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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Gokcem Yildiz

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Pediatrics|February 27, 2016

Congenital Mirror Movements in Gorlin Syndrome: A Case Report With DTI and Functional MRI FeaturesErdal Sag, Rahsan Gocmen, F Gokcem Yildiz, et al.

Acta Neurologica Belgica|December 30, 2016

New mutations and genotype-phenotype correlation in late-onset Pompe patientsCan Ebru Bekircan-Kurt, Hafize Nalan Güneş, F Gokcem Yildiz, et al.

Ideggyogyaszati Szemle|October 1, 2024

Recurrent simultaneous central nervous system demyelination with possible peripheral demyelination / nodopathy in a seronegative patientBerin Inan, Can Ebru Bekircan-Kurt, Fatma Gokcem Yildiz, et al.

Neuromuscular Disorders : NMD|January 4, 2022

The functional and structural evaluation of small fibers in asymptomatic carriers of TTR p.Val50Met (Val30Met) mutationCan Ebru Bekircan-Kurt, Ezgi Yilmaz, Doruk Arslan, et al.

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Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Pediatrics|February 27, 2016

Congenital Mirror Movements in Gorlin Syndrome: A Case Report With DTI and Functional MRI FeaturesErdal Sag, Rahsan Gocmen, F Gokcem Yildiz, et al.

Acta Neurologica Belgica|December 30, 2016

New mutations and genotype-phenotype correlation in late-onset Pompe patientsCan Ebru Bekircan-Kurt, Hafize Nalan Güneş, F Gokcem Yildiz, et al.

Ideggyogyaszati Szemle|October 1, 2024

Recurrent simultaneous central nervous system demyelination with possible peripheral demyelination / nodopathy in a seronegative patientBerin Inan, Can Ebru Bekircan-Kurt, Fatma Gokcem Yildiz, et al.

Neuromuscular Disorders : NMD|January 4, 2022

The functional and structural evaluation of small fibers in asymptomatic carriers of TTR p.Val50Met (Val30Met) mutationCan Ebru Bekircan-Kurt, Ezgi Yilmaz, Doruk Arslan, et al.

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