Found: 11
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Opsoclonus-myoclonus syndrome following rotavirus gastroenteritis.
- Published in:
- Pediatrics International, 2014, v. 56, n. 6, p. e86, doi. 10.1111/ped.12433
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- Publication type:
- Article
The management of elevated intracranial pressure and sinus vein thrombosis associated with mastoiditis: the experience of eighteen patients.
- Published in:
- Child's Nervous System, 2022, v. 38, n. 2, p. 421, doi. 10.1007/s00381-021-05402-6
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- Publication type:
- Article
Cerebral neoplasm in L-2-hydroxyglutaric aciduria: two different presentations.
- Published in:
- Child's Nervous System, 2020, v. 36, n. 7, p. 1545, doi. 10.1007/s00381-019-04466-9
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- Publication type:
- Article
Two Cases of Levetiracetam Overdose Without Any Serious Side Effects.
- Published in:
- 2017
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- Publication type:
- Case Study
Spastic Paraplegia with SPG1Î Gene delE39 in a Turkish Patient.
- Published in:
- Gazi Medical Journal, 2016, v. 27, n. 4, p. 205, doi. 10.12996/gmj.2016.64
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- Publication type:
- Article
Newly defined peroxisomal disease with novel ACBD5 mutation.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 1, p. 11, doi. 10.1515/jpem-2020-0352
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- Publication type:
- Article
Approaches for diagnosis and treatment in neurotransmitter disorders of childhood.
- Published in:
- Metabolic Brain Disease, 2021, v. 36, n. 8, p. 2255, doi. 10.1007/s11011-021-00838-w
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- Publication type:
- Article
A rare pediatric case of neurobrucellosis with bilateral optic neuritis.
- Published in:
- Turkish Journal of Pediatrics, 2020, v. 62, n. 6, p. 1094, doi. 10.24953/turkjped.2020.06.023
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- Publication type:
- Article
Two patients with glutaric aciduria type 3: a novel mutation and brain magnetic resonance imaging findings.
- Published in:
- Turkish Journal of Pediatrics, 2020, v. 62, n. 4, p. 657, doi. 10.24953/turkjped.2020.04.017
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- Publication type:
- Article
Magnetic resonance imaging patterns of subacute sclerosing panencephalitis may mimic metabolic disorders: clinical, electroencephalographic and imaging features of six cases.
- Published in:
- Acta Neurologica Belgica, 2021, v. 121, n. 4, p. 955, doi. 10.1007/s13760-020-01469-1
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- Publication type:
- Article
Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience.
- Published in:
- Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01349-9
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- Publication type:
- Article