Eserler

Adı Soyadı: HÜSEYİN PER

Doğum Tarihi: 18-01-1971 KAYSERİ

Öğrenim Durumu:

Derece	Bölüm/Program	Üniversite	Yıl
Lisans	Tıp	ERCİYES  ÜNİVERSİTESİ	1987-1994
Tıpta Uzmanlık	Çocuk Sağlığı Ve Hastalıkları	ERCİYES  ÜNİVERSİTESİ	1995-2000
Yan Dal	Çocuk Nöroloji	ERCİYES  ÜNİVERSİTESİ	2004-2010

Yüksek Lisans Tez Başlığı (özeti ekte) ve Tez Danışman(lar)ı  :

Doktora Tezi/S.Yeterlik Çalışması/Tıpta Uzmanlık Tezi Başlığı (özeti ekte)  ve  Danışman(lar)ı : Çocukluk Çağı Pnömonilerinde Serum Prokalsitonin Düzeylerinin Tanısal Değeri

Tez Danışmanı: Prof Dr Mustafa Öztürk

Yan Dal Uzmanlık Tezi: Çocukluk Çağı Dirençli Epilepsilerinde Serum ve İdrar Bor ve Selenyum Düzeyleri

Tez Danışmanı : Prof Dr Sefer Kumandaş

Görevler:

Görev Unvanı	Görev Yeri	Yıl
Ar.Gör.	Erciyes Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları ABD Araştırma Görevlisi	1995-2000
Uzman Dr	Özel İbni Sina Sağlık Merkezi	2000-2002
Uzman Dr	Kayseri Devlet Hastanesi	2002-2004
Yan Dal Arş Gör	Erciyes Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları ABD, Çocuk Nörolojisi Bilim Dalı Araştırma Görevlisi	2004- 2007
Uzman Dr	Kayseri Eğitim ve Araştırma Hastanesi	2007-2008
Uzman Dr	Kayseri Kadın Doğum ve Çocuk Hastalıkları Hastanesi	2008- 2009
Yard Doç Dr	Erciyes Üniversitesi Tıp Fakültesi	2009-2010
Doçent Dr	Erciyes Üniversitesi Tıp Fakültesi	2010-2015
Profesör Dr	Erciyes Üniversitesi Tıp Fakültesi	2015-

 

 

 

 

 

