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Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort.
Published in:
Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-18
By:
- Kehrer, Christiane;
- Groeschel, Samuel;
- Kustermann-Kuhn, Birgit;
- Bürger, Friederike;
- Köhler, Wolfgang;
- Kohlschütter, Alfried;
- Bley, Annette;
- Steinfeld, Robert;
- Gieselmann, Volkmar;
- Krägeloh-Mann, Ingeborg
Publication type:
Article
Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort.
Published in:
2014
By:
- Kehrer, Christiane;
- Groeschel, Samuel;
- Kustermann-Kuhn, Birgit;
- Bürger, Friederike;
- Köhler, Wolfgang;
- Kohlschütter, Alfried;
- Bley, Annette;
- Steinfeld, Robert;
- Gieselmann, Volkmar;
- Krägeloh-Mann, Ingeborg;
- German LEUKONET
Publication type:
journal article
Early clinical course after hematopoietic stem cell transplantation in children with juvenile metachromatic leukodystrophy.
Published in:
Molecular & Cellular Pediatrics, 2020, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40348-020-00103-7
By:
- Beschle, Judith;
- Döring, Michaela;
- Kehrer, Christiane;
- Raabe, Christa;
- Bayha, Ute;
- Strölin, Manuel;
- Böhringer, Judith;
- Bevot, Andrea;
- Kaiser, Nadja;
- Bender, Benjamin;
- Grimm, Alexander;
- Lang, Peter;
- Müller, Ingo;
- Krägeloh-Mann, Ingeborg;
- Groeschel, Samuel
Publication type:
Article
Phenotypic variation between siblings with Metachromatic Leukodystrophy.
Published in:
2019
By:
- Elgün, Saskia;
- Waibel, Jakob;
- Kehrer, Christiane;
- van Rappard, Diane;
- Böhringer, Judith;
- Beck-Wödl, Stefanie;
- Just, Jennifer;
- Schöls, Ludger;
- Wolf, Nicole;
- Krägeloh-Mann, Ingeborg;
- Groeschel, Samuel
Publication type:
journal article
Enlargement of peripheral nerves in Krabbe disease: The diagnostic value of nerve ultrasound.
Published in:
2020
By:
- Küpper, Hanna;
- Kaiser, Nadja;
- Winter, Natalie;
- Kehrer, Christiane;
- Groeschel, Samuel;
- Bevot, Andrea;
- Nägele, Thomas;
- Krägeloh‐Mann, Ingeborg;
- Grimm, Alexander;
- Krägeloh-Mann, Ingeborg
Publication type:
journal article
The natural course of gross motor deterioration in metachromatic leukodystrophy.
Published in:
Developmental Medicine & Child Neurology, 2011, v. 53, n. 9, p. 850, doi. 10.1111/j.1469-8749.2011.04028.x
By:
- KEHRER, CHRISTIANE;
- BLUMENSTOCK, GUNNAR;
- GIESELMANN, VOLKMAR;
- KRÄGELOH-MANN, INGEBORG
Publication type:
Article
Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy.
Published in:
Developmental Medicine & Child Neurology, 2011, v. 53, n. 2, p. 156, doi. 10.1111/j.1469-8749.2010.03821.x
By:
- KEHRER, CHRISTIANE;
- BLUMENSTOCK, GUNNAR;
- RAABE, CHRISTA;
- KRÄGELOH-MANN, INGEBORG
Publication type:
Article
Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort.
Published in:
Journal of Inherited Metabolic Disease Reports, 2021, v. 58, n. 1, p. 80, doi. 10.1002/jmd2.12189
By:
- Beck‐Wödl, Stefanie;
- Kehrer, Christiane;
- Harzer, Klaus;
- Haack, Tobias B.;
- Bürger, Friederike;
- Haas, Dorothea;
- Rieß, Angelika;
- Groeschel, Samuel;
- Krägeloh‐Mann, Ingeborg;
- Böhringer, Judith
Publication type:
Article
Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients.
Published in:
JAMA Neurology, 2016, v. 73, n. 9, p. 1133, doi. 10.1001/jamaneurol.2016.2067
By:
- Groeschel, Samuel;
- Kühl, Jörn-Sven;
- Bley, Annette E.;
- Kehrer, Christiane;
- Weschke, Bernhard;
- Döring, Michaela;
- Böhringer, Judith;
- Schrum, Johanna;
- Santer, René;
- Kohlschütter, Alfried;
- Krägeloh-Mann, Ingeborg;
- Müller, Ingo
Publication type:
Article
Demyelination load as predictor for disease progression in juvenile metachromatic leukodystrophy.
Published in:
Annals of Clinical & Translational Neurology, 2017, v. 4, n. 6, p. 403, doi. 10.1002/acn3.420
By:
- Strölin, Manuel;
- Krägeloh‐Mann, Ingeborg;
- Kehrer, Christiane;
- Wilke, Marko;
- Groeschel, Samuel
Publication type:
Article
The impact of severe rare chronic neurological disease in childhood on the quality of life of families-a study on MLD and PCH2.
Published in:
2021
By:
- Ammann-Schnell, Louisa;
- Groeschel, Samuel;
- Kehrer, Christiane;
- Frölich, Saskia;
- Krägeloh-Mann, Ingeborg
Publication type:
journal article
Natural history of Krabbe disease - a nationwide study in Germany using clinical and MRI data.
Published in:
2020
By:
- Krieg, Sarah Isabel;
- Krägeloh-Mann, Ingeborg;
- Groeschel, Samuel;
- Beck-Wödl, Stefanie;
- Husain, Ralf A.;
- Schöls, Ludger;
- Kehrer, Christiane
Publication type:
journal article
Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease.
Published in:
Journal of Inherited Metabolic Disease, 2020, v. 43, n. 6, p. 1298, doi. 10.1002/jimd.12298
By:
- Adang, Laura A.;
- Schlotawa, Lars;
- Groeschel, Samuel;
- Kehrer, Christiane;
- Harzer, Klaus;
- Staretz‐Chacham, Orna;
- Silva, Thiago Oliveira;
- Schwartz, Ida Vanessa D.;
- Gärtner, Jutta;
- De Castro, Mauricio;
- Costin, Carrie;
- Montgomery, Esperanza Font;
- Dierks, Thomas;
- Radhakrishnan, Karthikeyan;
- Ahrens‐Nicklas, Rebecca C.
Publication type:
Article
Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course.
Published in:
Journal of Inherited Metabolic Disease, 2011, v. 34, n. 5, p. 1095, doi. 10.1007/s10545-011-9361-1
By:
- Groeschel, Samuel;
- Kehrer, Christiane;
- Engel, Corinna;
- í Dali, Christine;
- Bley, Annette;
- Steinfeld, Robert;
- Grodd, Wolfgang;
- Krägeloh-Mann, Ingeborg
Publication type:
Article

Found: 14