Wissenschaftliche Arbeiten

Prof. Dr. Aycan Ünalp

216 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  1. Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.

    Europe PMC (PubMed Central), 2018

    PMID 30838351 14 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  2. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  3. 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 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  4. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  5. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  6. 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 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  7. 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 Frei zugänglicher VolltextQuelle: OpenAlex

  8. Alpha Sarcoglycanopathy in a Turkish Family

    SAJ Case Reports, 2018

    DOI 10.18875/2375-7043.5.102 Frei zugänglicher VolltextQuelle: OpenAlex

  9. 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 Zitationen (Europe PMC) Quelle: OpenAlex

  10. A Rare Cause of Seizure: Gitelman Syndrome

    Journal of Neuroscience and Neuropsychology, 2017

    DOI 10.18875/2577-7890.1.105 Frei zugänglicher VolltextQuelle: OpenAlex

  11. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  12. Ketogenic diet practices on childhood epilepsies

    Journal of Dr Behcet Uz Children s Hospital, 2017

    DOI 10.5222/buchd.2017.169 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  13. 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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  14. 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 Frei zugänglicher VolltextQuelle: OpenAlex

  15. Acil servise konvülzif epileptik nöbet ile başvuran çocukların özellikleri: Tek merkez çalışması

    2017

    Quelle: OpenAlex

  16. Bilateral frontoparietal polimikrogiride fenotipik değişkenlik ile ilişkili GPR56 homozigot nonsense mutasyonu p.R271*

    Van Yüzüncü Yıl University Academic Data Management System, 2017

    Quelle: OpenAlex

  17. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  18. Two Siblings with Beta-Ketothiolase Deficiency: One Genetic Defect Two Different Pictures

    The Journal of Pediatric Research, 2016

    DOI 10.4274/jpr.25338 4 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  19. Clinical, molecular, radiological investigations in patients with SURF1 mutations and muscle biopsy findings

    Neuromuscular Disorders, 2016

    DOI 10.1016/j.nmd.2016.06.320 Frei zugänglicher VolltextQuelle: OpenAlex

  20. 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 Quelle: OpenAlex

  21. 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 Frei zugänglicher VolltextQuelle: OpenAlex

  22. Etiological profile of the newborns who had convulsions and evaluation of their neurodevelopmental outcomes.

    2015

    1 Zitation (OpenAlex) Quelle: OpenAlex

  23. Yenidoğan döneminde konvülziyon geçiren olguların etiyolojik profili ve nörogelişimsel sonuçları açısından değerlendirilmesi

    İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2015

    Quelle: OpenAlex

  24. Serum concentration of brain-derived neurotrophic factor in epileptic children

    Journal of Pediatric Neurology, 2015

    DOI 10.3233/jpn-2009-0301 3 Zitationen (OpenAlex) Quelle: OpenAlex

  25. 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 Zitationen (OpenAlex) Quelle: OpenAlex

  26. Malnütrisyona Bağlı Büyüme Yetersizliği Olan Çocuklarda Yüksek Enerjili Lifli Pediatrik Enteral Beslenme Ürünü Kullanımının Gelişim Üzerine Etkisi

    AYBU AVESIS, 2015

    Quelle: OpenAlex

  27. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  28. Status epilepticus in an adolescent patient with adrenoleukodystrophy

    Journal of Pediatric Neurology, 2015

    DOI 10.1055/s-0035-1557422 1 Zitation (OpenAlex) Quelle: OpenAlex

  29. 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 Quelle: OpenAlex

  30. Risk Factors of Seizure Recurrence After Antiepileptic Drug Withdrawal

    Journal of Dr Behcet Uz Children s Hospital, 2015

    DOI 10.5222/buchd.2015.109 Frei zugänglicher VolltextQuelle: OpenAlex

  31. 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 Quelle: OpenAlex

  32. 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 Zitationen (OpenAlex) Quelle: OpenAlex

  33. 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 Zitationen (Europe PMC) Quelle: ORCID

  34. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  35. Vitamin B12 deficiency in a child presenting with epileptic spasms

    Journal of Pediatric Neurology, 2014

    DOI 10.3233/jpn-140641 3 Zitationen (OpenAlex) Quelle: ORCID

  36. G.P.224

    Neuromuscular Disorders, 2014

    DOI 10.1016/j.nmd.2014.06.300 Quelle: OpenAlex

  37. A case of propionic acidemia presenting with choreoathetoid movements

    Journal of Dr Behcet Uz Children s Hospital, 2013

    DOI 10.5222/buchd.2012.114 Quelle: OpenAlex

  38. Developmental problems in infants diagnosed as congenital cytomegalovirus infection

    Journal of Dr Behcet Uz Children s Hospital, 2013

    DOI 10.5222/buchd.2013.049 Quelle: OpenAlex

  39. 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 Frei zugänglicher VolltextQuelle: ORCID

  40. 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 Zitationen (Europe PMC) Quelle: ORCID

  41. Serum nerve growth factor levels in autistic children in Turkish population: A preliminary study

    Indian Journal of Medical Research, 2013

    PMID 24521633 19 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

  42. 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 Zitationen (OpenAlex) Quelle: OpenAlex

  43. Evaluation of the relationship between urogenital abnormalities and neuromuscular disorders Evaluation of the relationship between urogenital abnormalities and

    DergiPark (Istanbul University), 2013

    1 Zitation (OpenAlex) Quelle: OpenAlex

  44. Early-onset acute partial transverse myelitis: Case report

    Journal of Dr Behcet Uz Children s Hospital, 2013

    DOI 10.5222/buchd.2013.133 Quelle: OpenAlex

  45. Etiology of the children with chronic recurrent headaches

    Journal of Dr Behcet Uz Children s Hospital, 2013

    DOI 10.5222/buchd.2013.153 Quelle: OpenAlex

  46. Dyke-Davidoff-Masson syndrome: A case report

    Journal of Dr. Behcet Uz Children's Hospital, 2012

    DOI 10.5222/buchd.2012.194 1 Zitation (OpenAlex) Quelle: ORCID

  47. Koreoatetoik hareketler ile başvuran propiyonik asidemi olgusu

    İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2012

    Quelle: OpenAlex

  48. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  49. 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

    Quelle: ORCID

  50. Ventricular septal defect in crouzon syndrome: Case report

    Genetic Counseling, 2012

    PMID 23431754 3 Zitationen (OpenAlex) Quelle: ORCID