ESERLER

1. Uluslararası hakemli dergilerde yayımlanan makaleler :

A1 Gündüz Z, Kisaarslan FA, Düsünsel R, Poyrazoglu HM, Saraymen R, Per H. Effects of recombinant human erythropoietin on fibrinolytic system in children on continuous ambulatory peritoneal dialysis. Adv Perit Dial. 1999;15:278-82.A2 Caksen H, Oztürk MK, Uzüm K, Yüksel S, Ustünbaş HB, Per H. Septic arthritis in childhood. Pediatr Int. 2000;42:534-40A3 Narin N, Ciftci A, Patiroglu T, Ustünbas HB, Tutus A, Kilic H, Uzüm K, Per H. High neopterin levels in acute rheumatic fever. Clin Exp Rheumatol. 2000;18:652-3. A4 Kumandas S, Caksen H, Ciftçi A, Oztürk M, Per H. Lamotrigine in two cases of Rett syndrome. Brain Dev. 2001;23:240-2.A5 Kurtoğlu S, Caksen H, Per H, Narin N, Uzüm K. Asymmetric crying facies and congenital hypothyroidism: report of two patients. J Pediatr Endocrinol Metab. 2001;14:1177-81.A6 Aydin K, Per H, Kurtoglu S, Poyrazoglu MH, Narin N, Aslan D. Amitraz poisoning in children. Eur J Pediatr. 2002;161:349-50A7 Poyrazoğlu HM, Per H, Gündüz Z, Düşünsel R, Arslan D, Narin N, Gümüş H. Acute hemorrhagic edema of infancy. Pediatr Int. 2003;45:697-700.A8 Kurtoğlu S, Yüksel S, Gündüz Z, Per H, Narin N, Kontaş O, Ozdemir MA, Caksen H. Use of high-dose intravenous corticosteroid treatment in a child with scleredema. J Emerg Med. 2004;26:245-6A9 Gunduz Z, Canoz O, Per H, Dusunsel R, Poyrazoglu MH, Tez C, Saraymen R. The effects of pentoxifylline on diabetic renal changes in streptozotocin-induced diabetes mellitus. Ren Fail. 2004;26:597-605A10 Gümüş H, Kumandaş S, Coşkun A, Per H. Traumatic medial cerebral artery occlusion in a 4-year-old child. Am J Emerg Med. 2004;22:626-8. A11 Per H, Kumandaş S, Ozdemir MA, Gümüş H, Karakukcu M. Intracranial hemorrhage due to late hemorrhagic disease in two siblings. J Emerg Med. 2006 ;31:49-52.              A12 Per H, Gümüş H, Tucer B, Akgün H, Kurtsoy A, Kumandaş S. Calcified chronic subdural hematoma mimicking calvarial mass: a case report. Brain Dev. 2006;28:607-9               A13 Kumandaş S, Per H, Gümüş H, Tucer B, Yikilmaz A, Kontaş O, Coşkun A, Kurtsoy A. Torticollis secondary to posterior fossa and cervical spinal cord tumors: report of five cases and literature review. Neurosurg Rev. 2006;29(4):333-8A14 Kumandaş S, Kurtsoy A, Canöz O, Patiroğlu T, Yikilmaz A, Per H. Erdheim Chester disease: cerebral involvement in childhood. Brain Dev. 2007;29:227-30.A15 Gümüş H, Kumandaş S, Per H, Tahan F, Köklü E, Karakükçü M. Unusual presentation of herpes simplex virus encephalitis: bilateral thalamic involvement and normal imaging of early stage of the disease. Am J Emerg Med. 2007;25:87-9.A16 Per H, Gümüş H, Ichida K, Cağlayan O, Kumandaş S. Molybdenum cofactor deficiency: clinical features in a Turkish patient. Brain Dev. 2007;29:365-8.A17 Per H, Tucer B, Gümüs H, Kurtsoy A, Kumandas S. Transient sixth nerve palsies and torticollis secondary to parietal arteriovenous malformation. Pediatr Neurosurg. 2007;43:32-5.A18 Per H, Gumus H, Kumandas S, Tucer BL, Yikilmaz A, Menku A, Coskun A, Kurtsoy A. Gigantic cerebral hydatid cysts in childhood. Ann Saudi Med. 2007;27:60-1A19 Per H, Kurtoğlu S, Yağmur F, Gümüş H, Kumandaş S, Poyrazoğlu MH. Calcium carbide poisoning via food in childhood. J Emerg Med. 2007;32:179-80.A20 Per H, Kumandaş S, Gümüş H, Yikilmaz A, Kurtsoy A. Iatrogenic epidermoid tumor: late complication of lumbar puncture. J Child Neurol. 2007;22:332-6.A21 Gümüş H, Kumandaş S, Per H, Karakükçü M. Hemophagocytic syndrome associated with high-dose lamotrigine. Pediatr Int. 2007;49:672-3.A22 Gümüş H, Kumandaş S, Per H. Levetiracetam monotherapy in newly diagnosed cryptogenic West syndrome. Pediatr Neurol. 2007;37:350-3.A23 Kumandas S, Kose M, Gumus H, Per H, Saygin B. Cutaneous anthrax involving the genital area. Ann Trop Paediatr 2007;27:307-9A24 Per H, Kumandas S, Coskun A, Gümüs H, Oztop D. Neurologic sequelae of neonatal hypoglycemia in Kayseri, Turkey. J Child Neurol 2008;23:1406-12A25 Per H, Kumandaş S, Gümüş H, Kurtsoy A. Primary soliter and multiple intracranial cyst hydatid disease: report of five cases. Brain Dev 2009;31:228-33A26 Per H, Kumandaş S, Gümüş H, Oztürk MK, Coşkun A. Meningitis and Subgaleal, Subdural, Epidural Empyema due to Pasteurella Multocida. J Emerg Med 2008 May 15A27 Per H, Kontaş O, Kumandaş S, Kurtsoy A. A report of a desmoplastic non-infantile ganglioglioma in a 6-year-old boy with review of the literature. Neurosurg Rev 2009 Mar 12

A28 Gümüş H, Per H, Kumandaş S, Yikilmaz A. Reversible posterior leukoencephalopathy syndrome in childhood: report of nine cases and review of the literature. Neurol Sci. 2010 Apr;31(2):125-31.

A29 Yikilmaz A, Doganay S, Gumus H, Per H, Kumandas S, Coskun A. Magnetic resonance imaging of childhood Guillain-Barre syndrome. Childs Nerv Syst. 2010;26(8):1103-8.

A30 Gümüş H, Ghesquiere S, Per H, Kondolot M, Ichida K, Poyrazoğlu G, Kumandaş S,

Engelen J, Dundar M, Cağlayan AO. Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency. Dev Med Child Neurol. 2010;52(9):868-72.

