Shetty MS - Search Results

1

Freeman-Sheldon syndrome--prenatal and postnatal diagnosis.

Hegde SS, Shetty MS, Rama Murthy BS. Hegde SS, et al. Among authors: shetty ms. Indian J Pediatr. 2010 Feb;77(2):196-7. doi: 10.1007/s12098-009-0227-6. Epub 2009 Dec 11. Indian J Pediatr. 2010. PMID: 20012803

2

Upregulation of ASCL1 and inhibition of Notch signaling pathway characterize progressive astrocytoma.

Somasundaram K, Reddy SP, Vinnakota K, Britto R, Subbarayan M, Nambiar S, Hebbar A, Samuel C, Shetty M, Sreepathi HK, Santosh V, Hegde AS, Hegde S, Kondaiah P, Rao MR. Somasundaram K, et al. Oncogene. 2005 Oct 27;24(47):7073-83. doi: 10.1038/sj.onc.1208865. Oncogene. 2005. PMID: 16103883

3

Novel glioblastoma markers with diagnostic and prognostic value identified through transcriptome analysis.

Reddy SP, Britto R, Vinnakota K, Aparna H, Sreepathi HK, Thota B, Kumari A, Shilpa BM, Vrinda M, Umesh S, Samuel C, Shetty M, Tandon A, Pandey P, Hegde S, Hegde AS, Balasubramaniam A, Chandramouli BA, Santosh V, Kondaiah P, Somasundaram K, Rao MR. Reddy SP, et al. Clin Cancer Res. 2008 May 15;14(10):2978-87. doi: 10.1158/1078-0432.CCR-07-4821. Clin Cancer Res. 2008. PMID: 18483363

4

Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum.

Shetty M, Srikanth A, Kadandale J, Hegde S. Shetty M, et al. Mol Syndromol. 2015 Oct;6(4):187-92. doi: 10.1159/000440659. Epub 2015 Sep 11. Mol Syndromol. 2015. PMID: 26648835 Free PMC article.

5

Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.

Shetty M, Kadandale J, Hegde S. Shetty M, et al. Mol Syndromol. 2016 Feb;6(5):248-53. doi: 10.1159/000442506. Epub 2015 Dec 17. Mol Syndromol. 2016. PMID: 26997946 Free PMC article.

6

Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease.

Shetty M, Srikanth A, Kulshreshtha P, Kadandale J, Hegde S. Shetty M, et al. Indian J Pediatr. 2016 Nov;83(12-13):1484-1485. doi: 10.1007/s12098-016-2158-3. Epub 2016 Jun 8. Indian J Pediatr. 2016. PMID: 27272050 No abstract available.

7

Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.

Shetty M, Srikanth A, Kadandale J, Hegde S. Shetty M, et al. Cytogenet Genome Res. 2016;148(4):249-55. doi: 10.1159/000446162. Epub 2016 Jun 15. Cytogenet Genome Res. 2016. PMID: 27300488

8

A Homozygous Missense Variant in INPP5E Associated with Joubert Syndrome and Related Disorders.

Shetty M, Ramdas N, Sahni S, Mullapudi N, Hegde S. Shetty M, et al. Mol Syndromol. 2017 Nov;8(6):313-317. doi: 10.1159/000479673. Epub 2017 Sep 8. Mol Syndromol. 2017. PMID: 29230161 Free PMC article.

9

Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India.

Shetty M, Balakrishna S, Hegde S. Shetty M, et al. Indian J Hematol Blood Transfus. 2020 Apr;36(2):414-416. doi: 10.1007/s12288-019-01206-6. Epub 2019 Oct 5. Indian J Hematol Blood Transfus. 2020. PMID: 32425403 Free PMC article. No abstract available.

10

A multidisciplinary approach for prenatal diagnosis of FRASER SYNDROME-report of a novel variant in FRAS1.

Madan J, Shetty M, Ramamurthy BS, Managoli S. Madan J, et al. Taiwan J Obstet Gynecol. 2022 Jan;61(1):129-131. doi: 10.1016/j.tjog.2021.11.020. Taiwan J Obstet Gynecol. 2022. PMID: 35181022 Free article.

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