Detalhe da pesquisa
1.
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
Mov Disord
; 36(7): 1676-1688, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33624863
2.
A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiency.
Metab Brain Dis
; 32(3): 675-678, 2017 06.
Artigo
Inglês
| MEDLINE | ID: mdl-28281033
3.
Ictal urinary urge: localization and lateralization value in a pediatric case.
Childs Nerv Syst
; 31(12): 2383-5, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26206115
4.
PRUNE1: a disease-causing gene for secondary microcephaly.
Brain
; 140(10): e61, 2017 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28969376
5.
Changing views of cerebral palsy over 35 years: the experience of a center.
Turk J Pediatr
; 55(1): 8-15, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-23692827
6.
Video/EEG recording of myoclonic absences in GLUT1 deficiency syndrome with a hot-spot R126C mutation in the SLC2A1 gene.
Epilepsy Behav
; 21(2): 200-2, 2011 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-21546317
7.
A rare cause of recurrent stroke in childhood: left atrial rhabdomyosarcoma.
Acta Paediatr
; 100(10): e189-91, 2011 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-21352362
8.
Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis.
Childs Nerv Syst
; 32(9): 1567-8, 2016 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-27278281
9.
Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphisms.
Pediatr Neurol
; 40(2): 113-6, 2009 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-19135625
10.
Extreme delta brush activity: Could it be a marker for early diagnosis and prognosis of anti- NMDA (N-methyl-D-aspartate) encephalitis?
Turk Pediatri Ars
; 54(1): 61-65, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31217713
11.
Semiologic seizure classification: the effectiveness of a modular education program for health professionals in pediatrics.
Epilepsy Behav
; 13(2): 387-90, 2008 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-18524683
12.
The effect of depression on academic achievement in children with epilepsy.
Epilepsy Behav
; 13(3): 494-8, 2008 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-18599356
13.
Prevalence and severity of malnutrition in pediatric neurology outpatients with respect to underlying diagnosis and comorbid nutrition and feeding related problems.
Turk J Pediatr
; 60(6): 709-717, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-31365208
14.
Arterial ischemic stroke in childhood: risk factors and outcome in old versus new era.
J Child Neurol
; 22(10): 1204-8, 2007 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-17940247
15.
Miller Fisher syndrome: a case with pattern of pure sensory polyneuropathy concomitant with anti-GQ1B antibody.
Turk J Pediatr
; 49(1): 109-12, 2007.
Artigo
Inglês
| MEDLINE | ID: mdl-17479657
16.
Chronic inflammatory demyelinating polyradiculopathy: an atypical pediatric case complicated with phrenic nerve palsy.
Turk J Pediatr
; 49(2): 210-4, 2007.
Artigo
Inglês
| MEDLINE | ID: mdl-17907525
17.
Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy.
Acta Neurol Belg
; 117(1): 131-138, 2017 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-27734276
18.
Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights.
J Child Neurol
; 32(8): 759-765, 2017 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28464723
19.
Bone mineral status in pediatric outpatients on antiepileptic drug monotherapy.
J Child Neurol
; 21(5): 411-4, 2006 May.
Artigo
Inglês
| MEDLINE | ID: mdl-16901447
20.
Vigabatrin caused rapidly progressive deterioration in two cases with early myoclonic encephalopathy associated with nonketotic hyperglycinemia.
J Child Neurol
; 21(1): 82-4, 2006 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-16551461