H. Per

H. Per, M. Canpolat, D. Yalnızoǧlu, 2022, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Neurological features and management of Wilson disease in children: an evaluation of 12 cases.

H. Per, M. Canpolat, S. Kumandas, 2016, Turk pediatri arsivi.

Magnetic resonance imaging of childhood Guillain–Barre syndrome

H. Per, S. Kumandas, A. Coskun, 2010, Child's Nervous System.

Analysis of genotype-phenotype correlation in Walker-Warburg syndrome with a novel CRPPA mutation in different clinical manifestations

H. Per, A. Caglayan, N. Bayram, 2021, European journal of ophthalmology.

Genotype-phenotype correlations in ocular manifestations of Marinesco–Sjögren syndrome: Case report and literature review

H. Per, S. Çırak, H. Jungbluth, 2021, European journal of ophthalmology.

Magnetic resonance imaging of childhood Guillain–Barré syndrome

H. Per, S. Kumandas, A. Coskun, 2010, Child's Nervous System.

A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23

H. Per, M. Canpolat, S. Kumandas, 2014, Case Reports in Neurology.

Psychopathology and Life Quality in Children with Epilepsy and Psychopathology in Their Parents

E. Demirci, H. Per, Sevgi Özmen, 2018, Güncel Pediatri.

MR imaging findings in children with pseudotumor cerebri and comparison with healthy controls

H. Per, M. Canpolat, A. Coskun, 2015, Child's Nervous System.

Topical sirolimus for the treatment of angiofibromas in tuberous sclerosis

H. Per, M. Canpolat, Demet Kartal, 2017, Indian journal of dermatology, venereology and leprology.

Unusual presentation of herpes simplex virus encephalitis: bilateral thalamic involvement and normal imaging of early stage of the disease.

H. Per, S. Kumandas, F. Tahan, 2007, The American journal of emergency medicine.

Ehlers-Danlos Syndrome Type VI: A Case Report

H. Per, M. Canpolat, S. Kumandas, 2014 .

Ehlers-Danlos Syndrome Type VI: A Case Report Ehler-Danlos Sendromu Tip VI: Olgu Sunumu

H. Per, M. Canpolat, H. Gümüş, 2014 .

The Prevalence of Migraine and Tension-Type Headache Among Schoolchildren in Kayseri, Turkey

H. Per, M. Canpolat, S. Kumandas, 2015, Journal of child neurology.

Might BPA and phthalates have a role in etiopathogenesis of ADHD? Might BPA and phthalates have a role in etiopathogenesis of ADHD? ve fitalatların rolü

H. Per, Sevgi Özmen, M. Kondolot, 2018 .

The Effects of Pentoxifylline on Diabetic Renal Changes in Streptozotocin‐Induced Diabetes Mellitus

H. Per, O. Canoz, R. Dusunsel, 2004, Renal failure.

Hemophagocytic syndrome associated with high‐dose lamotrigine

H. Per, S. Kumandas, H. Gümüş, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

Serum and urine boron and selenium levels in children with resistant epilepsy.

H. Per, M. Canpolat, S. Kumandas, 2012, Saudi medical journal.

Intracranial hemorrhage in infants as a serious, and preventable consequence of late form of vitamin K deficiency: a selfie picture of Turkey, strategies for tomorrow

H. Per, M. Canpolat, E. Yılmaz, 2014, Child's Nervous System.

Intracranial hemorrhage in children with hemophilia

H. Per, Ekrem Ünal, A. Küçük, 2022, Journal of Translational and Practical Medicine.

Different etiologies of acquired torticollis in childhood

H. Per, M. Canpolat, Sevgi Özmen, 2014, Child's Nervous System.

Prevalence and risk factors of epilepsy among school children in Kayseri City Center, an urban area in Central Anatolia, Turkey

H. Per, M. Canpolat, S. Kumandas, 2014, Seizure.

Increased Serum Phthalates (MEHP, DEHP) and Bisphenol A Concentrations in Children With Autism Spectrum Disorder

E. Demirci, H. Per, M. Canpolat, 2016, Journal of child neurology.

Iatrogenic Epidermoid Tumor: Late Complication of Lumbar Puncture

H. Per, S. Kumandas, A. Yıkılmaz, 2007, Journal of child neurology.

Meningitis and subgaleal, subdural, epidural empyema due to Pasteurella multocida.

