Yasemin Akin

Kartal Dr. Lutfi Kirdar City Hospital
Kartal, Turkey

Last Updated: 09/26/2026

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Found 15 publications

A case of ocular flutter associated with sole anti-sulphatide antibody positivity: successful treatment with intravenous immunoglobulin in a pediatric patient.

A case of ocular flutter associated with sole anti-sulphatide antibody positivity: successful treatment with intravenous immunoglobulin in a pediatric patient.

Journal: Acta neurologica Belgica

Published: August 13, 2024

Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children.

Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children.

Journal: Scientific reports

Published: March 17, 2023

Novel guanosine diphosphate-mannose pyrophosphorylase A variant in an individual with achalasia, alacrima, and intellectual disability.

Novel guanosine diphosphate-mannose pyrophosphorylase A variant in an individual with achalasia, alacrima, and intellectual disability.

Journal: Clinical dysmorphology

Published: December 12, 2022

Infections in Pediatric Patients With Burn Injury: 6 Years of Experience.

Infections in Pediatric Patients With Burn Injury: 6 Years of Experience.

Journal: The Pediatric infectious disease journal

Published: December 08, 2022

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

Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease.

Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease.

Journal: Neurogenetics

Published: March 10, 2022

Intravenous Immunoglobulin Use in Hemolytic Disease Due to ABO Incompatibility to Prevent Exchange Transfusion.

Intravenous Immunoglobulin Use in Hemolytic Disease Due to ABO Incompatibility to Prevent Exchange Transfusion.

Journal: Frontiers in pediatrics

Published: January 28, 2022

Vaccine hesitancy and refusal among parents: An international ID-IRI survey.

Vaccine hesitancy and refusal among parents: An international ID-IRI survey.

Journal: Journal of infection in developing countries

Published: November 16, 2021

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

Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.

Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.

Journal: Clinical dysmorphology

Published: September 20, 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

Showing 1-12 of 15

Last Updated: 09/26/2026