N. Kaiser

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.

Improved upper limb function in non-ambulant children with SMA type 2 and 3 during nusinersen treatment: a prospective 3-years SMArtCARE registry study

B. Schlotter-Weigel, M. Blankenburg, P. Huppke, 2022, 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.

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

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

Neurocognitive development in isolated Robin sequence treated with the Tuebingen palatal plate

M. Krimmel, S. Reinert, C. Poets, 2022, Clinical Oral Investigations.

Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

Heinen, Heiko, Kehrer, 2023, medRxiv.

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.