Search Results - "Yildirim, Miraç"

Therapeutic plasma exchange in clinical pediatric neurology practice: Experience from a tertiary referral hospital by Yıldırım, Miraç, Bektaş, Ömer, Botan, Edin, Şahin, Süleyman, Gurbanov, Anar, Teber, Serap, Kendirli, Tanıl

“…This study aims to retrospectively evaluate the long-term efficacy, tolerability, and safety of therapeutic plasma exchange (TPE) in children with various…”
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Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis? by Koç Yekedüz, Merve, Köse, Engin, İnci, Aslı, Yüksel, Merve Feyza, Doğulu, Neslihan, Şen Akova, Birsel, Yeniay Süt, Nurşah, Öncül, Ümmühan, Yildirim, Miraç, Fitoz, Suat, Teber, Serap, Tümer, Leyla, Eminoğlu, Fatma Tuba

“…One of the most common causes of carpal tunnel syndrome (CTS) in childhood is mucopolysaccharidosis (MPS). While ultrasonography (US) can aid in the diagnosis…”
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Management of neurological problems in children on home invasive mechanical ventilation by Sayar, Yavuz, Yıldırım, Miraç, Teber, Serap

“…Home invasive mechanical ventilation (HIMV) has become a crucial long-term respiratory support for children with neurological disorders, but requires advanced…”
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Retrospective Evaluation of Children With Pseudotumor Cerebri: A Single Center Experience by Yıldırım, Miraç

“…Objectives: Pseudotumor cerebri is a rare neurological condition in which signs of increased intracranial pressure are observed and there are no intracranial…”
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Predictors of medical intractability in children with epilepsy onset during the first two years of life, excluding infantile epileptic spasm syndrome by Yıldırım, Miraç, Altıntaş, Mert, Uysal, Ece, Bektaş, Ömer, Teber, Serap

“…•In this study, a drug-resistant epilepsy rate of 33.1 % was observed in children with epilepsy onset during the first two years of life, excluding infantile…”
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Ketogenic diet-responsive drug-resistant epilepsy in a case of asparagine synthetase deficiency with a novel compound heterozygous missense variant by Altıntaş, Mert, Yıldırım, Miraç, Uçar, Çiğdem İlter, Köse, Engin, Bektaş, Ömer, Teber, Serap

“…Asparagine synthetase deficiency (ASNSD) is a rare autosomal recessive neurometabolic disorder caused by homozygous or compound heterozygous mutations in the…”
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A Case of Multidrug-Resistant Lance-Adams Syndrome Successfully Treated With Phenobarbital by Yeniay Süt, Nurşah, Yıldırım, Miraç, Bektaş, Ömer, Kendirli, Tanıl, Teber, Serap

“…Lance-Adams syndrome is a rare but devastating disorder characterized by rest, action, and stimulus-sensitive myoclonus after cardiorespiratory arrest. We…”
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Status dystonicus associated with CLN8 disease by Yıldırım, Miraç, Köse, Engin, Keçeli, Avni Merter, Balasar, Özgür, Şimşek, Nazmi

“…Status dystonicus is an underdiagnosed condition, probably due to heterogeneous etiology, presentation and course. Herein, we report the first case of CLN8…”
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Risk of seizure relapse and long-term outcomes after discontinuation of antiseizure medication in children with epilepsy by Yıldırım, Miraç, Bektaş, Ömer, Kartal, Ayşe Tuğba, Yeniay Süt, Nurşah, Teber, Serap

“…•We evaluated potential predictors of seizure relapse, some of which have rarely been evaluated.•Adolescent age at diagnosis, abnormal EEG findings after…”
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Clinical features and outcomes of opsoclonus myoclonus ataxia syndrome by Yıldırım, Miraç, Öncel, İbrahim, Bektaş, Ömer, Tanalı, Gizem, Şahin, Süleyman, Kutluk, Tezer, Teber, Serap, Anlar, Banu

