Showing 1 - 19 results of 19 for search 'Samuel Groeschel', query time: 0.06s
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Spatially regularized low-rank tensor approximation for accurate and fast tractography by Johannes Gruen, Samuel Groeschel, Thomas Schultz
Published 2023-05-01
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Reduced structural connectivity in non-motor networks in children born preterm and the influence of early postnatal human cytomegalovirus infection by Pablo Pretzel, Pablo Pretzel, Marko Wilke, Marko Wilke, J-Donald Tournier, J-Donald Tournier, Rangmar Goelz, Karen Lidzba, Till-Karsten Hauser, Samuel Groeschel, Samuel Groeschel
Published 2023-10-01
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Optimization of Enzyme Essays to Enhance Reliability of Activity Measurements in Leukocyte Lysates for the Diagnosis of Metachromatic Leukodystrophy and Gangliosidoses by Sebastian Strobel, Naomi Hesse, Vidiyaah Santhanakumaran, Samuel Groeschel, Gernot Bruchelt, Ingeborg Krägeloh-Mann, Judith Böhringer
Published 2020-11-01
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Corrigendum: Motor Abilities in Adolescents Born Preterm Are Associated With Microstructure of the Corpus Callosum by Samuel Groeschel, Linda Holmström, Gemma Northam, J-Donald Tournier, Torsten Baldeweg, Beatrice Latal, Jon Caflisch, Brigitte Vollmer, Brigitte Vollmer
Published 2020-03-01
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Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophy by Daphne H. Schoenmakers, Shanice Beerepoot, Ingeborg Krägeloh‐Mann, Saskia Elgün, Benjamin Bender, Marjo S. van derKnaap, Nicole I. Wolf, Samuel Groeschel
Published 2022-12-01
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Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR‐based urinary metabolomics by Lucia Laugwitz, Laimdota Zizmare, Vidiyaah Santhanakumaran, Claire Cannet, Judith Böhringer, Jürgen G. Okun, Manfred Spraul, Ingeborg Krägeloh‐Mann, Samuel Groeschel, Christoph Trautwein
Published 2022-03-01
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A connectome‐based approach to assess motor outcome after neonatal arterial ischemic stroke by Mariam Al Harrach, Pablo Pretzel, Samuel Groeschel, François Rousseau, Thijs Dhollander, Lucie Hertz‐Pannier, Julien Lefevre, Stéphane Chabrier, Mickael Dinomais, the AVCnn study group
Published 2021-05-01
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Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort by Stefanie Beck‐Wödl, Christiane Kehrer, Klaus Harzer, Tobias B. Haack, Friederike Bürger, Dorothea Haas, Angelika Rieß, Samuel Groeschel, Ingeborg Krägeloh‐Mann, Judith Böhringer
Published 2021-03-01
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Extremely low arylsulfatase A enzyme activity does not necessarily cause symptoms: A long‐term follow‐up and review of the literature by Lucia Laugwitz, Vidiyaah Santhanakumaran, Mareike Spieker, Judith Boehringer, Benjamin Bender, Volkmar Gieselmann, Stefanie Beck‐Woedl, Gernot Bruchelt, Klaus Harzer, Ingeborg Kraegeloh‐Mann, Samuel Groeschel
Published 2022-07-01
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Phenotypic variation between siblings with Metachromatic Leukodystrophy by Saskia Elgün, Jakob Waibel, Christiane Kehrer, Diane van Rappard, Judith Böhringer, Stefanie Beck-Wödl, Jennifer Just, Ludger Schöls, Nicole Wolf, Ingeborg Krägeloh-Mann, Samuel Groeschel
Published 2019-06-01
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Assessing White Matter Microstructure in Brain Regions with Different Myelin Architecture Using MRI. by Samuel Groeschel, Gisela E Hagberg, Thomas Schultz, Dávid Z Balla, Uwe Klose, Till-Karsten Hauser, Thomas Nägele, Oliver Bieri, Thomas Prasloski, Alex L MacKay, Ingeborg Krägeloh-Mann, Klaus Scheffler
Published 2016-01-01
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Inventory of current practices regarding hematopoietic stem cell transplantation in metachromatic leukodystrophy in Europe and neighboring countries by Daphne H. Schoenmakers, Fanny Mochel, Laura A. Adang, Jaap-Jan Boelens, Valeria Calbi, Erik A. Eklund, Sabine W. Grønborg, Francesca Fumagalli, Samuel Groeschel, Caroline Lindemans, Caroline Sevin, Ludger Schöls, Dipak Ram, Ayelet Zerem, Holm Graessner, Nicole I. Wolf
Published 2024-02-01
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Normative Observational Nerve Ultrasound Values in School-Age Children and Adolescents and Their Application to Hereditary Neuropathies by Anna-Sophie Grimm, Charlotte Schubert, Alexander Grimm, Jan-Hendrik Stahl, Jan-Hendrik Stahl, Hanna Küpper, Veronka Horber, Josua Kegele, Josua Kegele, Josua Kegele, Sophia Willikens, Sophia Willikens, Julia Wittlinger, Lina Serna-Higuita, Natalie Winter, Natalie Winter, Samuel Groeschel
Published 2020-04-01
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Modified Delphi procedure-based expert consensus on endpoints for an international disease registry for Metachromatic Leukodystrophy: The European Metachromatic Leukodystrophy init... by Daphne H. Schoenmakers, Shanice Beerepoot, Sibren van den Berg, Laura Adang, Annette Bley, Jaap-Jan Boelens, Francesca Fumagalli, Wim G. Goettsch, Sabine Grønborg, Samuel Groeschel, Peter M. van Hasselt, Carla E. M. Hollak, Caroline Lindemans, Fanny Mochel, Peter G. M. Mol, Caroline Sevin, Ayelet Zerem, Ludger Schöls, Nicole I. Wolf
Published 2022-02-01
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The European Reference Network for Rare Neurological Diseases by Carola Reinhard, Carola Reinhard, Anne-Catherine Bachoud-Lévi, Anne-Catherine Bachoud-Lévi, Anne-Catherine Bachoud-Lévi, Tobias Bäumer, Tobias Bäumer, Enrico Bertini, Alicia Brunelle, Alicia Brunelle, Annemieke I. Buizer, Antonio Federico, Thomas Gasser, Thomas Gasser, Samuel Groeschel, Sanja Hermanns, Sanja Hermanns, Thomas Klockgether, Ingeborg Krägeloh-Mann, G. Bernhard Landwehrmeyer, Isabelle Leber, Isabelle Leber, Alfons Macaya, Caterina Mariotti, Wassilios G. Meissner, Wassilios G. Meissner, Maria Judit Molnar, Jorik Nonnekes, Juan Dario Ortigoza Escobar, Belen Pérez Dueñas, Lori Renna Linton, Ludger Schöls, Rebecca Schuele, Rebecca Schuele, Marina A. J. Tijssen, Rik Vandenberghe, Rik Vandenberghe, Anna Volkmer, Anna Volkmer, Nicole I. Wolf, Holm Graessner, Holm Graessner
Published 2021-01-01
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