H. Per, S. Kumandas, A. Coskun, 2010, The Journal of emergency medicine.

Whole‐exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum

H. Per, M. Canpolat, S. Kumandas, 2013, Clinical genetics.

Biallelic Mutations in the 3’ Exonuclease TOE1 Cause Pontocerebellar Hypoplasia and Uncover a Role in snRNA Processing

Gene W. Yeo, S. Gabriel, F. Baas, 2016, Nature Genetics.

Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey

H. Per, M. Canpolat, S. Kumandas, 2016, Neuropediatrics.

Bone mineral density and bone metabolic markers’ status in children with neurofibromatosis type 1

H. Per, M. Canpolat, S. Kumandas, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Surgical timing of the subependymal giant cell astrocytoma (SEGA) with the patients of tuberous sclerosis complex.

H. Per, S. Kumandas, B. Tucer, 2011, Turkish neurosurgery.

Short Distance Falls and Shaken Baby Syndrome: Case Report

H. Per, M. Canpolat, A. Coskun, 2010 .

Intracranial hemorrhages and late hemorrhagic disease associated cholestatic liver disease

H. Per, S. Kumandas, A. Coskun, 2012, Neurological Sciences.

Intracranial hemorrhage due to late hemorrhagic disease in two siblings.

H. Per, S. Kumandas, H. Gümüş, 2006, The Journal of emergency medicine.

Clinical Communications: Pediatrics

H. Per, S. Kumandas, H. Gümüş, 2006 .

Primary soliter and multiple intracranial cyst hydatid disease: Report of five cases

H. Per, S. Kumandas, A. Kurtsoy, 2009, Brain and Development.

Idiopathic Brain Herniation

H. Per, S. Gorkem, A. Coskun, 2014, The neuroradiology journal.

ÇOCUKLARDA SEREBRAL TUZ KAYBI: İki Vaka Sunumu ve Literatürün Gözden Geçirilmesi Cerebral salt wasting in children: Report of two cases and review of literature

H. Per, M. A. Öztürk, H. Gümüş, 2002 .

The comparison of the effects of dexmedetomidine and midazolam sedation on electroencephalography in pediatric patients with febrile convulsion

H. Per, S. Kumandas, A. Akin, 2011, Paediatric anaesthesia.

Comparison of Effects of Different Dexmedetomidine and Chloral Hydrate Doses Used in Sedation on Electroencephalography in Pediatric Patients

H. Per, M. Canpolat, S. Kumandas, 2015, Journal of child neurology.

Sugammadex and general Anesthesia in Two Pediatric Patients withy Joubert Syndrome: case report

H. Per, M. Canpolat, S. Doğan, 2017 .

Cervical eosinophilic granuloma and torticollis: a case report and review of the literature.

H. Per, M. Canpolat, S. Kumandas, 2008, The Journal of emergency medicine.

Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors

S. Mane, H. Per, N. Šestan, 2015, Neuron.

Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors

S. Mane, H. Per, N. Šestan, 2014, Neuron.

Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking

H. Per, H. Galehdari, S. Efthymiou, 2019, Front. Neurosci..

Brain diffusion tensor imaging in children with tuberous sclerosis.

H. Per, M. Canpolat, S. Gorkem, 2016, Diagnostic and interventional imaging.

Neurofibromatosis type 1 with overlap Turner syndrome and Klinefelter syndrome.

