Demyelination load as predictor for disease progression in juvenile metachromatic leukodystrophy

por Strölin, Manuel, Krägeloh‐Mann, Ingeborg, Kehrer, Christiane, Wilke, Marko, Groeschel, Samuel
Publicado 2017

Fiber Visualization with LIC Maps Using Multidirectional Anisotropic Glyph Samples

por Höller, Mark, Otto, Kay-M., Klose, Uwe, Groeschel, Samuel, Ehricke, Hans-H.
Publicado 2014

The impact of severe rare chronic neurological disease in childhood on the quality of life of families—a study on MLD and PCH2

por Ammann-Schnell, Louisa, Groeschel, Samuel, Kehrer, Christiane, Frölich, Saskia, Krägeloh-Mann, Ingeborg
Publicado 2021

Optimization of Enzyme Essays to Enhance Reliability of Activity Measurements in Leukocyte Lysates for the Diagnosis of Metachromatic Leukodystrophy and Gangliosidoses

por Strobel, Sebastian, Hesse, Naomi, Santhanakumaran, Vidiyaah, Groeschel, Samuel, Bruchelt, Gernot, Krägeloh-Mann, Ingeborg, Böhringer, Judith
Publicado 2020

Reduced structural connectivity in non-motor networks in children born preterm and the influence of early postnatal human cytomegalovirus infection

por Pretzel, Pablo, Wilke, Marko, Tournier, J-Donald, Goelz, Rangmar, Lidzba, Karen, Hauser, Till-Karsten, Groeschel, Samuel
Publicado 2023

Brain morphometry in Pontocerebellar Hypoplasia type 2

por Ekert, Kaspar, Groeschel, Samuel, Sánchez-Albisua, Iciar, Frölich, Saskia, Dieckmann, Andrea, Engel, Corinna, Krägeloh-Mann, Ingeborg
Publicado 2016

Clinical application of advanced MR methods in children: points to consider

por Wilke, Marko, Groeschel, Samuel, Lorenzen, Anna, Rona, Sabine, Schuhmann, Martin U., Ernemann, Ulrike, Krägeloh‐Mann, Ingeborg
Publicado 2018

Is the Blood Oxygenation Level-Dependent fMRI Response to Motor Tasks Altered in Children After Neonatal Stroke?

por Al Harrach, Mariam, Rousseau, François, Groeschel, Samuel, Chabrier, Stéphane, Hertz-Pannier, Lucie, Lefevre, Julien, Dinomais, Mickael
Publicado 2020

Structural brain connectivity in children after neonatal stroke: A whole-brain fixel-based analysis

por Pretzel, Pablo, Dhollander, Thijs, Chabrier, Stéphane, Al-Harrach, Mariam, Hertz-Pannier, Lucie, Dinomais, Mickael, Groeschel, Samuel
Publicado 2022

Motor Abilities in Adolescents Born Preterm Are Associated With Microstructure of the Corpus Callosum

por Groeschel, Samuel, Holmström, Linda, Northam, Gemma, Tournier, J-Donald, Baldeweg, Torsten, Latal, Beatrice, Caflisch, Jon, Vollmer, Brigitte
Publicado 2019

Corrigendum: Motor Abilities in Adolescents Born Preterm Are Associated With Microstructure of the Corpus Callosum

por Groeschel, Samuel, Holmström, Linda, Northam, Gemma, Tournier, J-Donald, Baldeweg, Torsten, Latal, Beatrice, Caflisch, Jon, Vollmer, Brigitte
Publicado 2020

Natural history of Krabbe disease – a nationwide study in Germany using clinical and MRI data

por Krieg, Sarah Isabel, Krägeloh-Mann, Ingeborg, Groeschel, Samuel, Beck-Wödl, Stefanie, Husain, Ralf A., Schöls, Ludger, Kehrer, Christiane
Publicado 2020

MR-spectroscopy in metachromatic leukodystrophy: A model free approach and clinical correlation

por Feldmann, Joana, Martin, Pascal, Bender, Benjamin, Laugwitz, Lucia, Zizmare, Laimdota, Trautwein, Christoph, Krägeloh-Mann, Ingeborg, Klose, Uwe, Groeschel, Samuel
Publicado 2022

A connectome‐based approach to assess motor outcome after neonatal arterial ischemic stroke

por Al Harrach, Mariam, Pretzel, Pablo, Groeschel, Samuel, Rousseau, François, Dhollander, Thijs, Hertz‐Pannier, Lucie, Lefevre, Julien, Chabrier, Stéphane, Dinomais, Mickael
Publicado 2021

Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 study

por í Dali, Christine, Groeschel, Samuel, Moldovan, Mihai, Farah, Mohamed H., Krägeloh‐Mann, Ingeborg, Wasilewski, Margaret, Li, Jing, Barton, Norman, Krarup, Christian
Publicado 2020

Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophy

por Schoenmakers, Daphne H., Beerepoot, Shanice, Krägeloh‐Mann, Ingeborg, Elgün, Saskia, Bender, Benjamin, van der Knaap, Marjo S., Wolf, Nicole I., Groeschel, Samuel
Publicado 2022

Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort

por Kehrer, Christiane, Groeschel, Samuel, Kustermann-Kuhn, Birgit, Bürger, Friederike, Köhler, Wolfgang, Kohlschütter, Alfried, Bley, Annette, Steinfeld, Robert, Gieselmann, Volkmar, Krägeloh-Mann, Ingeborg
Publicado 2014

T2-Pseudonormalization and Microstructural Characterization in Advanced Stages of Late-infantile Metachromatic Leukodystrophy

por Martin, Pascal, Hagberg, Gisela E., Schultz, Thomas, Harzer, Klaus, Klose, Uwe, Bender, Benjamin, Nägele, Thomas, Scheffler, Klaus, Krägeloh-Mann, Ingeborg, Groeschel, Samuel
Publicado 2020

Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR‐based urinary metabolomics

por Laugwitz, Lucia, Zizmare, Laimdota, Santhanakumaran, Vidiyaah, Cannet, Claire, Böhringer, Judith, Okun, Jürgen G., Spraul, Manfred, Krägeloh‐Mann, Ingeborg, Groeschel, Samuel, Trautwein, Christoph
Publicado 2022

Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort

por Beck‐Wödl, Stefanie, Kehrer, Christiane, Harzer, Klaus, Haack, Tobias B., Bürger, Friederike, Haas, Dorothea, Rieß, Angelika, Groeschel, Samuel, Krägeloh‐Mann, Ingeborg, Böhringer, Judith
Publicado 2020