Author

Ozlem Mihriban Herguner

Observed names: Hergüner, Özlem, Hergüner, Özlem M., O Herguner, O Hergüner, O. Herguner, O.M. Hergüner, OZLEM HERGÜNER, Ozlem Herguner, Ozlem Hergüner, Ozlem M Herguner, Ozlem M Hergüner, Ozlem M. Herguner, Ozlem M. Hergüner, OzlemM Herguner, OzlemM Hergüner, Ö Hergüner, Ö. Hergüner, Özlem HERGÜNER, Özlem Hergüner, Özlem M Hergüner, Özlem M. Hergüner, Özlem Mihriban Hergüner

Institution: Cukurova University

Observed institutions: Adıyaman University, Cukurova University, University of Nebraska Medical Center, Hacettepe University

OpenAlex ID: A5111471392

A phase 3 randomized placebo-controlled trial of tadalafil for Duchenne muscular dystrophy

2017 · Ronald G. Victor, H. Lee Sweeney, et al. · Neurology · 79

PDF

Factors Affecting Epilepsy Development and Epilepsy Prognosis in Cerebral Palsy

2011 · Gulen Gul Mert, Faruk Incecik, et al. · Pediatric Neurology · 55

Hypertonic saline treatment in children with cerebral edema.

2006 · D Yildizdas, S Altunbasak, et al. · PubMed · 46

Asymptomatic Hyperammonemia in Children Treated With Valproic Acid

1997 · Sakir Altunbsak, Vildan Baytok, et al. · Journal of Child Neurology · 41

Retrospective evaluation of interferon-beta treatment in subacute sclerosing panencephalitis

2004 · Banu Anlar, Omer Faruk Aydin, et al. · Clinical Therapeutics · 37

Neurofibromatosis type 1 and cardiac manifestations

2015 · Faruk Incecik, Özlem M Hergüner, et al. · Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology · 33

Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

2017 · Ünsal Yılmaz, Banu Anlar, et al. · European Journal of Paediatric Neurology · 32

A Turkish newborn infant with cerebellar agenesis/neonatal diabetes mellitus and PTF1A mutation.

2009 · E Tutak, M Satar, et al. · PubMed · 32

Electroconvulsive therapy for refractory status epilepticus in a child: A case report

2015 · Faruk Incecik, Ozden O. Horoz, et al. · Annals of Indian Academy of Neurology · 23

Serum and hair zinc levels in epileptic children taking valproic acid

1997 · Sakir Altunbaşak, Ferhat Biatmakoui, et al. · Biological Trace Element Research · 23

Risk Factors Predicting Refractoriness in Epileptic Children with Partial Seizures

2007 · Sakir Altunbasak, Ozlem Herguner, et al. · Journal of Child Neurology · 22

Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients

2019 · Gülen Gül Mert, Neslihan Özcan, et al. · Acta Neurologica Belgica · 21

Risk of recurrence after discontinuation of antiepileptic drug therapy in children with epilepsy

2014 · Faruk Incecik, OzlemM Herguner, et al. · Journal of Pediatric Neurosciences · 21

Late-onset Leigh syndrome due to NDUFV1 mutation in a 10-year-old boy initially presenting with ataxia

2018 · Faruk Incecik, OzlemM Herguner, et al. · Journal of Pediatric Neurosciences · 19

Acute rhabdomyolysis associated with levetiracetam therapy in a child

2015 · Faruk Incecik, Ozlem M. Herguner, et al. · Acta Neurologica Belgica · 18

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience

2022 · Serap Bilge, Gülen Gül Mert, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 17

PDF

Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin

2015 · Ozden O. Horoz, Neslihan O. Mungan, et al. · Journal of Pediatric Endocrinology and Metabolism · 16

Prognosis of Patients With Seizures Occurring in the First 2 Years

2007 · Şakir Altunbaşak, Faruk Incecik, et al. · Journal of Child Neurology · 15

Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets

2024 · Ben Weisburd, Rakshya Sharma, et al. · Genetics in Medicine · 13

PDF

Factors affecting epilepsy prognosis in patients with tuberous sclerosis

2019 · Gülen Gül Mert, Şakir Altunbaşak, et al. · Child s Nervous System · 13

Four Gaucher disease type II patients with three novel mutations: a single centre experience from Turkey

2018 · Fatma Derya Bulut, Deniz Kör, et al. · Metabolic Brain Disease · 13

Limbic encephalitis with antibodies to glutamic acid decarboxylase presenting with brainstem symptoms

2015 · Faruk Incecik, OzlemM Hergüner, et al. · Annals of Indian Academy of Neurology · 13

Multiple sulfatase deficiency: A case series of four children

2013 · Faruk Incecik, MehmetN Ozbek, et al. · Annals of Indian Academy of Neurology · 13

Psoriasiform Drug Eruption Associated with Sodium Valproate

2013 · Gulen Gul Mert, Faruk Incecik, et al. · Case Reports in Pediatrics · 13

PDF

A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction

2020 · Faruk Ekinci, Riza Dincer Yildizdas, et al. · European Journal of Medical Genetics · 12

Works count: 104

Citation count: 875

H-index: 16

I10-index: 32