Connection
Co-Authors
This is a "connection" page, showing publications co-authored by Debopam Samanta and Raghu Hosahalli Ramakrishnaiah.
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Connection Strength |
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4.985 |
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Harada Y, Ramakrishnaiah R, Arya K, Samanta D. Extensive reversible myelopathy secondary to acute quadriventricular noncommunicating hydrocephalus. Childs Nerv Syst. 2019 11; 35(11):2023-2026.
Score: 0.689
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Samanta D, Ramakrishnaiah R, Frye RE. Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status. Neurol India. 2022 Sep-Oct; 70(5):2265-2267.
Score: 0.427
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Samanta D, Ramakrishnaiah R. Intravenous Immunoglobulin in the Treatment of Alternating Hemiplegia of Childhood. Clin Neuropharmacol. 2021 Jan-Feb 01; 44(1):23-26.
Score: 0.380
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Samanta D, Ramakrishnaiah R. Early-Onset Parkinsonism and Halo Sign: Beta-propeller Proteinassociated Neurodegeneration. J Pediatr Neurosci. 2020 Jul-Sep; 15(3):325-327.
Score: 0.376
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Samanta D, Ramakrishnaiah R. Recurrent Oral Ulcers in a Child With Seizures. Pediatr Neurol. 2020 02; 103:89-90.
Score: 0.338
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Samanta D, Ramakrishnaiah R, Schaefer B. The neurological aspects related to POGZ mutation: case report and review of CNS malformations and epilepsy. Acta Neurol Belg. 2020 Apr; 120(2):447-450.
Score: 0.336
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Samanta D, Ramakrishnaiah R, Crary SE, Sukumaran S, Burrow TA. Multiple Autoimmune Disorders in Aicardi-Gouti?res Syndrome. Pediatr Neurol. 2019 07; 96:37-39.
Score: 0.333
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Samanta D, Ramakrishnaiah R. Recurrent Encephalopathy with Spinal Cord Involvement: An Atypical Manifestation of Aicardi-Gouti?res Syndrome. Ann Indian Acad Neurol. 2019 Jan-Mar; 22(1):111-115.
Score: 0.331
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Samanta D, Ramakrishnaiah R, Frye RE. Complex heterozygous polymerase gamma mutation and cerebral folate deficiency in a child with refractory partial status. Neurol India. 2019 Jan-Feb; 67(1):259-260.
Score: 0.331
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Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76.
Score: 0.322
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Samanta D, Ramakrishnaiah R. Diffuse Carotid Arteriosclerosis and Stroke in a Patient With Schimke Immuno-osseous Dysplasia. Pediatr Neurol. 2017 Jun; 71:82-83.
Score: 0.293
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Samanta D, Ramakrishnaiah R. De novo R853Q mutation of SCN2A gene and West syndrome. Acta Neurol Belg. 2015 Dec; 115(4):773-6.
Score: 0.254
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Samanta D, Ramakrishnaiah R. Novel brain magnetic resonance imaging finding in a patient with trisomy 9p syndrome. Acta Neurol Belg. 2015 Sep; 115(3):431-2.
Score: 0.250
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Samanta D, Ramakrishnaiah R, Willis E, Frye RE. Myoclonic epilepsy evolved into West syndrome: a patient with a novel de novo KCNQ2 mutation. Acta Neurol Belg. 2015 Sep; 115(3):475-8.
Score: 0.244
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Malatesta LM, Samanta D, Ramakrishnaiah R. An Unusual Cause of Recurrent Facial Nerve Palsy. Pediatr Neurol. 2019 02; 91:68-69.
Score: 0.082
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Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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