Bilimsel çalışmalar
Prof. Dr. Aycan Ünalp
216 yayın. Her yayının yanında bilginin kaynağı yazar.
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Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.
Europe PMC (PubMed Central), 2018
PMID 30838351 14 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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High-fibre enteral feeding results in improved anthropometrics and favourable gastrointestinal tolerance in malnourished children with growth failure
Acta paediatrica (Oslo, Norway : 1992), 2018
DOI 10.1111/apa.14240 PMID 29364537 8 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Evaluation of patients admitted to the pediatric intensive care unit due to neurological problems
Journal of Dr Behcet Uz Children s Hospital, 2018
DOI 10.5222/buchd.2018.46872 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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A multicenter cross-sectional study to evaluate the clinical characteristics and nutritional status of children with cerebral palsy
Clinical Nutrition Espen, 2018
DOI 10.1016/j.clnesp.2018.05.002 PMID 29908679 26 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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GPR56 homozygous nonsense mutation p.R271* Associated with phenotypic variability in bilateral frontoparietal polymicrogyria
Turkish Journal of Pediatrics, 2018
DOI 10.24953/turkjped.2018.03.001 PMID 30511534 10 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Experience of the ketogenic diet therapy of the ketogenic diet team in a third-line children’s hospital
Journal of Dr Behcet Uz Children s Hospital, 2018
DOI 10.5222/buchd.2018.64935 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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The Evaluation Of Ventrikular Function Of Newly Diagnosed Idiopatic Generalized Epileptic Children With Tissue Doppler Imaging
Journal of Dr Behcet Uz Children s Hospital, 2018
DOI 10.5222/buchd.2018.023 Açık erişimli tam metinKaynak: OpenAlex
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Alpha Sarcoglycanopathy in a Turkish Family
SAJ Case Reports, 2018
DOI 10.18875/2375-7043.5.102 Açık erişimli tam metinKaynak: OpenAlex
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Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database
European Journal of Paediatric Neurology, 2017
DOI 10.1016/j.ejpn.2017.06.004 PMID 28694135 23 atıf (Europe PMC) Kaynak: OpenAlex
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A Rare Cause of Seizure: Gitelman Syndrome
Journal of Neuroscience and Neuropsychology, 2017
DOI 10.18875/2577-7890.1.105 Açık erişimli tam metinKaynak: OpenAlex
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Evaluation of polyneuropathy and associated risk factors in children with type 1 diabetes mellitus
Turkish Journal of Medical Sciences, 2017
DOI 10.3906/sag-1601-183 PMID 28618748 5 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Ketogenic diet practices on childhood epilepsies
Journal of Dr Behcet Uz Children s Hospital, 2017
DOI 10.5222/buchd.2017.169 2 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Characteristics of Children Admitted to the Emergency Department with Convulsive Epileptic Seizures: A Single-Center Study
Turkish Journal of Pediatric Emergency and Intensive Care Medicine, 2017
DOI 10.4274/cayd.86548 2 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Combined use of genetic and immunohistochemical analysis is a critical step in differential diagnosis of sarcoglycanopathies
Journal of Dr Behcet Uz Children s Hospital, 2017
DOI 10.5222/buchd.2017.247 Açık erişimli tam metinKaynak: OpenAlex
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Acil servise konvülzif epileptik nöbet ile başvuran çocukların özellikleri: Tek merkez çalışması
2017
Kaynak: OpenAlex
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Bilateral frontoparietal polimikrogiride fenotipik değişkenlik ile ilişkili GPR56 homozigot nonsense mutasyonu p.R271*
Van Yüzüncü Yıl University Academic Data Management System, 2017
Kaynak: OpenAlex
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Evaluation of the relationship between migraine disorder and oral comorbidities: Multicenter randomized clinical trial
Turkish Journal of Medical Sciences, 2016
DOI 10.3906/sag-1412-71 PMID 27513246 15 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Two Siblings with Beta-Ketothiolase Deficiency: One Genetic Defect Two Different Pictures
The Journal of Pediatric Research, 2016
DOI 10.4274/jpr.25338 4 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Clinical, molecular, radiological investigations in patients with SURF1 mutations and muscle biopsy findings
Neuromuscular Disorders, 2016
DOI 10.1016/j.nmd.2016.06.320 Açık erişimli tam metinKaynak: OpenAlex
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A histologically diagnosed case with limb-girdle muscular dystrophy type 1A: The youngest case in the literature
Neuromuscular Disorders, 2016
DOI 10.1016/j.nmd.2016.06.032 Kaynak: OpenAlex
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Assosiation of Cranial Magnetic Resonance Imaging and Clinical Findings of Children with Cerebral Palsy
Journal of Dr Behcet Uz Children s Hospital, 2016
DOI 10.5222/buchd.2016.119 Açık erişimli tam metinKaynak: OpenAlex
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Etiological profile of the newborns who had convulsions and evaluation of their neurodevelopmental outcomes.
