Gocmen R - Search Results

1

Acute Cerebellitis or Postinfectious Cerebellar Ataxia? Clinical and Imaging Features in Acute Cerebellitis.

Yildirim M, Gocmen R, Konuskan B, Parlak S, Yalnizoglu D, Anlar B. Yildirim M, et al. Among authors: gocmen r. J Child Neurol. 2020 May;35(6):380-388. doi: 10.1177/0883073820901407. Epub 2020 Mar 12. J Child Neurol. 2020. PMID: 32160830

2

Cerebral Hyperperfusion in a Child with Stroke-Like Migraine Attacks after Radiation Therapy Syndrome.

Ardicli D, Gocmen R, Oguz KK, Varan A, Yalnizoglu D. Ardicli D, et al. Among authors: gocmen r. Neuropediatrics. 2016 Aug;47(4):259-62. doi: 10.1055/s-0036-1582246. Epub 2016 Apr 22. Neuropediatrics. 2016. PMID: 27104483

3

Reversible Hypertensive Myelopathy-The Spinal Cord Variant of Posterior Reversible Encephalopathy Syndrome.

Gocmen R, Ardicli D, Erarslan Y, Duzova A, Anlar B. Gocmen R, et al. Neuropediatrics. 2017 Apr;48(2):115-118. doi: 10.1055/s-0036-1597612. Epub 2016 Dec 29. Neuropediatrics. 2017. PMID: 28033622

4

Clinical presentation of anti-N-methyl-d-aspartate receptor and anti-voltage-gated potassium channel complex antibodies in children: A series of 24 cases.

Konuskan B, Yildirim M, Topaloglu H, Erol I, Oztoprak U, Tan H, Gocmen R, Anlar B. Konuskan B, et al. Among authors: gocmen r. Eur J Paediatr Neurol. 2018 Jan;22(1):135-142. doi: 10.1016/j.ejpn.2017.10.009. Epub 2017 Nov 7. Eur J Paediatr Neurol. 2018. PMID: 29153996

5

Neurologic Involvement in Primary Immunodeficiency Disorders.

Yildirim M, Ayvaz DC, Konuskan B, Gocmen R, Tezcan I, Topcu M, Topaloglu H, Anlar B. Yildirim M, et al. Among authors: gocmen r. J Child Neurol. 2018 Apr;33(5):320-328. doi: 10.1177/0883073817754176. Epub 2018 Feb 8. J Child Neurol. 2018. PMID: 29421957

6

Retrospective analysis of children with myelin oligodendrocyte glycoprotein antibody-related disorders.

Konuskan B, Yildirim M, Gocmen R, Okur TD, Polat I, Kilic H, Saltik S, Ozturk Z, Gucuyener K, Altunbasak S, Celik T, Kose G, Yilmaz A, Komur M, Kayilioglu H, Anlar B. Konuskan B, et al. Among authors: gocmen r. Mult Scler Relat Disord. 2018 Nov;26:1-7. doi: 10.1016/j.msard.2018.07.022. Epub 2018 Sep 10. Mult Scler Relat Disord. 2018. PMID: 30212767

7

Concurrence of juvenile idiopathic arthritis and primary demyelinating disease in a young child.

Coşkun AN, Günbey C, Göçmen R, Turan KE, Sönmez HE, Özen S, Anlar B. Coşkun AN, et al. Among authors: gocmen r. Mult Scler Relat Disord. 2019 Jan;27:20-22. doi: 10.1016/j.msard.2018.10.002. Epub 2018 Oct 3. Mult Scler Relat Disord. 2019. PMID: 30300848

8

Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation.

Eroglu FK, Ozaltin F, Gönç N, Nalçacıoğlu H, Özçakar ZB, Yalnızoğlu D, Güçer Ş, Orhan D, Eminoğlu FT, Göçmen R, Alikaşifoğlu A, Topaloğlu R, Düzova A. Eroglu FK, et al. Among authors: gocmen r. Pediatr Neurol. 2018 Nov;88:71-74. doi: 10.1016/j.pediatrneurol.2018.07.008. Epub 2018 Jul 27. Pediatr Neurol. 2018. PMID: 30337132

9

Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' [Pediatric Neurology 88 (2018) 71-74].

Eroglu FK, Ozaltin F, Gönç N, Nalçacıoğlu H, Özçakar ZB, Yalnızoğlu D, Güçer Ş, Orhan D, Eminoğlu FT, Göçmen R, Alikaşifoğlu A, Topaloğlu R, Düzova A. Eroglu FK, et al. Among authors: gocmen r. Pediatr Neurol. 2019 May;94:84. doi: 10.1016/j.pediatrneurol.2018.12.017. Epub 2019 Feb 15. Pediatr Neurol. 2019. PMID: 30777605 No abstract available.

10

Diagnostic challenge: A case of late-onset spinal form cerebrotendinous xanthomatosis.

Mutlu D, Tuncer A, Gocmen R, Yalcin-Cakmakli G, Saygı S, Elibol B. Mutlu D, et al. Among authors: gocmen r. Neurology. 2019 Feb 26;92(9):438-439. doi: 10.1212/WNL.0000000000007015. Neurology. 2019. PMID: 30804055 No abstract available.

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