Paketci C - Search Results

1

Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease.

Keller N, Paketci C, Altmueller J, Fuhrmann N, Wunderlich G, Schrank B, Unver O, Yilmaz S, Boostani R, Karimiani EG, Motameny S, Thiele H, Nürnberg P, Maroofian R, Yis U, Wirth B, Karakaya M. Keller N, et al. Among authors: paketci c. Hum Mutat. 2021 Apr;42(4):460-472. doi: 10.1002/humu.24181. Epub 2021 Mar 3. Hum Mutat. 2021. PMID: 33600046

2

Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.

Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S. Yiş U, et al. Among authors: paketci c. Acta Myol. 2018 Sep 1;37(3):210-220. eCollection 2018 Sep. Acta Myol. 2018. PMID: 30838351 Free PMC article.

3

Changes of primary headache related white matter lesions in pediatric patients.

Bayram E, Yiş U, Paketçi C, Okur D, Polat İ, Çakmakcı H, Hız S, Anlar B. Bayram E, et al. Among authors: paketci c. Turk J Pediatr. 2018;60(4):380-384. doi: 10.24953/turkjped.2018.04.004. Turk J Pediatr. 2018. PMID: 30859761 Free article.

Bayram E, Yis U, Paketci C, Okur D, Polat I, Cakmakci H, Hiz S, Anlar B. Changes of primary headache related white matter lesions in pediatric patients. ...

Bayram E, Yis U, Paketci C, Okur D, Polat I, Cakmakci H, Hiz S, Anlar B. Changes of primary headache related white matter lesi …

4

A Drug Reaction With Eosinophilia and Systemic Symptoms Syndrome Associated With Clobazam.

Manyas H, Paketci C, Okur D, Bayram E, Hiz S, Yis U. Manyas H, et al. Among authors: paketci c. Pediatr Emerg Care. 2020 Mar;36(3):e175. doi: 10.1097/PEC.0000000000001754. Pediatr Emerg Care. 2020. PMID: 30870346 No abstract available.

5

Biallelic variant in AGTPBP1 causes infantile lower motor neuron degeneration and cerebellar atrophy.

Karakaya M, Paketci C, Altmueller J, Thiele H, Hoelker I, Yis U, Wirth B. Karakaya M, et al. Among authors: paketci c. Am J Med Genet A. 2019 Aug;179(8):1580-1584. doi: 10.1002/ajmg.a.61198. Epub 2019 May 18. Am J Med Genet A. 2019. PMID: 31102495 Review.

6

Herpes simplex virus-1 as a rare etiology of isolated acute cerebellitis: case report and literature review.

Paketci C, Edem P, Okumus C, Sarioglu FC, Bayram E, Hiz S, Yis U. Paketci C, et al. J Neurovirol. 2020 Apr;26(2):270-272. doi: 10.1007/s13365-019-00802-6. Epub 2019 Sep 12. J Neurovirol. 2020. PMID: 31515702 Review.

7

Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature.

Paketçi C, Edem P, Okur D, Sarıoğlu FC, Güleryüz H, Bayram E, Kurul SH, Yiş U. Paketçi C, et al. Turk J Pediatr. 2020;62(1):119-124. doi: 10.24953/turkjped.2020.01.017. Turk J Pediatr. 2020. PMID: 32253876 Free article. Review.

8

Neuroprotective Effects of Lacosamide and Memantine on Hyperoxic Brain Injury in Rats.

Polat İ, Cilaker Mıcılı S, Çalışır M, Bayram E, Yiş U, Ayanoğlu M, Okur D, Edem P, Paketçi C, Tuğyan K, Yılmaz O, Hız Kurul S. Polat İ, et al. Among authors: paketci c. Neurochem Res. 2020 Aug;45(8):1920-1929. doi: 10.1007/s11064-020-03056-5. Epub 2020 May 22. Neurochem Res. 2020. PMID: 32444924

9

Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies.

Paketci C, Karakaya M, Edem P, Bayram E, Keller N, Daimagüler HS, Cirak S, Jordanova A, Hiz S, Wirth B, Yiş U. Paketci C, et al. Rev Neurol (Paris). 2020 Dec;176(10):846-855. doi: 10.1016/j.neurol.2020.04.016. Epub 2020 Jul 21. Rev Neurol (Paris). 2020. PMID: 32709422

10

Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey.

Ünver O, Türkdoğan D, Güler S, Kipoğlu O, Güngör M, Paketçi C, Çarman KB, Öztürk G, Genç HM, Özkan M, Dündar NO, Işık U, Karatoprak E, Kılıç B, Özkale M, Bayram E, Yarar C, Sözen HG, Sağer G, Güneş AS, Kahraman Koytak P, Karadağ Saygı E, Ekinci G, Saltık S, Çalışkan M, Kara B, Yiş U, Aydınlı N. Ünver O, et al. Among authors: paketci c. Eur J Paediatr Neurol. 2021 Jan;30:113-120. doi: 10.1016/j.ejpn.2020.10.011. Epub 2020 Nov 4. Eur J Paediatr Neurol. 2021. PMID: 33218883

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