Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Mukhopadhyay, Rajarshi"'
Autor:
Mukhopadhyay, Rajarshi
Wireless communication is witnessing tremendous growth with the proliferation of various standards covering wide, local, and personal area networks, which operate at different frequency bands. Future wireless terminals will not only need to support m
Externí odkaz:
http://hdl.handle.net/1853/14097
Publikováno v:
In Expert Systems With Applications 30 December 2022 210
Publikováno v:
International Journal of Dynamics & Control; Aug2024, Vol. 12 Issue 8, p3017-3032, 16p
Publikováno v:
In Metabolic Syndrome 2024:585-595
Autor:
Acharya, Shamasunder, Arumugam, Somasundaram, Bagchi, Manashi, Bagchi, Debasis, Bala, Sapna, Balakrishnan, Grrishma, Bandopadhyay, Purbita, Bandyopadhyay, Arun, Banerjee, Mainak, Banik, Samudra P., Bhadada, Sanjay Kumar, Bhat, Sowrabha, Bhatnagar, Apoorva, Bhowmik, Eshita, Bir, Aritri, Biswas, Subhash Ch., Brodosi, Lucia, Burrage, Lauren, Buttari, Brigitta, Chakrabarti, Sankha Shubhra, Chakrabarti, Partha, Chakrabarti, Sasanka, Chakraborty, Sanjoy, Chatterjee, Aroup, Chatterjee, Sudip, Chattopadhyay, Dipanjan, Chaudhury, Tirthankar, Cherian, Kripa Elizabeth, Chowdhury, Amarta Shankar, Dabadghao, Preeti, Dabas, Aashima, Das, Snehasis, Das, Pamelika, Das, Jishna, Dasgupta, Riddhi, Dasgupta, I., Dissanayake, H.A., Downs, Bernard W., Dutta, Deep, Duttaroy, Asim K., Fariduddin, Maria M., Fazeli, Mostafa, Ferns, Gordon A., Ferrari, Carlos K.B., Gangopadhyay, Kalyan Kumar, Ganguly, Dipyaman, Ganguly, Anirban, Ganie, Mohd Ashraf, Garg, M.K., Gargari, Piyas, Geer, Mohammad Ishaq, Ghayour-Mobarhan, Majid, Ghosh, Amrit Raj, Ghosh, Arindam, Ghosh, Rituparna, Goswami, Soumik, Grover, B., Gupta, Sudhiranjan, Haldipur, Ashrita C., Hayer, M.K., Heller, Simon, Iqbal, Ahmed, Jacob, Jubbin J., Jebasingh, Felix, Jude, Edward B., Kanumilli, Naresh, Kapoor, Nitin, Kettler, Zelpha K., Khoo, C.M., Krishnaveni, G.V., Kumar, Sandeep, Kumar, Angad, Kushner, Steve, Lee, K.O., Li, Dong, Li, Li, Maisnam, Indira, Majumdar, Sujoy, Majumder, Anirban, Marchesini, Giulio, Marwaha, Raman Kumar, Mirshad, Reshma, Misra, A., Mitra, Sandip Kumar, Mittal, Madhukar, Mohan, Viswanathan, Mondal, Sunetra, Müller, Walter E., Mukherjee, Sutapa, Mukherjee, J.J., Mukhopadhyay, Rajarshi, Mukhopadhyay, Satinath, Muthiah, Mark, Naik, Ramachandra G., Pal, Rimesh, Palui, Rajan, Paul, Thomas V., Petroni, Maria Letizia, Prasanna, Vani Sai, Preuss, Harry G., Profumo, Elisabetta, Puppala, Alekhya, Rankawat, Sourbh, Rasool, Abid, Ray, Aleepta Guha, Ray, Sayantan, Ray, Sandipan, Raychaudhuri, Smriti K., Raychaudhuri, Siba P., Roy, Trina, Saberi-Karimian, Maryam, Safarian-Bana, Hamideh, Saha, Arpita, Saha, Sarmistha, Sahar, Tajali, Sahoo, J.P., Saikia, Uma Kaimal, Sanjeevi, Carani B., Sanyal, Arun J., Sarkar, Jit, Sarkar, Sulogna, Saso, Luciano, Satpathi, Tirthankar, Sharif, Adnan, Shetty, Shrinath Pratap, Singh, Awadhesh Kumar, Singh, Ritu, Sinha, Ashim, Somasundaram, N.P., Sreedhar, Remya, Srividya, N., Tabatabaeizadeh, Seyed-Amir, Tan, Eunice Xiang Xuan, Thomas, Nihal, Unnikrishnan, Ranjit, Velayutham, Ravichandiran, Vella, Adrian, Viswanathan, Vijay, Vora, Jiten, Wagle, S.S., Welch, Andrew, Yajnik, C.S., Yellurkar, Manoj Limbraj, Yousuf, Syed Douhath, Zhang, Jian
Publikováno v:
In Metabolic Syndrome 2024:xxi-xxv
Publikováno v:
Indian Journal of Dermatology, Vol 45, Iss 3, Pp 108-113 (2000)
Externí odkaz:
https://doaj.org/article/479df474280d47d0b4a58e67d6301c08
Akademický článek
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Autor:
Lodh, Moushumi, Mukhopadhyay, Rajarshi
Publikováno v:
Journal of Reproduction & Infertility
Background: McCune Albright syndrome is rare with an estimated prevalence of 1 in 100,000 to 1 in 1,000,000 persons. The classical clinical triad consists of fibrous dysplasia of the bone, café-au-lait skin spots and precocious puberty. However, in
Autor:
Mukhopadhyay, Rajarshi, Sergouniotis, Panagiotis I., Mackay, Donna S., Day, Alexander C., Wright, Genevieve, Devery, Sophie, Leroy, Bart P., Robson, Anthony G., Holder, Graham E., Li, Zheng, Webster, Andrew R.
Publikováno v:
Molecular Vision
Purpose To determine the spectrum of mutations and phenotypic variability within patients with mutations in membrane-type frizzled related protein gene (MFRP). Methods Individuals were initially ascertained based on a phenotype similar to that previo
Autor:
Omprakash, Anup P., Ildefonso, Adrian, Fleetwood, Zachary E., Tzintzarov, George N., Cardoso, Adilson S., Babcock, Jeffrey A., Mukhopadhyay, Rajarshi, Khachatrian, Ani, Warner, Jeffrey H., McMorrow, Dale, Buchner, Stephen P., Cressler, John D.
Publikováno v:
IEEE Transactions on Nuclear Science; Jan2019, Vol. 66 Issue 1, p389-396, 8p