Samuel Groeschel

Publication Activity (10 Years)

Years Active: 2014-2024
Publications (10 Years): 7

Top Topics

Magnetic Resonance Imaging

Hepatitis C Virus

Hematopoietic Stem Cell

Top Venues

Journal of inherited metabolic disease

Orphanet journal of rare diseases

International journal of biomedical imaging

Magnetic resonance in medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Samuel Groeschel, Shanice Beerepoot, Lucas Bastian Amedick, Ingeborg Krӓgeloh-Mann, Jing Li, David A H Whiteman, Nicole I Wolf, John D Port
The effect of intrathecal recombinant arylsulfatase A therapy on structural brain magnetic resonance imaging in children with metachromatic leukodystrophy. Journal of inherited metabolic disease 47 (4) (2024)
Samuel Groeschel, Shanice Beerepoot, Lucas Bastian Amedick, Ingeborg Krӓgeloh-Mann, Jing Li, David A H Whiteman, Nicole I Wolf, John D Port
The effect of intrathecal recombinant arylsulfatase A therapy on structural brain magnetic resonance imaging in children with metachromatic leukodystrophy. Journal of inherited metabolic disease (2024)
Theresa Kagermeier, Stefan Hauser, Kseniia Sarieva, Lucia Laugwitz, Samuel Groeschel, Wibke G Janzarik, Zeynep Yentür, Katharina Becker, Ludger Schöls, Ingeborg Kraegeloh-Mann, Simone Mayer
Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences. Disease models & mechanisms 17 (7) (2024)
Louisa Ammann-Schnell, Samuel Groeschel, Christiane Kehrer, Saskia Frölich, Ingeborg Krägeloh-Mann
The impact of severe rare chronic neurological disease in childhood on the quality of life of families-a study on MLD and PCH2. Orphanet journal of rare diseases 16 (1) (2021)
Judith Beschle, Michaela Döring, Christiane Kehrer, Christa Raabe, Ute Bayha, Manuel Strölin, Judith Böhringer, Andrea Bevot, Nadja Kaiser, Benjamin Bender, Alexander Grimm, Peter Lang, Ingo Müller, Ingeborg Krägeloh-Mann, Samuel Groeschel
Early clinical course after hematopoietic stem cell transplantation in children with juvenile metachromatic leukodystrophy. Molecular and cellular pediatrics 7 (1) (2020)
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
Phenotypic variation between siblings with Metachromatic Leukodystrophy. Orphanet journal of rare diseases 14 (1) (2019)
Alexandra Koch, Andrei Zhukov, Tony Stoecker, Samuel Groeschel, Thomas Schultz
SHORE-based detection and imputation of dropout in diffusion MRI. Magnetic resonance in medicine 82 (6) (2019)
Mark Höller, Kay-M Otto, Uwe Klose, Samuel Groeschel, Hans-H Ehricke
Fiber Visualization with LIC Maps Using Multidirectional Anisotropic Glyph Samples. International journal of biomedical imaging 2014 (2014)