Detalhe da pesquisa
1.
Diagnostic yield of muscle biopsy in infants: Retrospective analysis of clinical and histopathologic findings.
Clin Neuropathol
; 40(5): 286-291, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33860760
2.
Vanishing white matter disease with different faces.
Childs Nerv Syst
; 36(2): 353-361, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31385086
3.
A rare cause of arterial hypertension in a child with developmental delay: Answers.
Pediatr Nephrol
; 37(2): 333-336, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34668059
4.
A rare cause of arterial hypertension in a child with developmental delay: Questions.
Pediatr Nephrol
; 37(2): 329-331, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34668058
5.
BEND4 as a Candidate Gene for an Infection-Induced Acute Encephalopathy Characterized by a Cyst and Calcification of the Pons and Cerebellar Atrophy.
Mol Syndromol
; 13(1): 12-22, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35221871
6.
Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNA Lys Gene.
Mol Syndromol
; 13(4): 305-317, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-36158049
7.
Cytotoxic lesions of the corpus callosum in children: Etiology, clinical and radiological features, and prognosis.
Brain Dev
; 43(9): 919-930, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34120800
8.
Mild encephalitis/encephalopathy with a reversible splenial lesion in children.
Diagn Interv Radiol
; 24(2): 108-112, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29757148
9.
Long-term clinical and radiologic follow-up of Schilder's disease.
Mult Scler Relat Disord
; 13: 47-51, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28427702
10.
Severe neurodegenerative disease in brothers with homozygous mutation in POLR1A.
Eur J Hum Genet
; 25(3): 315-323, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28051070
11.
Clinical outcomes in children with herpes simplex encephalitis receiving steroid therapy.
J Clin Virol
; 80: 87-92, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27218417
12.
Head Circumference Charts for Turkish Children Aged Five to Eighteen Years.
Noro Psikiyatr Ars
; 53(1): 55-62, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28360767
13.
Clinical and neuroradiologic variability of Aicardi-Goutiéres syndrome: Two siblings with RNASEH2C mutation and a boy with TREX1 mutation.
Turk J Pediatr
; 57(5): 504-8, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-27411419
14.
TSEN54 gene-related pontocerebellar hypoplasia type 2 presenting with exaggerated startle response: report of two cases in a family.
Turk J Pediatr
; 57(3): 286-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26701950