Gunes G. Sager-Safiye

Ihlas Marmara Evleri - I. Kisim, Turkey

Last Updated: 09/26/2026

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Found 9 publications

Cardiac safety of low-dose ACTH therapy in infantile spasms: Evidence from electrocardiography and advanced echocardiography.

Cardiac safety of low-dose ACTH therapy in infantile spasms: Evidence from electrocardiography and advanced echocardiography.

Journal: Seizure

Published: August 19, 2025

Novel compound heterozygous P4HTM variants in a girl with developmental and epileptic encephalopathy: First case report of P4HTM variant-associated epileptic encephalopathy.

Novel compound heterozygous P4HTM variants in a girl with developmental and epileptic encephalopathy: First case report of P4HTM variant-associated epileptic encephalopathy.

Journal: Seizure

Published: August 18, 2024

Evaluation of long-term neurocognitive functions in patients with epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)/epileptic encephalopathy with spike-and-wave activation in sleep (EE-SWAS).

Evaluation of long-term neurocognitive functions in patients with epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)/epileptic encephalopathy with spike-and-wave activation in sleep (EE-SWAS).

Journal: Neurophysiologie clinique = Clinical neurophysiology

Published: November 13, 2022

Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood.

Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: August 26, 2022

A novel de novo TET3 loss-of-function variant in a Turkish boy presenting with neurodevelopmental delay and electrical status epilepticus during slow-wave sleep.

A novel de novo TET3 loss-of-function variant in a Turkish boy presenting with neurodevelopmental delay and electrical status epilepticus during slow-wave sleep.

Journal: Brain & development

Published: February 22, 2022

Auditory phoneme discrimination, articulation, and language disorders in patients with genetic epilepsy with febrile seizures plus: A case-control study.

Auditory phoneme discrimination, articulation, and language disorders in patients with genetic epilepsy with febrile seizures plus: A case-control study.

Journal: Epilepsy & behavior : E&B

Published: October 31, 2021

Neuropsychiatric comorbidities in genetic/idiopathic generalized epilepsies and their effects on psychosocial outcomes.

Neuropsychiatric comorbidities in genetic/idiopathic generalized epilepsies and their effects on psychosocial outcomes.

Journal: Epilepsy & behavior : E&B

Published: June 30, 2021

Correction to: HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

Correction to: HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

Journal: Acta neurologica Belgica

Published: May 07, 2021

HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

Journal: Acta neurologica Belgica

Published: December 11, 2020

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Last Updated: 09/26/2026