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Faruk Incecik

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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 22, 2023

Posttraumatic epilepsy in critically ill children with traumatic brain injuryNazan Ulgen Tekerek, Oguz Dursun, Nazik Asilioglu Yener, et al.

Cerebellum (London, England)|April 15, 2024

Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National StudyDilek Cavusoglu, Gulten Ozturk, Dilsad Turkdogan, et al.

Elife|May 31, 2015

Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndromeSusanne Roosing, Matan Hofree, Sehyun Kim, et al.

Nature Genetics|July 18, 2018

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, et al.

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Search research articles

Showing results (81-90 of 84) with videos related to

Sort By:

Pageof 9

You have reached the last page of results.This site can display upto 84 results.

Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 22, 2023

Posttraumatic epilepsy in critically ill children with traumatic brain injuryNazan Ulgen Tekerek, Oguz Dursun, Nazik Asilioglu Yener, et al.

Cerebellum (London, England)|April 15, 2024

Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National StudyDilek Cavusoglu, Gulten Ozturk, Dilsad Turkdogan, et al.

Elife|May 31, 2015

Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndromeSusanne Roosing, Matan Hofree, Sehyun Kim, et al.

Nature Genetics|July 18, 2018

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, et al.

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