H. Per, S. Kurtoğlu, M. Keskin, 2010, Journal of tropical pediatrics.

Tyrosinemia type II: Novel mutations in TAT in a boy with unusual presentation

H. Per, M. Kendirci, H. Poyrazoglu, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Torticollis in children: an alert symptom not to be turned away

H. Per, M. Canpolat, S. Kumandas, 2015, Child's Nervous System.

Transient Sixth Nerve Palsies and Torticollis Secondary to Parietal Arteriovenous Malformation

H. Per, S. Kumandas, B. Tucer, 2006, Pediatric Neurosurgery.

Uncontrolled Immigration Threatening Public Health: A Transverse Myelitis Case due to Measles

H. Per, M. Canpolat, Ö. Ceylan, 2017 .

The use of rapamycin in patients with tuberous sclerosis complex: Long-term results

H. Per, M. Canpolat, S. Kumandas, 2018, Epilepsy & Behavior.

Effects of Cornus mas L. and Morus rubra L. extracts on penicillin-induced epileptiform activity: an electrophysiological and biochemical study.

H. Per, F. Elmalı, M. Yıldırım, 2017, Acta neurobiologiae experimentalis.

Genetic Polymorphism of VKORC1-1639 in Children With Intracranial Hemorrhage Due to Vitamin K Deficiency

H. Per, S. Taheri, E. Unal, 2018, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Late-type vitamin K deficiency bleeding: experience from 120 patients

H. Per, T. Patiroglu, E. Unal, 2012, Child's Nervous System.

Characteristic and management of pediatric arachnoid cysts: A case series

H. Per, M. Canpolat, M. Çiftçi, 2022, Journal of Surgery and Medicine.

Evaluating the brainstem in children with breath-holding spells

H. Per, M. Canpolat, S. Kumandas, 2022, Northern clinics of Istanbul.

Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome

H. Per, M. Canpolat, S. Kumandas, 2021, Turkish archives of pediatrics.

Reversible posterior leukoencephalopathy syndrome in childhood: report of nine cases and review of the literature

H. Per, S. Kumandas, A. Yıkılmaz, 2010, Neurological Sciences.

Diffusion-weighted imaging in Sydenham’s chorea

H. Per, M. Canpolat, N. Narin, 2012, Child's Nervous System.

Levetiracetam monotherapy in newly diagnosed cryptogenic West syndrome.

H. Per, S. Kumandas, H. Gümüş, 2007, Pediatric neurology.

The relation between antiepileptic drug type and cognitive functions in childhood epilepsy: A prospective observational study

H. Per, M. Canpolat, S. Kumandas, 2019, Experimental Biomedical Research.

Neurologic Sequelae of Neonatal Hypoglycemia in Kayseri, Turkey

H. Per, S. Kumandas, A. Coskun, 2008, Journal of child neurology.

Gigantic cerebral hydatid cysts in childhood

H. Per, S. Kumandas, B. Tucer, 2007, Annals of Saudi medicine.

Clinical and EEG features, treatment, and outcome of hot water epilepsy in pediatric patients

H. Per, M. Canpolat, S. Kumandas, 2020 .

Loss of Protocadherin‐12 Leads to Diencephalic‐Mesencephalic Junction Dysplasia Syndrome

S. Gabriel, H. Per, N. Shomron, 2018, Annals of neurology.

Evaluation of Two Types of Drug Treatment with QEEG in Children with ADHD

Ramazan Aldemir, E. Demirci, H. Per, 2018, Translational neuroscience.

Efficiency of a Combination of Pharmacological Treatment and Nondrug Interventions in Childhood Narcolepsy

H. Per, M. Canpolat, M. Aksu, 2016, Neuropediatrics.

Traumatic Basilar Artery Dissection and Hypertrophic Olivary Degeneration

H. Per, M. Canpolat, S. Kumandas, 2015 .

Traumatic medial cerebral artery occlusion in a 4-year-old child.