“…Opsoclonus myoclonus ataxia syndrome (OMAS) is a rare neuroinflammatory disorder. We aimed to retrospectively evaluate clinical and laboratory data and…”
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Metabolic etiologies in children with infantile epileptic spasm syndrome: Experience at a tertiary pediatric neurology center by Yüksel, Merve Feyza, Doğulu, Neslihan, Yıldırım, Miraç, Köse, Engin, Bektaş, Ömer, Eminoğlu, Fatma Tuba, Teber, Serap

“…Infantile epileptic spasm syndrome (IESS), including West syndrome (WS) and infantile spasm (IS), causes a challenging prognosis, particularly when associated…”
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Periodic Lateralized Epileptiform Discharges: A Child with a Rare Manifestation of Posterior Reversible Encephalopathy Syndrome and Literature Review by Yıldırım, Miraç, Çiçek, Sultan, Havan, Merve, Kendirli, Tanıl, Teber, Serap

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VAMP1-Related Congenital Myasthenic Syndrome: A Case Report and Literature Review by Yıldırım, Miraç, Yarenci, Gülçin Bilicen, Genç, Mustafa Berk, Uçar, Çiğdem İlter, Bayav, Secahattin, Tekin, Merve Nur, Bektaş, Ömer, Teber, Serap

“…Congenital myasthenic syndrome-25 (CMS-25) is an autosomal recessive neuromuscular disorder caused by a homozygous mutation in gene. To date, only eight types…”
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Hypomelanosis of Ito presenting with unilateral dilation of Virchow-Robin spaces: a case report by Uçar, Çiğdem İlter, Yıldırım, Miraç, Sayar, Yavuz, Şahin, Süleyman, Teber, Serap Tıraş

“…Hypomelanosis of Ito is a rare heterogeneous neurocutaneous disorder often associated with central nervous and musculoskeletal system involvement. Herein, we…”
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The diagnostic challenges of congenital mirror movements and hand stereotypies in a case with TUBB3-associated tubulinopathy by Yeniay Süt, Nurşah, Yıldırım, Miraç, Bektaş, Ömer, Altıntaş, Mert, Teber, Serap

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Levetiracetam monotherapy in children with epilepsy: Experience from a tertiary pediatric neurology center by Yıldırım, Miraç, Bektaş, Ömer, Akıncı Göktaş, Özben, Yüksel, Merve Feyza, Şahin, Süleyman, Tıraş Teber, Serap

“…•Levetiracetam has high efficacy and tolerability as monotherapy in children.•Levetiracetam reduced seizures by more than 50% in 85% of the patients.•The…”
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Correlation between early computed tomography findings and neurological outcome in pediatric traumatic brain injury patients by Şahin, Süleyman, Botan, Edin, Gün, Emrah, Yüksel, Merve Feyza, Süt, Nurşah Yeniay, Kartal, Ayşe Tuğba, Gurbanov, Anar, Kahveci, Fevzi, Özen, Hasan, Havan, Merve, Yıldırım, Miraç, Şahap, Seda Kaynak, Bektaş, Ömer, Teber, Serap, Fitoz, Suat, Kendirli, Tanıl

“…Traumatic brain injury (TBI) is a leading cause of morbidity and mortality in children. Head computed tomography (CT) is frequently utilized for evaluating…”
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Glucose Transporter Type 1 Deficiency Syndrome: A Single-Center Case Series by Yıldırım, Miraç, Babayiğit, Ömür, Ilgaz, Fatma, Yalnızoğlu, Dilek, Topçu, Meral

“…Glucose transporter type 1 deficiency syndrome is a neurometabolic encephalopathy characterized by movement disorders, intractable seizures, and acquired…”
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A sydenham chorea attack associated with COVID-19 infection by Yüksel, Merve Feyza, Yıldırım, Miraç, Bektaş, Ömer, Şahin, Süleymen, Teber, Serap

“…The coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 appeared in Wuhan, China in December 2019 and quickly spread around the world and is considered a…”
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Mild congenital myopathy due to a novel variation in SPEG gene by Yildirim, Mirac, Balasar, Ozgur, Kose, Engin, Dogan, Melih Timucin

“…Centronuclear myopathies (CNMs) are a subgroup of congenital myopathies (CMs) characterized by muscle weakness, genetic heterogeneity, and predominant type 1…”
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