Seshadri S - Search Results

1

Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.

Yadav RM, Gupta M, Dalvi A, Bargir UA, Hule G, Shabrish S, Aluri J, Kulkarni M, Kambli P, Uppuluri R, Seshadri S, Jagadeesh S, Suresh B, Raja J, Taur P, Malaischamy S, Ghosh P, Mahalingam S, Kadam P, Lashkari HP, Tamhankar P, Tamhankar V, Mithbawkar S, Bhattad S, Jhawar P, Makam A, Bansal V, Prasad M, Govindaraj G, Guhan B, Bharadwaj Tallapaka K, Desai M, Raj R, Madkaikar MR. Yadav RM, et al. Among authors: seshadri s. Front Immunol. 2020 Dec 7;11:612316. doi: 10.3389/fimmu.2020.612316. eCollection 2020. Front Immunol. 2020. PMID: 33365035 Free PMC article. Review.

2

Triple X syndrome with rare phenotypic presentation.

Jagadeesh S, Jabeen G, Bhat L, Vasikarla M, Suresh A, Seshadri S, Lata S. Jagadeesh S, et al. Among authors: seshadri s. Indian J Pediatr. 2008 Jun;75(6):629-31. doi: 10.1007/s12098-008-0120-8. Epub 2008 Aug 31. Indian J Pediatr. 2008. PMID: 18759093

3

Biotinidase deficiency: an atypical presentation.

Jagadeesh S, Suresh B, Seshadri S, Suzuki Y. Jagadeesh S, et al. Among authors: seshadri s. Natl Med J India. 2013 Jan-Feb;26(1):29-30. Natl Med J India. 2013. PMID: 24066991

4

Citrullinemia type 1: genetic diagnosis and prenatal diagnosis in subsequent pregnancy.

Karthikeyan G, Jagadeesh S, Seshadri S, Häberle J. Karthikeyan G, et al. Among authors: seshadri s. Indian Pediatr. 2013 Oct;50(10):965-6. doi: 10.1007/s13312-013-0239-1. Indian Pediatr. 2013. PMID: 24222285 Free article.

5

Usefulness of fetal autopsy in the diagnosis of blomstrand chondrodysplasia: a report of three cases.

Beena S, Murlidhar L, Seshadri S, Jagadeesh S, Suresh I. Beena S, et al. Among authors: seshadri s. J Matern Fetal Neonatal Med. 2017 May;30(9):1041-1044. doi: 10.1080/14767058.2016.1199675. Epub 2016 Aug 10. J Matern Fetal Neonatal Med. 2017. PMID: 27353973

6

Persistent Left Superior Vena Cava in Fetuses: An Autopsy Series.

Ramakrishnan D, Chidambarathanu S, Murli L, Micheal J, Jagadeesh S, Suresh I, Seshadri S. Ramakrishnan D, et al. Among authors: seshadri s. Fetal Pediatr Pathol. 2017 Aug;36(4):304-310. doi: 10.1080/15513815.2017.1324546. Epub 2017 Jun 1. Fetal Pediatr Pathol. 2017. PMID: 28569558

7

Utility and performance of bacterial artificial chromosomes-on-beads assays in chromosome analysis of clinical prenatal samples, products of conception and blood samples.

Rose R, Venkatesh A, Pietilä S, Jabeen G, Jagadeesh SM, Seshadri S. Rose R, et al. Among authors: seshadri s. J Obstet Gynaecol Res. 2019 Apr;45(4):830-840. doi: 10.1111/jog.13920. Epub 2019 Jan 10. J Obstet Gynaecol Res. 2019. PMID: 30632238

8

Mucopolysaccharidoses type IV A (Morquio syndrome): a case series of three siblings.

Rekka P, Rathna PV, Jagadeesh S, Seshadri S. Rekka P, et al. Among authors: seshadri s. J Indian Soc Pedod Prev Dent. 2012 Jan-Mar;30(1):66-9. doi: 10.4103/0970-4388.95586. J Indian Soc Pedod Prev Dent. 2012. PMID: 22565520

9

Utility of Various Ultrafast Magnetic Resonance Sequences in the Detection of Fetal Intracranial Hemorrhage.

Baburaj R, Rangasami R, Chandrasekharan A, Suresh I, Suresh S, Seshadri S. Baburaj R, et al. Among authors: seshadri s. Ann Indian Acad Neurol. 2018 Oct-Dec;21(4):275-279. doi: 10.4103/aian.AIAN_431_17. Ann Indian Acad Neurol. 2018. PMID: 30532356 Free PMC article.

10

Imaging spectrum of posterior fossa anomalies on foetal magnetic resonance imaging with an algorithmic approach to diagnosis.

Mahalingam HV, Rangasami R, Seshadri S, Suresh I. Mahalingam HV, et al. Among authors: seshadri s. Pol J Radiol. 2021 Mar 30;86:e183-e194. doi: 10.5114/pjr.2021.105014. eCollection 2021. Pol J Radiol. 2021. PMID: 33828631 Free PMC article. Review.

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