2015
1 atıf (OpenAlex) Kaynak: OpenAlex
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Yenidoğan döneminde konvülziyon geçiren olguların etiyolojik profili ve nörogelişimsel sonuçları açısından değerlendirilmesi
İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2015
Kaynak: OpenAlex
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Serum concentration of brain-derived neurotrophic factor in epileptic children
Journal of Pediatric Neurology, 2015
DOI 10.3233/jpn-2009-0301 3 atıf (OpenAlex) Kaynak: OpenAlex
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Evaluation of short-term neurodevelopmental outcomes in the premature patients with periventricular-intraventricular hemorrhage
Journal of Pediatric Neurology, 2015
DOI 10.1055/s-0035-1557481 2 atıf (OpenAlex) Kaynak: OpenAlex
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Malnütrisyona Bağlı Büyüme Yetersizliği Olan Çocuklarda Yüksek Enerjili Lifli Pediatrik Enteral Beslenme Ürünü Kullanımının Gelişim Üzerine Etkisi
AYBU AVESIS, 2015
Kaynak: OpenAlex
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Investigation of iron's neurotoxicity during cerebral maturation in the neonatal rat model of haemolysis
Folia Neuropathologica, 2015
DOI 10.5114/fn.2015.54623 PMID 26443317 5 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Status epilepticus in an adolescent patient with adrenoleukodystrophy
Journal of Pediatric Neurology, 2015
DOI 10.1055/s-0035-1557422 1 atıf (OpenAlex) Kaynak: OpenAlex
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P117 – 2587: Assessment of patients who were admitted to pediatric intensive care unit with neurological disorders
European Journal of Paediatric Neurology, 2015
DOI 10.1016/s1090-3798(15)30430-x Kaynak: OpenAlex
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Risk Factors of Seizure Recurrence After Antiepileptic Drug Withdrawal
Journal of Dr Behcet Uz Children s Hospital, 2015
DOI 10.5222/buchd.2015.109 Açık erişimli tam metinKaynak: OpenAlex
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P54 – 2942: Controlled evaluation of serum lipid levels and carotid artery intima media thickness in idiopathic epileptic children treated with valproic acid, carbamazepine and levetiracetam
European Journal of Paediatric Neurology, 2015
DOI 10.1016/s1090-3798(15)30367-6 Kaynak: OpenAlex
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Efficacy and Safety of IV Levetiracetam in Children With Acute Repetitive Seizures
Pediatric Neurology, 2014
DOI 10.1016/j.pediatrneurol.2014.07.021 PMID 25172096 15 atıf (OpenAlex) Kaynak: OpenAlex
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Childhood headaches and brain magnetic resonance imaging findings
European Journal of Paediatric Neurology, 2014
DOI 10.1016/j.ejpn.2013.11.003 PMID 24268890 26 atıf (Europe PMC) Kaynak: ORCID
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Histopathological and genetic features of patients with limb girdle muscular dystrophy type 2C,Kavşak tipi müsküler distrofi tip 2C hastalari{dotless}ni{dotless}n histopatolojik ve genetik özellikleri
Turk Patoloji Dergisi Turkish Journal of Pathology, 2014
DOI 10.5146/tjpath.2014.01239 PMID 24638197 4 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Vitamin B12 deficiency in a child presenting with epileptic spasms
Journal of Pediatric Neurology, 2014
DOI 10.3233/jpn-140641 3 atıf (OpenAlex) Kaynak: ORCID
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G.P.224
