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JCEM Case Reports
|
July 17, 2025
Cerebrotendinous Xanthomatosis With a Heterozygous Frameshift Mutation Involving <i>CYP27A1(C.526del)</i>
Ajitesh Roy, Sounak Kumar Roy, Soumyadip Das
Indian Journal of Pediatrics
|
December 31, 2013
Labial neurofibroma as the presenting feature of genital and orbitotemporal neurofibromatosis
Deep Dutta, Ajitesh Roy, Satinath Mukhopadhyay, et al.
Indian Journal of Dermatology
|
December 19, 2012
Leprechaunism - a case report
Sumit Sen, Ajitesh Roy, Anusree Gangopadhyay, et al.
Postgraduate Medical Journal
|
May 14, 2017
Pseudoacromegaly: an unusual presenting manifestation of long-standing undiagnosed primary hypothyroidism
Partha Pratim Chakraborty, Rana Bhattacharjee, Ajitesh Roy, et al.
JCEM Case Reports
|
April 23, 2026
Betel leaf (paan) chewing: an unusual cause of refractory hypothyroidism in levothyroxine-treated patient
Neeti Agrawal, Ajitesh Roy, Partha Pratim Chakraborty, et al.
BMJ Case Reports
|
December 6, 2023
Marked increase in bone mineral density with oral phosphate and calcitriol in tumour-induced osteomalacia
Partha Pratim Chakraborty, Rana Bhattacharjee, Ajitesh Roy, et al.
BMJ Case Reports
|
May 15, 2016
Blount's disease: a rickets mimicker
Rana Bhattacharjee, Partha Pratim Chakraborty, Ajitesh Roy, et al.
Journal of Obstetrics and Gynaecology of India
|
November 3, 2016
Male Factor Infertility: Clues to Diagnose 46, XX Male
Partha P Chakraborty, Rana Bhattacharjee, Ajitesh Roy, et al.
Journal of the American Podiatric Medical Association
|
December 19, 2017
Reversible Secondary Osteolysis in Diabetic Foot Infection
Partha P Chakraborty, Ajitesh Roy, Rana Bhattacharjee, et al.
Journal of the Endocrine Society
|
November 21, 2022
Glial Cell Missing Homolog 2 Mutation Causing Severe Hypoparathyroidism: Report of Two Cases With Novel Mutations
Pankaj Singhania, Arunava Ghosh, Debaditya Das, et al.
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of 4
Search research articles
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Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
JCEM Case Reports
|
July 17, 2025
Cerebrotendinous Xanthomatosis With a Heterozygous Frameshift Mutation Involving <i>CYP27A1(C.526del)</i>
Ajitesh Roy, Sounak Kumar Roy, Soumyadip Das
Indian Journal of Pediatrics
|
December 31, 2013
Labial neurofibroma as the presenting feature of genital and orbitotemporal neurofibromatosis
Deep Dutta, Ajitesh Roy, Satinath Mukhopadhyay, et al.
Indian Journal of Dermatology
|
December 19, 2012
Leprechaunism - a case report
Sumit Sen, Ajitesh Roy, Anusree Gangopadhyay, et al.
Postgraduate Medical Journal
|
May 14, 2017
Pseudoacromegaly: an unusual presenting manifestation of long-standing undiagnosed primary hypothyroidism
Partha Pratim Chakraborty, Rana Bhattacharjee, Ajitesh Roy, et al.
JCEM Case Reports
|
April 23, 2026
Betel leaf (paan) chewing: an unusual cause of refractory hypothyroidism in levothyroxine-treated patient
Neeti Agrawal, Ajitesh Roy, Partha Pratim Chakraborty, et al.
BMJ Case Reports
|
December 6, 2023
Marked increase in bone mineral density with oral phosphate and calcitriol in tumour-induced osteomalacia
Partha Pratim Chakraborty, Rana Bhattacharjee, Ajitesh Roy, et al.
BMJ Case Reports
|
May 15, 2016
Blount's disease: a rickets mimicker
Rana Bhattacharjee, Partha Pratim Chakraborty, Ajitesh Roy, et al.
Journal of Obstetrics and Gynaecology of India
|
November 3, 2016
Male Factor Infertility: Clues to Diagnose 46, XX Male
Partha P Chakraborty, Rana Bhattacharjee, Ajitesh Roy, et al.
Journal of the American Podiatric Medical Association
|
December 19, 2017
Reversible Secondary Osteolysis in Diabetic Foot Infection
Partha P Chakraborty, Ajitesh Roy, Rana Bhattacharjee, et al.
Journal of the Endocrine Society
|
November 21, 2022
Glial Cell Missing Homolog 2 Mutation Causing Severe Hypoparathyroidism: Report of Two Cases With Novel Mutations
Pankaj Singhania, Arunava Ghosh, Debaditya Das, et al.
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of 4