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Journal of Child Neurology|June 26, 2003
Subacute sclerosing panencephalitis presenting with hemiparesis in childhood: case reportHamit Ozyürek, Aydan Değerliyurt, Guzide Turanli
The Turkish Journal of Pediatrics|February 28, 2020
Ataxia, tremor, intellectual disability: a case of STXBP1 encephalopathy with a new mutationAydan Değerliyurt, Gamze Gezgen Kesen, Serdar Ceylaner
Pediatric Neurology|April 22, 2009
Hypomelanosis of Ito and Sturge-Weber syndrome without facial nevus: an association or a new syndrome?Aydan Değerliyurt, Asli Kantar, Serdar Ceylaner, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Serological follow-up in juvenile myasthenia: clinical and acetylcholine receptor antibody status of patients followed for at least 2 yearsBanu Anlar, Nesrin Senbil, Gülşen Köse, et al.
Epilepsy & Behavior : E&B|May 21, 2014
Panayiotopoulos syndrome: a case series from TurkeyAydan Değerliyurt, Serap Teber, Omer Bektaş, et al.
The International Journal of Neuroscience|June 27, 2022
Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A geneAydan Değerliyurt, Nadide Başak Gülleroğlu, Ayşe Esin Kibar Gül
The Turkish Journal of Pediatrics|January 18, 2020
Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosisAydan Değerliyurt, Mehmet Gündüz, Serdar Ceylaner, et al.
The Turkish Journal of Pediatrics|March 7, 2012
Assessment of bone density in children with cerebral palsy by areal bone mineral density measurementIhsan Esen, Fatma Demirel, Alev Güven, et al.
Neurocase|August 16, 2021
Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutationAydan Değerliyurt, Özlem Yayıcı Köken, Neslihan Düzkale Teker, et al.
Turkish Neurosurgery|December 25, 2008
Posttraumatic infarction in the basal ganglia after a minor head injury in a child: case reportHakan Seçkin, Adnan Yalçin Demirci, Aydan Değerliyurt, et al.
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