C. Kehrer

发表

Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course

W. Grodd, S. Groeschel, I. Krägeloh-Mann, 2011, Journal of Inherited Metabolic Disease.

Early clinical course after hematopoietic stem cell transplantation in children with juvenile metachromatic leukodystrophy

S. Groeschel, I. Krägeloh-Mann, A. Grimm, 2020, Molecular and Cellular Pediatrics.

Phenotypic variation between siblings with Metachromatic Leukodystrophy

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2019, Orphanet Journal of Rare Diseases.

Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients.

B. Weschke, S. Groeschel, I. Krägeloh-Mann, 2016, JAMA neurology.

Juvenile metachromatic leukodystrophy 10 years post transplant compared with a non-transplanted cohort

T. Nägele, S. Groeschel, I. Krägeloh-Mann, 2013, Bone Marrow Transplantation.

Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challenges.

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2022, Molecular genetics and metabolism.

Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy

C. Krarup, M. Wilke, S. Groeschel, 2012, Neurology.

Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy

I. Krägeloh-Mann, G. Blumenstock, C. Kehrer, 2011, Developmental medicine and child neurology.

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

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2020, Orphanet Journal of Rare Diseases.

Demyelination load as predictor for disease progression in juvenile metachromatic leukodystrophy

M. Wilke, S. Groeschel, I. Krägeloh-Mann, 2017, Annals of clinical and translational neurology.

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

S. Groeschel, I. Krägeloh-Mann, C. Kehrer, 2021, Orphanet Journal of Rare Diseases.

Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2020, Neurology.

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

S. Groeschel, I. Krägeloh-Mann, V. Gieselmann, 2014, Orphanet Journal of Rare Diseases.

The natural course of gross motor deterioration in metachromatic leukodystrophy

I. Krägeloh-Mann, V. Gieselmann, G. Blumenstock, 2011, Developmental medicine and child neurology.

Enlargement of peripheral nerves in Krabbe disease: The diagnostic value of nerve ultrasound

T. Nägele, S. Groeschel, I. Krägeloh-Mann, 2020, Muscle & nerve.

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

S. Groeschel, I. Krägeloh-Mann, T. Haack, 2020, JIMD reports.

Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency

I. Krägeloh-Mann, R. Trollmann, J. Böhringer, 2017, Neuropediatrics.

Hematopoietic stem cell transplantation with mesenchymal stromal cells in children with metachromatic leukodystrophy.

S. Groeschel, I. Krägeloh-Mann, R. Handgretinger, 2022, Stem cells and development.

Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease

T. Dierks, S. Groeschel, J. Gärtner, 2020, Journal of inherited metabolic disease.

Hematopoietic Stem Cell Therapy In Eight Patients with Metachromatic Leukodystrophy – Relevance of Post-Transplant Medication.

I. Krägeloh-Mann, A. Erbacher, R. Handgretinger, 2010 .

Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy

I. Krägeloh-Mann, G. Blumenstock, C. Kehrer, 2011, Developmental medicine and child neurology.

Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophy

M. Poe, M. Ruzhnikov, J. Boulanger, 2024, Molecular Genetics and Metabolism.