Laxmi' V - Search Results

1

Meta-QTL and ortho analysis unravels the genetic architecture and key candidate genes for cold tolerance at seedling stage in rice.

Kumari A, Sharma P, Rani M, Laxmi V, Sahil, Sahi C, Satturu V, Katiyar-Agarwal S, Agarwal M. Kumari A, et al. Among authors: laxmi v. Physiol Mol Biol Plants. 2024 Jan;30(1):93-108. doi: 10.1007/s12298-024-01412-1. Epub 2024 Feb 2. Physiol Mol Biol Plants. 2024. PMID: 38435852

2

Cogan's Lid Twitch Sign in a Child with Congenital Myasthenia.

Manjunathan S, Gunasekaran PK, Laxmi V, Kumar A, Saini L. Manjunathan S, et al. Among authors: laxmi v. Neuropediatrics. 2024 Apr;55(2):148. doi: 10.1055/s-0043-1778649. Epub 2024 Jan 16. Neuropediatrics. 2024. PMID: 38228156 No abstract available.

3

Primary Diffuse Leptomeningeal Melanomatosis in an Indian Child With Review of Literature.

Kumar A, Gunasekaran PK, Aggarwal D, Janu V, Manjunathan S, Laxmi V, Tiwari S, Saini L. Kumar A, et al. Among authors: laxmi v. Pediatr Neurol. 2024 Mar;152:23-29. doi: 10.1016/j.pediatrneurol.2023.12.007. Epub 2023 Dec 14. Pediatr Neurol. 2024. PMID: 38176225 Review.

4

Teaching NeuroImage: Neuroimaging Features of Wilson Disease.

Gunasekaran PK, Tiwari S, Kumar A, Laxmi V, Saini L. Gunasekaran PK, et al. Among authors: laxmi v. Neurology. 2024 Feb 13;102(3):e208078. doi: 10.1212/WNL.0000000000208078. Epub 2024 Jan 4. Neurology. 2024. PMID: 38175989

5

Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene.

Gunasekaran PK, Kumar A, Uk KK, Laxmi V, Tiwari S, Saini L. Gunasekaran PK, et al. Among authors: laxmi v. Indian J Pediatr. 2024 Mar;91(3):317. doi: 10.1007/s12098-023-04970-6. Epub 2023 Dec 6. Indian J Pediatr. 2024. PMID: 38052954 No abstract available.

6

Acute Flaccid Paralysis due to Pyruvate Dehydrogenase E1-Alpha Deficiency.

Laxmi V, Gunasekaran PK, Kumar A, Manjunathan S, Tiwari S, Saini L. Laxmi V, et al. Indian J Pediatr. 2024 May;91(5):518. doi: 10.1007/s12098-023-04853-w. Epub 2023 Oct 3. Indian J Pediatr. 2024. PMID: 37787965 No abstract available.

7

Emerging Field of Nanotechnology in Environment.

Laxmi V, Singhvi N, Ahmad N, Sinha S, Negi T, Gupta V, Mubashshir M, Ahmad A, Sharma S. Laxmi V, et al. Indian J Microbiol. 2023 Sep;63(3):244-252. doi: 10.1007/s12088-023-01092-7. Epub 2023 Sep 2. Indian J Microbiol. 2023. PMID: 37781004 Review.

8

Knobloch Syndrome - Triad of Occipital Encephalocele, Retino-Choroidal Detachment and Epilepsy.

Gunasekaran PK, Jindal P, Laxmi V, Manjunathan S, Kumar A, Tandon M, Yadav T, Saini L. Gunasekaran PK, et al. Among authors: laxmi v. Indian J Pediatr. 2024 Mar;91(3):306. doi: 10.1007/s12098-023-04861-w. Epub 2023 Sep 20. Indian J Pediatr. 2024. PMID: 37726637 No abstract available.

9

Associated movement disorder as a clue for the diagnosis of paroxysmal kinesigenic dyskinesia in a child with focal epilepsy.

Laxmi V, Gunasekaran PK, Manjunathan S, Gupta R, Kumar A, Saini L. Laxmi V, et al. J Neurosci Rural Pract. 2023 Jul-Sep;14(3):558-559. doi: 10.25259/JNRP_118_2023. Epub 2023 May 31. J Neurosci Rural Pract. 2023. PMID: 37692800 Free PMC article. No abstract available.

10

Clinical Profile, Follow-up, and Role of Neuroimaging in Pediatric Guillain-Barré Syndrome in the COVID Era: An Ambispective Study.

Saini L, Krishna D, Gunasekaran PK, Tiwari S, Kumar P, Goyal JP, Khera D, Choudhary B, Didel S, Gaur R, Laxmi V, Panda S, Singh K. Saini L, et al. Among authors: laxmi v. J Child Neurol. 2023 May;38(6-7):407-413. doi: 10.1177/08830738231184089. Epub 2023 Jun 26. J Child Neurol. 2023. PMID: 37365810

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