A31 Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizoğlu D, Tüysüz

B, Cağlayan AO, Gökben S, Kaymakçalan H, Barak T, Bakircioğlu M, Yasuno K, Ho W,

Sanders S, Zhu Y, Yilmaz S, Dinçer A, Johnson MH, Bronen RA, Koçer N, Per H, Mane

S, Pamir MN, Yalçinkaya C, Kumandaş S, Topçu M, Ozmen M, Sestan N, Lifton RP,

State MW, Günel M. Whole-exome sequencing identifies recessive WDR62 mutations in

severe brain malformations. Nature. 2010;467:207-10.

A32 Aksu R, Kumandas S, Akin A, Bicer C, Gümüş H, Güler G, Per H, Bayram A, Boyaci A. The comparison of the effects of dexmedetomidine and midazolam sedation on electroencephalography in pediatric patients with febrile convulsion. Paediatr Anaesth. 2011;21(4):373-8.

A33 Ekici MA, Kumandas S, Per H, Ekici A, Tucer B, Gumus H, Canoz O, Kurtsoy A. Surgical timing of the subependymal giant cell astrocytoma (SEGA) with the patients of tuberous sclerosis complex. Turk Neurosurg. 2011;21:315-24.

A34 Ozdemir MA, Karakukcu M, Per H, Unal E, Gumus H, Patiroglu T. Late-type vitamin K deficiency bleeding: experience from 120 patients. Childs Nerv Syst. 2012;28:247-51

A35 Mavili E, Coskun A, Per H, Donmez H, Kumandas S, Yikilmaz A. Polymicrogyria:

correlation of magnetic resonance imaging and clinical findings. Childs Nerv

Syst. 2012;28(6):905-9.

A36 Per H, Arslan D, Gümüş H, Coskun A, Kumandaş S. Intracranial hemorrhages and

late hemorrhagic disease associated cholestatic liver disease. Neurol Sci. 2012 Feb 11.

A37 Gumus H, Gumus G, Per H, Yikilmaz A, Canpolat M, Poyrazoglu G, Narin N. Diffusion-weighted imaging in Sydenham's chorea. Childs Nerv Syst. 2013 Jan;29(1):125-30.

A38  Per H, Canpolat M, Gümüş H, Poyrazoğlu HG, Yıkılmaz A, Karaküçük S, Doğan H,  Kumandaş S. Clinical spectrum of the pseudotumor cerebri in children: etiological, clinical features, treatment and prognosis. Brain Dev. 2013 Jun;35(6):561-8.

A39 Caglayan AO, Per H, Akgumus G, Gumus H, Baranoski J, Canpolat M, Calik M, Yikilmaz A, Bilguvar K, Kumandas S, Gunel M. Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum. Clin Genet. 2013 Oct;84(4):394-5.

A40 Canpolat M, Kumandas S, Yikilmaz A, Gumus H, Koseoglu E, Poyrazoğlu HG, Kose M, Per H. Transverse myelitis and acute motor sensory axonal neuropathy due to Legionella pneumophila: A case report. Pediatr Int. 2013 Dec;55(6):778-82.

A41 Bayrakli F, Canpolat M, Per H, Gumus H, Kumandas S, Kartal U, Balaban H. A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23. Case Rep Neurol. 2014 Jan 23;6(1):18-22.

A42 Canpolat M, Per H, Gumus H, Yikilmaz A, Unal E, Patiroglu T, Cinar L, Kurtsoy A, Kumandas S. Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex: results of 7 children from a cohort of 86. Childs Nerv Syst. 2014 Feb;30(2):227-40.

A43 Per H, Canpolat M, Tümtürk A, Gumuş H, Gokoglu A, Yikilmaz A, Özmen S, Kaçar Bayram A, Poyrazoğlu HG, Kumandas S, Kurtsoy A. Different etiologies of acquired  torticollis in childhood. Childs Nerv Syst. 2014 Mar;30(3):431-40.

A44 Per H, Unal E, Poyrazoglu HG, Ozdemir MA, Donmez H, Gumus H, Uzum K, Canpolat M, Akyildiz BN, Coskun A, Kurtsoy A, Kumandas S. Childhood stroke: results of 130 children from a reference center in Central Anatolia, Turkey. Pediatr Neurol. 2014 Jun;50(6):595-600.

A45 Unal E, Ozsoylu S, Bayram A, Ozdemir MA, Yilmaz E, Canpolat M, Tumturk A, Per H. Intracranial hemorrhage in infants as a serious, and preventable consequence of late form of vitamin K deficiency: a selfie picture of Turkey, strategies for tomorrow. Childs Nerv Syst. 2014 Aug;30(8):1375-82.

A46 Canpolat M, Kumandas S, Poyrazoglu HG, Gumus H, Elmali F, Per H. Prevalence and risk factors of epilepsy among school children in Kayseri City Center, an urban area in Central Anatolia, Turkey. Seizure. 2014 Oct;23(9):708-16.

