Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Apurba, Ghosh"'
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 20, Iss 1 (2024)
Measles, mumps, and rubella (MMR) are highly infectious viral diseases affecting young children and have high secondary attack rates. Present MMR vaccines show consistent seroconversion rates for anti-measles and anti-rubella antibodies with variable
Externí odkaz:
https://doaj.org/article/7093428b00aa48bc8099b3038e06a76e
Publikováno v:
Indian Journal of Public Health, Vol 68, Iss 1, Pp 21-25 (2024)
Background: Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. Immunophenotype (IPT) and cytogenetics are essential for diagnosis, risk stratification, and management for ALL. Objectives: Evaluating the burden of immunophenotypic
Externí odkaz:
https://doaj.org/article/2804a465d3f447c1b88f07e2c8ff3993
Autor:
Hitt J Sharma, Sameer Parekh, Pramod Pujari, Sunil Shewale, Shivani Desai, Anand Kawade, Mandyam Ravi, Jitendra Oswal, Saji James, N. Mahantashetti, Renuka Munshi, Apurba Ghosh, Venkateshwar Rao, Sundaram Balsubramaniam, P. Varughese, A. Somshekhar, Amy Sarah Ginsburg, Harish Rao, Manish Gautam, Sunil Gairola, Umesh Shaligram
Publikováno v:
Expert Review of Vaccines, Vol 22, Iss 1, Pp 278-287 (2023)
Background This study assessed safety and immunogenicity of Serum Institute of India Pvt Ltd (SIIPL)’s tetanus toxoid (TT), diphtheria toxoid (DT), and acellular pertussis booster vaccine (Tdap). Research Design and Methods In this Phase II/III, mu
Externí odkaz:
https://doaj.org/article/e0cedde7b1a44c5e8540564550c33c7a
Publikováno v:
Asian Journal of Medical Sciences, Vol 14, Iss 6, Pp 250-256 (2023)
A nevus is characterized by collection of partially differentiated or well-differentiated cells normally found in the skin. Some nevi are associated with disorders such as autism, epilepsy, ophthalmogical disorders, intracranial abnormalities, and ot
Externí odkaz:
https://doaj.org/article/f6f3a96104bc4d3a964047903475c0d0
Publikováno v:
Indian Pediatrics Case Reports, Vol 3, Iss 2, Pp 72-76 (2023)
Background: Rapid-onset obesity with hypoventilation, hypothalamic dysfunction, and autonomic dysregulation (ROHHAD) syndrome is a rare cause of obesity, characterized by early and rapid onset of obesity, hypoventilation, hypothalamic dysfunction, an
Externí odkaz:
https://doaj.org/article/792d45784bfa47f08cdf492e28c0b86d
Autor:
Nijalingappa K. Kalappanavar, Apurba Ghosh, Monika Sharma, Latha Ravichandran, Nirmal Choraria, Saravanan P, Madhukar Pandey, Pradeep N, Prachee Shah, Sneha Nair, Ashfaque Shaikh, Serge van de Witte
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 18, Iss 6 (2022)
Efficacy and safety data on quadrivalent influenza vaccines (QIVs) for immunization of Indian children are scarce. This phase 3, registration study evaluated the immunogenicity, safety, and tolerability of a QIV in Indian children aged 6–35 months
Externí odkaz:
https://doaj.org/article/21993a0117aa4b7dbc34ca15077f88c8
Autor:
Kakali Roy, Surupa Basu, Nabendu Murmu, Jyotirmoy Adhikari, Sumantra Adhikari, Ritabrata Kundu, Apurba Ghosh
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 16, Iss 8, Pp SC20-SC23 (2022)
Introduction: Children are most susceptible to Lead (Pb) toxicity. Exposure to lead in the environment still exists in various pockets of urban cities due to continued practices of using lead in jewellery making, paints, battery smelting and in cosme
Externí odkaz:
https://doaj.org/article/64ebc3db3beb4ae782ee8e6394366476
Publikováno v:
Advances in Difference Equations, Vol 2021, Iss 1, Pp 1-12 (2021)
Abstract In this work, we present new necessary and sufficient conditions for the oscillation of a class of second-order neutral delay impulsive differential equations. Our oscillation results complement, simplify and improve recent results on oscill
Externí odkaz:
https://doaj.org/article/0e7fdd6de9f645cba467a448887247d4
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 23, Iss 1, Pp 77-79 (2022)
Triple-A syndrome (Allgrove syndrome) is a rare, autosomal recessive disorder classically described with the triad of alacramia, achalasia, and ACTH-resistant adrenal insufficiency. Very few cases have been reported so far in the literature. Rarity l
Externí odkaz:
https://doaj.org/article/229c1af87a984777a4ebfd6785173921
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 23, Iss 2, Pp 126-128 (2022)
Infantile systemic hyalinosis (ISH; MIM #236490) and juvenile hyaline fibromatosis (MIM #228600) represent two spectrums of the rare autosomal recessive disorder, the hyaline fibromatosis syndrome caused by mutations in ANTXR2/CMG2 encoding capillary
Externí odkaz:
https://doaj.org/article/5003a1e4a4f54acf9ca4f13fe47675a7