Dayal D - Search Results

1

Short Stature Syndromes: Case Series from India.

Panigrahi I, Kaur P, Chaudhry C, Shariq M, Naorem DD, Gowtham BC, Kaur A, Dayal D. Panigrahi I, et al. Among authors: dayal d. J Pediatr Genet. 2021 Apr 14;11(4):279-286. doi: 10.1055/s-0041-1726037. eCollection 2022 Dec. J Pediatr Genet. 2021. PMID: 36267864 Free PMC article.

2

Acquired syndactyly in epidermolysis bullosa dystrophica.

Panigrahi I, Kulkarni K, Dayal D. Panigrahi I, et al. Among authors: dayal d. BMJ Case Rep. 2009;2009:bcr04.2009.1785. doi: 10.1136/bcr.04.2009.1785. Epub 2009 Jun 21. BMJ Case Rep. 2009. PMID: 21691395 Free PMC article. No abstract available.

3

Thyroid dysfunction in Indian children with Down syndrome.

Dayal D, Jain P, Panigrahi I, Bhattacharya A, Sachdeva N. Dayal D, et al. Indian Pediatr. 2014 Sep;51(9):751-2. doi: 10.1007/s13312-014-0495-8. Indian Pediatr. 2014. PMID: 25228616 Free article. Review.

4

An Indian girl with Fanconi-Bickel syndrome without SLC2A2 gene mutation.

Dayal D, Dekate P, Sharda S, Das A, Attri S. Dayal D, et al. J Pediatr Genet. 2013 Jun;2(2):109-12. doi: 10.3233/PGE-13056. J Pediatr Genet. 2013. PMID: 27625848 Free PMC article.

5

Concentrations of leptin, adiponectin and other metabolic parameters in non-obese children with Down syndrome.

Tenneti N, Dayal D, Sharda S, Panigrahi I, Didi M, Attri SV, Sachdeva N, Bhalla AK. Tenneti N, et al. Among authors: dayal d. J Pediatr Endocrinol Metab. 2017 Aug 28;30(8):831-837. doi: 10.1515/jpem-2016-0422. J Pediatr Endocrinol Metab. 2017. PMID: 28749784

6

Severe Early Onset Obesity due to a Novel Missense Mutation in Exon 3 of the Leptin Gene in an Infant from Northwest India.

Dayal D, Seetharaman K, Panigrahi I, Muthuvel B, Agarwal A. Dayal D, et al. J Clin Res Pediatr Endocrinol. 2018 Jul 31;10(3):274-278. doi: 10.4274/jcrpe.5501. Epub 2017 Dec 8. J Clin Res Pediatr Endocrinol. 2018. PMID: 29217499 Free PMC article.

7

Simple virilising congenital adrenal hyperplasia in monozygotic twins: A rare report and review of previous cases.

Muthuvel B, Gautam A, Pal R, Panigrahi I, Dayal D. Muthuvel B, et al. Among authors: dayal d. Pediatr Endocrinol Diabetes Metab. 2020;26(1):58-62. doi: 10.5114/pedm.2020.93248. Pediatr Endocrinol Diabetes Metab. 2020. PMID: 32272826 Free article. Review. English.

8

Managing syndromic congenital ichthyosis at a tertiary care institute-Genotype-phenotype correlations, and novel treatments.

Dabas G, Mahajan R, De D, Handa S, Kumar R, Dayal D, Suthar R, Panigrahi I. Dabas G, et al. Among authors: dayal d. Dermatol Ther. 2020 Nov;33(6):e13816. doi: 10.1111/dth.13816. Epub 2020 Jul 7. Dermatol Ther. 2020. PMID: 32533806

9

Ten-year use of recombinant parathyroid hormone for the treatment of hypoparathyroidism in a boy with partial Jacobsen syndrome.

Dayal D, Panigrahi I, Varma T, Gupta S, Gupta A, Kumar R, Sachdeva N. Dayal D, et al. Pediatr Endocrinol Diabetes Metab. 2021;27(1):57-61. doi: 10.5114/pedm.2020.100402. Pediatr Endocrinol Diabetes Metab. 2021. PMID: 33191722 Free PMC article.

10

Characterization of the CYP21A2 Gene Mutations in Children with Classic Congenital Adrenal Hyperplasia.

Saraf S, Srivastava P, Panigrahi I, Seenappa V, Kumar R, Yadav J, Daniel R, Dayal D. Saraf S, et al. Among authors: dayal d. Indian J Pediatr. 2024 Feb;91(2):137-142. doi: 10.1007/s12098-021-03975-3. Epub 2022 Jan 30. Indian J Pediatr. 2024. PMID: 35094236

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