Ayse İpek Polat

Ayse İpek Polat

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Ayse İpek Polat

Ayse İpek Polat

Publications by authors named "Ayse İpek Polat"

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11Publications

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Identification of the largest homozygous glycine decarboxylase gene deletion in a Turkish infant.

Pediatr Neonatol 2018 12 31;59(6):632-633. Epub 2018 Jan 31.

Department of Pediatric Genetics, Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey.

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http://dx.doi.org/10.1016/j.pedneo.2018.01.011DOI Listing
December 2018

Importance of neurologic and cutaneous signs in the diagnosis of Schimke immuno-osseous dysplasia.

Turk J Pediatr 2015 Sep-Oct;57(5):509-13

Division of Pediatric Neurology, Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.

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September 2017

Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA.

Brain Dev 2017 Apr 19;39(4):361-364. Epub 2016 Nov 19.

Children's National Medical Center, Research Center for Genetic Medicine, 20010 Washington DC, USA; University Children's Hospital Cologne, 50931 Cologne, Germany; Center for Molecular Medicine, 50931 Cologne, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2016.11.002DOI Listing
April 2017

An infant with hypomotor seizures and cutaneous lesions.

Acta Neurol Belg 2015 Dec 31;115(4):687-8. Epub 2014 Dec 31.

Division of Child Neurology, Department of Pediatrics, School of Medicine, Dokuz Eylül University, İzmir, Turkey.

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http://dx.doi.org/10.1007/s13760-014-0414-8DOI Listing
December 2015

Parieto-occipital encephalomalacia in children; clinical and electrophysiological features of twenty-seven cases.

J Pediatr Neurosci 2015 Apr-Jun;10(2):103-7

Department of Pediatric Neurology, Dokuz Eylul University Medical School, 35340, Inciraltı, Izmir, Turkey.

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http://www.pediatricneurosciences.com/text.asp?2015/10/2/103
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http://dx.doi.org/10.4103/1817-1745.159187DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489049PMC
July 2015