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Science (New York, N.Y.)
|
September 28, 2013
Volatile, isotope, and organic analysis of martian fines with the Mars Curiosity rover
L A Leshin, P R Mahaffy, C R Webster, et al.
Nature
|
March 14, 2008
Stream denitrification across biomes and its response to anthropogenic nitrate loading
Patrick J Mulholland, Ashley M Helton, Geoffrey C Poole, et al.
Journal of Neurointerventional Surgery
|
August 2, 2022
Multicenter investigation of technical and clinical outcomes after thrombectomy for distal vessel occlusion by frontline technique
Ali M Alawieh, Reda M Chalhoub, Sami Al Kasab, et al.
Journal of Neurointerventional Surgery
|
February 17, 2021
Is a picture-perfect thrombectomy necessary in acute ischemic stroke?
Ching-Jen Chen, Reda Chalhoub, Dale Ding, et al.
Ophthalmology Science
|
February 3, 2025
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom
William A Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 16, 2019
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides
Riccardo Sangermano, Alejandro Garanto, Mubeen Khan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations
William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
The British Journal of Ophthalmology
|
October 18, 2023
<i>KCNV2</i>-associated retinopathy: genotype-phenotype correlations - <i>KCNV2</i> study group report 3
Thales A C de Guimaraes, Michalis Georgiou, Anthony G Robson, et al.
American Journal of Human Genetics
|
October 6, 2020
Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa
Suzanne E de Bruijn, Alessia Fiorentino, Daniele Ottaviani, et al.
American Journal of Ophthalmology
|
March 19, 2021
KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints-KCNV2 Study Group Report 2
Michalis Georgiou, Kaoru Fujinami, Ajoy Vincent, et al.
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Showing results (1201-1210 of 1,250) with videos related to
Sort By:
Page
of 125
Science (New York, N.Y.)
|
September 28, 2013
Volatile, isotope, and organic analysis of martian fines with the Mars Curiosity rover
L A Leshin, P R Mahaffy, C R Webster, et al.
Nature
|
March 14, 2008
Stream denitrification across biomes and its response to anthropogenic nitrate loading
Patrick J Mulholland, Ashley M Helton, Geoffrey C Poole, et al.
Journal of Neurointerventional Surgery
|
August 2, 2022
Multicenter investigation of technical and clinical outcomes after thrombectomy for distal vessel occlusion by frontline technique
Ali M Alawieh, Reda M Chalhoub, Sami Al Kasab, et al.
Journal of Neurointerventional Surgery
|
February 17, 2021
Is a picture-perfect thrombectomy necessary in acute ischemic stroke?
Ching-Jen Chen, Reda Chalhoub, Dale Ding, et al.
Ophthalmology Science
|
February 3, 2025
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom
William A Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 16, 2019
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides
Riccardo Sangermano, Alejandro Garanto, Mubeen Khan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations
William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
The British Journal of Ophthalmology
|
October 18, 2023
<i>KCNV2</i>-associated retinopathy: genotype-phenotype correlations - <i>KCNV2</i> study group report 3
Thales A C de Guimaraes, Michalis Georgiou, Anthony G Robson, et al.
American Journal of Human Genetics
|
October 6, 2020
Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa
Suzanne E de Bruijn, Alessia Fiorentino, Daniele Ottaviani, et al.
American Journal of Ophthalmology
|
March 19, 2021
KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints-KCNV2 Study Group Report 2
Michalis Georgiou, Kaoru Fujinami, Ajoy Vincent, et al.
Page
of 125