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Year | Number of Results |
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2023 | 3 |
2024 | 1 |
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Page 1
Lathosterolosis - A Rare Treatable Cause for Global Developmental Delay, Cataract, and Liver Dysfunction Masquerading as Galactosemia.
Indian J Pediatr. 2023 Aug;90(8):837. doi: 10.1007/s12098-023-04623-8. Epub 2023 Apr 21.
Indian J Pediatr. 2023.
PMID: 37083887
No abstract available.
Reversible Basal Ganglia Changes in a Child With Infantile Tremor Syndrome.
Gowda VK, Bylappa AY, Kinhal U, Srinivasan VM.
Gowda VK, et al. Among authors: kinhal u.
Indian Pediatr. 2023 Sep 15;60(9):770-771.
Indian Pediatr. 2023.
PMID: 37705272
Free article.
No abstract available.
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In silico characterization and identification of compound heterozygous variants in H/ACA Ribonucleoprotein Assembly Factor (SHQ1) from Indian population.
Gowda VK, Srinivasan VM, Srivastava S, Ghali N, Kinhal U, Shamnur A, Srivastava A.
Gowda VK, et al. Among authors: kinhal u.
J Family Med Prim Care. 2024 Jan;13(1):208-220. doi: 10.4103/jfmpc.jfmpc_979_23. Epub 2024 Feb 8.
J Family Med Prim Care. 2024.
PMID: 38482315
Free PMC article.
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Mitochondrial Complex I Deficiency Masquerading as Stroke-Like Episode Clinically and as Alexander Disease Radiologically Following Chicken Pox.
Gowda VK, Bylappa AY, Kinhal U, Srinivasan VM, Vamyanmane DK.
Gowda VK, et al. Among authors: kinhal u.
Ann Indian Acad Neurol. 2023 Nov-Dec;26(6):977-979. doi: 10.4103/aian.aian_339_23. Epub 2023 Aug 11.
Ann Indian Acad Neurol. 2023.
PMID: 38229652
Free PMC article.
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