Danda S - Search Results

1

Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India.

Mohan S, Danda S, Mathai S, Simon A. Mohan S, et al. Among authors: danda s. Natl Med J India. 2019 May-Jun;32(3):141-143. doi: 10.4103/0970-258X.278692. Natl Med J India. 2019. PMID: 32129306 Free article.

2

Juvenile ankylosing spondylitis in Turner syndrome.

Sandhya P, Danda D, Danda S, Srivastava VM. Sandhya P, et al. Among authors: danda d, danda s. Natl Med J India. 2013 Nov-Dec;26(6):338-9. Natl Med J India. 2013. PMID: 25073991

3

Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India.

Danda S, Mohan S, Devaraj P, Dutta AK, Nampoothiri S, Yesodharan D, Phadke SR, Jalan AB, Thangaraj K, Verma IC, Danda D, Jebaraj I. Danda S, et al. Among authors: danda d. Clin Rheumatol. 2020 Sep;39(9):2743-2749. doi: 10.1007/s10067-020-05020-8. Epub 2020 Mar 24. Clin Rheumatol. 2020. PMID: 32212000

4

Hepatic Glycogenoses Among Children-Clinical and Biochemical Characterization: Single-Center Study.

Korula S, Danda S, Paul PG, Mathai S, Simon A. Korula S, et al. Among authors: danda s. J Clin Exp Hepatol. 2020 May-Jun;10(3):222-227. doi: 10.1016/j.jceh.2019.07.007. Epub 2019 Jul 25. J Clin Exp Hepatol. 2020. PMID: 32405178 Free PMC article.

5

Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study.

Barney AM, Danda S, Abraham A, Fouzia NA, Gowdra A, Abraham SSC, Sony M, Das S, Korula S, Mathai S, Simon A, Kumar S. Barney AM, et al. Among authors: danda s. Public Health Genomics. 2021;24(3-4):139-148. doi: 10.1159/000514507. Epub 2021 Apr 6. Public Health Genomics. 2021. PMID: 33823526 Free article.

6

Imaging findings in TRPM6-Related hypomagnesemia with secondary hypocalcemia.

Malik P, Bidkar SU, Yoganathan S, Mathai S, Danda S, Koshy B. Malik P, et al. Among authors: danda s. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):247-248. doi: 10.4103/aian.AIAN_243_20. Epub 2021 Apr 28. Ann Indian Acad Neurol. 2021. PMID: 34220071 Free PMC article. No abstract available.

7

Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent.

Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Abraham SSC, et al. Among authors: danda s. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. Eur J Med Genet. 2021. PMID: 34303877

8

Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinent.

Das S, Thomas M, Yoganathan S, Muthusamy K, Barney AM, A SSC, Dutta AK, A R, Mohan S, Danda S. Das S, et al. Among authors: danda s. Eur J Med Genet. 2023 Jun;66(6):104766. doi: 10.1016/j.ejmg.2023.104766. Epub 2023 Apr 17. Eur J Med Genet. 2023. PMID: 37075885

9

High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia.

Ravichandran L, Paul S, A R, Hs A, Mathai S, Simon A, Danda S, Thomas N, Chapla A. Ravichandran L, et al. Among authors: danda s. Endocrine. 2024 Jul;85(1):363-369. doi: 10.1007/s12020-024-03747-x. Epub 2024 Mar 5. Endocrine. 2024. PMID: 38441846

10

Advocating Targeted Sequential Screening over Whole Exome Sequencing in 21-Hydroxylase Deficiency.

Ravichandran L, Paul S, Rekha A, Varghese D, Parthiban R, Asha HS, Mathai S, Simon A, Danda S, Thomas N, Chapla A. Ravichandran L, et al. Among authors: danda s. Indian J Pediatr. 2024 Sep 20. doi: 10.1007/s12098-024-05249-0. Online ahead of print. Indian J Pediatr. 2024. PMID: 39302536

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