Yayınlar & Eserler

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SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Exploring metabolic alterations in PYCR2 deficiency: Unveiling pathways and clinical presentations of hypomyelinating leukodystrophy 10

Gurbuz B. B., GÜLBAKAN B., ÖZGÜL R. K., YALNIZOĞLU D., Yilmaz D. Y., GÖÇMEN R., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , sa.9, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

Frequency and Characteristics of Sleep Apnea Syndrome in Pediatric Patients with Duchenne Muscular Dystrophy

Yavuz B. C., Yildiz S. O., Buyuksahin H. N., ÖZEL E., EMİRALİOĞLU ORDUKAYA N., AYKAN H. H., et al.
EUROPEAN RESPIRATORY JOURNAL , 2024 (SCI-Expanded) identifier

Predictors of Clinically Important Neuroimaging Findings in Children Presenting Pediatric Emergency Department

GÜNGÖR E., Haliloglu G., YALNIZOĞLU D., Oguz K. K., TEKŞAM Ö.
PEDIATRIC EMERGENCY CARE , sa.6, ss.474-479, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

Delineation of <i>ADPRHL2</i> Variants: Report of Two New Patients with Review of the Literature

Yildiz S. O., Yalnizoglu D., ŞİMŞEK KİPER P. Ö., GÖÇMEN R., Sogukpinar M., Utine G. E., et al.
NEUROPEDIATRICS , sa.02, ss.117-123, 2024 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier

Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency

YILDIZ Y., Ardıçlı D., GÖÇMEN R., YALNIZOĞLU D., Topçu M., Coşkun T., et al.
European Journal of Paediatric Neurology , cilt.49, ss.66-72, 2024 (SCI-Expanded) identifier identifier

Non-epileptic paroxysmal events at pediatric video-electroencephalography monitoring unit over a 15-year period

Yavuz P., GÜNBEY C., KARAHAN S., TOPÇU M., Turanli G., YALNIZOĞLU D.
Seizure , cilt.108, ss.89-95, 2023 (SCI-Expanded) identifier identifier

Claude Syndrome in Childhood Associated with Probable Neuro-Behcet Disease

Yavuz P., SOLMAZ İ., Kaya U. A., Akgoz A., Oguz K. K., Aytac S., et al.
Neuropediatrics , cilt.54, sa.1, ss.82-87, 2023 (SCI-Expanded) identifier identifier identifier

Clinically important intracranial abnormalities in children presenting with first focal seizure

Kasap T., TEKŞAM Ö., Turanlı G., KONUŞKAN B., Oğuz K. K., Haliloğlu G., et al.
Turkish Journal of Pediatrics , cilt.65, sa.1, ss.96-108, 2023 (SCI-Expanded) Creative Commons License identifier identifier identifier identifier

Practices of pediatric emergency physicians on the first febrile and afebrile seizures: a research in European Pediatric Emergency Medicine Survey Study

TEKŞAM Ö., Serdaroglu E., Haliloglu G., KONUŞKAN B., YALNIZOĞLU D.
EUROPEAN JOURNAL OF EMERGENCY MEDICINE , cilt.29, sa.6, ss.455-457, 2022 (SCI-Expanded) identifier identifier identifier

Neurologic manifestations in children with COVID-19

Gürlevik S. L., GÜNBEY C., ÖZSÜREKCİ Y., KESİCİ S., GÖÇMEN R., TEMUÇİN Ç. M., et al.
European Journal of Paediatric Neurology , cilt.39, ss.118-119, 2022 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

Synthetic MRI in children with tuberous sclerosis complex

ÇOBAN ÇİFÇİ G., GÜMELER E., PARLAK SAĞOL Ş., KONUŞKAN B., KARAKAYA KARABULUT J., YALNIZOĞLU D., et al.
INSIGHTS INTO IMAGING , cilt.13, sa.1, 2022 (SCI-Expanded) Creative Commons License identifier identifier identifier

Evaluation of changes in physician behavior after introduction of pediatric syncope approach protocol in the emergency department

Yildiz L. A., Haliloglu G., YALNIZOĞLU D., ERTUĞRUL İ., ALEHAN D., TEKŞAM Ö.
AMERICAN JOURNAL OF EMERGENCY MEDICINE , cilt.55, ss.57-63, 2022 (SCI-Expanded) identifier identifier identifier

