Schaper J - Search Results

1

Rituximab as a highly effective treatment in a female adolescent with severe multiple sclerosis.

Karenfort M, Kieseier BC, Tibussek D, Assmann B, Schaper J, Mayatepek E. Karenfort M, et al. Among authors: schaper j. Dev Med Child Neurol. 2009 Feb;51(2):159-61. doi: 10.1111/j.1469-8749.2008.03246.x. Dev Med Child Neurol. 2009. PMID: 19191848 Free article. No abstract available.

2

Clinical findings and a therapeutic trial in the first patient with beta-ureidopropionase deficiency.

Assmann B, Göhlich G, Baethmann M, Wevers RA, Van Gennip AH, Van Kuilenburg AB, Dietrich C, Wagner L, Rotteveel JJ, Schaper J, Mayatepek E, Hoffmann GF, Voit T. Assmann B, et al. Among authors: schaper j. Neuropediatrics. 2006 Feb;37(1):20-5. doi: 10.1055/s-2006-923933. Neuropediatrics. 2006. PMID: 16541364

3

Infantile onset neurofibromatosis type 2 presenting with peripheral facial palsy, skin patches, retinal hamartoma and foot drop.

Tibussek D, Hübsch S, Berger K, Schaper J, Rosenbaum T, Mayatepek E. Tibussek D, et al. Among authors: schaper j. Klin Padiatr. 2009 Jul-Aug;221(4):247-50. doi: 10.1055/s-0028-1112155. Epub 2009 Jul 23. Klin Padiatr. 2009. PMID: 19629903

4

Posterior reversible encephalopathy syndrome in early infancy.

Kummer S, Schaper J, Mayatepek E, Tibussek D. Kummer S, et al. Among authors: schaper j. Klin Padiatr. 2010 Jul;222(4):269-70. doi: 10.1055/s-0030-1249031. Epub 2010 May 31. Klin Padiatr. 2010. PMID: 20514606 No abstract available.

5

Paraneoplastic limbic encephalitis with SOX1 and PCA2 antibodies and relapsing neurological symptoms in an adolescent with Hodgkin lymphoma.

Kunstreich M, Kreth JH, Oommen PT, Schaper J, Karenfort M, Aktas O, Tibussek D, Distelmaier F, Borkhardt A, Kuhlen M. Kunstreich M, et al. Among authors: schaper j. Eur J Paediatr Neurol. 2017 Jul;21(4):661-665. doi: 10.1016/j.ejpn.2017.03.005. Epub 2017 Mar 27. Eur J Paediatr Neurol. 2017. PMID: 28389060

6

"Crying without tears" as an early diagnostic sign-post of triple A (Allgrove) syndrome: two case reports.

Tibussek D, Ghosh S, Huebner A, Schaper J, Mayatepek E, Koehler K. Tibussek D, et al. Among authors: schaper j. BMC Pediatr. 2018 Jan 15;18(1):6. doi: 10.1186/s12887-017-0973-y. BMC Pediatr. 2018. PMID: 29334914 Free PMC article.

7

Aplasia cutis congenita of the scalp: how much therapy is necessary in large defects?

Bernbeck B, Schwabe J, Groninger A, Schaper J, Messing-Jünger H, Mayatepek E, Rosenbaum T. Bernbeck B, et al. Among authors: schaper j. Acta Paediatr. 2005 Jun;94(6):758-60. doi: 10.1111/j.1651-2227.2005.tb01977.x. Acta Paediatr. 2005. PMID: 16188781

8

Persistent right umbilical vein associated with complex congenital cardiac malformation.

Hoehn T, Lueder M, Schmidt KG, Schaper J, Mayatepek E. Hoehn T, et al. Among authors: schaper j. Am J Perinatol. 2006 Apr;23(3):181-2. doi: 10.1055/s-2006-934096. Epub 2006 Mar 29. Am J Perinatol. 2006. PMID: 16586233

9

Diagnostic and therapeutic implications of neurological complications following paediatric haematopoietic stem cell transplantation.

Weber C, Schaper J, Tibussek D, Adams O, Mackenzie CR, Dilloo D, Meisel R, Göbel U, Laws HJ. Weber C, et al. Among authors: schaper j. Bone Marrow Transplant. 2008 Feb;41(3):253-9. doi: 10.1038/sj.bmt.1705905. Epub 2007 Nov 5. Bone Marrow Transplant. 2008. PMID: 17982498

10

Cat scratch disease--heterogeneous in clinical presentation: five unusual cases of an infection caused by Bartonella henselae.

Weinspach S, Tenenbaum T, Schönberger S, Schaper J, Engers R, Rueggeberg J, Mackenzie CR, Wolf A, Mayatepek E, Schroten H. Weinspach S, et al. Among authors: schaper j. Klin Padiatr. 2010 Mar;222(2):73-8. doi: 10.1055/s-0029-1233488. Epub 2009 Sep 29. Klin Padiatr. 2010. PMID: 19790029

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