Dubey S - Search Results

1

Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders.

Goswami R, Goswami D, Kabra M, Gupta N, Dubey S, Dadhwal V. Goswami R, et al. Among authors: dubey s. Fertil Steril. 2003 Oct;80(4):1052-4. doi: 10.1016/s0015-0282(03)01121-x. Fertil Steril. 2003. PMID: 14556833 Free article.

2

Detection of complex chromosomal rearrangements in a woman with repeated spontaneous abortions.

Dubey S, Mathur R, Kabra M, Menon PS. Dubey S, et al. Acta Obstet Gynecol Scand. 2001 May;80(5):478-9. Acta Obstet Gynecol Scand. 2001. PMID: 11328231 No abstract available.

3

Rapid prenatal karyotyping using foetal blood obtained by cordocentesis.

Mathur R, Dubey S, Hamilton S, Singh G, Deka D, Kriplani A, Kabra M, Menon PS. Mathur R, et al. Among authors: dubey s. Natl Med J India. 2002 Mar-Apr;15(2):75-7. Natl Med J India. 2002. PMID: 12044120

4

Serum leptin levels in obese Indian children relation to clinical and biochemical parameters.

Dubey S, Kabra M, Bajpai A, Pandey RM, Hasan M, Gautam RK, Menon PS. Dubey S, et al. Indian Pediatr. 2007 Apr;44(4):257-62. Indian Pediatr. 2007. PMID: 17468520 Free article.

5

Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients.

Gupta N, Singh PK, Kumar M, Shastri S, Gulati S, Kumar A, Agarwala A, Kapoor S, Nair M, Sapra S, Dubey S, Singh A, Kaur P, Kabra M. Gupta N, et al. Among authors: dubey s. JIMD Rep. 2015;21:45-55. doi: 10.1007/8904_2014_377. Epub 2015 Mar 12. JIMD Rep. 2015. PMID: 25762492 Free PMC article.

6

Erratum to: Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients.

Gupta N, Singh PK, Kumar M, Shastri S, Gulati S, Kumar A, Agarwala A, Kapoor S, Nair M, Sapra S, Dubey S, Singh A, Kaur P, Kabra M. Gupta N, et al. Among authors: dubey s. JIMD Rep. 2015;21:129. doi: 10.1007/8904_2015_448. Epub 2015 May 27. JIMD Rep. 2015. PMID: 26013749 Free PMC article. No abstract available.

7

Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.

Dubey S, Tardy V, Chowdhury MR, Gupta N, Jain V, Deka D, Sharma P, Morel Y, Kabra M. Dubey S, et al. Indian J Med Res. 2017 Feb;145(2):194-202. doi: 10.4103/ijmr.IJMR_329_16. Indian J Med Res. 2017. PMID: 28639595 Free PMC article.

8

Improved method for study of chromosomes of chorionic villus samples.

Chowdhury MR, Mathur R, Prabhakara K, Singh G, Dubey S, Verma IC. Chowdhury MR, et al. Among authors: dubey s. Indian J Med Res. 1996 Oct;104:269-72. Indian J Med Res. 1996. PMID: 8952181

9

CDKN1C -Related Beckwith-Wiedemann Syndrome: First Patient from India.

Arora V, Takkar A, Dubey S, Gupta D, Saxena R, Verma IC. Arora V, et al. Among authors: dubey s. J Pediatr Genet. 2023 Mar 31;13(4):330-334. doi: 10.1055/s-0043-1764126. eCollection 2024 Dec. J Pediatr Genet. 2023. PMID: 39502854 Free PMC article.

10

Nutritional value, phytochemical content, and pharmacological screening of Borassus flabellifer L. fruits.

Dubey S, Shukla A, Shukla RK, Kumar A. Dubey S, et al. Nat Prod Res. 2025 Jan 18:1-8. doi: 10.1080/14786419.2025.2453511. Online ahead of print. Nat Prod Res. 2025. PMID: 39825638

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