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Saskia Elgün

Showing results (1-10 of 5) with videos related to

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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.
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.
Molecular Genetics and Metabolism|October 14, 2022
Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challengesVidiyaah Santhanakumaran, Samuel Groeschel, Klaus Harzer, et al.
Orphanet Journal of Rare Diseases|June 13, 2019
Phenotypic variation between siblings with Metachromatic LeukodystrophySaskia Elgün, Jakob Waibel, Christiane Kehrer, et al.
Molecular Genetics and Metabolism|February 5, 2023
Corrigendum to "Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challenges" Mol Genet Metab/Vol 137/Issue 3/2022/ 273-282Vidiyaah Santhanakumaran, Samuel Groeschel, Klaus Harzer, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
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.
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.
Molecular Genetics and Metabolism|October 14, 2022
Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challengesVidiyaah Santhanakumaran, Samuel Groeschel, Klaus Harzer, et al.
Orphanet Journal of Rare Diseases|June 13, 2019
Phenotypic variation between siblings with Metachromatic LeukodystrophySaskia Elgün, Jakob Waibel, Christiane Kehrer, et al.
Molecular Genetics and Metabolism|February 5, 2023
Corrigendum to "Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challenges" Mol Genet Metab/Vol 137/Issue 3/2022/ 273-282Vidiyaah Santhanakumaran, Samuel Groeschel, Klaus Harzer, et al.
Pageof 1