Passi GR - Search Results

1

Progressive Unilateral Foot Drop in a Child due to Neuromuscular Choristoma.

Passi GR, Maheshwari S, Udani V. Passi GR, et al. Ann Indian Acad Neurol. 2024 Sep 1;27(5):580-582. doi: 10.4103/aian.aian_226_24. Epub 2024 Oct 15. Ann Indian Acad Neurol. 2024. PMID: 39445895 Free PMC article.

2

Tocilizumab in a Child with Acute Leukoencephalopathy with Restricted Diffusion.

Jaiswal A, Patel S, Khare S, Passi GR. Jaiswal A, et al. Among authors: passi gr. Ann Indian Acad Neurol. 2023 Jan-Feb;26(1):95-96. doi: 10.4103/aian.aian_795_22. Epub 2023 Jan 4. Ann Indian Acad Neurol. 2023. PMID: 37034033 Free PMC article. No abstract available.

3

Case Report of Congenital Kyphoscoliosis with Myotonic Dystrophy Type 1: Perioperative and Anesthetic Considerations.

Agrawal A, Dhawale T, Kaur V, Passi GR. Agrawal A, et al. Among authors: passi gr. J Pediatr Neurosci. 2021 Oct-Dec;16(4):281-284. doi: 10.4103/jpn.JPN_119_20. Epub 2021 Jul 12. J Pediatr Neurosci. 2021. PMID: 36531760 Free PMC article.

4

Treatment of Seizures in the Neonate: Special Report From the ILAE Task Force on Neonatal Seizures, 2022.

Jajoo M, Anand P, Passi GR. Jajoo M, et al. Among authors: passi gr. Indian Pediatr. 2023 Aug 15;60(8):675-678. Indian Pediatr. 2023. PMID: 37565439 Free article.

5

Cerebral creatine deficiency disorders - A clinical, genetic and follow up study from India.

Passi GR, Pandey S, Devi ARR, Konanki R, Jain AR, Bhatnagar S, Tripathi R, Jain V. Passi GR, et al. Brain Dev. 2022 Apr;44(4):271-280. doi: 10.1016/j.braindev.2021.12.004. Epub 2021 Dec 30. Brain Dev. 2022. PMID: 34974949

6

Clinical and Genetic Spectrum of 50 Children with Inborn Errors of Metabolism from Central India.

Passi GR, Wakchaure A, Jaiswal SP. Passi GR, et al. Indian J Pediatr. 2022 Feb;89(2):184-191. doi: 10.1007/s12098-021-03958-4. Epub 2021 Nov 25. Indian J Pediatr. 2022. PMID: 34822107

7

What Percentage of Patients with Duchene Muscular Dystrophy are Potentially Treatable with Gene Therapies?

Passi GR, Paharia M, Jaiswal SP. Passi GR, et al. Ann Indian Acad Neurol. 2021 Jul-Aug;24(4):601-603. doi: 10.4103/aian.AIAN_727_20. Epub 2021 Apr 16. Ann Indian Acad Neurol. 2021. PMID: 34728964 Free PMC article. No abstract available.

8

Management of Neurocysticercosis in Children: Association of Child Neurology Consensus Guidelines.

Sankhyan N, Kadwa RA, Kamate M, Kannan L, Kumar A, Passi GR, Sharawat IK, Singhi P; For Association of Child Neurology Delphi Group for Neurocysticerosis in Childhood. Sankhyan N, et al. Among authors: passi gr. Indian Pediatr. 2021 Sep 15;58(9):871-880. Epub 2021 Aug 2. Indian Pediatr. 2021. PMID: 34338221 Free article.

9

Dominant SCN2A mutation with variable phenotype in two generations.

Passi GR, Mohammad SS. Passi GR, et al. Brain Dev. 2021 Jan;43(1):166-169. doi: 10.1016/j.braindev.2020.08.009. Epub 2020 Sep 4. Brain Dev. 2021. PMID: 32893078

10

An Indian child with Coats plus syndrome due to mutations in STN1.

Passi GR, Shamim U, Rathore S, Joshi A, Mathur A, Parveen S, Sharma P, Crow YJ, Faruq M. Passi GR, et al. Am J Med Genet A. 2020 Sep;182(9):2139-2144. doi: 10.1002/ajmg.a.61737. Epub 2020 Jul 6. Am J Med Genet A. 2020. PMID: 32627942

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