Sait H - Search Results

1

Factors Associated with Transient Neonatal Hyperthyrotropinemia.

Garg R, Sait H, Jindal A, Juneja M, Gupta S, Thelma BK, Kapoor S. Garg R, et al. Among authors: sait h. Indian J Pediatr. 2020 Jun;87(6):482-483. doi: 10.1007/s12098-019-03095-z. Epub 2019 Nov 8. Indian J Pediatr. 2020. PMID: 31705380 No abstract available.

2

Association Between Neonatal Thyroid Stimulating Hormone Status and Maternal Urinary Iodine Status.

Sait H, Kapoor S, Jindal A, Garg R, Belwal RS, Yadav S, Gupta S, Thelma BK. Sait H, et al. Indian Pediatr. 2019 Jun 15;56(6):472-475. Indian Pediatr. 2019. PMID: 31278226 Free article.

3

Portal Hypertension in a Case of Klippel Trenaunay Syndrome.

Sait H, Sahi PK, Kapoor S. Sait H, et al. Indian Pediatr. 2020 Aug 15;57(8):754-755. doi: 10.1007/s13312-020-1925-4. Indian Pediatr. 2020. PMID: 32844765 Free PMC article. No abstract available.

4

Biallelic cGMP-dependent type II protein kinase gene (PRKG2) variants cause a novel acromesomelic dysplasia.

Díaz-González F, Wadhwa S, Rodriguez-Zabala M, Kumar S, Aza-Carmona M, Sentchordi-Montané L, Alonso M, Ahmad I, Zahra S, Kumar D, Kushwah N, Shamim U, Sait H, Kapoor S, Roldán B, Nishimura G, Offiah AC, Faruq M, Heath KE. Díaz-González F, et al. Among authors: sait h. J Med Genet. 2022 Jan;59(1):28-38. doi: 10.1136/jmedgenet-2020-107177. Epub 2020 Oct 26. J Med Genet. 2022. PMID: 33106379

5

Bartter-Like Renal Phenotype in a Child with Donnai-Barrow Syndrome.

Sait H, Singh R, Kapoor S. Sait H, et al. Indian J Pediatr. 2021 Apr;88(4):390. doi: 10.1007/s12098-020-03589-1. Epub 2021 Jan 6. Indian J Pediatr. 2021. PMID: 33403612 No abstract available.

6

Phenotypic and genotypic spectrum of CTSK variants in a cohort of twenty-five Indian patients with pycnodysostosis.

Sait H, Srivastava P, Gupta N, Kabra M, Kapoor S, Ranganath P, Rungsung I, Mandal K, Saxena D, Dalal A, Roy A, Pabbati J, Phadke SR. Sait H, et al. Eur J Med Genet. 2021 Jul;64(7):104235. doi: 10.1016/j.ejmg.2021.104235. Epub 2021 May 1. Eur J Med Genet. 2021. PMID: 33945887

7

An Unusual Occurrence of Protein C Deficiency and Cytomegalovirus Infection in a Case of Purpura Fulminans.

Sait H, Singh R, Kapoor S. Sait H, et al. Indian J Dermatol. 2021 Mar-Apr;66(2):201-203. doi: 10.4103/ijd.IJD_463_19. Indian J Dermatol. 2021. PMID: 34188281 Free PMC article. No abstract available.

8

Loes Score: Clinical and Radiological Profile of 22 Patients of X-Linked Adrenoleukodystrophy: Case Series from a Single Center.

Kumar S, Sait H, Polipalli SK, Pradhan GS, Pruthi S, Kapoor S. Kumar S, et al. Among authors: sait h. Indian J Radiol Imaging. 2021 Apr;31(2):383-390. doi: 10.1055/s-0041-1734366. Epub 2021 Jul 28. Indian J Radiol Imaging. 2021. PMID: 34556923 Free PMC article.

9

Anastrozole-mediated modulation of mitochondrial activity by inhibition of mitochondrial permeability transition pore opening: an initial perspective.

Kumar S, Choudhary N, Faruq M, Kumar A, Saran RK, Indercanti PK, Singh V, Sait H, Jaitley S, Valis M, Kuca K, Polipalli SK, Kumar M, Singh T, Suravajhala P, Sharma R, Kapoor S. Kumar S, et al. Among authors: sait h. J Biomol Struct Dyn. 2023;41(23):14063-14079. doi: 10.1080/07391102.2023.2176927. Epub 2023 Feb 23. J Biomol Struct Dyn. 2023. PMID: 36815262

10

Inborn Errors of Ketogenesis: Novel Variants, Clinical Presentation, and Follow-Up in a Series of Four Patients.

Sait H, Srivastava S, Kumar S, Varughese B, Pandey M, Venkatramaiah M, Chaudhary P, Moirangthem A, Mandal K, Kapoor S. Sait H, et al. J Pediatr Genet. 2022 Jul 12;13(1):22-28. doi: 10.1055/s-0042-1749362. eCollection 2024 Mar. J Pediatr Genet. 2022. PMID: 38567177 Free PMC article.

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