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Kehrer, Christiane
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1

Validation of GMFC-MLD scale as a measure of gross motor fu..:

Mutua, Sylvia ; Sevagamoorthy, Anjana ; Gavazzi, Francesco...
Molecular Genetics and Metabolism.  141 (2024)  2 - p. 107976 , 2024
Link: https://doi.org/10.1016/..
 
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2

Corrigendum to "Predicting clinical phenotypes of metachrom..:

Santhanakumaran, Vidiyaah ; Groeschel, Samuel ; Harzer, Klaus...
Molecular Genetics and Metabolism.  138 (2023)  3 - p. 107372 , 2023
Link: https://doi.org/10.1016/..
 
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3

Developmental delay can precede neurologic regression in me..:

Adang, Laura A. ; Groeschel, Samuel ; Grzyb, Chloe...
Molecular Genetics and Metabolism.  138 (2023)  2 - p. 106989 , 2023
Link: https://doi.org/10.1016/..
 
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4

Predicting clinical phenotypes of metachromatic leukodystro..:

Santhanakumaran, Vidiyaah ; Groeschel, Samuel ; Harzer, Klaus...
Molecular Genetics and Metabolism.  137 (2022)  3 - p. 273-282 , 2022
Link: https://doi.org/10.1016/..
 
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5

Association of Age at Onset and First Symptoms With Disease..:

Kehrer, Christiane ; Elgün, Saskia ; Raabe, Christa...
Neurology.  96 (2021)  2 - p. , 2021
Link: https://doi.org/10.1212/..
 
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6

The impact of severe rare chronic neurological disease in c..:

Ammann-Schnell, Louisa ; Groeschel, Samuel ; Kehrer, Christiane..
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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7

Enlargement of peripheral nerves in Krabbe disease: The dia..:

Küpper, Hanna ; Kaiser, Nadja ; Winter, Natalie...
Muscle & Nerve.  61 (2020)  4 - p. , 2020
Link: https://doi.org/10.1002/..
 
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8

Natural history of Krabbe disease – a nationwide study in G..:

Krieg, Sarah Isabel ; Krägeloh-Mann, Ingeborg ; Groeschel, Samuel...
Orphanet Journal of Rare Diseases.  15 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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9

Early clinical course after hematopoietic stem cell transpl..:

Beschle, Judith ; Döring, Michaela ; Kehrer, Christiane...
Molecular and Cellular Pediatrics.  7 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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10

Long‐term disease course of two patients with multiple sulf..:

Beck‐Wödl, Stefanie ; Kehrer, Christiane ; Harzer, Klaus...
JIMD Reports.  58 (2020)  1 - p. 80-88 , 2020
Link: https://doi.org/10.1002/..
 
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11

Natural history of multiple sulfatase deficiency: Retrospec..:

Adang, Laura A. ; Schlotawa, Lars ; Groeschel, Samuel...
Journal of Inherited Metabolic Disease.  43 (2020)  6 - p. 1298-1309 , 2020
Link: https://doi.org/10.1002/..
 
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12

Phenotypic variation between siblings with Metachromatic Le..:

Elgün, Saskia ; Waibel, Jakob ; Kehrer, Christiane...
Orphanet Journal of Rare Diseases.  14 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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13

Demyelination load as predictor for disease progression in ..:

Strölin, Manuel ; Krägeloh‐Mann, Ingeborg ; Kehrer, Christiane..
Annals of Clinical and Translational Neurology.  4 (2017)  6 - p. 403-410 , 2017
Link: https://doi.org/10.1002/..
 
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14

Thickening of the peripheral nerves in metachromatic leukod..:

Grimm, Alexander ; Schäffer, Eva ; Just, Jennifer...
Journal of the Neurological Sciences.  368 (2016)  - p. 399-401 , 2016
Link: https://doi.org/10.1016/..
 
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15

Language and cognition in children with metachromatic leuko..:

Kehrer, Christiane ; Groeschel, Samuel ; Kustermann-Kuhn, Birgit...
Orphanet Journal of Rare Diseases.  9 (2014)  1 - p. 18 , 2014
Link: https://doi.org/10.1186/..
 
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