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Judith Böhringer

Human multipotent mesenchymal stromal cells use galectin-1 to inhibit immune effector cells
2010 · Friederike Gieseke, Judith Böhringer, et al. · Blood · 265
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Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients
2016 · Samuel Groeschel, Jörn-Sven Kühl, et al. · JAMA Neurology · 153
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Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy
2020 · Christiane Kehrer, Saskia Elgün, et al. · Neurology · 86
The Mutation Matters: CSF Profiles of GCase , Sphingolipids, α‐Synuclein in PD GBA
2021 · Stefanie Lerche, Claudia Schulte, et al. · Movement Disorders · 73
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Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy
2012 · Samuel Groeschel, Christine í Dali, et al. · Neurology · 58
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Early clinical course after hematopoietic stem cell transplantation in children with juvenile metachromatic leukodystrophy
2020 · Judith Beschle, Michaela Döring, et al. · Molecular and Cellular Pediatrics · 47
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Phenotypic variation between siblings with Metachromatic Leukodystrophy
2019 · Saskia Elgün, Jakob Waibel, et al. · Orphanet Journal of Rare Diseases · 47
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SERAC1 deficiency causes complicated HSP: evidence from a novel splice mutation in a large family
2017 · Benjamin Roeben, Rebecca Schüle, et al. · Journal of Medical Genetics · 40
Enzymatic characterization of novel arylsulfatase A variants using human arylsulfatase A‐deficient immortalized mesenchymal stromal cells
2017 · Judith Böhringer, René Santer, et al. · Human Mutation · 25
Optimization of Enzyme Essays to Enhance Reliability of Activity Measurements in Leukocyte Lysates for the Diagnosis of Metachromatic Leukodystrophy and Gangliosidoses
2020 · Sebastian Strobel, Naomi Hesse, et al. · Cells · 16
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Hematopoietic Stem Cell Transplantation with Mesenchymal Stromal Cells in Children with Metachromatic Leukodystrophy
2022 · Karin Melanie Cabanillas Stanchi, Judith Böhringer, et al. · Stem Cells and Development · 13
A Mutation-Agnostic Hematopoietic Stem Cell Gene Therapy for Metachromatic Leukodystrophy
2021 · Justin S. Antony, Alberto Daniel-Moreno, et al. · The CRISPR Journal · 12
Clinical, Imaging, Genetic, and Disease Course Characteristics in Patients With GM2 Gangliosidosis
2023 · Jan Kern, Judith Böhringer, et al. · Neurology · 10
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Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency
2017 · Christiane Kehrer, Wibke Kustermann, et al. · Neuropediatrics · 10
Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort
2020 · Stefanie Beck‐Wödl, Christiane Kehrer, et al. · JIMD Reports · 8
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Chitotriosidase is a biomarker for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia
2022 · Stefanie N. Hayer, Vidiyaah Santhanakumaran, et al. · Annals of Clinical and Translational Neurology · 7
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Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR ‐based urinary metabolomics
2022 · Lucia Laugwitz, Laimdota Zizmare, et al. · JIMD Reports · 6
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Late onset Krabbe disease due to the new GALC p.Ala543Pro mutation, with intriguingly high residual GALC activity in vitro
2017 · Inge Krägeloh-Mann, Klaus Harzer, et al. · European Journal of Paediatric Neurology · 6
Measurement of recombinant human arylsulfatase A and leukocyte sulfatase activities by analytical isotachophoresis
2019 · Sandra Pajarola, Christine Weißenberg, et al. · Journal of Chromatography B · 5
Generation of two iPSC lines derived from two unrelated patients with Gaucher disease
2018 · Maike Nagel, Jennifer Reichbauer, et al. · Stem Cell Research · 5
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Challenges in Biochemical Diagnosis of Krabbe and Gaucher Disease
2021 · V. Santhanakumaran, M. Pechan, et al. · Neuropediatrics · 1
Hematopoietic Stem Cell Therapy In Eight Patients with Metachromatic Leukodystrophy – Relevance of Post-Transplant Medication.
2010 · Judith Böhringer, Birgit Kustermann-Kuhn, et al. · Blood · 1
Influence of Age and Type of First Symptoms on Disease Progression in Metachromatic Leukodystrophy
2019 · Saskia Elgün, Christiane Kehrer, et al. · Neuropediatrics
OP1 – 2527: Phenotypic variation between siblings with metachromatic leukodystrophy
2015 · S. Groeschel, J. Waibel, et al. · European Journal of Paediatric Neurology
GM2-Activator Deficiency Mimics Tay–Sachs Disease
2015 · C. Kehrer, J. Böhringer, et al. · Neuropediatrics
Works count: 31
Citation count: 896
H-index: 12
I10-index: 14
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