Pakize Karaoğlu, M.D.
13.05.2024

Name Surname: Pakize Karaoğlu
Date of birth:1982
Language skills: English
Place of duty: University of Health Sciences, Dr.Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital

A.      EDUCATION

·         Hacettepe University Faculty of Medicine (2000-2006)

·         Dokuz Eylül University Faculty of Medicine, Department of Pediatrics (Residency, 2006-2011)

·         Dokuz Eylül University Faculty of Medicine, Department of Pediatrics, Child Neurology Unit (Fellowship, 2011-2014)

 

B.      WORK EXPERIENCE

·         2006-2011; Dokuz Eylül University Faculty of Medicine, Department of Pediatrics

·         2011; Manisa Alaşehir State Hospital

·         2011-2014; Dokuz Eylül University Faculty of Medicine, Department of Pediatrics, Child Neurology Unit

·         2014-2016 Van İpekyolu Maternity and Children’s Hospital

·         2016-currently; University of Health Sciences, Dr.Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital

         C. CLINICAL RESEARCH

  1. Ayar D, Ünalp A, Bektaş M, Yılmaz Ü, Karaoğlu P, Yalçıntuğ FM. Psychometric properties of a Turkish version of the quality of life in childhood epilepsy questionnaire. J Pediatr Nurs. 2022;62:91-97. doi: 10.1016/j.pedn.2021.09.009. 
  2. Tekin HG, Karaoğlu P, Edem P. Clinical and Electrophysiological Prognostic Factors of Childhood Absence Epilepsy. The Journal of Pediatric Research. 2021; 8(3):320-325.
  3. Polat İ, Karaoğlu P, Şışman AR, Yış U, Hız Kurul S. Inflammation and endothelial dysfunction in pediatric migraine patients. Pediatr Int. 2021 Aug 6. doi: 10.1111/ped.14946. 
  4. Kose M, Isik E, Aykut A, Durmaz A, Kose E, Ersoy M, Diniz G, Adebali O, Ünalp A, Yilmaz Ü, Karaoğlu P, Edizer S, Tekin HG, Özdemir TR, Atik T, Onay H, Özkınay F. The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum. J Pediatr Endocrinol Metab. 2021;34(4):417-430. doi: 10.1515/jpem-2020-0410.
  5. Karaoğlu P, Yaş U, Polat Aİ, Ayanoğlu M, Hız S. Clinical predictors of drug-resistant epilepsy in children. Turk J Med Sci. 2021;51(3):1249-1252. doi: 10.3906/sag-2010-27.
  6. Tekin HG, Karaoğlu P, Bolat E. A rare central nervous system tumor of childhood with spongiform appearance on brain magnetic resonance imaging; primary diffuse leptomeningeal oligodendrogliomatosis. Neurocirugia (Astur : Engl Ed). 2021 F:S1130-1473(21)00006-3. English, Spanish. doi: 10.1016/j.neucir.2020.12.004. 
  7. Tekin HG, Karaoğlu P. COVID-19 Pandemisinin Çocukluk Çağı Epilepsi Yönetimi Üzerindeki Etkileri; Anket Çalışması. Osmangazi Journal of Medicine. 2021; 43(4), 318-323. doi: 10.20515/otd.823760.
  8. Polat, I., Karaoglu, P., Ayanoglu, M., Cirali, C., Bayram, E., Yis, U., & Hız, S. (2021). Inflammation and anemia in simple febrile seizures and complex febrile seizures. Annals of Medical Research, 28(10), 1835–1839. 
  9. Kose M, Kose E, Ünalp A, Yılmaz Ü, Edizer S, Tekin HG, Karaoğlu P, Özdemir TR, Er E, Onay H, Yildirim ES. Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey. Neurol Sci. 2021;42(3):1103-1111. doi: 10.1007/s10072-021-05067-8. 
  10. Ünalp A, Gazeteci Tekin H, Karaoğlu P, Akışın Z. Benefits of ketogenic diet in a pediatric patient with Ehlers-Danlos syndrome and STXBP1-related epileptic encephalopathy. Int J Neurosci. 2020 Dec 9:1-3. doi: 10.1080/00207454.2020.1858825.
  11. Terzioğlu MA, Karaoğlu P. A case of pediatric neuroboreliosis presenting with psychiatric symptoms. Alpha Psychiatry. 2020; 21: 553-556
  12. Karaoğlu P, Köse M. Expanding the spectrum of VAC14 related pediatric-onset neurological disease; striatonigral degeneration with brainstem involvement. Eur J Med Genet. 2021;64(1):104117. doi: 10.1016/j.ejmg.2020.104117. 
  13. Karaoğlu P, Hız S, İşcan B, Polat AI, Ayanoğlu M, Duman N, Yiş U. Intravenous Levetiracetam for Treatment of Seizures in Term and Preterm Neonates. J Pediatr Neurosci. 2020 ;15(1):15-20. doi: 10.4103/JPN.JPN_66_19. 
  14. Çubukçu D, Karaoğlu P. The Effects of Neuro-Developmental Treatment Based Rehabilitation on Gross Motor Function in Spastic Cerebral Palsy Children Rehabilitation. Behcet Uz Cocuk Hast Derg. 2020; 10(1): 47-52.
  15. Karaoglu P, Quizon N, Pergande M, Wang H, Polat AI, Ersen A, Özer E, Willkomm L, Hiz Kurul S, Heredia R, Yis U, Selcen D, Çirak S. Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA. Brain Dev. 2017;39(4):361-364. doi: 10.1016/j.braindev.2016.11.002. 
  16. Polat İ, Karaoğlu P, Yiş U, Kurul SH. Schwartz-Jampel syndrome with gastroduodenal bleeding. J Pediatr Neurosci. 2016;11(3):255-257. doi: 10.4103/1817-1745.193351. 
  17. Polat İ, Yiş U, Karaoğlu P, Ayanoğlu M, Öztürk T, Güleryüz H, Kurul SH. Myelin Oligodendrocyte Glycoprotein Antibody Persistency in a Steroid-Dependent ADEM Case. Pediatrics. 2016;137(5):e20151958. doi: 10.1542/peds.2015-1958.