H. Per, S. Kumandas, A. Coskun, 2004, The American journal of emergency medicine.

Neonatal septic arthritis

H. Per, M. Halıcı, S. Kabak, 2001 .

The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency Syndrome

H. Per, M. Canpolat, A. Caglayan, 2015, Neuropediatrics.

Lamotrigine in two cases of Rett syndrome

H. Per, S. Kumandas, H. Çaksen, 2001, Brain and Development.

Calcified chronic subdural hematoma mimicking calvarial mass: A case report

H. Per, S. Kumandas, H. Akgün, 2006, Brain and Development.

COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by CoQ10 Administration

Jun Z. Li, H. Per, A. Caglayan, 2019, The Cerebellum.

Investigating the prevalence of febrile convulsion in Kayseri, Turkey: An assessment of the risk factors for recurrence of febrile convulsion and for development of epilepsy

H. Per, M. Canpolat, S. Kumandas, 2018, Seizure.

Electroencephalography in Pediatric Patients Comparison of Effects of Different Dexmedetomidine and Chloral Hydrate Doses Used in Sedation on

H. Per, M. Canpolat, S. Kumandas, 2014 .

Shuddering attacks in children: A retrospective analysis of 19 cases from a single-center in Turkey

H. Per, H. Gumuş, S. Ozturk, 2021, Epilepsy & Behavior.

Calcium carbide poisoning via food in childhood.

H. Per, S. Kumandas, S. Kurtoğlu, 2007, Journal of Emergency Medicine.

Asymmetric Crying Facies and Congenital Hypothyroidism: Report of Two Patients

H. Per, N. Narin, S. Kurtoğlu, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Anti-Ganglioside, Anti-Glutamate, and Anti-Gad Antibody Levels in Attention-Deficit Hyperactivity Disorder

E. Demirci, H. Per, Sevgi Özmen, 2014 .

Molybdenum cofactor deficiency: Clinical features in a Turkish patient

H. Per, S. Kumandas, O. Çağlayan, 2007, Brain and Development.

Gliomatosis Cerebri Mimicking Encephalopathy in a Teenager Boy

Mehmet, H. Per, E. Unal, 2020, Gazi Medical Journal.

Concomitant Heart and Brain Hydatid Cyst without Other Organ Involvement: A Case Report

H. Per, S. Kumandas, B. Tucer, 2011 .

Stretch Syncope: A Rare Case Mimicking Seizure

H. Per, M. Canpolat, S. Kumandas, 2016 .

An analysis of 109 fetuses with prenatal diagnosis of complete agenesis of corpus callosum

H. Per, M. Canpolat, S. Kumandas, 2020, Neurological Sciences.

Apparent diffusion coefficient in differentiation of pediatric posterior fossa tumors

H. Per, S. Saraçoğlu, A. Coskun, 2017, Japanese Journal of Radiology.

Determination of restless legs syndrome prevalence in children aged 13–16 years in the provincial center of Kayseri

H. Per, O. Günay, D. Öztop, 2017, Brain and Development.

Determination of restless legs syndrome prevalence in children aged 13–16years in the provincial center of Kayseri

H. Per, D. Oztop, O. Gunay, 2017, Brain and Development.

Spinal Cord Injury without Radiographic Abnormality Sciwora in Chilhood Case Report

H. Per, M. Canpolat, S. Kumandas, 2015 .

Investigation of the Prevalence of Sleep Disorders in Medical Students and Examination of Its Change by Classes, Gender and Body Mass Index

H. Per, G. Zararsiz, Fatih Yavuz, 2019, Journal of Turkish Sleep Medicine.

Neutropenia and Increased Mean Corpuscular Volume (MCV) With Abnormal Neurologic Findings: A Case of Cobalamin D Deficiency

H. Per, M. Kendirci, F. Kardaş, 2019, Journal of pediatric hematology/oncology.

Septic arthritis in childhood

H. Per, H. Çaksen, H. B. Üstünbaş, 2000, Pediatrics international : official journal of the Japan Pediatric Society.

Diagnosis of intracranial calcification and hemorrhage in pediatric patients: Comparison of quantitative susceptibility mapping and phase images of susceptibility-weighted imaging.

