Zobrazeno 1 - 10
of 59
pro vyhledávání: '"ARJUN BAIDYA"'
Autor:
Ajitesh Roy, Amarta Shankar Chowdhury, Arindam Ray, Arjun Baidya, Bibek Roychowdhury, Dasarathi Sarkar, Debmalya Sanyal, Indira Maisnam, Kaushik Biswas, Kaushik Pandit, Mainak Banerjee, Moutusi Raychaudhuri, Nilanjan Sengupta, Partha Pratim Chakraborty, Pradip Mukhopadhyay, Pradip Raychaudhuri, Pranab Kumar Sahana, Rajan Palui, Rana Bhattacharjee, Sarmistha Mukhopadhyay, Satinath Mukhopadhyay, Sayantan Ray, Soumik Goswami, Subhankar Chowdhury, Subhodip Pramanik, Subir Chandra Swar, Sujoy Ghosh, Sunetra Mondal, Tapas Chandra Das
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 5, Pp 284-307 (2024)
Rickets, one of the leading causes of bony deformities and short stature, can be calciopenic (inciting event is defective intestinal calcium absorption) or phosphopenic (inciting event is phosphaturia). Early diagnosis and timely treatment of rickets
Externí odkaz:
https://doaj.org/article/311ee5adb89b4e1a9aea18fdddf4116a
Publikováno v:
BMJ Open, Vol 14, Iss 6 (2024)
Introduction Diabetic neuropathy is frequently underdiagnosed and undertreated. Logistic problems accompany the routine use of the biothesiometer. Hence, we attempted to find a more easily available alternative.Research design and methods 149 patient
Externí odkaz:
https://doaj.org/article/2cd01b95f8c044229b9e8b2953aaa41f
Autor:
Rajdeep Basu, Soumik Goswami, Nilanjan Sengupta, Arjun Baidya, Sunetra Mondal, Kumar Swapnil, Rajat Deb, Vibhu Ranjan Khare, Joydip Datta
Publikováno v:
Bone Reports, Vol 21, Iss , Pp 101768- (2024)
Osteogenesis imperfecta (OI) commonly involving defects in COL1A1 and COL1A2 is a rare hereditary disease of bone fragility affecting 6–7 per 100,000 population. On the other hand, hypopituitarism is a separate entity that manifests with reduced le
Externí odkaz:
https://doaj.org/article/09622f4b2a1d4e3fa9ef643cbdd4181d
Autor:
Niladri Das, Silima Subhasnigdha Tarenia, Souvik Saha, Prashant Manohar Gaikwad, Deep Kamlesh Hathi, Soumik Goswami, Arjun Baidya, Nilanjan Sengupta
Publikováno v:
Journal of the ASEAN Federation of Endocrine Societies, Vol 38, Iss 2 (2023)
Primary growth hormone (GH) resistance or growth hormone insensitivity syndrome, also called Laron syndrome, is a hereditary disease caused by mutations in the GH receptor or in the post-receptor signaling pathway. This disorder is characterized by p
Externí odkaz:
https://doaj.org/article/aa48d7ff5ed4437eaf168b646e9f35dd
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 07, Pp 29-32 (2021)
Introduction: Idiopathic hypogonadotropic hypogonadism is a rare gonadal dysgenesis in which puberty does not take place naturally. It occurs due to insufficient pulsatile secretion of Gonadotrophin-Releasing Hormone (GnRH) and the resulting Foll
Externí odkaz:
https://doaj.org/article/a072630b093c45fbb2c5c9298cefb118
Autor:
Arjun Baidya, Santosh Kumar Singh, Sarita Bajaj, Abdul Hamid Zargar, Parminder Singh, Sambit Das, Anand Shankar
Publikováno v:
Journal of the ASEAN Federation of Endocrine Societies, Vol 35, Iss 1 (2020)
Coronavirus Disease 2019 (COVID-19) is an emerging disease and since its first identification in Wuhan, China, in December 2019, there has been a rapid increase in cases and deaths across the world. COVID-19 has been shown to have an immense impact i
Externí odkaz:
https://doaj.org/article/733f2a31707b4928a5fdb7491a5b69e4
Autor:
Chitra Selvan, Deep Dutta, Indira Maisnam, Anubhav Thukral, P P Chakraborthy, Ajitesh Roy, Rakesh Arora, Soumik Dutta, Arjun Baidya, Sujoy Ghosh, Satinath Mukhopadhyay, Subhankar Chowdhury
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 9, Pp 657-659 (2013)
Thyroid associated orbitopathy, although seen most commonly with thyrotoxicosis, is also known to occur in primary hypothyroidism. Myasthenia gravis is an autoimmune condition with an established association with autoimmune thyroid disease. We report
Externí odkaz:
https://doaj.org/article/94985e6905ab4744b515fd5f2f794e9f
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 8, Pp 402-404 (2012)
Introduction: Renal phosphate-wasting disorders are the most common form of hereditary rickets and osteomalacia in western countries, but are rarely reported in India. Therefore, we report here a case of hypophosphatemic rickets. Aim and objective: T
Externí odkaz:
https://doaj.org/article/a7c762237e8b41208ea3b9a47299b123
Autor:
Saumik Datta, Rakesh Arora, S Chitra, Partha Chakraborty, Arjun Baidya, Dibakar Biswas, Sujoy Ghosh
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 333-334 (2013)
A 42-year-old lady, a known diabetic presented with generalized body ache, severe burning sensation over her lower limbs, loss of weight (approximately 8 kg), loss of appetite, nausea, frequent vomiting, and altered bowel habits without history of fe
Externí odkaz:
https://doaj.org/article/1ab3a003c05c4bda8574264d4f5a3f55
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 8, Pp 416-417 (2012)
Introduction: Vitamin D deficiency has been documented across all age groups and both sexes from India. However, there is paucity of data on vitamin D deficiency in a particular cohort of population. Objectives: To assess the vitamin D status in a co
Externí odkaz:
https://doaj.org/article/28d1f643492e4bf78eaa0a15085e69c7