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vedantham v
(113 results)?
Genomics of rare genetic diseases-experiences from India.
Hum Genomics. 2019 Sep 25;14(1):52. doi: 10.1186/s40246-019-0215-5.
Hum Genomics. 2019.
PMID: 31554517
Free PMC article.
Review.
Utility of the RIPS Scale and 2CAN Score for In-Hospital Stroke Prediction.
Chinta VR, Krishnan P, Murgod U, Mahadevappa M, Roy AK, Srinivasan M, Vedartham V.
Chinta VR, et al. Among authors: vedartham v.
Ann Indian Acad Neurol. 2023 Mar-Apr;26(2):151-155. doi: 10.4103/aian.aian_879_22. Epub 2023 Mar 17.
Ann Indian Acad Neurol. 2023.
PMID: 37179682
Free PMC article.
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Hypodensities within Hematoma is Time-Dependent and Predicts Outcome after Spontaneous Intracerebral Hemorrhage.
Vedartham V, Kesav P, Maniangatt S, Nagesh C, Sreedharan SE, Jayadevan ER, Sarma S, Sylaja PN.
Vedartham V, et al.
Neurol India. 2021 May-Jun;69(3):676-680. doi: 10.4103/0028-3886.319222.
Neurol India. 2021.
PMID: 34169867
Free article.
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Homozygous sequestosome 1 (SQSTM1) mutation: a rare cause for childhood-onset progressive cerebellar ataxia with vertical gaze palsy.
Vedartham V, Sundaram S, Nair SS, Ganapathy A, Mannan A, Menon R.
Vedartham V, et al.
Ophthalmic Genet. 2019 Aug;40(4):376-379. doi: 10.1080/13816810.2019.1666414. Epub 2019 Sep 16.
Ophthalmic Genet. 2019.
PMID: 31525130
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Rare anatomical variation in transverse sinuses (duplication on right, hypoplasia of left) falsely mimicking transverse sinus thrombosis probably due to resultant slow flow.
Monigari N, Deshpande A, Vedartham V, Nalabothu M.
Monigari N, et al. Among authors: vedartham v.
BMJ Case Rep. 2014 Jan 17;2014:bcr2013202937. doi: 10.1136/bcr-2013-202937.
BMJ Case Rep. 2014.
PMID: 24443342
Free PMC article.
No abstract available.
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