Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Rathika D Shenoy"'
Publikováno v:
Journal of International Advanced Otology, Vol 19, Iss 4, Pp 355-359 (2023)
Externí odkaz:
https://doaj.org/article/cc2797bb4bbe48a78d70017438739dc5
Autor:
Abhishek Sreekumar, Gundyadka Moideen Safwan, Shilpa J Shetty, Suchetha Kumari, Rathika D Shenoy, Vijaya Shenoy
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 3, Pp SC38-SC40 (2023)
Introduction: Childhood Nephrotic Syndrome (NS) is a podocytopathy. Micro Ribonucleic Acid (miRNA), composed of 21-25 non coding nucleotides, regulates gene expression by inhibiting protein transcription by binding to complementary messenger RNA. The
Externí odkaz:
https://doaj.org/article/705c47920ad14c45b41db2089e5a21a2
Publikováno v:
Indian Journal of Community Medicine, Vol 47, Iss 1, Pp 87-91 (2022)
Objectives: To compare the cord serum ferritin and fetal iron status in newborns with and without maternal occupational smokeless tobacco exposure and determine the influencing factors. Methods: This cross-sectional study included mother–infant dya
Externí odkaz:
https://doaj.org/article/5fe754f1e59a4e11b8386a91f4c822cc
Publikováno v:
Indian Journal of Pediatrics.
Autor:
Prince Jacob, Gandham SriLakshmi Bhavani, Prajna Udupa, Zheng Wang, Sankar V. Hariharan, Kishan Delampady, Ashwin Dalal, Nutan Kamath, Shiro Ikegawa, Rathika D. Shenoy, Koushik Handattu, Hitesh Shah, Katta M. Girisha
Publikováno v:
Indian Journal of Pediatrics.
Objective To understand the phenotypic and genotypic spectrum of genetic forms of rickets in 10 families. Methods Detailed clinical, radiographic, and biochemical evaluation of 10 families with phenotypes suggestive of a genetic cause of rickets was
Autor:
Yatheesha Bl, Ali Kumble, Michelle C. do Rosario, Anupriya Kaur, Leslie Lewis, Rajagopal Kadavigere, Ratna Dua Puri, K Shreedhara Avabratha, Sunita Bijarnia Mahay, Girish Subramaniam, Suvasini Sharma, K C Rakshith, Siddaramappa J. Patil, Sheela Nampoothiri, Mahesh Kamate, Shrikiran A, Hitesh Shah, Rajesh Shetty, Katta M. Girisha, Nutan Kamath, Anju Shukla, Shruti Bajaj, Stephanie L. Bielas, Narayanaswami Suresh, Malavika Hebbar, Shivanand Pai, Mamta N. Muranjan, Parneet Kaur, Ramesh Bhat Y, Rathika D. Shenoy, Neethukrishna Kausthubham, Karthik Nair
Publikováno v:
Clin Genet
Genetic disorders with predominant central nervous system white matter abnormalities (CNS WMAs), also called leukodystrophies, are heterogeneous entities. We ascertained 117 individuals with CNS WMAs from 104 unrelated families. Targeted genetic test
Autor:
Praveen Nayak, Rathika D. Shenoy, Ankeeta Menona Jacob, Swathi Sunil Rao, Shivakumar Hiremath
Publikováno v:
Journal of Health and Allied Sciences NU. 12:38-41
A pandemic leads to disruption and stretching of an existing health care system and its resources. Coronavirus disease 2019 (COVID-19) data show distinct and severe manifestations in children necessitating critical care. Children need prioritization
Publikováno v:
Indian Pediatrics. 57:918-921
To assess the effect of maternal occupational tobacco handling (bidi rolling) on cord serum leptin levels. We enrolled 64 neonates born to women who were bidi-rollers, and 64 small for gestational age (SGA) neonates and 57 term appropriate for gestat
Publikováno v:
Asian Journal of Clinical Pediatrics and Neonatology. 8:6-10
Background: Cerebral hypoxia can result in anaerobic glycolysis which leads to decreased phosphorylase production and increased uric acid which gets excreted in the urine where it can be easily detected. The aim of the study is to assess the utility
Publikováno v:
Sudan J Paediatr
This study was designed to assess iodine status of mother-fetus dyad by estimation of spot urine iodine concentration (UIC) in the study district. It is a cross-sectional study of 250 pregnant women with euthyroid status and their term neonates resid