<p>Lesional resective epilepsy surgery in childhood: Comparison of two decades and long-term seizure outcome from a single center</p>

GÜNBEY C., BİLGİNER B., Oguz K. K., Soylemezoglu F., Ergun E. L., AKALAN N., et al.
EPILEPSY RESEARCH , cilt.181, 2022 (SCI-Expanded) identifier identifier identifier

Comparison of physical fitness, activity, and quality of life of the children with epilepsy and their healthy peers

SIRTBAŞ G., YALNIZOĞLU D., LİVANELİOĞLU A.
Epilepsy Research , cilt.178, 2021 (SCI-Expanded) identifier identifier identifier

Biallelic mutations in ELFN1 gene associated with developmental and epileptic encephalopathy and joint laxity

DURSUN A., YALNIZOĞLU D., Yilmaz D. Y., Oguz K. K., GÜLBAKAN B., KOŞUKCU C., et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.64, sa.11, 2021 (SCI-Expanded) identifier identifier identifier

Long-term effects of vagus nerve stimulation in refractory pediatric epilepsy: A single-center experience

YALNIZOĞLU D., ARDIÇLI D., BİLGİNER B., KONUŞKAN B., Oguz K. K., AKALAN N., et al.
EPILEPSY & BEHAVIOR , cilt.110, 2020 (SCI-Expanded) identifier identifier identifier

The training and organization of Paediatric Neurology in Europe: Special report of the European Paediatric Neurology Society & Committee of National Advisors

Craiu D., Haataja L., Hollody K., Krsek P., Lagae L., Mall V., et al.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.28, ss.6-15, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

Acute Cerebellitis or Postinfectious Cerebellar Ataxia? Clinical and Imaging Features in Acute Cerebellitis

Yildirim M., GÖÇMEN R., KONUŞKAN B., PARLAK Ş., YALNIZOĞLU D., Anlar B.
JOURNAL OF CHILD NEUROLOGY , cilt.35, sa.6, ss.380-388, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Risk factors for seizure recurrence in a pediatric observation unit

GÜLTEKİNGİL KESER A., TEKŞAM Ö., Haliloglu G., YALNIZOĞLU D.
AMERICAN JOURNAL OF EMERGENCY MEDICINE , cilt.37, sa.12, ss.2151-2154, 2019 (SCI-Expanded) identifier identifier identifier

Clinical highlights of a very rare phospolipid remodeling disease due to MBOAT7 gene defect

DURSUN A., YALNIZOĞLU D., ÖZGÜL R. K., Oguz K. K., Yucel-Yilmaz D.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 2019 (SCI-Expanded) identifier identifier identifier

Epilepsy in neurofibromatosis type 1: Diffuse cerebral dysfunction?

Serdaroglu E., KONUŞKAN B., Oguz K. K., Gurler G., YALNIZOĞLU D., Anlar B.
EPILEPSY & BEHAVIOR , cilt.98, ss.6-9, 2019 (SCI-Expanded) identifier identifier identifier

Expanding the phenotype of phospholipid remodelling disease due to MBOAT7 gene defect

YALNIZOĞLU D., ÖZGÜL R. K., Oguz K. K., Ozer B., Yucel-Yilmaz D., Gurbuz B., et al.
JOURNAL OF INHERITED METABOLIC DISEASE , cilt.42, sa.2, ss.381-388, 2019 (SCI-Expanded) identifier identifier identifier

Behavioral problems of preschool children with new-onset epilepsy and one-year follow-up - A prospective study

Yoldas T. C., GÜNBEY C., Degerliyurt A., Erol N., Ozmert E., YALNIZOĞLU D.
EPILEPSY & BEHAVIOR , cilt.92, ss.171-175, 2019 (SCI-Expanded) identifier identifier identifier

Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation

Eroglu F. K., ÖZALTIN F., Gonc N., Nalcacioglu H., Ozcakar Z. B., YALNIZOĞLU D., et al.
PEDIATRIC NEUROLOGY , cilt.88, ss.71-74, 2018 (SCI-Expanded) identifier identifier identifier

Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span

Yucel-Yilmaz D., Yucesan E., YALNIZOĞLU D., Oguz K. K., Sagiroglu M. S., Ozbek U., et al.
BRAIN & DEVELOPMENT , cilt.40, sa.6, ss.458-464, 2018 (SCI-Expanded) identifier identifier identifier

Electroencephalographic findings in anti-N-methyl-D-aspartate receptor encephalitis in children: A series of 12 patients

