Dry beriberi preceded Wernicke’s encephalopathy: Thiamine deficiency after laparoscopic sleeve gastrectomy.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Works matching IS 18171745 AND DT 2015 AND VI 10 AND IP 3
Results: 26
1
2
Magnetic resonance imaging depiction of acquired Dyke–Davidoff-Masson syndrome with crossed cerebro‑cerebellar diaschisis: Report of two cases.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
3
Giant pediatric glioblastoma multiforme causing primary calvarial erosion and sutural diastasis presenting with enlarged head.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
4
Fatal cerebellar hemorrhage as an initial presentation of medulloblastoma in a child.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
5
Bilateral symmetrical infratentorial subdural empyema: Delay proves detrimental.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
6
Neonatal brain abscess: An atypical presentation.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
7
A rare cause of acute flaccid paralysis: Human coronaviruses.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
8
Childhood‑onset (Juvenile) Huntington's disease: A rare case report.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
9
Rare association of thin corpus callosum with infantile tremor syndrome in a 5.5‑month‑old infant.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
10
Bilateral occipital extradural hematoma in a child.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
11
Intracranial extradural hematoma: Spontaneous rapid decompression - not resolution.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
12
Split calvarial fracture: A rare cause of hypovolemic shock in an infant.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
13
Linear undisplaced fracture of temporoparietal bone acting as spontaneous early decompressive craniotomy in a neonate.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
14
Neurobehavioral phenotype in cyclin‑dependent kinase‑like 5 syndrome: Case report and review of literature.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
15
A case of mitochondrial cytopathy with exertion induced dystonia.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
16
Posterior fossa infected dermoid with congenital heart disease: A novel hypothesis of an unusual association.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
17
Rare case of anterior fontanelle epidermoid/ dermoid.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
18
Middle interhemispheric variant of holoprosencephaly: A rare midline malformation.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
19
Acute onset of postoperative syringohydromyelia.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
20
Diastematomyelia with hemimyelomeningocele: An exceptional and complex spinal dysraphism.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
21
Symmetrical central tegmental tract hyperintensities on magnetic resonance imaging.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 3, p. 235, doi. 10.4103/1817-1745.165666
- By:
- Publication type:
- Article
22
Pattern, etiological factors and determinants of mortality among sick newborns with seizures in Ilesa, Nigeria.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 3, p. 227, doi. 10.4103/1817-1745.165663
- By:
- Publication type:
- Article
23
Parameters of metabolic syndrome in Indian children with epilepsy on valproate or phenytoin monotherapy.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 3, p. 222, doi. 10.4103/1817-1745.165661
- By:
- Publication type:
- Article
24
Pediatric intramedullary spinal cord lesions: Pathological spectrum and outcome of surgery.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 3, p. 214, doi. 10.4103/1817-1745.165660
- By:
- Publication type:
- Article
25
Novel mutation detection of fibroblast growth factor receptor 1 (FGFR1) gene, FGFR2IIIa, FGFR2IIIb, FGFR2IIIc, FGFR3, FGFR4 gene for craniosynostosis: A prospective study in Asian Indian patient.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 3, p. 207, doi. 10.4103/1817-1745.165659
- By:
- Publication type:
- Article
26
Analysis of survival in pediatric high‑grade brainstem gliomas: A population‑based study.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 3, p. 199, doi. 10.4103/1817-1745.165656
- By:
- Publication type:
- Article