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Adnan Yuksel

Showing results (1-10 of 32) with videos related to

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Klinische Padiatrie|June 16, 2026
Ayhan Yaman, Abdullah Sert, Adnan Yuksel
Journal of Child Neurology|January 27, 2009
Magnetic resonance imaging, magnetic resonance spectroscopy, and facial dysmorphism in a case of Lowe syndrome with novel OCRL1 gene mutationAdnan Yuksel, Ender Karaca, M Sait Albayram
American Journal of Medical Genetics. Part A|December 21, 2013
Report of a patient with Temple-Baraitser syndromeGozde Yesil, Serhat Guler, Adnan Yuksel, et al.
Acta Biochimica Polonica|September 15, 2020
New mutations in KCNT2 gene causing early infantile epileptic encephalopathy type 57: Case study and literature reviewMeryem Alagoz, Nasim Kherad, Sureyya Bozkurt, et al.
Journal of Molecular Neuroscience : MN|June 15, 2020
The New CIC Mutation Associates with Mental Retardation and Severity of Seizure in Turkish Child with a Rare Class I Glucose-6-Phosphate Dehydrogenase DeficiencyMeryem Alagoz, Nasim Kherad, Ezgi Gunger, et al.
Experimental and Therapeutic Medicine|April 30, 2020
A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencingMeryem Alagoz, Nasim Kherad, Selda Turkmen, et al.
Epilepsy Research|October 30, 2012
Deficiency of selenium and zinc as a causative factor for idiopathic intractable epilepsyMehmet Seven, Sarenur Y Basaran, Mujgan Cengiz, et al.
Molecular Diagnosis & Therapy|December 17, 2013
The effect of genetic polymorphisms of cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on drug-resistant epilepsy in Turkish childrenMehmet Seven, Bahadir Batar, Selin Unal, et al.
Archives of Medical Science : AMS|May 15, 2013
Involvement of the corpus callosum splenium in a case with SSPE: magnetic resonance spectroscopy findingsAlpay Alkan, Rasul Sharifov, Serhat Guler, et al.
Molecular Biology Reports|November 12, 2013
The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish childrenMehmet Seven, Bahadir Batar, Selin Unal, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Klinische Padiatrie|June 16, 2026
Ayhan Yaman, Abdullah Sert, Adnan Yuksel
Journal of Child Neurology|January 27, 2009
Magnetic resonance imaging, magnetic resonance spectroscopy, and facial dysmorphism in a case of Lowe syndrome with novel OCRL1 gene mutationAdnan Yuksel, Ender Karaca, M Sait Albayram
American Journal of Medical Genetics. Part A|December 21, 2013
Report of a patient with Temple-Baraitser syndromeGozde Yesil, Serhat Guler, Adnan Yuksel, et al.
Acta Biochimica Polonica|September 15, 2020
New mutations in KCNT2 gene causing early infantile epileptic encephalopathy type 57: Case study and literature reviewMeryem Alagoz, Nasim Kherad, Sureyya Bozkurt, et al.
Journal of Molecular Neuroscience : MN|June 15, 2020
The New CIC Mutation Associates with Mental Retardation and Severity of Seizure in Turkish Child with a Rare Class I Glucose-6-Phosphate Dehydrogenase DeficiencyMeryem Alagoz, Nasim Kherad, Ezgi Gunger, et al.
Experimental and Therapeutic Medicine|April 30, 2020
A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencingMeryem Alagoz, Nasim Kherad, Selda Turkmen, et al.
Epilepsy Research|October 30, 2012
Deficiency of selenium and zinc as a causative factor for idiopathic intractable epilepsyMehmet Seven, Sarenur Y Basaran, Mujgan Cengiz, et al.
Molecular Diagnosis & Therapy|December 17, 2013
The effect of genetic polymorphisms of cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on drug-resistant epilepsy in Turkish childrenMehmet Seven, Bahadir Batar, Selin Unal, et al.
Archives of Medical Science : AMS|May 15, 2013
Involvement of the corpus callosum splenium in a case with SSPE: magnetic resonance spectroscopy findingsAlpay Alkan, Rasul Sharifov, Serhat Guler, et al.
Molecular Biology Reports|November 12, 2013
The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish childrenMehmet Seven, Bahadir Batar, Selin Unal, et al.
Pageof 4