Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Animesh Maiti"'
Autor:
Rana Bhattacharjee, Partha P. Chakraborty, Neeti Agrawal, Ajitesh Roy, Animesh Maiti, Subhankar Chowdhury
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 2, Pp 184-191 (2024)
Introduction: We aimed to describe the clinical, biochemical and etiological profile of patients referred with a provisional diagnosis of rickets in tertiary care centres. In addition, we tried to propose a diagnostic algorithm for the evaluation of
Externí odkaz:
https://doaj.org/article/495a077c965749c9b118611e8b8326db
Autor:
Avivar Awasthi, Partha Pratim Chakraborty, Neeti Agrawal, Anirban Sinha, Anuj Kumar Pandey, Animesh Maiti
Publikováno v:
Thyroid Research, Vol 16, Iss 1, Pp 1-10 (2023)
Abstract Background One of the common causes of suboptimal control of thyroid stimulating hormone (TSH) in levothyroxine-treated hypothyroidism is coadministration of proton pump inhibitors (PPIs). Morning administration of pantoprazole has been show
Externí odkaz:
https://doaj.org/article/2eb36d5a4fa44a749cf0b3006ab56261
Autor:
Sayan Ghosh, Partha Pratim Chakraborty, Biswabandhu Bankura, Animesh Maiti, Rajkrishna Biswas, Madhusudan Das
Publikováno v:
JCRPE, Vol 13, Iss 4, Pp 456-460 (2021)
Isolated growth hormone deficiency (IGHD) type 1A is a rare, autosomal recessive disorder caused by deletion of the GH1 gene and characterized by early onset severe short stature and typical phenotype. Lack of exposure to GH during fetal life often l
Externí odkaz:
https://doaj.org/article/083a3bf876a44f999bf8ba1ffdfca02d
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 24, Iss 2, Pp 220-222 (2020)
Externí odkaz:
https://doaj.org/article/36ad4233917043b98aaac85b9dae11bf
Publikováno v:
BMJ case reports. 15(11)
Enamel renal syndrome (ERS) due to loss of function (LOF) mutation of FAM20A gene typically consists of hypoplastic amelogenesis imperfecta (AI) and bilateral nephrolithiasis/nephrocalcinosis. Recent evidence suggests that FAM20A interacts with FAM20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::107b55883ee914216ed6deec6959ae95
https://pubmed.ncbi.nlm.nih.gov/36351670
https://pubmed.ncbi.nlm.nih.gov/36351670
Autor:
null Animesh Maiti
Publikováno v:
Journal of Ayurveda and Integrated Medical Sciences. 8:15-18
Asrigdara is a disease of excessive and prolonged blood loss per vagina during menstrual and inter menstrual period. In modern era, Asrigdara is similar just like a Menorrhagia. In my comparative study I had chosen to evaluate the role of both drugs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b06b9f96ac54ed7b26b0257441288986
https://doi.org/10.21760/jaims.8.3.2
https://doi.org/10.21760/jaims.8.3.2
Autor:
null Animesh Maiti
Publikováno v:
Journal of Ayurveda and Integrated Medical Sciences. 7:09-12
Swetapradara is a common and major problem in our country of female especially reproductive age. Total patients (60) were divided into three group i.e. Gr-A, Gr- B and Gr- C with clinical features of white vaginal discharge, itching of vulva, burning
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f04aa2ac266c5579ad161f170241d0bf
https://doi.org/10.21760/jaims.7.10.2
https://doi.org/10.21760/jaims.7.10.2
Autor:
null Animesh Maiti
Publikováno v:
Journal of Ayurveda and Integrated Medical Sciences. 7:31-33
Upapluta Yoni Vyapad has mentioned in many Samhita. The genital organs are afflicted by Kapha & Vata, the ailment of the woman is called Upapluta which clinical features are simulated description of Monilial Vulvovaginitis specially caused by Candida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ff38812a8828ee2824a1428c3e574aa
https://doi.org/10.21760/jaims.7.11.5
https://doi.org/10.21760/jaims.7.11.5
Publikováno v:
International Journal of Diabetes in Developing Countries.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98f23dc74eadd242b807afb52174e3a1
https://doi.org/10.1007/s13410-023-01187-3
https://doi.org/10.1007/s13410-023-01187-3
Autor:
Madhusudan Das, Animesh Maiti, Sayan Ghosh, Partha Pratim Chakraborty, Biswabandhu Bankura, Rajkrishna Biswas
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 13, Iss 4, Pp 456-460 (2021)
JCRPE, Vol 13, Iss 4, Pp 456-460 (2021)
Isolated growth hormone (GH) deficiency type I A is a rare autosomal recessive disorder caused by deletion of the GH1 gene and characterized by early onset severe short stature and typical phenotype. Lack of exposure to GH during fetal life often lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45d8e7e8c8d7f670e0cdfe29dff57b07
http://europepmc.org/articles/PMC8638633
http://europepmc.org/articles/PMC8638633