Correa ARE - Search Results

1

The spectrum of neurological manifestations and genotype-phenotype correlation in Indian children with Gaucher disease.

Venkatachari M, Chakraborty S, Correa ARE, Mishra P, Kocchar KP, Kabra M, Chakrabarty B, Kalaivani M, Sapra S, Mishra P, Gulati S, Gupta N. Venkatachari M, et al. Among authors: correa are. Am J Med Genet A. 2023 Apr;191(4):1038-1043. doi: 10.1002/ajmg.a.63115. Epub 2023 Jan 13. Am J Med Genet A. 2023. PMID: 36637080

2

Report of a Novel Homozygous Nonsense DDR2 Mutation in an Indian Adult Male with Spondylo-meta-epiphyseal Dysplasia, Short Limb-Abnormal Calcification Type.

Gupta N, Correa ARE, Jana M, Kabra M. Gupta N, et al. Among authors: correa are. J Pediatr Genet. 2019 Sep;8(3):153-156. doi: 10.1055/s-0039-1683382. Epub 2019 Mar 12. J Pediatr Genet. 2019. PMID: 31406622 Free PMC article.

3

Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases.

Correa ARE, Mishra P, Kabra M, Gupta N. Correa ARE, et al. Indian J Pediatr. 2020 Mar;87(3):175-178. doi: 10.1007/s12098-019-03148-3. Epub 2020 Jan 29. Indian J Pediatr. 2020. PMID: 31997239

4

Methylene Tetrahydrofolate Reductase Deficiency.

Kaur R, Correa ARE, Thakur S, Kabra M, Gupta N. Kaur R, et al. Among authors: correa are. Indian J Pediatr. 2020 Nov;87(11):951-953. doi: 10.1007/s12098-020-03290-3. Epub 2020 May 26. Indian J Pediatr. 2020. PMID: 32451826

5

Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum.

Correa ARE, Endrakanti M, Naini K, Kabra M, Gupta N. Correa ARE, et al. Ann Hum Genet. 2021 May;85(3-4):138-145. doi: 10.1111/ahg.12417. Epub 2021 Mar 2. Ann Hum Genet. 2021. PMID: 33655537

6

Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalis.

Correa ARE, Naini K, Mishra P, Dadhwal V, Agarwal R, Shukla R, Kabra M, Gupta N. Correa ARE, et al. Prenat Diagn. 2021 Oct;41(11):1414-1424. doi: 10.1002/pd.6022. Epub 2021 Aug 2. Prenat Diagn. 2021. PMID: 34302381

7

Mevalonate Kinase Deficiency as Cause of Periodic Fever in Two Siblings.

Correa ARE, Gupta N, Bagri N, Vignesh P, Alam S, Yamaguchi S. Correa ARE, et al. Indian Pediatr. 2020 Feb 15;57(2):180-181. Indian Pediatr. 2020. PMID: 32060250 Free article.

8

First case report of Penttinen syndrome from India.

Aggarwal B, Correa ARE, Gupta N, Jana M, Kabra M. Aggarwal B, et al. Among authors: correa are. Am J Med Genet A. 2022 Feb;188(2):683-687. doi: 10.1002/ajmg.a.62558. Epub 2021 Nov 19. Am J Med Genet A. 2022. PMID: 34799960

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