Works matching IS 18171745 AND DT 2020 AND VI 15 AND IP 2
Results: 25
Increased hemoglobin and plateletcrit levels indicating hemoconcentration in pediatric patients with migraine.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 99, doi. 10.4103/jpn.JPN_73_19
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Clinico-radiological profile of children with pontocerebellar hypoplasia.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 94, doi. 10.4103/jpn.JPN_6_19
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Facebook and WhatsApp in identifying current practices of neurological physiotherapy intervention in neonatal intensive care units: In Indian scenario.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 90, doi. 10.4103/jpn.JPN_175_18
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Clinical features and molecular genetics of autosomal recessive ataxia in the Turkish population.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 86, doi. 10.4103/jpn.JPN_145_18
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Effect of levetiracetam usage on serum creatine phosphokinase concentration in patients with epilepsy.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 81, doi. 10.4103/jpn.JPN_133_18
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Craniosynostosis: To study the spectrum and outcome of surgical intervention at a tertiary referral institute in India.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 72, doi. 10.4103/jpn.JPN_101_18
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COVID-19. The missing link.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 69, doi. 10.4103/jpn.JPN_158_20
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James Goodrich: A personal tribute.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 166, doi. 10.4103/jpn.JPN_143_20
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Autism spectrum disorder and mammalian target of rapamycin system.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 164, doi. 10.4103/jpn.JPN_172_19
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West syndrome and neurocutaneous syndromes: A never-ending association.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 162, doi. 10.4103/jpn.JPN_147_19
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Amniotic band syndrome with placenta–encephalocele adhesion: An uncommon case.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 160, doi. 10.4103/jpn.JPN_163_19
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A rare case report of Guillain–Barré syndrome presenting as unilateral facial palsy with isolated acute bulbar palsy.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 157, doi. 10.4103/jpn.JPN_129_19
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A rare case of peripheral nerve hyperexcitability in childhood: Isaacs syndrome.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 153, doi. 10.4103/jpn.JPN_128_19
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Cerebral venous sinus thrombosis following primary varicella infection in a child.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 150, doi. 10.4103/jpn.JPN_136_19
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A rare case of intramedullary lipoma of brainstem to thoracic cord––What to do?
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 145, doi. 10.4103/jpn.JPN_134_19
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Delayed diagnosis of cobalamin E defect in an adolescent patient.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 140, doi. 10.4103/jpn.JPN_132_19
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Split cord malformation type 2 with double dorsal lipoma: A sequela or a chance.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 135, doi. 10.4103/jpn.JPN_131_19
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Primary hypokalemic periodic paralysis: Long-term management and complications in a child.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 132, doi. 10.4103/jpn.JPN_101_19
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Moebius syndrome: A rare entity or a missed diagnosis?
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 128, doi. 10.4103/jpn.JPN_72_19
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Intracranial rhabdomyosarcoma of the cerebellopontine angle in a 6-year-old child: A case report.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 124, doi. 10.4103/jpn.JPN_70_19
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A novel SCN1A mutation: A case report.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 120, doi. 10.4103/jpn.JPN_118_18
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Acute cerebral venous sinus thrombosis: A rare complication of primary varicella zoster virus infection.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 116, doi. 10.4103/jpn.JPN_167_18
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Infantile presentation of Lehman syndrome with multiple lateral meningoceles, dural ectasias, and herniation of conus: A rare case report.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 111, doi. 10.4103/jpn.JPN_152_18
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Facial dysmorphism, hirsutism, and failure to thrive as manifestation of Leigh syndrome in a child with SURF1 mutation.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 108, doi. 10.4103/jpn.JPN_137_18
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Multiple cerebral hemorrhages during the course of Guillain–Barre syndrome: A case report.
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- Journal of Pediatric Neurosciences, 2020, v. 15, n. 2, p. 105, doi. 10.4103/jpn.JPN_143_18
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