Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Sundaramoorthy Gopi"'
Autor:
Ramasamy Aarthy, Kathryn Aston-Mourney, Anandakumar Amutha, Antonina Mikocka-Walus, Ranjit Mohan Anjana, Ranjit Unnikrishnan, Saravanan Jebarani, Ulagamathesan Venkatesan, Sundaramoorthy Gopi, Venkatesan Radha, Viswanathan Mohan
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Maturity Onset Diabetes of the Young (MODY) is a monogenic form of diabetes which is detected by genetic testing. We looked at clinical and biochemcial variables that could help detect possible MODY among Asian Indians with youth-onset diabe
Externí odkaz:
https://doaj.org/article/29b3a93d56344a86acc26f95d0ee78f1
Autor:
Babu Kavitha, Sampathkumar Ranganathan, Sundaramoorthy Gopi, Umashankar Vetrivel, Nagarajan Hemavathy, Viswanathan Mohan, Venkatesan Radha
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundHNF1A is an essential component of the transcription factor network that controls pancreatic β-cell differentiation, maintenance, and glucose stimulated insulin secretion (GSIS). A continuum of protein malfunction is caused by variations i
Externí odkaz:
https://doaj.org/article/14d3494cf9024ecf8ef34b3e32eeb811
Autor:
Omkar Patil, Karnam Guruswamy Ravikumar, Sundaramoorthy Gopi, Thulasi Raman, Venkatesan Radha, Viswanathan Mohan
Publikováno v:
Journal of Diabetology, Vol 11, Iss 1, Pp 45-48 (2020)
Thiamine-responsive megaloblastic anemia (TRMA) syndrome is a rare autosomal recessive disorder characterized by a cardinal triad consisting of megaloblastic anemia, sensorineural deafness, and diabetes mellitus. TRMA is caused by mutations in the ge
Externí odkaz:
https://doaj.org/article/202cf23e023e4baa94b7f8bde49a4b13
Autor:
Venkatesan Radha, Bhuvanagiri Ramya, Sundaramoorthy Gopi, Babu Kavitha, Somayajula Preetika, Kalpana Thai, Ranjit Unnikrishnan, Viswanathan Mohan, Prasanna Kumar Gupta
Publikováno v:
Journal of Diabetology, Vol 9, Iss 2, Pp 65-67 (2018)
Neonatal diabetes mellitus (NDM) is a monogenic form of diabetes mellitus that occurs in the first 6 months of life. It is a rare condition with a prevalence of 1 in 100,000–500,000 live births. We report a 3-month-old girl child with high blood gl
Externí odkaz:
https://doaj.org/article/0389530990004ed38db100c7afde76d0
Autor:
Samreen Siddiqui, Swati Waghdhare, Sundaramoorthy Gopi, Amit Bhargava, Manju Panda, Venkatesan Radha, Viswanathan Mohan, Shweta Dubey, Sujeet Jha
Publikováno v:
Clinical Medicine Insights: Endocrinology and Diabetes, Vol 11 (2018)
Background: GCK gene variants have been reported to be associated with gestational diabetes mellitus (GDM) in the Caucasian population. There are no reports exploring this association in the Indian population. Methods: This cross-sectional study incl
Externí odkaz:
https://doaj.org/article/b7674960fe7246f99bc394a5121b68e7
Autor:
Ramasamy Aarthy, Kathryn Aston-Mourney, Anandakumar Amutha, Antonina Mikocka-Walus, Ranjit Mohan Anjana, Ranjit Unnikrishnan, Saravanan Jebarani, Ulagamathesan Venkatesan, Sundaramoorthy Gopi, Venkatesan Radha, Viswanathan Mohan
Publikováno v:
Primary Care Diabetes.
Autor:
Jamuna Kalpana, Sundaramoorthy Gopi, Lalitha Krishnan, Nishanth Rajan, Venkatesan Radha, Vishwanathan Mohan
Publikováno v:
Journal of Nepal Paediatric Society. 41:107-110
Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is one of the commonest reasons for severe, intractable hypoglycemia in neonates. Dysregulated insulin secretion is the major underlying pathogenesis which results in hyperinsulinemia, hypoke
Autor:
Swati Kanodia, Sanket Pendsey, Sundaramoorthy Gopi, Rajesh Kumar, Babu Kavitha, Rajesh Joshi, Sharad Pendsey, Alagarsamy Kannan, Venkatesan Radha, Sekar Kanthimathi, Viswanathan Mohan, Archana Dayal Arya, P Raghupathy
Publikováno v:
Pediatric Diabetes. 22:82-92
Background There are very few reports pertaining to Indian patients with neonatal diabetes mellitus (NDM). Activating or gain of function mutations of KATP channel genes namely KCNJ11 and ABCC8 are most predominant cause of permanent neonatal diabete
Autor:
Karnam Guruswamy Ravikumar, Viswanathan Mohan, Omkar Patil, Sundaramoorthy Gopi, Venkatesan Radha, Thulasi Raman
Publikováno v:
Journal of Diabetology, Vol 11, Iss 1, Pp 45-48 (2020)
Thiamine-responsive megaloblastic anemia (TRMA) syndrome is a rare autosomal recessive disorder characterized by a cardinal triad consisting of megaloblastic anemia, sensorineural deafness, and diabetes mellitus. TRMA is caused by mutations in the ge
Autor:
Babu Kavitha, Viswanathan Mohan, Rakesh Kumar, Rajesh Joshi, Archana Dayal Arya, Sanket Pendsey, Swati Kanodia, Sundaramoorthy Gopi, Sekar Kanthimathi, Alagarsamy Kannan, Sharad Pendsey, P Raghupathy, V Radha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdd8335ca6f89bbfbcfab95f6d9ce39b
https://doi.org/10.1111/pedi.13109/v2/response1
https://doi.org/10.1111/pedi.13109/v2/response1