18.    Ozyurt G, Bayram E, Karaoglu P, Kurul SH, Yis U. Quality of life and sleep in children diagnosed with duchenne muscular dystrophy and their mothers’ level of anxiety: a case-control study. Dusunen Adam The Journal of Psychiatry and Neurological Sciences 2015;28:362-368.

19.    Yis U, Polat I, Karaoglu P, Ayanaoglu M, Unsal E, Ozkutuk AA, Kurul SH. An 11-Year-Old Boy with Headache, Fever, and Neck Pain. Pediatr Ann. 2015;44(10):426-7, 432. doi: 10.3928/00904481-20151012-05.

  1. Yiş U, Karaoğlu P, Kurul SH, Soylu A, Çakmakçi H, Kavukçu S. Posterior reversible leukoencephalopathy syndrome with spinal cord involvement in a 9-year-old girl. Brain Dev. 2016;38(1):154-7. doi: 10.1016/j.braindev.2015.07.001.
  2. Karaoğlu P, Polat Aİ, Yiş U, Hız S. Parieto-occipital encephalomalacia in children; clinical and electrophysiological features of twenty-seven cases. J Pediatr Neurosci. 2015;10(2):103-7. doi: 10.4103/1817-1745.159187.
  3. Polat I, Karaoglu P, Ayanoglu M, Yis U, Hiz S. Life-Threatening and Rare Adverse Effects of Phenytoin. Pediatr Emerg Care. 2015;31(7):e3. doi:  10.1097/PEC.0000000000000495.
  4. Polat İ, Karaoglu P, Ayanoglu M, Yis U, Hiz S. Williams Syndrome with Infantile Spasms. Indian J Pediatr. 2015;82(8):757-8. doi: 10.1007/s12098-015-1740-4. 
  5. Topçu Y, Bayram E, Karaoğlu P, Yiş U, Kurul SH. Importance of acylcarnitine profile analysis for disorders of lipid metabolism in adolescent patients with recurrent rhabdomyolysis: Report of two cases. Ann Indian Acad Neurol. 2014;17(4):437-40. doi: 10.4103/0972-2327.144031. 
  6. Topçu Y, Bayram E, Ozbal S, Yiş U, Tuğyan K, Karaoğlu P, Kumral A, Yılmaz O, Kurul SH. Zonisamide attenuates hyperoxia-induced apoptosis in the developing rat brain. Neurol Sci. 2014;35(11):1769-75. doi: 10.1007/s10072-014-1834-1. 
  7. Topçu Y, Bayram E, Karaoğlu P, Yiş U, Bayram M, Kurul SH. Carnitine palmitoyl transferase II deficiency in an adolescent presenting with rhabdomyolysis and acute renal failure. Pediatr Emerg Care. 2014;30(5):343-4. doi: 10.1097/PEC.0000000000000127.
  8. Topcu Y, Bayram E, Karaoglu P, Yis U, Kurul SH. Kabuki syndrome and perisylvian cortical dysplasia in a Turkish girl. J Pediatr Neurosci. 2013;8(3):259-60. doi: 10.4103/1817-1745.123710. 
  9. Bayram E, Topçu Y, Karaoğlu P, Yiş U, Hız Kurul S, Yılmaz N, Kır M. The Utility of Head Up Tilt Test with Video Electroencephalography in Children with Recurrent Loss of Consciousness. Hong Kong Journal of Paediatrics 18(4):217-222
  10. Topcu Y, Bayram E, Karaoglu P, Yis U, Kurul SH. The combination of thermal dysregulation and agenesis of corpus callosum: Shapiro's or/and reverse Shapiro's syndrome. Ann Indian Acad Neurol. 2013;16(4):716-9. doi:10.4103/0972-2327.120451. 