H. Per, S. Gorkem, A. Coskun, 2017, Diagnostic and interventional imaging.

Insights from genotype–phenotype correlations by novel SPEG mutations causing centronuclear myopathy

E. Bertini, H. Per, J. Bevilacqua, 2017, Neuromuscular Disorders.

Three Patients With Lafora Disease

H. Per, M. Canpolat, S. Kumandas, 2015, Journal of child neurology.

Multiple Sclerosis with Onset Younger Than 10 Years in Turkey

H. Per, M. Canpolat, S. Gökben, 2017, Neuropediatrics.

Lack of serum antineuronal antibodies in children with autism.

E. Demirci, H. Per, M. Canpolat, 2016, Bratislavske lekarske listy.

Assessment of Psychopathology and Quality of Life in Children and Adolescents With Migraine

H. Per, D. Öztop, Nilfer Sahin, 2016, Journal of Child Neurology.

Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study.

H. Per, M. Canpolat, U. Yiş, 2023, Pediatric neurology.

Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment

H. Per, H. Canatan, Ekrem Ünal, 2022, Genes and Immunity.

A case of DRESS syndrome associated with carbamazepine treatment.

H. Per, B. Akyıldız, A. Dursun, 2018, Turk pediatri arsivi.

Evaluation of Adolescents with Restless Legs Syndrome: Relation to School Success

H. Per, F. Kardaş, Neslihan Günay, 2021, The Journal of Pediatric Academy.

Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene

H. Per, S. Kumandas, A. Dağçınar, 2015, Journal of Human Genetics.

COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by CoQ10 Administration

Jun Z. Li, H. Per, A. Caglayan, 2019, The Cerebellum.

Polymicrogyria: correlation of magnetic resonance imaging and clinical findings

H. Per, S. Kumandas, A. Coskun, 2012, Child's Nervous System.

Meningitis and subdural empyema caused by Salmonella typhi in infancy

H. Per, S. Kumandas, H. Gümüş, 2007, Journal of Pediatric Neurology.

Clinical and genetic studies of thiamine metabolism dysfunction syndrome-4: case series and review of the literature

H. Per, M. Canpolat, A. Caglayan, 2022, Clinical dysmorphology.

A case of Rhiozomelic Chondrodysplasia Punctata.

H. Per, M. Canpolat, S. Kumandas, 2012 .

Clinical Presentation of Epileptic Seizures in a Child with a Final Diagnosis of Atrial Fibrillation: A Pediatric Case Report

H. Per, M. Canpolat, S. Kumandas, 2016 .

Erdheim Chester disease: Cerebral involvement in childhood

H. Per, S. Kumandas, T. Patiroglu, 2007, Brain and Development.

A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenon.

H. Per, M. Canpolat, S. Kumandas, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Electroencephalogram abnormalities in patients with NREM parasomnias.

H. Per, F. Erdoğan, R. Yılmaz, 2019, Sleep Medicine.

Evaluation of Micronutrient Levels in Children with Cerebral Palsy.

H. Per, A. Cansu, H. Tekgul, 2021, Pediatrics international : official journal of the Japan Pediatric Society.

A report of a desmoplastic non-infantile ganglioglioma in a 6-year-old boy with review of the literature

H. Per, S. Kumandas, A. Kurtsoy, 2009, Neurosurgical Review.

Evaluation of Immunization Status in Patients with Cerebral Palsy: Multicenter CP-VACC Study

H. Per, M. Canpolat, S. Kumandas, 2021 .

Effects of recombinant human erythropoietin on fibrinolytic system in children on continuous ambulatory peritoneal dialysis.

H. Per, H. Poyrazoğlu, R. Düşünsel, 1999, Advances in peritoneal dialysis. Conference on Peritoneal Dialysis.

Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations.

H. Per, M. Canpolat, Selcan Öztürk, 2022, Pediatric neurology.