YILDIRIM M., KONUŞKAN B., YALNIZOĞLU D., Topaloglu H., Erol I., Anlar B.
EPILEPSY & BEHAVIOR , cilt.78, ss.118-123, 2018 (SCI-Expanded) identifier identifier identifier

A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutation

DURSUN A., YALNIZOĞLU D., Gerdan O. F., Yucel-Yilmaz D., Sagiroglu M. S., YUKSEL B., et al.
CLINICAL DYSMORPHOLOGY , cilt.26, sa.1, ss.1-12, 2017 (SCI-Expanded) identifier identifier identifier

The seizure semiology consistent with frontal lobe symptomatogenic zone in children

Oztoprak Ü., Yalnızoğlu D., Oguz K. K., Ergün E., Soylemezoglu F., Bilginer B., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.6, ss.583-591, 2016 (SCI-Expanded) Creative Commons License identifier identifier

Cerebral Hyperperfusion in a Child with Stroke-Like Migraine Attacks after Radiation Therapy Syndrome

Ardicli D., GÖÇMEN R., Oguz K. K., VARAN A., YALNIZOĞLU D.
NEUROPEDIATRICS , cilt.47, sa.4, ss.259-262, 2016 (SCI-Expanded) identifier identifier identifier

SPECT-PET in Epilepsy and Clinical Approach in Evaluation

ERGUN E. L., SAYGI S., YALNIZOĞLU D., OGUZ K. K., Erbas B.
SEMINARS IN NUCLEAR MEDICINE , cilt.46, sa.4, ss.294-307, 2016 (SCI-Expanded) identifier identifier identifier

Acute Abducens Nerve Paralysis in the Pediatric Emergency Department Analysis of 14 Patients

TEKŞAM Ö., GÜLTEKİNGİL KESER A., KONUŞKAN B., Haliloglu G., Oguz K. K., YALNIZOĞLU D.
PEDIATRIC EMERGENCY CARE , cilt.32, sa.5, ss.307-311, 2016 (SCI-Expanded) identifier identifier identifier

Evaluation of central nervous system in patients with glycogen storage disease type 1a

Aydemir Y., Gurakan F., Temizel İ. N., DEMİR H., Oguz K. K., YALNIZOĞLU D., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.1, ss.12-18, 2016 (SCI-Expanded) Creative Commons License identifier identifier identifier

Mesenchymal stem cell application in children with subacute sclerosing panencephalitis

KUSKONMAZ B. B., UCKAN D., YALNIZOĞLU D., GUENEL M., OGUZ K. K., Konuskan B., et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY , cilt.57, sa.9, ss.880-883, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Childhood epilepsy with occipital paroxysm: classification, atypical evolution and long-term prognosis in 35 patients

Aksoy A., Haliloglu G., YALNIZOĞLU D., Turanli G.
TURKISH JOURNAL OF PEDIATRICS , cilt.57, sa.5, ss.439-452, 2015 (SCI-Expanded) identifier identifier identifier

Intelligence quotient improves after antiepileptic drug withdrawal following pediatric epilepsy surgery

Boshuisen K., van Schooneveld M. M. J., Uiterwaal C. S. P. M., Cross J. H., Harrison S., Polster T., et al.
ANNALS OF NEUROLOGY , cilt.78, sa.1, ss.104-114, 2015 (SCI-Expanded) identifier identifier identifier

Electrical status epilepticus during sleep: A study of 22 patients

Degerliyurt A., YALNIZOĞLU D., Bakar E. E., TOPÇU M., Turanli G.
BRAIN & DEVELOPMENT , cilt.37, sa.2, ss.250-264, 2015 (SCI-Expanded) identifier identifier identifier

Semiological seizure classification of epileptic seizures in children admitted to video-EEG monitoring unit

Alan S., YALNIZOĞLU D., Turanli G., Karli-Oguz K., Lay-Ergun E., Soylemezoglu F., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.57, sa.4, ss.317-323, 2015 (SCI-Expanded) identifier identifier identifier

Human intracellular ISG15 prevents interferon-alpha/beta over-amplification and auto-inflammation

Zhang X., Bogunovic D., Payelle-Brogard B., Francois-Newton V., Speer S. D., Yuan C., et al.
NATURE , cilt.517, sa.7532, ss.89-103, 2015 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 genemutation.