A47 Poyrazoğlu HG, Karaca E, Per H, Gümüs H, Onay H, Canpolat M, Canöz O, Ozkınay F, Kumandas S. Three Patients With Lafora Disease: Different Clinical Presentations and a Novel Mutation. J Child Neurol. 2014 Jul 10. [Epub ahead of print] DOI: 10.1177/0883073814535489,  PubMed PMID: 25015673.

A48 Canpolat M, Ceylan O, Per H, Koc G, Tumturk A, Kumandas S, Patiroglu T, Doganay S, Gumus H, Unal E, Kose M, Gorkem SB, Kurtsoy A, Ozturk MK. Brain Abscesses in Children: Results of 24 Children From a Reference Center in Central Anatolia, Turkey. J Child Neurol. 2014 Sep 15. [Epub ahead of print] DOI: 10.1177/0883073814549247, PubMed PMID: 25223695.

A49 Gumus H, Bayram AK, Poyrazoglu HG, Canpolat DG, Per H, Canpolat M, Yildiz K, Kumandas S. Comparison of Effects of Different Dexmedetomidine and Chloral Hydrate Doses Used in Sedation on Electroencephalography in Pediatric Patients. J Child Neurol. 2014 Sep 22. A50 Poyrazoğlu HG, Kumandas S, Canpolat M, Gümüs H, Elmali F, Kara A, Per H. The Prevalence of Migraine and Tension-Type Headache Among Schoolchildren in Kayseri, Turkey: An Evaluation of Sensitivity and Specificity Using Multivariate Analysis. J Child Neurol. 2014 Oct 7. [Epub ahead of print] DOI: 10.1177/0883073814549240,  PubMed PMID: 25296924.

A 51 Per H, Canpolat M, Sahin U, Gumus H, Konuskan B, Kumandas S. Serum and urine  boron and selenium levels in children with resistant epilepsy. Saudi Med J. 2012 Sep;33(9):942-7.

A52 Görkem SB, Doğanay S, Canpolat M, Koc G, Dogan MS, Per H, Coşkun A. MR imaging findings in children with pseudotumor cerebri and comparison with healthy

controls. Childs Nerv Syst. 2014 Oct 31. [Epub ahead of print] PubMed PMID:

25358812.

A53 Koc G, Doganay S, Bayram AK, Gorkem SB, Dogan MS, Per H, Coskun A. Idiopathic

brain herniation. A report of two paediatric cases. Neuroradiol J. 2014 Oct;27(5):586-9.

A 54 Mishra-Gorur K, Çağlayan AO, Schaffer AE, Chabu C, Henegariu O, Vonhoff F,

Akgümüş GT, Nishimura S, Han W, Tu S, Baran B, Gümüş H, Dilber C, Zaki MS, Hossni

HA, Rivière JB, Kayserili H, Spencer EG, Rosti RÖ, Schroth J, Per H, Çağlar C,

Çağlar Ç, Dölen D, Baranoski JF, Kumandaş S, Minja FJ, Erson-Omay EZ, Mane SM,

Lifton RP, Xu T, Keshishian H, Dobyns WB, Chi NC, Šestan N, Louvi A, Bilgüvar K,

Yasuno K, Gleeson JG, Günel M. Mutations in KATNB1 Cause Complex Cerebral

Malformations by Disrupting Asymmetrically Dividing Neural Progenitors. Neuron.

2014 Dec 17;84(6):1226-39.

A55 Dogan MS, Gumus K, Koc G, Doganay S, Per H, Gorkem SB, Canpolat M, Bayram AK,

Coskun A. Brain diffusion tensor imaging in children with tuberous sclerosis.

Diagn Interv Imaging. 2015 Apr 27. pii: S2211-5684(15)00135-7. doi:

10.1016/j.diii.2015.04.002. [Epub ahead of print] PubMed PMID: 25936891.

A56 Tumturk A, Kaya Ozcora G, Kacar Bayram A, Kabaklioglu M, Doganay S, Canpolat

M, Gumus H, Kumandas S, Unal E, Kurtsoy A, Per H. Torticollis in children: an

alert symptom not to be turned away. Childs Nerv Syst. 2015 Sep;31(9):1461-70.

doi: 10.1007/s00381-015-2764-9. Epub 2015 Jun 5. PubMed PMID: 26043711.

A57 Kaçar Bayram A, Per H, Quon J, Canpolat M, Ülgen E, Doğan H, Gumus H, Kumandas

S, Bayram N, Bilguvar K, Çağlayan AO. A rare case of congenital fibrosis of

extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking

phenomenon. Eur J Paediatr Neurol. 2015 Nov;19(6):743-6.

