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Hypophosphatasia: is it an underdiagnosed disease even by expert physicians?

Journal of bone and mineral metabolism, 2021-07, Vol.39 (4), p.598-605

2021

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Opsoclonus–myoclonus syndrome following rotavirus gastroenteritis

Pediatrics international, 2014-12, Vol.56 (6), p.e86-e87

2014

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The Relation of Epilepsy Type with Depression and Anxiety in Children

Gazi tıp dergisi, 2021-05, Vol.32 (2A), p.273-275

2021

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Matrix Metalloproteinase-7 and Matrix Metalloproteinase-9 in Pediatric Multiple Sclerosis

Pediatric neurology, 2012-09, Vol.47 (3), p.171-176

2012

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The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

Nature genetics, 2000-11, Vol.26 (3), p.370-374

2000

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The Effect of Topiramate on Body Weight and Ghrelin, Leptin, and Neuropeptide-Y Levels of Prepubertal Children With Epilepsy

Pediatric neurology, 2014-08, Vol.51 (2), p.220-224

2014

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Sacral aneurysmal bone cyst in a child presenting with radiculopathy

The spine journal, 2016-06, Vol.16 (6), p.e391-e392

2016

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Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations

Orphanet journal of rare diseases, 2011-06, Vol.6 (1), p.40-40, Article 40

2011

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Effect of Antiepileptic Drugs on Plasma Lipids, Lipoprotein (a), and Liver Enzymes

Journal of child neurology, 2006-01, Vol.21 (1), p.70-74

2006

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Spastic Paraplegia with SPG11 Gene delE39 in a Turkish Patient

Gazi tıp dergisi, 2016-01, Vol.27 (4)

2016

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Case: Valproat-Induced Hyperammonemic Encephalopathy

Gazi tıp dergisi, 2016-01, Vol.27 (2)

2016

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Matrix Metalloproteinase-7, Matrix Metalloproteinase-9, and Disease Activity in Pediatric Multiple Sclerosis

Pediatric neurology, 2013-03, Vol.48 (3), p.255-256

2013

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Autism Spectrum Disorder Management Practices and Level of Knowledge Among General Pediatricians

Gazi tıp dergisi, 2015-01, Vol.26 (4)

2015

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Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia

American journal of human genetics, 2017-09, Vol.101 (3), p.441-450

2017

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Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

Brain (London, England : 1878), 2011-01, Vol.134 (Pt 1), p.143-156

2011

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Evaluation of state and trait anxiety levels of parents and children before electroencephalography procedures: A prospective study from a tertiary epilepsy center

Epilepsy & behavior, 2020-11, Vol.112, p.107338-107338, Article 107338

2020

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Internal carotid artery dissection without intracranial infarct following a minor shoulder trauma: The second pediatric case and review of the literature

Journal of clinical neuroscience, 2018-10, Vol.56, p.172-175

2018

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Regional brain volume reduction and cognitive outcomes in preterm children at low risk at 9 years of age

Child's nervous system, 2017-08, Vol.33 (8), p.1317-1326

2017

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An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation

Neurology Asia, 2022-03, Vol.27 (1), p.199-202

2022

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Thymic carcinoma presenting with overlap polyarthritis and myositis: A rare paraneoplastic syndrome in childhood

International journal of rheumatic diseases, 2024-05, Vol.27 (5), p.e15187-n/a

2024

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Milk of calcium: A rare manifestation of juvenile dermatomyositis

Archives of rheumatology, 2021-06, Vol.36 (2), p.302-304

2021

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Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes

European journal of paediatric neurology, 2022-11, Vol.41, p.8-18

2022

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Dikkat eksikliği hiperaktivite bozukluğu olan hastaların nöropsikolojik test performansının değerlendirilmesi

Gazi tıp dergisi, 2019-02, Vol.30 (2), p.114-118

2019

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Automatic Positioning of Mobile Users via GSM Signal Measurements

Balkan journal of electrical & computer engineering, 2021-04, Vol.9 (2), p.152-160

2021

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Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy

American journal of human genetics, 2002-06, Vol.70 (6), p.1446-1458

2002

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Hypophosphatasia: is it an underdiagnosed disease even by expert physicians?

Opsoclonus–myoclonus syndrome following rotavirus gastroenteritis

The Relation of Epilepsy Type with Depression and Anxiety in Children

Matrix Metalloproteinase-7 and Matrix Metalloproteinase-9 in Pediatric Multiple Sclerosis

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

The Effect of Topiramate on Body Weight and Ghrelin, Leptin, and Neuropeptide-Y Levels of Prepubertal Children With Epilepsy

Sacral aneurysmal bone cyst in a child presenting with radiculopathy

Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations

Effect of Antiepileptic Drugs on Plasma Lipids, Lipoprotein (a), and Liver Enzymes

Spastic Paraplegia with SPG11 Gene delE39 in a Turkish Patient

Case: Valproat-Induced Hyperammonemic Encephalopathy

Matrix Metalloproteinase-7, Matrix Metalloproteinase-9, and Disease Activity in Pediatric Multiple Sclerosis

Autism Spectrum Disorder Management Practices and Level of Knowledge Among General Pediatricians

Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

Evaluation of state and trait anxiety levels of parents and children before electroencephalography procedures: A prospective study from a tertiary epilepsy center

Internal carotid artery dissection without intracranial infarct following a minor shoulder trauma: The second pediatric case and review of the literature

Regional brain volume reduction and cognitive outcomes in preterm children at low risk at 9 years of age

An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation

Thymic carcinoma presenting with overlap polyarthritis and myositis: A rare paraneoplastic syndrome in childhood

Milk of calcium: A rare manifestation of juvenile dermatomyositis

Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes

Dikkat eksikliği hiperaktivite bozukluğu olan hastaların nöropsikolojik test performansının değerlendirilmesi

Automatic Positioning of Mobile Users via GSM Signal Measurements

Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy

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