Krägeloh-Mann I - Search Results

1

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

Ammann-Schnell L, Groeschel S, Kehrer C, Frölich S, Krägeloh-Mann I. Ammann-Schnell L, et al. Orphanet J Rare Dis. 2021 May 10;16(1):211. doi: 10.1186/s13023-021-01828-y. Orphanet J Rare Dis. 2021. PMID: 33971942 Free PMC article.

2

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

Kehrer C, Blumenstock G, Raabe C, Krägeloh-Mann I. Kehrer C, et al. Dev Med Child Neurol. 2011 Feb;53(2):156-60. doi: 10.1111/j.1469-8749.2010.03821.x. Epub 2010 Nov 18. Dev Med Child Neurol. 2011. PMID: 21087233 Free article.

3

Relationship between functional connectivity and sensory impairment: red flag or red herring?

Dinomais M, Groeschel S, Staudt M, Krägeloh-Mann I, Wilke M. Dinomais M, et al. Hum Brain Mapp. 2012 Mar;33(3):628-38. doi: 10.1002/hbm.21227. Epub 2011 Mar 9. Hum Brain Mapp. 2012. PMID: 21391277 Free PMC article.

4

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

Groeschel S, Kehrer C, Engel C, I Dali C, Bley A, Steinfeld R, Grodd W, Krägeloh-Mann I. Groeschel S, et al. J Inherit Metab Dis. 2011 Oct;34(5):1095-102. doi: 10.1007/s10545-011-9361-1. Epub 2011 Jun 23. J Inherit Metab Dis. 2011. PMID: 21698385

5

The natural course of gross motor deterioration in metachromatic leukodystrophy.

Kehrer C, Blumenstock G, Gieselmann V, Krägeloh-Mann I; GERMAN LEUKONET. Kehrer C, et al. Dev Med Child Neurol. 2011 Sep;53(9):850-855. doi: 10.1111/j.1469-8749.2011.04028.x. Epub 2011 Jun 27. Dev Med Child Neurol. 2011. PMID: 21707604 Free article. Clinical Trial.

6

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

Krägeloh-Mann I, Groeschel S, Kehrer C, Opherk K, Nägele T, Handgretinger R, Müller I. Krägeloh-Mann I, et al. Bone Marrow Transplant. 2013 Mar;48(3):369-75. doi: 10.1038/bmt.2012.155. Epub 2012 Sep 3. Bone Marrow Transplant. 2013. PMID: 22941383

7

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

Groeschel S, í Dali C, Clas P, Böhringer J, Duno M, Krarup C, Kehrer C, Wilke M, Krägeloh-Mann I. Groeschel S, et al. Neurology. 2012 Oct 16;79(16):1662-70. doi: 10.1212/WNL.0b013e31826e9ad2. Epub 2012 Sep 19. Neurology. 2012. PMID: 22993277 Free PMC article.

8

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

Kehrer C, Groeschel S, Kustermann-Kuhn B, Bürger F, Köhler W, Kohlschütter A, Bley A, Steinfeld R, Gieselmann V, Krägeloh-Mann I; German LEUKONET. Kehrer C, et al. Orphanet J Rare Dis. 2014 Feb 5;9:18. doi: 10.1186/1750-1172-9-18. Orphanet J Rare Dis. 2014. PMID: 24499656 Free PMC article.

9

Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts.

Synofzik M, Schüle R, Schulze M, Gburek-Augustat J, Schweizer R, Schirmacher A, Krägeloh-Mann I, Gonzalez M, Young P, Züchner S, Schöls L, Bauer P. Synofzik M, et al. Orphanet J Rare Dis. 2014 Apr 17;9:57. doi: 10.1186/1750-1172-9-57. Orphanet J Rare Dis. 2014. PMID: 24742043 Free PMC article.

10

Natural course of pontocerebellar hypoplasia type 2A.

Sánchez-Albisua I, Frölich S, Barth PG, Steinlin M, Krägeloh-Mann I. Sánchez-Albisua I, et al. Orphanet J Rare Dis. 2014 May 5;9:70. doi: 10.1186/1750-1172-9-70. Orphanet J Rare Dis. 2014. PMID: 24886362 Free PMC article.

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