A58 Gumus H, Bayram AK, Kardas F, Canpolat M, Çağlayan AO, Kumandas S, Kendirci M,

Per H. The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other

Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency

Syndrome. Neuropediatrics. 2015 Oct;46(5):313-20.

A59 Bayram AK, Yilmaz E, Per H, Ito M, Uchino H, Doganay S, Houkin K, Unal E.

Familial moyamoya disease in two Turkish siblings with same polymorphism in

RNF213 gene but different clinical features. Childs Nerv Syst. 2015 Aug 16. [Epub

ahead of print] PubMed PMID: 26277359.

A60 Bayrakli F, Poyrazoglu HG, Yuksel S, Yakicier C, Erguner B, Sagiroglu MS,

Yuceturk B, Ozer B, Doganay S, Tanrikulu B, Seker A, Akbulut F, Ozen A, Per H,

Kumandas S, Altuner Torun Y, Bayri Y, Sakar M, Dagcinar A, Ziyal I. Hereditary

spastic paraplegia with recessive trait caused by mutation in KLC4 gene. J Hum

Genet. 2015 Oct 1. doi: 10.1038/jhg.2015.109. [Epub ahead of print] PubMed PMID:

26423925.

A61 Bayram AK, Canpolat M, Karacabey N, Gumus H, Kumandas S, Doğanay S, Arslan D,

Per H. Misdiagnosis of gastroesophageal reflux disease as epileptic seizures in

children. Brain Dev. 2015 Oct 3. pii: S0387-7604(15)00208-9. doi:

10.1016/j.braindev.2015.09.009. [Epub ahead of print] PubMed PMID: 26443628.

A62 Kardas F, Bayram AK, Demirci E, Akin L, Ozmen S, Kendirci M, Canpolat M, Oztop

DB, Narin F, Gumus H, Kumandas S, Per H. Increased Serum Phthalates (MEHP, DEHP)

and Bisphenol A Concentrations in Children With Autism Spectrum Disorder: The

Role of Endocrine Disruptors in Autism Etiopathogenesis. J Child Neurol. 2015 Oct

8. pii: 0883073815609150. [Epub ahead of print] PubMed PMID: 26450281.

A63 Per H, Canpolat M, Bayram AK, Ulgen E, Baran B, Kardas F, Gumus H, Kumandas S,

Bilguvar K, Çağlayan AO. Clinical, Electrodiagnostic, and Genetic Features of

Tangier Disease in an Adolescent Girl with Presentation of Peripheral Neuropathy.

Neuropediatrics. 2015 Oct 19. [Epub ahead of print] PubMed PMID: 26479764.

A 64 Bayram AK, Canpolat M, Çınar SL, Tahan F, Gumus H, Kumandaş S, Per H. Drug

Reaction with Eosinophilia and Systemic Symptoms Syndrome Induced by

Levetiracetam in a Pediatric Patient. J Emerg Med. 2016 Feb;50(2):e61-6.

A 65 Öztop DB, Taşdelen Bİ, PoyrazoğLu HG, Ozsoy S, Yilmaz R, Şahın N, Per H,

Bozkurt S. Assessment of Psychopathology and Quality of Life in Children and

Adolescents With Migraine. J Child Neurol. 2016 Jun;31(7):837-42.

A66 Bayram AK, Pamukcu O, Per H. Current approaches to the clinical assessment of

syncope in pediatric population. Childs Nerv Syst. 2016 Mar;32(3):427-36.

A 67 Bayram AK, Kardas F, Demirci EO, Gokahmetoglu S, Ozmen S, Canpolat M, Oztop

DB, Kumandas S, Gumus H, Per H. Lack of serum antineuronal antibodies in

children with autism. Bratisl Lek Listy. 2016;117(2):77-9.

A 68 Bayram AK, Gümüş H, Arslan D, Özçora GK, Kumandaş S, Karacabey N, Canpolat

M, Per H. Neurological features and management of Wilson disease in children: an

evaluation of 12 cases. Turk Pediatri Ars. 2016 Mar 1;51(1):15-21.

A 69 Gokay S, Kendirci M, Ustkoyuncu PS, Kardas F, Bayram AK, Per H, Poyrazoğlu

1. Tyrosinemia type II: Novel mutations in TAT in a boy with unusual

presentation. Pediatr Int. 2016 Oct;58(10):1069-1072.

A 70 Kardas F, Bayram AK, Demirci E, Akin L, Ozmen S, Kendirci M, Canpolat M,

Oztop DB, Narin F, Gumus H, Kumandas S, Per H. Increased Serum Phthalates (MEHP,

DEHP) and Bisphenol A Concentrations in Children With Autism Spectrum Disorder:

The Role of Endocrine Disruptors in Autism Etiopathogenesis. J Child Neurol.