  11. Karaoğlu P, Polat Aİ, Ayanoğlu M, Yiş U, Hız S. Evaluation of vitamin D status in children with refractory epilepsy. Behcet Uz Cocuk Hast Derg. 2014; 4(3): 167-170
  12. Yiş U, Kalemci O, Polat I, Karaoğlu P, Oztura I, Güleryüz H, Kurul SH. Chronic spinal epidural hematoma. J Pediatr. 2014;164(1):215-215.e1. doi: 10.1016/j.jpeds.2013.08.043. 
  13. Karaoğlu P, Yiş U, Öztura I, Akdoğan Ö, Bayram E, Topçu Y, Hiz S. Phrenic nerve palsy associated with brachial plexus avulsion in a pediatric patient with multitrauma. Pediatr Emerg Care. 2013;29(8):922-3. doi: 10.1097/PEC.0b013e31829ec20b.
  14. Topcu Y, Bayram E, Karaoglu P, Yis U, Guleryuz H, Kurul SH. Coexistence of myositis, transverse myelitis, and Guillain Barré syndrome following Mycoplasma pneumoniae infection in an adolescent. J Pediatr Neurosci. 2013;8(1):59-63. doi: 10.4103/1817-1745.111428. 
  15. Bayram E, Topcu Y, Karaoglu P, Yis U, Cakmakci Guleryuz H, Kurul SH. Incidental white matter lesions in children presentıng with headache. Headache. 2013;53(6):970-6. doi: 10.1111/head.12089. 
  16. Bayram E, Topçu Y, Karaoglu K, Yiş U, Güleryüz HÇ, Kurul SH. Van der Knaap disease: Case report. Behcet Uz Cocuk Hast Derg. 2013; 3(1): 60-62.
  17. Bayram E, Topcu Y, Karakaya P, Yiş U, Çakmakçı H, Kurul SH. Canavan disease in the differential diagnosis of macrocephaly: Case report. Behcet Uz Cocuk Hast Derg. 2012; 2(2): 107-110.
  18. Karaoğlu P, Topçu Y, Bayram E, Yis U, Akarsu S, Atalay E, Koroğlu T, Cakmakçi H, Ozer E, Hız S. Severe neurologic involvement of Degos disease in a pediatric patient. J Child Neurol. 2014;29(4):550-4. doi: 10.1177/0883073812474692.
  19. Yiş U, Polat İ, Karakaya P, Ayanoğlu M, Hiz AS. Importance of acrocyanosis in delayed walking. J Pediatr Neurosci. 2015;10(1):80-1. doi: 10.4103/1817-1745.154368. 
  20. Yiş U, Karaoğlu P, Polat Aİ, Güleryüz H, Hız S. Transient striatal involvement with frequent seizures and fast recovery associated with Mycoplasma pneumoniae infection. Behcet Uz Cocuk Hast Derg. 2014; 4(2): 135-138.
  21. Bayram E, Yiş U, Öztura İ, Akdoğan Ö, Topçu Y, Karaoğlu P, Kurul SH. Severe axonal neuropathy resultıng from folic acid deficiency in a case with restrictive type anorexia nervosa. Behcet Uz Cocuk Hast Derg. 2014; 4(1): 72-74.
  22. Hız S, Yiş U, Özer E, Karaoğlu P, Polat AI. Clinical features and psychomotor development at one year of age in infants born from a mother with chorioamnionitis. Behcet Uz Cocuk Hast Derg. 2014; 4(1): 15-19
  23. Yiş U, Ezgü FS, Karakaya P, Polat İ, Arslan N, Çankaya T, Bozkaya ÖG, Kurul SH. A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with Prader Willi syndrome. J Child Neurol. 2015;30(3):378-81. doi: 10.1177/0883073814530499.

