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Fesih Aktar

Showing results (21-30 of 31) with videos related to

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Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|December 25, 2015
Urinary Kidney Injury Molecules in Children with Iron-Deficiency AnemiaAli Güneş, Aydın Ece, Fesih Aktar, et al.
Biomed Research International|March 17, 2016
Determining the Independent Risk Factors and Mortality Rate of Nosocomial Infections in Pediatric PatientsFesih Aktar, Recep Tekin, Ali Güneş, et al.
Italian Journal of Pediatrics|April 19, 2015
Assessment of epicardial adipose tissue thickness and the mean platelet volume in children with familial Mediterranean feverÜnal Uluca, Fikri Demir, Aydın Ece, et al.
Italian Journal of Pediatrics|January 13, 2016
Diagnostic role of inflammatory markers in pediatric Brucella arthritisFesih Aktar, Recep Tekin, Mehmet Selçuk Bektaş, et al.
Journal of Infection in Developing Countries|November 4, 2022
Evaluation of inflammatory and hematological parameters in patients diagnosed with COVID-19Çiğdem Mermutluoğlu, Recep Dursun, Fesih Aktar, et al.
Journal of Human Genetics|August 9, 2020
METAP1 mutation is a novel candidate for autosomal recessive intellectual disabilityAhmet Okay Caglayan, Fesih Aktar, Kaya Bilguvar, et al.
Neuropsychiatric Disease and Treatment|May 5, 2016
Protective effects of l-glutamine against toxicity of deltamethrin in the cerebral tissueSefer Varol, Hasan Hüseyin Özdemir, Mehmet Uğur Çevik, et al.
Hepatology Forum|May 30, 2023
First year real life experience with tenofovir alafenamide fumarate: The pythagorean cohortOmer Karasahin, Irem Akdemir Kalkan, Tuba Dal, et al.
Pediatric Neurology|December 3, 2014
Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutationsAhmet Okay Caglayan, Jacob F Baranoski, Fesih Aktar, et al.
Cell|April 29, 2014
CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegenerationAshleigh E Schaffer, Veerle R C Eggens, Ahmet Okay Caglayan, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|December 25, 2015
Urinary Kidney Injury Molecules in Children with Iron-Deficiency AnemiaAli Güneş, Aydın Ece, Fesih Aktar, et al.
Biomed Research International|March 17, 2016
Determining the Independent Risk Factors and Mortality Rate of Nosocomial Infections in Pediatric PatientsFesih Aktar, Recep Tekin, Ali Güneş, et al.
Italian Journal of Pediatrics|April 19, 2015
Assessment of epicardial adipose tissue thickness and the mean platelet volume in children with familial Mediterranean feverÜnal Uluca, Fikri Demir, Aydın Ece, et al.
Italian Journal of Pediatrics|January 13, 2016
Diagnostic role of inflammatory markers in pediatric Brucella arthritisFesih Aktar, Recep Tekin, Mehmet Selçuk Bektaş, et al.
Journal of Infection in Developing Countries|November 4, 2022
Evaluation of inflammatory and hematological parameters in patients diagnosed with COVID-19Çiğdem Mermutluoğlu, Recep Dursun, Fesih Aktar, et al.
Journal of Human Genetics|August 9, 2020
METAP1 mutation is a novel candidate for autosomal recessive intellectual disabilityAhmet Okay Caglayan, Fesih Aktar, Kaya Bilguvar, et al.
Neuropsychiatric Disease and Treatment|May 5, 2016
Protective effects of l-glutamine against toxicity of deltamethrin in the cerebral tissueSefer Varol, Hasan Hüseyin Özdemir, Mehmet Uğur Çevik, et al.
Hepatology Forum|May 30, 2023
First year real life experience with tenofovir alafenamide fumarate: The pythagorean cohortOmer Karasahin, Irem Akdemir Kalkan, Tuba Dal, et al.
Pediatric Neurology|December 3, 2014
Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutationsAhmet Okay Caglayan, Jacob F Baranoski, Fesih Aktar, et al.
Cell|April 29, 2014
CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegenerationAshleigh E Schaffer, Veerle R C Eggens, Ahmet Okay Caglayan, et al.
Pageof 4