Krägeloh-Mann I - Search Results

1

Cerebral palsy and congenital malformations.

Garne E, Dolk H, Krägeloh-Mann I, Holst Ravn S, Cans C; SCPE Collaborative Group. Garne E, et al. Eur J Paediatr Neurol. 2008 Mar;12(2):82-8. doi: 10.1016/j.ejpn.2007.07.001. Epub 2007 Sep 19. Eur J Paediatr Neurol. 2008. PMID: 17881257 Review.

2

Trends in cerebral palsy among infants of very low birthweight (<1500 g) or born prematurely (<32 weeks) in 16 European centres: a database study.

Platt MJ, Cans C, Johnson A, Surman G, Topp M, Torrioli MG, Krageloh-Mann I. Platt MJ, et al. Lancet. 2007 Jan 6;369(9555):43-50. doi: 10.1016/S0140-6736(07)60030-0. Lancet. 2007. PMID: 17208641

3

Trends in Prevalence and Severity of Pre/Perinatal Cerebral Palsy Among Children Born Preterm From 2004 to 2010: A SCPE Collaboration Study.

Arnaud C, Ehlinger V, Delobel-Ayoub M, Klapouszczak D, Perra O, Hensey O, Neubauer D, Hollódy K, Virella D, Rackauskaite G, Greitane A, Himmelmann K, Ortibus E, Dakovic I, Andersen GL, Papavasiliou A, Sellier E, Platt MJ, Krägeloh-Mann I. Arnaud C, et al. Front Neurol. 2021 May 20;12:624884. doi: 10.3389/fneur.2021.624884. eCollection 2021. Front Neurol. 2021. PMID: 34093391 Free PMC article.

4

Brain lesions in preterms: origin, consequences and compensation.

Krägeloh-Mann I, Toft P, Lunding J, Andresen J, Pryds O, Lou HC. Krägeloh-Mann I, et al. Acta Paediatr. 1999 Aug;88(8):897-908. doi: 10.1080/08035259950168856. Acta Paediatr. 1999. PMID: 10503692

5

Brain magnetic resonance imaging in children with optimally controlled hyperphenylalaninaemia.

Toft PB, Lou HC, Krägeloh-Mann I, Andresen J, Güttler F, Guldberg P, Henriksen O. Toft PB, et al. J Inherit Metab Dis. 1994;17(5):575-83. doi: 10.1007/BF00711594. J Inherit Metab Dis. 1994. PMID: 7837764

6

The cognitive outcome of very preterm children: how to interpret results.

Krägeloh-Mann I. Krägeloh-Mann I. Acta Paediatr. 2002;91(12):1285-7. doi: 10.1111/j.1651-2227.2002.tb02818.x. Acta Paediatr. 2002. PMID: 12578279 No abstract available.

7

Late onset Krabbe disease due to the new GALC p.Ala543Pro mutation, with intriguingly high residual GALC activity in vitro.

Krägeloh-Mann I, Harzer K, Rostásy K, Beck-Wödl S, Bornemann A, Böhringer J, Bevot A, Beck V, Merkel G, Pechan M. Krägeloh-Mann I, et al. Eur J Paediatr Neurol. 2017 May;21(3):522-529. doi: 10.1016/j.ejpn.2016.12.012. Epub 2017 Jan 6. Eur J Paediatr Neurol. 2017. PMID: 28109651 Free article.

8

The second report of a new hypomyelinating disease due to a defect in the VPS11 gene discloses a massive lysosomal involvement.

Hörtnagel K, Krägeloh-Mann I, Bornemann A, Döcker M, Biskup S, Mayrhofer H, Battke F, du Bois G, Harzer K. Hörtnagel K, et al. J Inherit Metab Dis. 2016 Nov;39(6):849-857. doi: 10.1007/s10545-016-9961-x. Epub 2016 Jul 29. J Inherit Metab Dis. 2016. PMID: 27473128 Free PMC article.

9

Generation of two iPSC lines derived from two unrelated patients with Gaucher disease.

Nagel M, Reichbauer J, Böhringer J, Schelling Y, Krägeloh-Mann I, Schüle R, Ulmer U. Nagel M, et al. Stem Cell Res. 2019 Mar;35:101336. doi: 10.1016/j.scr.2018.10.021. Epub 2018 Nov 18. Stem Cell Res. 2019. PMID: 30606667 Free article.

10

Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences.

Kagermeier T, Hauser S, Sarieva K, Laugwitz L, Groeschel S, Janzarik WG, Yentür Z, Becker K, Schöls L, Krägeloh-Mann I, Mayer S. Kagermeier T, et al. Among authors: krageloh mann i. Dis Model Mech. 2024 Jul 1;17(7):dmm050740. doi: 10.1242/dmm.050740. Epub 2024 Jul 22. Dis Model Mech. 2024. PMID: 39034883 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

242 results

Search Page

Filters