43.    Bayram E, Topcu Y, Tufekci O, Karaoglu P, Yis U , Oren H, Kurul S.H. Levetiracetam in hematologic disorders. J Paediatr Child Health, 2014;50: 553-556. https://doi.org/10.1111/jpc.12494.

44.    Yiş U, Karaoğlu P, Polat Aİ, Ayanoğlu M, Güleryüz H, Hız S. Fisher-Bickerstaff syndrome with negative anti-ganglioside antibody test results associated with mycoplasma pneumoniae infection. Behcet Uz Cocuk Hast Derg. 2014; 4(3): 218-222.

  1. Karakaya P, Yılmaz S, Tüfekçi O, Kır M, Böber E, Irken G, Oren H. Endocrinological and cardiological late effects among survivors of childhood acute lymphoblastic leukemia. Turk J Haematol. 2013;30(3):290-9. doi: 10.4274/Tjh.2012.0094. 
  2. Yiş U, Bayram E, Topçu Y, Karakaya P, Hız Kurul S. A case of atypical Miller Fisher syndrome with negative anti-GQ1b immunoglobulin G and importance of H reflex. Turk J Pediatr. 2013;55(2):235-6. 
  3. Yiş U, Topçu Y, Özbal S, Tuğyan K, Bayram E, Karakaya P, Yilmaz O, Kurul SH. Caffeic acid phenethyl ester prevents apoptotic cell death in the developing rat brain after pentylenetetrazole-induced status epilepticus. Epilepsy Behav. 2013;29(2):275-80. doi: 10.1016/j.yebeh.2013.08.002. 
  4. Bayram E, Topcu Y, Karaoğlu P, Yiş U, Kurul SH. Evaluation of the quality of sleep in patients diagnosed with epilepsy and their mothers. Behcet Uz Cocuk Hast Derg. 2013; 3(2): 87-92
  5. Yiş U, Topçu Y, Bayram E, Karakaya P, Cakmakçı H, Hız-Kurul S. Pneumatosis intestinalis due to rotavirus infection in a child with Prader-Willi syndrome. Turk J Pediatr. 2012;54(6):679-81.
  6. Bayram E, Karakaya P, Topcu Y, Yis U, Hiz S. Acute cervical dystonia after the first dose of butamirate citrate. Pediatr Emerg Care. 2013;29(1):80-1. doi: 10.1097/PEC.0b013e31827b5635. 
  7. Yis U, Topcu Y, Bayram E, Karakaya P, Cakmakci H, Kurul SH. Importance of diazepam administration during electroencephalography in the differential diagnosis of cortical visual loss. J Child Neurol. 2014;29(1):114-7. doi: 10.1177/0883073812467690. 
  8. Bayram E, Topcu Y, Karakaya P, Yis U, Cakmakci H, Ichida K, Kurul SH. Molybdenum cofactor deficiency: review of 12 cases (MoCD and review). Eur J Paediatr Neurol. 2013;17(1):1-6. doi: 10.1016/j.ejpn.2012.10.003. 
  9. Karaoğlu P, Topçu Y, Bayram E, Yiş U, Güleryüz H, Hız S. Klippel Treunanay Syndrome in differential diagnosis of cerebral palsy. Behcet Uz Cocuk Hast Derg. 2015; 5(2): 125-128
  10. Bayram E, Topcu Y, Karakaya P, Bayram MT, Sahin E, Gunduz N, Yis U, Peker O, Kurul SH. Correlation between motor performance scales, body composition, and anthropometry in patients with Duchenne muscular dystrophy. Acta Neurol Belg. 2013;113(2):133-7. doi: 10.1007/s13760-012-0125-y.
  11. Karakaya P, Yiş U, Kurul SH, Türkmen MA. Rhabdomyolysis associated with olanzapine treatment in a child with Autism. Pediatr Emerg Care. 2010;26(1):41-2. doi: 10.1097/PEC.0b013e3181c39a22.