Soumik Goswami
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Explore the profile of Soumik Goswami including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
143
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Recent Articles
1.
Singh A, Das A, Murthy L, Ghosal S, Sahay R, Harikumar K, et al.
Adv Ther
. 2024 Dec;
42(2):801-812.
PMID: 39636567
Introduction: A slower adoption rate of fixed dose combinations (FDC) in diabetes management is partly due to insufficient data. This study evaluates the safety and efficacy of an FDC of...
2.
Roy A, Chowdhury A, Ray A, Baidya A, Roychowdhury B, Sarkar D, et al.
Ann Pediatr Endocrinol Metab
. 2024 Nov;
29(5):284-307.
PMID: 39506343
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...
3.
Deb R, Goswami S, Sengupta N, Baidya A, Khare V, Datta J, et al.
Indian J Endocrinol Metab
. 2024 Oct;
28(4):385-390.
PMID: 39371654
Introduction: There is high prevalence of non-alcoholic fatty liver disease in individuals with type 2 diabetes mellitus (T2D), and available evidence suggests higher prevalence of NASH and advanced stages of...
4.
Chattopadhyay S, Goswami S, Sengupta N, Baidya A
BMJ Open
. 2024 Jun;
14(6):e082193.
PMID: 38862223
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...
5.
Basu R, Goswami S, Sengupta N, Baidya A, Mondal S, Swapnil K, et al.
Bone Rep
. 2024 May;
21:101768.
PMID: 38706521
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...
6.
Ghosh S, Yasmin M, Sen K, Goswami S, Das T, Swar S, et al.
Indian J Endocrinol Metab
. 2023 Dec;
27(5):398-403.
PMID: 38107729
Introduction: A structured dedicated health programme for Type 1 diabetes mellitus (T1DM) has been initiated in the state of West Bengal, India. Aim: The aim is to provide comprehensive healthcare...
7.
Das N, Tarenia S, Saha S, Gaikwad P, Hathi D, Goswami S, et al.
J ASEAN Fed Endocr Soc
. 2023 Dec;
38(2):124-127.
PMID: 38045665
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...
8.
Goswami S, Chowdhury J
Future Virol
. 2023 Nov;
PMID: 37970095
The unprecedented scale of the SARS-CoV-2 pandemic has driven considerable investigation into novel antiviral treatments since effective vaccination strategies cannot completely eradicate the virus. Apitherapy describes the medicinal use of...
9.
Tarenia S, Chattopadhyay S, Das N, Hathi D, Baidya A, Chakrabarty P, et al.
J ASEAN Fed Endocr Soc
. 2023 May;
38(1):108-113.
PMID: 37252405
Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but with the presence of typical Müllerian structures in a phenotypically female individual....
10.
Baidya A, Basu A, Bhattacharjee R, Biswas D, Biswas K, Chakraborty P, et al.
J Pediatr Endocrinol Metab
. 2022 Nov;
36(1):4-18.
PMID: 36424806
Objectives: 46, XY difference/disorder of sex development (DSD) is a relatively uncommon group of heterogeneous disorders with varying degree of underandrogenization of male genitalia. Such patients should be approached systematically...