Dwivedi A - Search Results

1

NEDRIHF syndrome or PURA syndrome : A rare cause of central hypotonia.

Richa S, Dwivedi A, Shaw SC, Singh D. Richa S, et al. Among authors: dwivedi a. Med J Armed Forces India. 2024 Dec;80(Suppl 1):S325-S328. doi: 10.1016/j.mjafi.2023.08.009. Epub 2023 Oct 3. Med J Armed Forces India. 2024. PMID: 39734905

2

Correlation of renal length with anthropometric and demographic data in healthy children: A prospective cross sectional study.

Dwivedi A, Kanitkar M, Singh D, Sharma M, Kalra S. Dwivedi A, et al. Med J Armed Forces India. 2023 Dec;79(Suppl 1):S202-S208. doi: 10.1016/j.mjafi.2022.06.005. Epub 2022 Aug 1. Med J Armed Forces India. 2023. PMID: 38144613 Free PMC article.

3

A Term Neonate with Ambiguous Genitalia.

Datta S, Shaw SC, Dwivedi A. Datta S, et al. Among authors: dwivedi a. Neoreviews. 2024 Jul 1;25(7):e438-e442. doi: 10.1542/neo.25-7-e438. Neoreviews. 2024. PMID: 38945973 No abstract available.

4

Diagnosis of 22q11.2 deletion syndrome in children with congenital heart diseases and facial dysmorphisms.

Agarwal M, Kumar V, Dwivedi A. Agarwal M, et al. Among authors: dwivedi a. Med J Armed Forces India. 2023 Dec;79(Suppl 1):S196-S201. doi: 10.1016/j.mjafi.2022.05.014. Epub 2022 Aug 1. Med J Armed Forces India. 2023. PMID: 38144635 Free PMC article.

5

Partial Trisomy 16q21-q24.3 with Novel Cardiac Manifestation of Left Ventricular Noncompaction Cardiomyopathy: A Case Report.

Dwivedi A, Kumar V, Ramamurthy HR. Dwivedi A, et al. J Pediatr Genet. 2020 Sep 2;10(4):326-330. doi: 10.1055/s-0040-1714362. eCollection 2021 Dec. J Pediatr Genet. 2020. PMID: 34849281 Free PMC article.

6

Monogenic lupus with neuroregression in an infant due to rare compound heterozygous variants in C1QA gene: Case-based review.

Jain H, Kartik S, Kumar A, Dwivedi A, Jayaprakash S, Vasdev V, Chandwani A. Jain H, et al. Among authors: dwivedi a. Mod Rheumatol Case Rep. 2025 Jan 16;9(1):57-62. doi: 10.1093/mrcr/rxae039. Mod Rheumatol Case Rep. 2025. PMID: 39096524 Review.

7

Hypomagnesemia with Secondary Hypoparathyroidism and Hypocalcemia due to Novel Variants in the Transient Receptor Potential Cation Channel Subfamily M Member 6 ( TRPM6 ) Gene.

Jain G, Das G, Malhotra R, Ramchandran S, Phani NM, Appaswamy G, Sridharan U, Dwivedi A. Jain G, et al. Among authors: dwivedi a. J Pediatr Genet. 2021 Aug 31;13(1):35-42. doi: 10.1055/s-0041-1733949. eCollection 2024 Mar. J Pediatr Genet. 2021. PMID: 38567178 Free PMC article.

8

Early presentation of urological abnormalities in a case of Wolfram syndrome.

Lalwani S, Shekhawat VS, Nachankar A, Dwivedi A. Lalwani S, et al. Among authors: dwivedi a. BMJ Case Rep. 2024 Sep 20;17(9):e260822. doi: 10.1136/bcr-2024-260822. BMJ Case Rep. 2024. PMID: 39306336

9

A sib-pair with Al Kaissi syndrome caused by homozygosity for a novel CDK10 splice variant.

Beriwal A, Chauhan L, Kumar A, Dwivedi A. Beriwal A, et al. Among authors: dwivedi a. Clin Dysmorphol. 2023 Jan 1;32(1):32-35. doi: 10.1097/MCD.0000000000000439. Epub 2022 Nov 3. Clin Dysmorphol. 2023. PMID: 36503922 No abstract available.

10

Acrorenal Syndrome: Unusual Association of Limb and Renal Anomaly.

Bhandari S, Kalra S, Dwivedi A. Bhandari S, et al. Among authors: dwivedi a. Indian J Nephrol. 2022 Mar-Apr;32(2):182-183. doi: 10.4103/ijn.IJN_38_21. Epub 2022 Mar 23. Indian J Nephrol. 2022. PMID: 35603114 Free PMC article. No abstract available.

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