ÜNAL Ö., ÖZGÜL R. K., YÜCEL YILMAZ D., YALNIZOĞLU D., TOKATLI A., SİVRİ H. S., et al.
Turkish Journal Of Pediatrics , cilt.57, ss.388-393, 2015 (SCI-Expanded)

Successful Treatment of Severe Myasthenia Gravis Developed After Allogeneic Hematopoietic Stem Cell Transplantation With Plasma Exchange and Rituximab

ÜNAL Ş., SAĞ E., KUSKONMAZ B. B., Kesici S., BAYRAKCİ B., AYVAZ D. N., et al.
PEDIATRIC BLOOD & CANCER , cilt.61, sa.5, ss.928-930, 2014 (SCI-Expanded) identifier identifier identifier

Usefulness of long-term video-EEG monitoring in children at a tertiary care center

Onay S., YALNIZOĞLU D., TOPÇU M., Turanli G.
TURKISH JOURNAL OF PEDIATRICS , cilt.55, sa.6, ss.591-597, 2013 (SCI-Expanded) identifier identifier identifier

Developmental abnormalities and mental retardation: diagnostic strategy

TOPÇU M., YALNIZOĞLU D.
PEDIATRIC NEUROLOGY, PT I , cilt.111, ss.211-217, 2013 (SCI-Expanded) identifier

Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing

DUNDAR H., ÖZGÜL R. K., YALNIZOĞLU D., Erdem S., Oguz K. K., Tuncel D., et al.
PEDIATRIC NEUROLOGY , cilt.46, sa.3, ss.172-177, 2012 (SCI-Expanded) identifier identifier identifier

The classification and differential diagnosis of absence seizures with short-term video-EEG monitoring during childhood

UYSAL SOYER Ö., YALNIZOĞLU D., Turanli G.
TURKISH JOURNAL OF PEDIATRICS , cilt.54, sa.1, ss.7-14, 2012 (SCI-Expanded) identifier identifier identifier

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

Bilguvar K., Ozturk A. K., Louvi A., Kwan K. Y., Choi M., Tatli B., et al.
NATURE , cilt.467, sa.7312, ss.207-211, 2010 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

ASSOCIATION OF POLYNEUROPATHY, MENTAL RETARDATION, SENSORINEURAL HEARING LOSS, 6th NERVE PALSY, CONVULSIONS, AND ORAL DYSKINESIA; A PROPABLE NEW NEUROMETABOLIC DISORDER

DURSUN A., YALNIZOĞLU D., DÜNDAR H., ERDEM S., AKARSU A. N., ÖZGÜL R. K.
JOURNAL OF INHERITED METABOLIC DISEASE , cilt.33, 2010 (SCI-Expanded) identifier

Surgery for epilepsy in children with dysembryoplastic neuroepithelial tumor: clinical spectrum, seizure outcome, neuroradiology, and pathology

BİLGİNER B., YALNIZOĞLU D., Soylemezoglu F., TURANLI G., CİLA A., TOPÇU M., et al.
CHILDS NERVOUS SYSTEM , cilt.25, sa.4, ss.485-491, 2009 (SCI-Expanded) identifier identifier identifier

Lamotrigine in children with refractory epilepsy

Celebi A., YALNIZOĞLU D., Turanli G., Topaloglu H., AYSÜN S., TOPÇU M.
TURKISH JOURNAL OF PEDIATRICS , cilt.50, sa.5, ss.426-431, 2008 (SCI-Expanded) identifier

Neuropsychiatric involvement in juvenile systemic lupus erythematosus

Demirkaya E., BİLGİNER Y., AKTAY AYAZ N., YALNIZOĞLU D., Karli-Oguz K., IŞIKHAN V., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.50, sa.2, ss.126-131, 2008 (SCI-Expanded) identifier identifier identifier

Interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) levels and IL-6, TNF-polymorphisms in children with thrombosis

Una S., GÜMRÜK F., Aytac Ş. S., YALNIZOĞLU D., GÜRGEY A.
Journal of Pediatric Hematology/Oncology , cilt.30, sa.1, ss.26-31, 2008 (SCI-Expanded) identifier identifier identifier

Familial isolated non-compaction of myocardium presenting as restrictive cardiomyopathy

Ozkutlu S., Hascelik S., Yalnizoglu D., Altinok G.
PEDIATRICS INTERNATIONAL , cilt.49, sa.4, ss.536-539, 2007 (SCI-Expanded) identifier identifier identifier