2016 Apr;31(5):629-35.

A 71 Zitouni S, Koc G, Doganay S, Saracoglu S, Gumus KZ, Ciraci S, Coskun A, Unal

E, Per H, Kurtsoy A, Kontas O. Apparent diffusion coefficient in differentiation

of pediatric posterior fossa tumors. Jpn J Radiol. 2017 Aug;35(8):448-453.

A 72 Yılmaz Ü, Anlar B, Gücüyener K; Turkish Pediatric Multiple Sclerosis Study

Group. Characteristics of pediatric multiple sclerosis: The Turkish pediatric

multiple sclerosis database. Eur J Paediatr Neurol. 2017 Nov;21(6):864-872.

A 73 Poyrazoğlu HG, Baş VN, Arslan A, Bastug F, Canpolat M, Per H, Gümüs H,

Kumandas S. Bone mineral density and bone metabolic markers' status in children

with neurofibromatosis type 1. J Pediatr Endocrinol Metab. 2017 Feb

1;30(2):175-180.

A 74 Per H, Gunay N, Ismailogullari S, Oztop DB, Gunay O. Determination of

restless legs syndrome prevalence in children aged 13-16years in the provincial

center of Kayseri. Brain Dev. 2017 Feb;39(2):154-160.

A 75 Cinar SL, Kartal D, Bayram AK, Canpolat M, Borlu M, Ferahbas A, Per H.

Topical sirolimus for the treatment of angiofibromas in tuberous sclerosis.

Indian J Dermatol Venereol Leprol. 2017 Jan-Feb;83(1):27-32.

A 76 Wang H, Castiglioni C, Kaçar Bayram A, Fattori F, Pekuz S, Araneda D, Per H,

Erazo R, Gümüş H, Zorludemir S, Becker K, Ortega X, Bevilacqua JA, Bertini E,

Cirak S. Insights from genotype-phenotype correlations by novel SPEG mutations

causing centronuclear myopathy. Neuromuscul Disord. 2017 Sep;27(9):836-842.

A 77 Tubaş F, Per S, Taşdemir A, Bayram AK, Yıldırım M, Uzun A, Saraymen R, Gümüş

H, Elmalı F, Per H. Effects of Cornus mas L. and Morus rubra L. extracts on

penicillin-induced epileptiform activity: an electrophysiological and

biochemical study. Acta Neurobiol Exp (Wars). 2017;77(1):45-56.

A 78 Ciraci S, Gumus K, Doganay S, Dundar MS, Kaya Ozcora GD, Gorkem SB, Per H,

Coskun A. Diagnosis of intracranial calcification and hemorrhage in pediatric

patients: Comparison of quantitative susceptibility mapping and phase images of

susceptibility-weighted imaging. Diagn Interv Imaging. 2017 Oct;98(10):707-714.

A 79 Lardelli RM, Schaffer AE, Eggens VR, Zaki MS, Grainger S, Sathe S, Van

Nostrand EL, Schlachetzki Z, Rosti B, Akizu N, Scott E, Silhavy JL, Heckman LD,

Rosti RO, Dikoglu E, Gregor A, Guemez-Gamboa A, Musaev D, Mande R, Widjaja A,

Shaw TL, Markmiller S, Marin-Valencia I, Davies JH, de Meirleir L, Kayserili H,

Altunoglu U, Freckmann ML, Warwick L, Chitayat D, Blaser S, Çağlayan AO,

Bilguvar K, Per H, Fagerberg C, Christesen HT, Kibaek M, Aldinger KA, Manchester

D, Matsumoto N, Muramatsu K, Saitsu H, Shiina M, Ogata K, Foulds N, Dobyns WB,

Chi NC, Traver D, Spaccini L, Bova SM, Gabriel SB, Gunel M, Valente EM, Nassogne

MC, Bennett EJ, Yeo GW, Baas F, Lykke-Andersen J, Gleeson JG. Biallelic

mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and

uncover a role in snRNA processing. Nat Genet. 2017 Mar;49(3):457-464.

 

A 80 Tumturk A, Ozdemir MA, Per H, Unal E, Kucuk A, Ulutabanca H, Karakukcu M,

Canoz O, Gumus H, Coskun A, Kurtsoy A. Pediatric central nervous system tumors

in the first 3 years of life: pre-operative mean platelet volume,

neutrophil/lymphocyte count ratio, and white blood cell count correlate with the

presence of a central nervous system tumor. Childs Nerv Syst. 2017

Feb;33(2):233-238.

