Gowda VK - Search Results

1

A Rare Case of Neuronal Ceroid Lipofuscinosis-Type 1 (NCL-1) with Vitamin D-Dependent Rickets-Type 1 (VDDR-1), Complex 1 Mitochondrial Deficiency, and Mixed Variant-Checkerboard and Phylloid Type of Pigmentary Mosaicism.

Gowda VK, K AR, Srinivasan VM, Vamyanmane DK, Srinivas SM, Chickabasaviah Y, Santhoshkumar R, Mittal P, Chikara SK, Vishwanathan GB. Gowda VK, et al. J Pediatr Genet. 2024 May 30;13(4):291-299. doi: 10.1055/s-0044-1787196. eCollection 2024 Dec. J Pediatr Genet. 2024. PMID: 39502845

2

Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South India.

Gowda VK, Vegda H, Sugumar K, Narayanappa G, Srinivasan VM, Santhoshkumar R, Bhat M, Balu S, Naveen MR. Gowda VK, et al. J Pediatr Genet. 2020 Aug 4;10(4):266-273. doi: 10.1055/s-0040-1715575. eCollection 2021 Dec. J Pediatr Genet. 2020. PMID: 34849271 Free PMC article.

3

A Treatable Cause of Myelopathy: Biotinidase Deficiency Presenting as Acute Flaccid Paralysis.

Gowda VK, Kerur C, Vamyanmane DK, Kumar P, Nagarajappa VH, Shivappa SK. Gowda VK, et al. J Pediatr Genet. 2020 Oct 8;11(3):257-260. doi: 10.1055/s-0040-1718537. eCollection 2022 Sep. J Pediatr Genet. 2020. PMID: 35990026 Free PMC article.

4

Cohort of Phenotype, Genotype, and Outcome of SCN Developmental and Epileptic Encephalopathies from Southern Part of India.

Gowda VK, Battina M, Vegda H, Srinivasan VM, Chikara SK, Mishra A, Shivappa SK, Benakappa N. Gowda VK, et al. J Pediatr Genet. 2021 Jun 22;12(1):32-41. doi: 10.1055/s-0041-1731020. eCollection 2023 Mar. J Pediatr Genet. 2021. PMID: 36684540 Free PMC article.

5

Infantile Systemic Hyalinosis Presenting as Pseudo-Paralysis in Infancy: Study of Six Cases.

Gowda VK, Srinivas SM, Gupta P, Srinivasan VM, Shivappa SK, Vishwanathan GB. Gowda VK, et al. J Pediatr Genet. 2021 Nov 9;12(3):199-205. doi: 10.1055/s-0041-1736558. eCollection 2023 Sep. J Pediatr Genet. 2021. PMID: 37575643 Free PMC article.

6

Recurrent Bilateral Lower Motor Neuron Type of Facial Palsy with Hearing Impairment: Hyperphosphatemic Familial Tumoral Calcinosis.

Gowda VK, Raj A, Vamyanmane DK, Nagarajappa VH, Srinivas SM, Tirumale R, Ranganath J, Gaddehosur C, Vishwanathan GB. Gowda VK, et al. J Pediatr Genet. 2022 Jan 7;12(4):280-287. doi: 10.1055/s-0041-1741522. eCollection 2023 Dec. J Pediatr Genet. 2022. PMID: 38162162 Free PMC article.

7

Compressive Myelopathy Secondary to TRPV4 Skeletal Dysplasia: Spondylometaphyseal Dysplasia, Kozlowski Type.

Gowda VK, Srinivasan VM, Reddy VM, Vamyanmane DK, Shivappa SK, Ramesh RH, Vishwanathan GB. Gowda VK, et al. J Pediatr Genet. 2022 Jan 6;13(2):158-165. doi: 10.1055/s-0041-1741424. eCollection 2024 Jun. J Pediatr Genet. 2022. PMID: 38721578 Free PMC article.

8

Giant melanocytic nevi with neurocutaneous melanosis masquerading as neurofibromas.

Gowda VK, Basude A, Srinivas SM, Bhat M. Gowda VK, et al. J Pediatr Neurosci. 2016 Jul-Sep;11(3):258-260. doi: 10.4103/1817-1745.193357. J Pediatr Neurosci. 2016. PMID: 27857802 Free PMC article.

9

Macrophagic Myofasciitis: A Report of Two South Indian Infants.

Gowda VK, Srinivasan VM, Muthane Y, Narayanappa G. Gowda VK, et al. J Pediatr Neurosci. 2020 Jul-Sep;15(3):279-282. doi: 10.4103/jpn.JPN_141_19. Epub 2020 Nov 6. J Pediatr Neurosci. 2020. PMID: 33531946 Free PMC article.

10

Siblings with Glutaric Aciduria Type 1 with Atypical Phenotype with Novel Pathogenic Variant in GCDH Gene.

Gowda VK, Nagarajan B, Srinivasan VM, Bhat M. Gowda VK, et al. J Pediatr Neurosci. 2021 Jan-Mar;16(1):75-78. doi: 10.4103/jpn.JPN_63_20. Epub 2021 Jun 25. J Pediatr Neurosci. 2021. PMID: 34316315 Free PMC article.

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