annals of Clinical and Translational Neurology
|
May 23, 2015
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
Tobias B Haack, Christopher B Jackson, Kei Murayama, et al.
Human Mutation
|
September 24, 2017
Molecular and clinical spectra of FBXL4 deficiency
Ayman W El-Hattab, Hongzheng Dai, Mohammed Almannai, et al.
Nature Communications
|
January 11, 2022
Robust and durable serological response following pediatric SARS-CoV-2 infection
Hanna Renk, Alex Dulovic, Alina Seidel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 26, 2019
Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients
Christian Staufner, Bianca Peters, Matias Wagner, et al.
American Journal of Human Genetics
|
July 16, 2020
The Genetic Landscape and Epidemiology of Phenylketonuria
Alicia Hillert, Yair Anikster, Amaya Belanger-Quintana, et al.
Neurology
|
July 5, 2023
Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in <i>STXBP1</i>
Kim M Thalwitzer, Jan H Driedger, Julie Xian, et al.
Brain : a Journal of Neurology
|
February 27, 2016
EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy
Susan Byrne, Lara Jansen, Jean-Marie U-King-Im, et al.
Page
of 108
Search research articles
Search
Showing results (1031-1040 of 1,073) with videos related to
Sort By:
Page
of 108
Brain : a Journal of Neurology
|
October 21, 2017
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy
Steffen Syrbe, Frederike L Harms, Elena Parrini, et al.
The Lancet. Digital Health
|
December 26, 2024
The potential of Generative Pre-trained Transformer 4 (GPT-4) to analyse medical notes in three different languages: a retrospective model-evaluation study
Maria Clara Saad Menezes, Alexander F Hoffmann, Amelia L M Tan, et al.
Journal of Extracellular Vesicles
|
January 5, 2023
Special considerations for studies of extracellular vesicles from parasitic helminths: A community-led roadmap to increase rigour and reproducibility
Ruby White, Javier Sotillo, María Eugenia Ancarola, et al.
Annals of Clinical and Translational Neurology
|
May 23, 2015
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
Tobias B Haack, Christopher B Jackson, Kei Murayama, et al.
Human Mutation
|
September 24, 2017
Molecular and clinical spectra of FBXL4 deficiency
Ayman W El-Hattab, Hongzheng Dai, Mohammed Almannai, et al.
Nature Communications
|
January 11, 2022
Robust and durable serological response following pediatric SARS-CoV-2 infection
Hanna Renk, Alex Dulovic, Alina Seidel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 26, 2019
Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients
Christian Staufner, Bianca Peters, Matias Wagner, et al.
American Journal of Human Genetics
|
July 16, 2020
The Genetic Landscape and Epidemiology of Phenylketonuria
Alicia Hillert, Yair Anikster, Amaya Belanger-Quintana, et al.
Neurology
|
July 5, 2023
Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in <i>STXBP1</i>
Kim M Thalwitzer, Jan H Driedger, Julie Xian, et al.
Brain : a Journal of Neurology
|
February 27, 2016
EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy
Susan Byrne, Lara Jansen, Jean-Marie U-King-Im, et al.
Page
of 108