A 81 Canpolat M, Gumus H, Gunduz Z, Dusunsel R, Kumandas S, Bayram AK, Yel S,

Poyrazoglu HG, Yilmaz K, Doganay S, Yikilmaz A, Dundar M, Per H. Neurological

Manifestations in Familial Mediterranean Fever: Results of 22 Children from a

Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.

Neuropediatrics. 2017 Apr;48(2):79-85

Erratum in: Neuropediatrics. 2017 Oct;48(5):402. PMID: 27656843.

A 83 Işıkay S, Işıkay N, Per H, Çarman KB, Kocamaz H. Restless leg syndrome in

children with celiac disease. Turk J Pediatr. 2018;60(1):70-75.

A 84 Per H, Günay N, İsmailoğulları S, Öztop DB, Günay O. Determination of

restless legs syndrome prevalence in children aged 13-16 years in the provincial

center of Kayseri. Brain Dev. 2018 Mar;40(3):256-257.

A 85 Canpolat M, Per H, Gumus H, Elmali F, Kumandas S. Investigating the

prevalence of febrile convulsion in Kayseri, Turkey: An assessment of the risk

factors for recurrence of febrile convulsion and for development of epilepsy.

Seizure. 2018 Feb;55:36-47.

A 86 Aldemir R, Demirci E, Bayram AK, Canpolat M, Ozmen S, Per H, Tokmakci M.

Evaluation of Two Types of Drug Treatment with QEEG in Children with ADHD.

Transl Neurosci. 2018 Sep 1;9:106-116.

A 87 Yilmaz E, Bayram Kacar A, Bozpolat A, Zararsiz G, Gorkem BS, Karakukcu M,

Patiroglu T, Gumus H, Ozdemir MA, Ozcan A, Per H, Unal E. The relationship

between hematological parameters and prognosis of children with acute ischemic

stroke. Childs Nerv Syst. 2018 Apr;34(4):655-661.

A 88 Aydin K; Turkish Cerebral Palsy Study Group. A multicenter cross-sectional

study to evaluate the clinical characteristics and nutritional status of

children with cerebral palsy. Clin Nutr ESPEN. 2018 Aug;26:27-34.

A 89 Aldemir R, Demirci E, Per H, Canpolat M, Özmen S, Tokmakçı M. Investigation

of attention deficit hyperactivity disorder (ADHD) sub-types in children via EEG

frequency domain analysis. Int J Neurosci. 2018 Apr;128(4):349-360.

A 90 Guemez-Gamboa A, Çağlayan AO, Stanley V, Gregor A, Zaki MS, Saleem SN, Musaev

D, McEvoy-Venneri J, Belandres D, Akizu N, Silhavy JL, Schroth J, Rosti RO,

Copeland B, Lewis SM, Fang R, Issa MY, Per H, Gumus H, Bayram AK, Kumandas S,

Akgumus GT, Erson-Omay EZ, Yasuno K, Bilguvar K, Heimer G, Pillar N, Shomron N,

Weissglas-Volkov D, Porat Y, Einhorn Y, Gabriel S, Ben-Zeev B, Gunel M, Gleeson

1. Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction

Dysplasia Syndrome. Ann Neurol. 2018 Nov;84(5):638-647.

A 91 Dursun A, Bayram AK, Tekerek NÜ, Akyıldız BN, Per H. A case of DRESS

syndrome associated with carbamazepine treatment. Turk Pediatri Ars. 2018 Mar

1;53(1):48-50.

A 92 Berber U, Özdemir MA, Unal E, Taheri S, Yildiz S, Bayramov KK, Güler Y, Per

1. Genetic Polymorphism of VKORC1-1639 in Children With Intracranial

Hemorrhage Due to Vitamin K Deficiency. Clin Appl Thromb Hemost. 2018

Dec;24(9_suppl):89S-93S.

A 93 Canpolat M, Gumus H, Kumandas S, Coskun A, Per H. The use of rapamycin in

patients with tuberous sclerosis complex: Long-term results. Epilepsy Behav.

2018 Nov;88:357-364.

A 94 Bozpolat A, Unal E, Topaloglu T, Taheri S, Bayram AK, Ozcan A, Karakukcu M,

Ozdemir MA, Per H. The relationship between the prognosis of children with acute

arterial stroke and polymorphisms of CDKN2B, HDAC9, NINJ2, NAA25 genes. J Thromb

Thrombolysis. 2019 May;47(4):578-584.

A 95 Caglayan AO, Gumus H, Sandford E, Kubisiak TL, Ma Q, Ozel AB, Per H, Li JZ,

Shakkottai VG, Burmeister M. COQ4 Mutation Leads to Childhood-Onset Ataxia

Improved by CoQ10 Administration. Cerebellum. 2019 Jun;18(3):665-669.

