Kohlschütter A - Search Results

1

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

Groeschel S, Kühl JS, Bley AE, Kehrer C, Weschke B, Döring M, Böhringer J, Schrum J, Santer R, Kohlschütter A, Krägeloh-Mann I, Müller I. Groeschel S, et al. Among authors: kohlschutter a. JAMA Neurol. 2016 Sep 1;73(9):1133-40. doi: 10.1001/jamaneurol.2016.2067. JAMA Neurol. 2016. PMID: 27400410

2

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. Among authors: kohlschutter a. 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.

3

Long-term neuroimaging follow-up on an asymptomatic juvenile metachromatic leukodystrophy patient after hematopoietic stem cell transplantation: evidence of myelin recovery and ongoing brain maturation.

Ding XQ, Bley A, Kohlschütter A, Fiehler J, Lanfermann H. Ding XQ, et al. Among authors: kohlschutter a. Am J Med Genet A. 2012 Jan;158A(1):257-60. doi: 10.1002/ajmg.a.34389. Epub 2011 Dec 2. Am J Med Genet A. 2012. PMID: 22140054 No abstract available.

4

Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.

Kohlschütter A, Bley A, Brockmann K, Gärtner J, Krägeloh-Mann I, Rolfs A, Schöls L. Kohlschütter A, et al. Brain Dev. 2010 Feb;32(2):82-9. doi: 10.1016/j.braindev.2009.03.014. Epub 2009 May 7. Brain Dev. 2010. PMID: 19427149 Review.

5

A child with night blindness: preventing serious symptoms of Refsum disease.

Kohlschütter A, Santer R, Lukacs Z, Altenburg C, Kemper MJ, Rüther K. Kohlschütter A, et al. J Child Neurol. 2012 May;27(5):654-6. doi: 10.1177/0883073811424799. Epub 2011 Dec 7. J Child Neurol. 2012. PMID: 22156782

6

Stabilization of juvenile metachromatic leukodystrophy after bone marrow transplantation: a 13-year follow-up.

Görg M, Wilck W, Granitzny B, Suerken A, Lukacs Z, Ding X, Schulte-Markwort M, Kohlschütter A. Görg M, et al. Among authors: kohlschutter a. J Child Neurol. 2007 Sep;22(9):1139-42. doi: 10.1177/0883073807306256. J Child Neurol. 2007. PMID: 17890417

7

Lysosomal leukodystrophies: Krabbe disease and metachromatic leukodystrophy.

Kohlschütter A. Kohlschütter A. Handb Clin Neurol. 2013;113:1611-8. doi: 10.1016/B978-0-444-59565-2.00029-0. Handb Clin Neurol. 2013. PMID: 23622382 Review.

8

First Recognized Patient with Genetic Vitamin E Deficiency Stable after 36 Years of Controlled Supplement Therapy.

Kohlschütter A, Finckh B, Nickel M, Bley A, Hübner C. Kohlschütter A, et al. Neurodegener Dis. 2020;20(1):35-38. doi: 10.1159/000508080. Epub 2020 Jul 3. Neurodegener Dis. 2020. PMID: 32623435

9

Metachromatic Leukodystrophy: An Assessment of Disease Burden.

Eichler FS, Cox TM, Crombez E, Dali CÍ, Kohlschütter A. Eichler FS, et al. Among authors: kohlschutter a. J Child Neurol. 2016 Nov;31(13):1457-1463. doi: 10.1177/0883073816656401. Epub 2016 Jul 7. J Child Neurol. 2016. PMID: 27389394

10

The natural history of Canavan disease: 23 new cases and comparison with patients from literature.

Bley A, Denecke J, Kohlschütter A, Schön G, Hischke S, Guder P, Bierhals T, Lau H, Hempel M, Eichler FS. Bley A, et al. Among authors: kohlschutter a. Orphanet J Rare Dis. 2021 May 19;16(1):227. doi: 10.1186/s13023-020-01659-3. Orphanet J Rare Dis. 2021. PMID: 34011350 Free PMC article.

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