Detalhe da pesquisa
1.
High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases.
Brain
; 145(4): 1507-1518, 2022 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34791078
2.
Sural Sparing Pattern and Sensory Ratio as Electrodiagnostic and Prognostic Markers in Pediatric Guillain-Barré Syndrome.
Neuropediatrics
; 54(1): 20-30, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36096153
3.
The Effect of Nusinersen Therapy on Laboratory Parameters of Patients with Spinal Muscular Atrophy.
Neuropediatrics
; 53(5): 321-329, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35871521
4.
Inflammation and endothelial dysfunction in pediatric migraine patients.
Pediatr Int
; 64(1): e14946, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34358404
5.
Risk Factors of Post-Stroke Epilepsy in Children; Experience from a Tertiary Center and a Brief Review of the Literature.
J Stroke Cerebrovasc Dis
; 30(1): 105438, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33197802
6.
Neuroprotective Effects of Lacosamide and Memantine on Hyperoxic Brain Injury in Rats.
Neurochem Res
; 45(8): 1920-1929, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32444924
7.
A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing Panencephalitis.
Neuropediatrics
; 46(6): 377-84, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26479761
8.
The Paediatric migraine disability assessment score is a useful tool for evaluating prophylactic migraine treatment.
Acta Paediatr
; 103(11): e484-9, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25048365
9.
Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing Panels.
Mol Syndromol
; 15(1): 14-21, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38357257
10.
The fate of spikes in self-limited epilepsy with centrotemporal spikes: Are clinical and baseline EEG features effective?
Epilepsy Res
; 193: 107165, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37201400
11.
Immunization status of patients with spinal muscular atrophy receiving nusinersen therapy.
Arch Pediatr
; 30(5): 291-296, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37147157
12.
Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in Turkey.
Acta Neurol Belg
; 123(6): 2325-2335, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37656362
13.
DPAGT1-CDG: Report of Two New Pediatric Patients and Brief Review of the Literature.
Mol Syndromol
; 14(4): 322-330, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37766827
14.
Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study.
Pediatr Neurol
; 145: 3-10, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37245275
15.
Anti-GQ1b-negative Miller Fisher syndrome presented with one-sided horizontal gaze palsy.
Turk J Pediatr
; 52(3): 317-20, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20718193
16.
Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish population.
Turk J Pediatr
; 52(2): 179-83, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20560255
17.
A case of atypical Miller Fisher syndrome with negative anti-GQ1b immunoglobulin G and importance of H reflex.
Turk J Pediatr
; 55(2): 235-6, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24192691
18.
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.
Turk J Pediatr
; 60(3): 229-237, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30511534
19.
Expanding spectrum of SCN1A-related phenotype with novel mutations.
Turk J Pediatr
; 59(5): 570-575, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29745119
20.
Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2.
Turk J Pediatr
; 59(3): 338-341, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29376585