A 96 Wang H, Kaçar Bayram A, Sprute R, Ozdemir O, Cooper E, Pergande M, Efthymiou

S, Nedic I, Mazaheri N, Stumpfe K, Azizi Malamiri R, Shariati G, Zeighami J,

Bayram N, Naghibzadeh SK, Tajik M, Yaşar M, Sami Güven A, Bibi F, Sultan T,

Salpietro V, Houlden H, Per H, Galehdari H, Shalbafan B, Jamshidi Y, Cirak S.

Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to

MTMR2 Mutations and Implications in Membrane Trafficking. Front Neurosci.

2019 Oct 14;13:974.

A 97 Soylu Ustkoyuncu P, Kendirci M, Kardas F, Gokay S, Per H, Kacar Bayram A.

Neutropenia and Increased Mean Corpuscular Volume (MCV) With Abnormal Neurologic

Findings: A Case of Cobalamin D Deficiency. J Pediatr Hematol Oncol. 2019;41(1):e54-e56.

A 98 Bayram AK, Kütük MS, Doganay S, Özgün MT, Gümüş H, Başbuğ M, Kumandaş S,

Canpolat M, Per H. An analysis of 109 fetuses with prenatal diagnosis of complete agenesis of corpus callosum. Neurol Sci. 2020 ;41(6):1521-1529.

A 99 Sarilar AC, Ismailogullari S, Yilmaz R, Erdogan FF, Per H.Electroencephalogram abnormalities in patients with NREM parasomnias. Sleep Med. 2021 Jan;77:256-260.

A 100 Ozturk S, Peduk Y, Gumus H, Per H. Shuddering attacks in children: A retrospective analysis of 19 cases from a single-center in Turkey. Epilepsy Behav. 2021 Apr;117:107827.

A 101 Tumturk A, Gorkem SB, Ozmansur EN, Peduk Y, Arslan U, Gok V, Dogan H, Cetin

BS, Sahin A, Gumus H, Guney A, Unal E, Kurtsoy A, Per H. The Spectrum of

Underlying Diseases in Children with Torticollis. Turk Neurosurg. 2021;31(3):389-398.

A 102 Bayram N, Kaçar Bayram A, Daimagüler HS, Salimi Dafsari H, Bamborschke D,

Uyanik G, Erdogan M, Özsaygılı C, Pangal E, Yuvaci İ, Doğanay S, Gümüş H, Per H,

Jungbluth H, Çırak S. Genotype-phenotype correlations in ocular manifestations of Marinesco-Sjögren syndrome: Case report and literature review. Eur J Ophthalmol. 2021 Jun.

A 103 Bayram N, Bayram AK, Per H, Gümüş H, Ozsaygili C, Doğan MS, Çağlayan AO.

Analysis of genotype-phenotype correlation in Walker-Warburg syndrome with a novel CRPPA mutation in different clinical manifestations. Eur J Ophthalmol. 2021 May

A 104 Öztürk Z, Yılmaz Ü, Konuşkan B., Gücüyener K., Demir E., Anlar B., Turkish P., "Multiple Sclerosis with Onset Younger Than 10 Years in Turkey.", Neuropediatrics, cilt.49, ss.51-58, 2018

A105 Oztop DB, Demirci E, Ozmen S, Kondolot M, Kardaş F, Per H. Might BPA and phthalates have a role in etiopathogenesis of ADHD, Anadolu Psikiatri dergisi, 2018;19-300-306

A 106  Bayram AK, Per H, İsmailoğulları S, Canpolat M, Gümüş H, Aksu M "Efficiency of a Combination of Pharmacological Treatment and Nondrug Interventions in Childhood Narcolepsy", Neuropediatrics 2016;47:380-387

A 107 Bozkaya-Yilmaz S, Karadag-Oncel E, Olgac-Dundar N, Gencpinar P, Sarioglu B,

Arican P, Ersen A, Yilmaz-Ciftdoğan D, Yuksel MF, Bektas O, Teber S, Kilic B,

Calik M, Karaca M, Canpolat M, Kumandas S, Per H, Gumus H, Ozturk S, Okuyaz C,

Komur M, Ipek R, Ozbudak P, Arhan E, Ince H, Gurbuz G, Mert GG, Ozcan N, Turker

AO, Gazeteci-Tekin H, Kırık S, Günbey C, Çarman KB, Yarar C, Çavuşoğlu D.

Evaluation of immunization status in patients with cerebral palsy: a multicenter

CP-VACC study. Eur J Pediatr. 2021 Aug 5