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Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.
J Pediatr Genet. 2021 Sep;10(3):213-221. doi: 10.1055/s-0040-1715528. Epub 2020 Sep 2.
J Pediatr Genet. 2021.
PMID: 34504725
Free PMC article.
Expanding the spectrum of HEXA mutations in Indian patients with Tay-Sachs disease.
Sheth J, Mistri M, Datar C, Kalane U, Patil S, Kamate M, Shah H, Nampoothiri S, Gupta S, Sheth F.
Sheth J, et al. Among authors: kalane u.
Mol Genet Metab Rep. 2014 Sep 29;1:425-430. doi: 10.1016/j.ymgmr.2014.09.004. eCollection 2014.
Mol Genet Metab Rep. 2014.
PMID: 27896118
Free PMC article.
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Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.
Garg D, Yoganathan S, Shamim U, Mankad K, Gulati P, Bonifati V, Botre A, Kalane U, Saini AG, Sankhyan N, Srivastava K, Gowda VK, Juneja M, Kamate M, Padmanabha H, Panigrahi D, Pachapure S, Udani V, Kumar A, Pandey S, Thomas M, Danda S, Iqbalahmed SA, Subramanian A, Pemde H, Singh V, Faruq M, Sharma S.
Garg D, et al. Among authors: kalane u.
Mov Disord Clin Pract. 2022 Aug 12;9(7):886-899. doi: 10.1002/mdc3.13516. eCollection 2022 Oct.
Mov Disord Clin Pract. 2022.
PMID: 36247901
Free PMC article.
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Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India.
Nagarajan B, Gowda VK, Yoganathan S, Sharawat IK, Srivastava K, Vora N, Badheka R, Danda S, Kalane U, Kaur A, Madaan P, Mehta S, Negi S, Panda PK, Rajadhyaksha S, Saini AG, Saini L, Shah S, Srinivasan VM, Suthar R, Thomas M, Vyas S, Sankhyan N, Sahu JK.
Nagarajan B, et al. Among authors: kalane u.
Epilepsia Open. 2023 Dec;8(4):1383-1404. doi: 10.1002/epi4.12811. Epub 2023 Aug 25.
Epilepsia Open. 2023.
PMID: 37583270
Free PMC article.
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Clinical and Electrophysiological Factors Predicting Prolonged Recovery in Children with Guillain-Barré Syndrome.
Agarwal E, Bhagat A, Srivastava K, Thakore B, Jagtap S, Kalane U, Rajadhyaksha S.
Agarwal E, et al. Among authors: kalane u.
Indian J Pediatr. 2022 May;89(5):452-458. doi: 10.1007/s12098-021-03804-7. Epub 2021 Jun 7.
Indian J Pediatr. 2022.
PMID: 34097234
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First reported case of Charcot Marie Tooth disease type 4C in a child from India with SH3TC2 mutation but absent spinal deformities.
Kalane UD, Datar C, Mahadevan A.
Kalane UD, et al.
Neurol India. 2015 May-Jun;63(3):395-8. doi: 10.4103/0028-3886.158222.
Neurol India. 2015.
PMID: 26053813
Free article.
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Dengue Encephalitis in a Newborn.
Kalane SU, Gokhale AN, Kalane UD.
Kalane SU, et al. Among authors: kalane ud.
Indian J Pediatr. 2021 Jul;88(7):716. doi: 10.1007/s12098-021-03791-9. Epub 2021 May 20.
Indian J Pediatr. 2021.
PMID: 34018130
No abstract available.
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Rhombencephalosynapsis: A rare cerebellar malformation associated with aqueductal stenosis and obstructive hydrocephalus.
Kalane U, Atre A.
Kalane U, et al.
Neurol India. 2016 Nov-Dec;64(6):1381-1383. doi: 10.4103/0028-3886.193837.
Neurol India. 2016.
PMID: 27841240
Free article.
No abstract available.
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