Temucin C - Search Results

1

Early-onset chronic axonal neuropathy, strokes, and hemolysis: inherited CD59 deficiency.

Haliloglu G, Maluenda J, Sayinbatur B, Aumont C, Temucin C, Tavil B, Cetin M, Oguz KK, Gut I, Picard V, Melki J, Topaloglu H. Haliloglu G, et al. Among authors: temucin c. Neurology. 2015 Mar 24;84(12):1220-4. doi: 10.1212/WNL.0000000000001391. Epub 2015 Feb 25. Neurology. 2015. PMID: 25716358

2

Peripheral neuropathy in a patient with D-2-hydroxyglutaric aciduria.

Haliloglu G, Temucin CM, Oguz KK, Celiker A, Coskun T, Sass JO, Fischer J, Topcu M. Haliloglu G, et al. Among authors: temucin cm. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S21-5. doi: 10.1007/s10545-009-0933-2. Epub 2009 Jan 26. J Inherit Metab Dis. 2009. PMID: 19169842

3

Identification of a novel Twinkle mutation in a family with infantile onset spinocerebellar ataxia by whole exome sequencing.

Dündar H, Ozgül RK, Yalnızoğlu D, Erdem S, Oğuz KK, Tuncel D, Temuçin CM, Dursun A. Dündar H, et al. Pediatr Neurol. 2012 Mar;46(3):172-7. doi: 10.1016/j.pediatrneurol.2011.12.006. Pediatr Neurol. 2012. PMID: 22353293

4

Tract-based spatial statistics of diffusion tensor imaging in hereditary spastic paraplegia with thin corpus callosum reveals widespread white matter changes.

Oğuz KK, Sanverdi E, Has A, Temuçin Ç, Türk S, Doerschner K. Oğuz KK, et al. Among authors: temucin c. Diagn Interv Radiol. 2013 May-Jun;19(3):181-6. doi: 10.5152/dir.2013.046. Diagn Interv Radiol. 2013. PMID: 23302284 Free article.

5

Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Oguz KK, Haliloglu G, Temucin C, Gocmen R, Has AC, Doerschner K, Dolgun A, Alikasifoglu M. Oguz KK, et al. Among authors: temucin c. AJNR Am J Neuroradiol. 2013 Oct;34(10):1952-7. doi: 10.3174/ajnr.A3488. Epub 2013 Apr 18. AJNR Am J Neuroradiol. 2013. PMID: 23598833 Free PMC article.

6

Fulminant Central Plus Peripheral Nervous System Demyelination without Antibodies to Neurofascin.

Vural A, Göçmen R, Kurne AT, Oğuz KK, Temuçin ÇM, Tan E, Karabudak R, Meinl E, Erdem Özdamar S. Vural A, et al. Can J Neurol Sci. 2016 Jan;43(1):149-56. doi: 10.1017/cjn.2015.238. Epub 2015 Aug 14. Can J Neurol Sci. 2016. PMID: 26271726

7

Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defects.

Haliloglu G, Becker K, Temucin C, Talim B, Küçükşahin N, Pergande M, Motameny S, Nürnberg P, Aydingoz U, Topaloglu H, Cirak S. Haliloglu G, et al. Among authors: temucin c. J Hum Genet. 2017 Apr;62(4):497-501. doi: 10.1038/jhg.2016.153. Epub 2016 Dec 15. J Hum Genet. 2017. PMID: 27974811

8

Neonatal-Onset Recurrent Guillain-Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency.

Ardicli D, Taskiran EZ, Kosukcu C, Temucin C, Oguz KK, Haliloglu G, Alikasifoglu M, Topaloglu H. Ardicli D, et al. Among authors: temucin c. Neuropediatrics. 2017 Dec;48(6):477-481. doi: 10.1055/s-0037-1604483. Epub 2017 Aug 11. Neuropediatrics. 2017. PMID: 28800659 No abstract available.

9

Tracking Pain in Resting State Networks in Patients with Hereditary and Diabetic Neuropathy.

Sağ AT, Has AC, Öztekin N, Temuçin ÇM, Oğuz KK. Sağ AT, et al. Noro Psikiyatr Ars. 2018 Jul 9;56(2):92-98. doi: 10.5152/npa.2017.22660. eCollection 2019 Jun. Noro Psikiyatr Ars. 2018. PMID: 31223239 Free PMC article.

10

Isolated spinal cord granulomatous angiitis: a case report and review of the literature.

Ayvacıoğlu Cagan C, Temucin CM, Arslan D, Gocmen R, Bolek EC, Söylemezoğlu F, Topçuoğlu MA. Ayvacıoğlu Cagan C, et al. Among authors: temucin cm. J Neurol. 2022 Jun;269(6):3175-3179. doi: 10.1007/s00415-021-10912-z. Epub 2022 Jan 9. J Neurol. 2022. PMID: 34999955 Review.

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