Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 86

1.

The use of rapamycin in patients with tuberous sclerosis complex: Long-term results.

Canpolat M, Gumus H, Kumandas S, Coskun A, Per H.

Epilepsy Behav. 2018 Nov;88:357-364. doi: 10.1016/j.yebeh.2018.09.020. Epub 2018 Oct 7.

PMID:
30305233
2.

Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.

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 JG.

Ann Neurol. 2018 Nov;84(5):638-647. doi: 10.1002/ana.25327. Epub 2018 Oct 4.

PMID:
30178464
3.

PEX10-related autosomal recessive cerebellar ataxia with hearing loss.

Kaya Özçora GD, Miyatake S, Matsumoto N, Canpolat M, Erdoğan M, Bayramov R, Kumandaş S.

Acta Neurol Belg. 2018 Jul 19. doi: 10.1007/s13760-018-0987-8. [Epub ahead of print] No abstract available.

PMID:
30022445
4.

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.

Canpolat M, Per H, Gumus H, Elmali F, Kumandas S.

Seizure. 2018 Feb;55:36-47. doi: 10.1016/j.seizure.2018.01.007. Epub 2018 Jan 10.

PMID:
29353090
5.

Erratum: Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.

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.

Neuropediatrics. 2017 Oct;48(5):402. doi: 10.1055/s-0037-1599783. Epub 2017 Aug 24. No abstract available.

PMID:
28837982
6.

Glutaric Acidemia Type 1: A Case of Infantile Stroke.

Kaya Ozcora GD, Gokay S, Canpolat M, Kardaş F, Kendirci M, Kumandaş S.

JIMD Rep. 2018;38:7-12. doi: 10.1007/8904_2017_26. Epub 2017 Apr 15.

7.

Bone mineral density and bone metabolic markers' status in children with neurofibromatosis type 1.

Poyrazoğlu HG, Baş VN, Arslan A, Bastug F, Canpolat M, Per H, Gümüs H, Kumandas S.

J Pediatr Endocrinol Metab. 2017 Feb 1;30(2):175-180. doi: 10.1515/jpem-2016-0092.

PMID:
28125404
8.

Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.

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.

Neuropediatrics. 2017 Apr;48(2):79-85. doi: 10.1055/s-0036-1593374. Epub 2016 Sep 22. Erratum in: Neuropediatrics. 2017 Oct;48(5):402.

PMID:
27656843
9.

The Role of Diffusion-Weighted Imaging in the Evaluation of the Whole Brain in Isolated Unilateral Polymicrogyria.

Görkem SB, Doganay S, Gumus K, Bayram A, Kumandas S, Coskun A.

J Child Neurol. 2016 Dec;31(14):1575-1578. Epub 2016 Sep 12.

PMID:
27625015
10.

Neurological features and management of Wilson disease in children: an evaluation of 12 cases.

Bayram AK, Gümüş H, Arslan D, Özçora GK, Kumandaş S, Karacabey N, Canpolat M, Per H.

Turk Pediatri Ars. 2016 Mar 1;51(1):15-21. doi: 10.5152/TurkPediatriArs.2016.3080. eCollection 2016 Mar.

11.

Lack of serum antineuronal antibodies in children with autism.

Bayram AK, Kardas F, Demirci EO, Gokahmetoglu S, Ozmen S, Canpolat M, Oztop DB, Kumandas S, Gumus H, Per H.

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

PMID:
26830036
12.

Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome Induced by Levetiracetam in a Pediatric Patient.

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

J Emerg Med. 2016 Feb;50(2):e61-6. doi: 10.1016/j.jemermed.2015.10.004. Epub 2015 Nov 18.

PMID:
26597350
13.

Clinical, Electrodiagnostic, and Genetic Features of Tangier Disease in an Adolescent Girl with Presentation of Peripheral Neuropathy.

Per H, Canpolat M, Bayram AK, Ulgen E, Baran B, Kardas F, Gumus H, Kumandas S, Bilguvar K, Çağlayan AO.

Neuropediatrics. 2015 Dec;46(6):420-3. doi: 10.1055/s-0035-1565275. Epub 2015 Oct 19.

PMID:
26479764
14.

Increased Serum Phthalates (MEHP, DEHP) and Bisphenol A Concentrations in Children With Autism Spectrum Disorder: The Role of Endocrine Disruptors in Autism Etiopathogenesis.

Kardas F, Bayram AK, Demirci E, Akin L, Ozmen S, Kendirci M, Canpolat M, Oztop DB, Narin F, Gumus H, Kumandas S, Per H.

J Child Neurol. 2016 Apr;31(5):629-35. doi: 10.1177/0883073815609150. Epub 2015 Oct 8.

PMID:
26450281
15.

Misdiagnosis of gastroesophageal reflux disease as epileptic seizures in children.

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

Brain Dev. 2016 Mar;38(3):274-9. doi: 10.1016/j.braindev.2015.09.009. Epub 2015 Oct 9.

PMID:
26443628
16.

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

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.

J Hum Genet. 2015 Dec;60(12):763-8. doi: 10.1038/jhg.2015.109. Epub 2015 Oct 1.

PMID:
26423925
17.

The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency Syndrome.

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

Neuropediatrics. 2015 Oct;46(5):313-20. doi: 10.1055/s-0035-1558435. Epub 2015 Aug 12.

PMID:
26267703
18.

A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenon.

Kaçar Bayram A, Per H, Quon J, Canpolat M, Ülgen E, Doğan H, Gumus H, Kumandas S, Bayram N, Bilguvar K, Çağlayan AO.

Eur J Paediatr Neurol. 2015 Nov;19(6):743-6. doi: 10.1016/j.ejpn.2015.06.003. Epub 2015 Jul 9.

PMID:
26190014
19.

Torticollis in children: an alert symptom not to be turned away.

Tumturk A, Kaya Ozcora G, Kacar Bayram A, Kabaklioglu M, Doganay S, Canpolat M, Gumus H, Kumandas S, Unal E, Kurtsoy A, Per H.

Childs Nerv Syst. 2015 Sep;31(9):1461-70. doi: 10.1007/s00381-015-2764-9. Epub 2015 Jun 5.

PMID:
26043711
20.

Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors.

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 HAA, 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.

Neuron. 2015 Jan 7;85(1):228. doi: 10.1016/j.neuron.2014.12.046. Epub 2015 Jan 7. No abstract available.

Supplemental Content

Loading ...
Support Center