Mitesh Shetty
Overview
Explore the profile of Mitesh Shetty including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
15
Citations
148
Followers
0
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Recent Articles
1.
Murthy M, Banerjee B, Shetty M, Mariappan M, Sekhsaria A
Epileptic Disord
. 2024 Jun;
26(5):609-625.
PMID: 38923778
Objective: Studies on the genetic yield of developmental and epileptic encephalopathy and Epileptic encephalopathies using next-generation sequencing techniques are sparse from the Indian subcontinent. Hence, the study was conducted to...
2.
Prabhu S, Banerjee B, Shetty M
Ann Indian Acad Neurol
. 2023 Nov;
26(5):814-816.
PMID: 38022434
No abstract available.
3.
Prabhu P, Ballal S, Augustine R, Shetty M
Indian J Nephrol
. 2023 Oct;
33(5):377-380.
PMID: 37881737
A 39-year-old male was incidentally detected to have hypertension and chronic kidney disease (CKD) with left solitary functioning kidney in 2017. He has bilateral sensorineural hearing loss since adolescence. He...
4.
Prabhu S, Banerjee B, Acharya U, Hegde P, Shetty M
Indian J Radiol Imaging
. 2022 Dec;
32(4):625-626.
PMID: 36451939
No abstract available.
5.
Madan J, Shetty M, Ramamurthy B, Managoli S
Taiwan J Obstet Gynecol
. 2022 Feb;
61(1):129-131.
PMID: 35181022
Objective: With this case report, we would like to highlight the importance of a multidisciplinary approach and atypical findings of congenital high airway obstruction sequence (CHAOS), anhydramnios, and renal dysgenesis...
6.
Shetty M, Balakrishna S, Hegde S
Indian J Hematol Blood Transfus
. 2020 May;
36(2):414-416.
PMID: 32425403
No abstract available.
7.
Shetty M, Ramdas N, Sahni S, Mullapudi N, Hegde S
Mol Syndromol
. 2017 Dec;
8(6):313-317.
PMID: 29230161
Joubert syndrome and related disorders (JSRD; ORPHA 140874) is a complex set of neurodevelopmental disorders with multiple organ involvement. JSRD is a type of ciliopathy which is caused by the...
8.
Bose D, D V, Shetty M, J K, Kutty A
Mutat Res
. 2017 Aug;
803-805:26-34.
PMID: 28843068
Congenital Heart Disease (CHD) is the most common birth defect among congenital anomalies that arise before birth. GATA4 transcription factor plays an important role in foetal heart development. Mutational analysis...
9.
Shetty M, Srikanth A, Kadandale J, Hegde S
Cytogenet Genome Res
. 2016 Jun;
148(4):249-55.
PMID: 27300488
Congenital heart defect (CHD) is the most common form of birth defects. There is a high association between increased nuchal translucency and CHD in fetuses, and CHD in the antenatal...
10.
Shetty M, Srikanth A, Kulshreshtha P, Kadandale J, Hegde S
Indian J Pediatr
. 2016 Jun;
83(12-13):1484-1485.
PMID: 27272050
No abstract available.