Neurologic outcome in patients with MRI pattern of damage typical for neonatal hypoglycemia

Yalnizoglu D., Halilo G., Turanli G., Cila A., Topcu M.
BRAIN & DEVELOPMENT , cilt.29, sa.5, ss.285-292, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Evaluation of central nervous system in patients with glycogen storage disease type IA

Gurakan F., Aydemir Y., YÜCE A., Saltik-Temizel İ. N., DEMİR H., YALNIZOĞLU D., et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION , cilt.44, ss.163, 2007 (SCI-Expanded) identifier

Malformations of cortical development and epilepsy: evaluation of 101 cases (Part II)

Guengoer S., Yalnizoglu D., Turanli G., Saatci I., Erdogan-Bakar E., Topcu M.
TURKISH JOURNAL OF PEDIATRICS , cilt.49, sa.2, ss.131-140, 2007 (SCI-Expanded) identifier identifier identifier

Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I)

Guengoer S., Yalnizoglu D., Turanli G., Saatci I., Erdogan-Bakar E., Topcu M.
TURKISH JOURNAL OF PEDIATRICS , cilt.49, sa.2, ss.120-130, 2007 (SCI-Expanded) identifier

Outcome and long term follow-up after corpus callosotomy in childhood onset intractable epilepsy

Turanli G., Yalnizoglu D., Genc-Acikgoz D., Akalan N., Topcu M.
CHILDS NERVOUS SYSTEM , cilt.22, sa.10, ss.1322-1327, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier
Diğer Dergilerde Yayınlanan Makaleler

Pediatric cardiology consultation at long-term video EEG monitoring

GÜNBEY C., AYKAN H. H., KARAGÖZ T., TURANLI G., TOPÇU M., YALNIZOĞLU D.
Annals of Medical Research , cilt.30, sa.1, ss.116-120, 2023 (Hakemli Dergi) identifier

Glucose Transporter Type 1 Deficiency Syndrome: A Single-Center Case Series

Yildirim M., Babayigit O., ILGAZ F., YALNIZOĞLU D., TOPÇU M.
TURKISH JOURNAL OF NEUROLOGY , cilt.27, sa.3, ss.343-346, 2021 (ESCI) Creative Commons License identifier identifier identifier

Intertechnique Agreement in Epilepsy Imaging

GÜNEŞ A., YALNIZOĞLU D., GÜNBEY C., VOLKAN SALANCI B., SÖYLEMEZOĞLU A. F., BİLGİNER B., et al.
Türkiye Çocuk Hastalıkları Dergisi , cilt.13, sa.4, ss.292-301, 2019 (Hakemli Dergi) Creative Commons License

HOMOZYGOUS GNAL MUTATION ASSOCIATED WITH FAMILIAL CHILDHOOD-ONSET GENERALIZED DYSTONIA

MASUHO I., FANG M., GENG C., ZHANG J., JİANG H., ÖZGÜL R. K., et al.
NEUROLOGY-GENETICS , cilt.2, sa.3, 2016 (ESCI) Creative Commons License identifier identifier

A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay

OZANTÜRK A., Davis E. E., Sabo A., Weiss M. M., Muzny D., Dugan-Perez S., et al.
COLD SPRING HARBOR MOLECULAR CASE STUDIES , cilt.2, sa.2, 2016 (ESCI) Creative Commons License identifier

Intractable Epilepsy in Childhood: Presurgical Evaluation and Treatment

YALNIZOĞLU D., HIRFANOĞLU T., SERDAROĞLU A., Turanli G., TOPÇU M.
EPILEPSI , cilt.18, ss.7-14, 2012 (ESCI) identifier
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Central Nervous System Vasculitis in Primary Immune Deficiency

Uzunyayla-Sayici B., Oz S., GÖÇMEN R., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N., ESENBOĞA S., et al.
Pediatric Neurology, Ankara, Türkiye, 21 Temmuz 2022

CMV Miyokarditi ve Ağır Hipotonisi Olan Bir Hastada ORAI1 Defekti

ESENBOĞA S., DEVECİ K., AKARSU A., OCAK M., BİLDİK H. N., YAZ İ., et al.
7. Klinik İmmünoloji Kongresi, Türkiye, 6 - 09 Ekim 2021, ss.64-65

Comparison of physical fitness, activity andquality of life of the children with epilepsy andtheir healthy peers