Neuromuscular Disorders, 2014
DOI 10.1016/j.nmd.2014.06.300 Kaynak: OpenAlex
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A case of propionic acidemia presenting with choreoathetoid movements
Journal of Dr Behcet Uz Children s Hospital, 2013
DOI 10.5222/buchd.2012.114 Kaynak: OpenAlex
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Developmental problems in infants diagnosed as congenital cytomegalovirus infection
Journal of Dr Behcet Uz Children s Hospital, 2013
DOI 10.5222/buchd.2013.049 Kaynak: OpenAlex
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Alternating facial paralysis in a girl with hypertension. Case report,Parálisis facial alternante en una niña con hipertensión arterial. Informe de un caso
Archivos Argentinos De Pediatria, 2013
DOI 10.5546/aap.2013.eng.e133 PMID 24196770 Açık erişimli tam metinKaynak: ORCID
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Nemaline myopathy in a newborn infant: A rare muscle disorder,Miopatia nemalinowa u noworodka - Opis rzadkiej choroby
Neurologia I Neurochirurgia Polska, 2013
DOI 10.5114/ninp.2013.38229 PMID 24166571 4 atıf (Europe PMC) Kaynak: ORCID
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Serum nerve growth factor levels in autistic children in Turkish population: A preliminary study
Indian Journal of Medical Research, 2013
PMID 24521633 19 atıf (OpenAlex) Açık erişimli tam metinKaynak: ORCID
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The evaluation of muscle biopsy findings in children with neuromuscular disorders
Journal of Dr Behcet Uz Children s Hospital, 2013
DOI 10.5222/buchd.2012.062 17 atıf (OpenAlex) Kaynak: OpenAlex
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Evaluation of the relationship between urogenital abnormalities and neuromuscular disorders Evaluation of the relationship between urogenital abnormalities and
DergiPark (Istanbul University), 2013
1 atıf (OpenAlex) Kaynak: OpenAlex
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Early-onset acute partial transverse myelitis: Case report
Journal of Dr Behcet Uz Children s Hospital, 2013
DOI 10.5222/buchd.2013.133 Kaynak: OpenAlex
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Etiology of the children with chronic recurrent headaches
Journal of Dr Behcet Uz Children s Hospital, 2013
DOI 10.5222/buchd.2013.153 Kaynak: OpenAlex
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Dyke-Davidoff-Masson syndrome: A case report
Journal of Dr. Behcet Uz Children's Hospital, 2012
DOI 10.5222/buchd.2012.194 1 atıf (OpenAlex) Kaynak: ORCID
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Koreoatetoik hareketler ile başvuran propiyonik asidemi olgusu
İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2012
Kaynak: OpenAlex
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Lack of association of childhood partial epilepsy with brain derived neurotrophic factor gene
Scientific World Journal, 2012
DOI 10.1100/2012/414797 PMID 22654603 2 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Subacute sclerosing panencephalitis cases diagnosed by increased csf/serum measles antibody indices,Yüksek BOS/Serum Kizamik Antikor indeksi ile Tanimlanan Subakut Skierozan Panensefalit Olgulari
Mikrobiyoloji Bulteni, 2012
Kaynak: ORCID
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Ventricular septal defect in crouzon syndrome: Case report
Genetic Counseling, 2012
PMID 23431754 3 atıf (OpenAlex) Kaynak: ORCID