Krägeloh-Mann I - Search Results

1

In vitro analysis of multipotent mesenchymal stromal cells as potential cellular therapeutics in neurometabolic diseases in pediatric patients.

Müller I, Kustermann-Kuhn B, Holzwarth C, Isensee G, Vaegler M, Harzer K, Krägeloh-Mann I, Handgretinger R, Bruchelt G. Müller I, et al. Exp Hematol. 2006 Oct;34(10):1413-9. doi: 10.1016/j.exphem.2006.06.007. Exp Hematol. 2006. PMID: 16982334 Free article. Clinical Trial.

2

Niemann-Pick disease type A and B are clinically but also enzymatically heterogeneous: pitfall in the laboratory diagnosis of sphingomyelinase deficiency associated with the mutation Q292 K.

Harzer K, Rolfs A, Bauer P, Zschiesche M, Mengel E, Backes J, Kustermann-Kuhn B, Bruchelt G, van Diggelen OP, Mayrhofer H, Krägeloh-Mann I. Harzer K, et al. Neuropediatrics. 2003 Dec;34(6):301-6. doi: 10.1055/s-2003-44668. Neuropediatrics. 2003. PMID: 14681755

3

Clinical findings in Niemann-Pick disease type B.

Müssig K, Harzer K, Mayrhofer H, Krägeloh-Mann I, Häring HU, Machicao F. Müssig K, et al. Intern Med J. 2006 Feb;36(2):135-6. doi: 10.1111/j.1445-5994.2005.01013.x. Intern Med J. 2006. PMID: 16472269 No abstract available.

4

Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations.

Kuchar L, Ledvinová J, Hrebícek M, Mysková H, Dvoráková L, Berná L, Chrastina P, Asfaw B, Elleder M, Petermöller M, Mayrhofer H, Staudt M, Krägeloh-Mann I, Paton BC, Harzer K. Kuchar L, et al. Am J Med Genet A. 2009 Feb 15;149A(4):613-21. doi: 10.1002/ajmg.a.32712. Am J Med Genet A. 2009. PMID: 19267410 Free PMC article.

5

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

6

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.

7

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. JAMA Neurol. 2016 Sep 1;73(9):1133-40. doi: 10.1001/jamaneurol.2016.2067. JAMA Neurol. 2016. PMID: 27400410

8

Enzymatic characterization of novel arylsulfatase A variants using human arylsulfatase A-deficient immortalized mesenchymal stromal cells.

Böhringer J, Santer R, Schumacher N, Gieseke F, Cornils K, Pechan M, Kustermann-Kuhn B, Handgretinger R, Schöls L, Harzer K, Krägeloh-Mann I, Müller I. Böhringer J, et al. Hum Mutat. 2017 Nov;38(11):1511-1520. doi: 10.1002/humu.23306. Epub 2017 Sep 6. Hum Mutat. 2017. PMID: 28762252

9

Measurement of recombinant human arylsulfatase A and leukocyte sulfatase activities by analytical isotachophoresis.

Pajarola S, Weißenberg C, Baysal F, Bruchelt G, Krägeloh-Mann I, Böhringer J. Pajarola S, et al. J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Aug 15;1124:109-113. doi: 10.1016/j.jchromb.2019.05.035. Epub 2019 May 30. J Chromatogr B Analyt Technol Biomed Life Sci. 2019. PMID: 31195190

10

Early clinical course after hematopoietic stem cell transplantation in children with juvenile metachromatic leukodystrophy.

Beschle J, Döring M, Kehrer C, Raabe C, Bayha U, Strölin M, Böhringer J, Bevot A, Kaiser N, Bender B, Grimm A, Lang P, Müller I, Krägeloh-Mann I, Groeschel S. Beschle J, et al. Mol Cell Pediatr. 2020 Sep 3;7(1):12. doi: 10.1186/s40348-020-00103-7. Mol Cell Pediatr. 2020. PMID: 32910272 Free PMC article.

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