SIRTBAŞ G., YALNIZOĞLU D., LİVANELİOĞLU A.
32nd European Academy Of Childhood Disability Annual Meeting 2020, Poznan, Polonya, 25 Kasım 2020, cilt.62, ss.40

Severe Motor Mental Retardation with Microcepahlyand Hypomyelination due to PYCR2 Gene variant in aLarge Family

BİLGİNER GÜRBÜZ B., EROĞLU ERTUĞRUL N. G., KOŞUKCU C., YÜCEL YILMAZ D., ÖZGÜL R. K., YALNIZOĞLU D., et al.
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism 2019 (SSIEM-2019), Rotterdam, Hollanda, 3 - 06 Eylül 2019, cilt.42, ss.1-479 identifier identifier

Epilepsili Çocukların ve Sağlıklı Yaşıtlarının Fiziksel Aktivite, Uygunluk, Performans ve Yaşam Kalitelerinin Karşılaştırılması

SIRTBAŞ G., LİVANELİOĞLU A., YALNIZOĞLU D.
XVII. Fizyoterapi ve Rehabilitasyonda Gelişmeler Kongresi 2018, Antalya, Türkiye, 25 - 28 Nisan 2018

Acute cerebellitis in children: A series of eight cases

YILDIRIM M., GÖÇMEN R., KONUŞKAN B., YALNIZOĞLU D., ANLAR F. B.
12th The European Paediatric Neurology Society (EPNS) Congress, Lyon, Fransa, 20 - 24 Haziran 2017, cilt.21, ss.121

Ethylmalonic encephalopathy without ethylmalonic aciduria

YÜCEL YILMAZ D., ÖZGÜL R. K., PEKTAŞ E., serdaroğlu e., YALNIZOĞLU D., DURSUN A.
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM), 6 - 09 Eylül 2016

ethymelanonic encephaopathy without etilmelanoc acitüria

YÜCEL YILMAZ D., ÖZGÜL R. K., PEKTAŞ E., SERDARDĞLu e., YALNIZOĞLU D., DURSUN A.
SSIEM ROMA, 6 - 09 Eylül 2016

Pontocerebellar hypoplasia type 6 a case with neonatal seizures hypotonia and microcephaly diagnosed by exome sequencing

SERDAROĞLU E., ÖZGÜL R. K., YÜCEL YILMAZ D., YALNIZOĞLU D., DURSUN A.
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM), 6 - 09 Eylül 2016

A case with psychomotor regression and leukoencephalopathy due to RNASEH2B gene defect

ÖZGÜL R. K., YÜCEL YILMAZ D., SERDAROĞLU E., YALNIZOĞLU D., TOPÇU M., DURSUN A.
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM), 6 - 09 Eylül 2016

pontocerebellar hypoplasia type 6 a case with meonatal seizures hypotonia and microcephaly diagnosed by exome sequencing

DURSUN A., sedaroğlu e., ÖZGÜL R. K., YÜCEL YILMAZ D., YALNIZOĞLU D.
SSIEM roma, 6 - 09 Eylül 2016

Thalamic Lesions Associated with Epilepsy and ESES

YILDIRIM M., GÖÇMEN R., TOPÇU M., YALNIZOĞLU D.
14th International Child Neurology Congress, Amsterdam, Hollanda, 1 - 05 Mayıs 2016

Ekzom Dizi Analizi ile ATP8A2 Aminofosfolipid Transporter Protein Geninde Saptanan Yeni Bir Splaysing Mutasyonu

YÜCEL YILMAZ D., DURSUN A., YALNIZOĞLU D., serdaroğlu e.
3. Nörometabolik Dismorfoloji Sempozyumu, Türkiye, 10 - 12 Mart 2016

ANALYSIS of MRI and 18F FDG PET Scan IN NON TRAUMATIC NON TUMORAL TEMPORAL LOBE EPILEPSY experience from an epilepsy center

GÜNEŞ A., VOLKAN SALANCI B., TEZER FİLİK F. İ., YALNIZOĞLU D., GÖÇMEN R., SAYGI S., et al.
The 2016 European Congress of Radiology, Viyana, Avusturya, 2 - 06 Mart 2016

Splicing mutation in aminophospholipid transporter protein ATP8A2 in a Turkish family

DURSUN A., YALNIZOĞLU D., YÜCEL YILMAZ D., serdaroğlu E., Unal Ö., görmez Z., et al.
SSIEM, 4 - 06 Eylül 2015

SNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family

ÖZGÜL R. K., YÜCEL YILMAZ D., Ömer g., YALNIZOĞLU D., Mahmut s., DURSUN A.
SSIEM, 4 - 07 Eylül 2015

Vacuolar storage material in a family with juvenile parkinsonism andmutations in FBXO7

ESRA S., ÖZGÜL R. K., YALNIZOĞLU D., MADEO M., MALANDRİNİ A., KLEE E., et al.
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM), 1 - 04 Eylül 2015

SMART syndrome A rare complication of cranial radiotherapy

ARDIÇLI D., GÖÇMEN R., VARAN A., YALNIZOĞLU D.
The European Paediatric Neurology Society (EPNS), 27 - 30 Mayıs 2015, cilt.19, ss.42

Magnetic resonance imaging findings in pediatric tuberoussclerosis patients

ANLAR F. B., GÖÇMEN R., SERDAROĞLU E., KONUŞKAN B., YALNIZOĞLU D.
The European Paediatric Neurology Society (EPNS), 27 - 30 Mayıs 2015, cilt.19, ss.131

Dirençli Hipoglisemi Hipertrofik Kardiyomiyopati ve Ensefalopatili Bir Hastada Ekzom Dizileme ile Mitokondriyal TSFM Gen Defekti

DURSUN A., ÖMER FARUK G., MELİS P., YÜCEL YILMAZ D., TOPÇU M., YALNIZOĞLU D., et al.
Uluslararası Katılımlı XIII.Ulusal Metabolik Hastalıklar Ve Beslenme Kongresi, Türkiye, 14 - 18 Nisan 2015

Ekzom Dizi Analizi ile MTO1 Mitochondriyal tRNA Modifier Geninde Saptanan Yeni Bir Mutasyon

YÜCEL YILMAZ D., ÖZGÜL R. K., ÖMER FARUK G., ESRA S., BETÜL Y., SAĞIROĞLU M., et al.
Uluslararası Katılımlı XIII.Ulusal Metabolik Hastalıklar Ve Beslenme Kongresi, Türkiye, 14 - 18 Nisan 2015

Lizozom Otofagozom Defekti Sonucu Serebellar Atrofiye Neden Olan Yeni Bir Gen SNX14 Tanımlanması

ÖZGÜL R. K., YÜCEL YILMAZ D., YALNIZOĞLU D., MAHMUT S., DURSUN A.
Uluslararası Katılımlı XIII.Ulusal Metabolik Hastalıklar Ve Beslenme Kongresi, 1, Türkiye, 14 - 18 Nisan 2015

Klasik Glutarik Asidüri Tip I GA I Bulguları Göstermeyen Bir Ailede GCDH Gen Defekti

ÖZGÜL R. K., YÜCEL YILMAZ D., SANİYE Ö., YALNIZOĞLU D., TURANLI G., ESRA S., et al.
Uluslararası Katılımlı XIII.Ulusal Metabolik Hastalıklar Ve Beslenme Kongresi, Türkiye, 14 - 18 Nisan 2015

Hereditary spastic paraplegia with predominant cerebel lar signs due to KIF1C mutation in two brothers

ÖZGÜL R. K., Esra s., YALNIZOĞLU D., YÜCEL YILMAZ D., TOPÇU M., ZZ G., et al.
SSIEM, 4 - 07 Eylül 2015

VAGUS NERVE STIMULATION IN CHILDREN WITH RETT SYNDROME

TOPÇU M., YALNIZOĞLU D., Turanli G., Bilginer B., Akalan N.
62nd Annual Meeting of the American-Epilepsy-Society, Washington, Amerika Birleşik Devletleri, 5 - 09 Aralık 2008, cilt.49, ss.297 identifier

Classification and follow-up of pediatric patients with absence epilepsy

Soyuer O. U., Turanli G., Yalnizoglu D., Bakar E. E., Topcu M.
60th Annual Meeting of the American-Epilepsy-Society, California, Amerika Birleşik Devletleri, 1 - 05 Aralık 2006, cilt.47, ss.152 identifier
Metrikler

Yayın

88

Atıf (WoS)

917

H-İndeks (WoS)

12

Atıf (Scopus)

235

H-İndeks (Scopus)

10

Proje

10

Açık Erişim

13
BM Sürdürülebilir Kalkınma Amaçları