Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Samuel Groeschel

Showing results (41-50 of 86) with videos related to

Pageof 9
Sort By:
Annals of Clinical and Translational Neurology|December 17, 2020
Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 studyChristine Í Dali, Samuel Groeschel, Mihai Moldovan, et al.
Annals of Clinical and Translational Neurology|March 31, 2021
A connectome-based approach to assess motor outcome after neonatal arterial ischemic strokeMariam Al Harrach, Pablo Pretzel, Samuel Groeschel, et al.
Stroke|May 12, 2016
Does Contralesional Hand Function After Neonatal Stroke Only Depend on Lesion Characteristics?Mickael Dinomais, Lucie Hertz-Pannier, Samuel Groeschel, et al.
Annals of Clinical and Translational Neurology|November 5, 2022
Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophyDaphne H Schoenmakers, Shanice Beerepoot, Ingeborg Krägeloh-Mann, et al.
JIMD Reports|March 14, 2022
Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR-based urinary metabolomicsLucia Laugwitz, Laimdota Zizmare, Vidiyaah Santhanakumaran, et al.
Human Brain Mapping|October 30, 2015
Long term motor function after neonatal stroke: Lesion localization above allMickael Dinomais, Lucie Hertz-Pannier, Samuel Groeschel, et al.
Orphanet Journal of Rare Diseases|February 7, 2014
Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohortChristiane Kehrer, Samuel Groeschel, Birgit Kustermann-Kuhn, et al.
Journal of Inherited Metabolic Disease|February 7, 2024
The effect of intrathecal recombinant arylsulfatase A therapy on structural brain magnetic resonance imaging in children with metachromatic leukodystrophySamuel Groeschel, Shanice Beerepoot, Lucas Bastian Amedick, et al.
Clinical Neuroradiology|November 23, 2020
T2-Pseudonormalization and Microstructural Characterization in Advanced Stages of Late-infantile Metachromatic LeukodystrophyPascal Martin, Gisela E Hagberg, Thomas Schultz, et al.
Neurology|October 13, 2020
Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic LeukodystrophyChristiane Kehrer, Saskia Elgün, Christa Raabe, et al.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
Annals of Clinical and Translational Neurology|December 17, 2020
Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 studyChristine Í Dali, Samuel Groeschel, Mihai Moldovan, et al.
Annals of Clinical and Translational Neurology|March 31, 2021
A connectome-based approach to assess motor outcome after neonatal arterial ischemic strokeMariam Al Harrach, Pablo Pretzel, Samuel Groeschel, et al.
Stroke|May 12, 2016
Does Contralesional Hand Function After Neonatal Stroke Only Depend on Lesion Characteristics?Mickael Dinomais, Lucie Hertz-Pannier, Samuel Groeschel, et al.
Annals of Clinical and Translational Neurology|November 5, 2022
Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophyDaphne H Schoenmakers, Shanice Beerepoot, Ingeborg Krägeloh-Mann, et al.
JIMD Reports|March 14, 2022
Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR-based urinary metabolomicsLucia Laugwitz, Laimdota Zizmare, Vidiyaah Santhanakumaran, et al.
Human Brain Mapping|October 30, 2015
Long term motor function after neonatal stroke: Lesion localization above allMickael Dinomais, Lucie Hertz-Pannier, Samuel Groeschel, et al.
Orphanet Journal of Rare Diseases|February 7, 2014
Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohortChristiane Kehrer, Samuel Groeschel, Birgit Kustermann-Kuhn, et al.
Journal of Inherited Metabolic Disease|February 7, 2024
The effect of intrathecal recombinant arylsulfatase A therapy on structural brain magnetic resonance imaging in children with metachromatic leukodystrophySamuel Groeschel, Shanice Beerepoot, Lucas Bastian Amedick, et al.
Clinical Neuroradiology|November 23, 2020
T2-Pseudonormalization and Microstructural Characterization in Advanced Stages of Late-infantile Metachromatic LeukodystrophyPascal Martin, Gisela E Hagberg, Thomas Schultz, et al.
Neurology|October 13, 2020
Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic LeukodystrophyChristiane Kehrer, Saskia Elgün, Christa Raabe, et al.
Pageof 9