Mayatepek E - 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: mayatepek e. 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

Glucose transporter type 1 deficiency syndrome with carbohydrate-responsive symptoms but without epilepsy.

Koy A, Assmann B, Klepper J, Mayatepek E. Koy A, et al. Among authors: mayatepek e. Dev Med Child Neurol. 2011 Dec;53(12):1154-6. doi: 10.1111/j.1469-8749.2011.04082.x. Epub 2011 Aug 12. Dev Med Child Neurol. 2011. PMID: 21838819 Free article.

3

Hereditary sensory and autonomic neuropathy with autonomic crises: a Turkish variant of familial dysautonomia?

Koy A, Freynhagen R, Mayatepek E, Tibussek D. Koy A, et al. Among authors: mayatepek e. J Child Neurol. 2012 Feb;27(2):191-6. doi: 10.1177/0883073811416664. Epub 2011 Dec 2. J Child Neurol. 2012. PMID: 22140130

4

Clinical reasoning: shuddering attacks in infancy.

Tibussek D, Karenfort M, Mayatepek E, Assmann B. Tibussek D, et al. Among authors: mayatepek e. Neurology. 2008 Mar 25;70(13):e38-41. doi: 10.1212/01.wnl.0000306698.75592.6e. Neurology. 2008. PMID: 18362276 No abstract available.

5

Posterior reversible encephalopathy syndrome in early infancy.

Kummer S, Schaper J, Mayatepek E, Tibussek D. Kummer S, et al. Among authors: mayatepek e. 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.

6

Probable pseudotumor cerebri complex in 25 children. Further support of a concept.

Tibussek D, Distelmaier F, Karenfort M, Harmsen S, Klee D, Mayatepek E. Tibussek D, et al. Among authors: mayatepek e. Eur J Paediatr Neurol. 2017 Mar;21(2):280-285. doi: 10.1016/j.ejpn.2016.10.004. Epub 2016 Oct 27. Eur J Paediatr Neurol. 2017. PMID: 27825557

7

Brown-Vialetto-Van Laere syndrome: a riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene.

Koy A, Pillekamp F, Hoehn T, Waterham H, Klee D, Mayatepek E, Assmann B. Koy A, et al. Among authors: mayatepek e. Pediatr Neurol. 2012 Jun;46(6):407-9. doi: 10.1016/j.pediatrneurol.2012.03.008. Pediatr Neurol. 2012. PMID: 22633641

8

Neuromyelitis optica and pregnancy during therapeutic B cell depletion: infant exposure to anti-AQP4 antibody and prevention of rebound relapses with low-dose rituximab postpartum.

Ringelstein M, Harmel J, Distelmaier F, Ingwersen J, Menge T, Hellwig K, Kieseier B, Mayatepek E, Hartung HP, Kuempfel T, Aktas O. Ringelstein M, et al. Among authors: mayatepek e. Mult Scler. 2013 Oct;19(11):1544-7. doi: 10.1177/1352458513498125. Epub 2013 Jul 25. Mult Scler. 2013. PMID: 23886825

9

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: mayatepek e. Klin Padiatr. 2009 Jul-Aug;221(4):247-50. doi: 10.1055/s-0028-1112155. Epub 2009 Jul 23. Klin Padiatr. 2009. PMID: 19629903

10

Presumed Arterial Gas Embolism After Breath-Hold Diving in Shallow Water.

Harmsen S, Schramm D, Karenfort M, Christaras A, Euler M, Mayatepek E, Tibussek D. Harmsen S, et al. Among authors: mayatepek e. Pediatrics. 2015 Sep;136(3):e687-90. doi: 10.1542/peds.2014-4095. Epub 2015 Aug 10. Pediatrics. 2015. PMID: 26260715

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