Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Shrutiprajna Kar"'
Publikováno v:
Indian Pediatrics Case Reports, Vol 4, Iss 3, Pp 142-144 (2024)
Background: Thyroid hemiagenesis (THA) is a rare aberration in the development of the thyroid gland, denoted by the absence of either thyroid lobe with or without the isthmus, common in females, predominantly involving left lobe of thyroid, usually m
Externí odkaz:
https://doaj.org/article/10d63d941cf24f14bbb54faf2a9c9997
Autor:
Tanushree Sahoo, Pankaj Kumar Mohanty, Tapas Kumar Som, Usha Devi, Shrutiprajna Kar, Jagdish Prasad Sahoo, Veneza Zareen Lyngdoh Jarain, Soumi Karmakar, Saranya Jeyaraman, Sangeeta Acharya
Publikováno v:
BMJ Open Quality, Vol 13, Iss Suppl 1 (2024)
Externí odkaz:
https://doaj.org/article/04c1fa6446524585b918f1bd540beee4
Publikováno v:
Indian Pediatrics Case Reports, Vol 3, Iss 3, Pp 142-145 (2023)
Background: Non-Rhesus D antigen non-ABO, minor blood group alloimmunization in pregnant women is being increasingly recognized as a significant contributor to the development of the hemolytic disease of the fetus and newborn (HDFN). We report severe
Externí odkaz:
https://doaj.org/article/50e17b003a7341a18a0e35eb8dc5818c
Publikováno v:
BMJ case reports. 15(12)
A full-term male baby was administered furosemide and enalapril for treatment of cardiac failure secondary to a ventricular septal defect. He also received piperacillin-tazobactam and amikacin for 7 days for suspected early-onset neonatal sepsis. He
Publikováno v:
Indian Journal of Pediatrics.
Autor:
Shrutiprajna Kar, Pavithra Ayyanar, Tanushree Sahoo, Usha Devi, Tapas Som, Pankaj Kumar Mohanty
Publikováno v:
Medical Journal Armed Forces India.
Autor:
Shrutiprajna Kar, Sriram Krishnamurthy, Malini Maya, Pediredla Karunakar, Yamini Agarwal, Abarna Thangaraj
Publikováno v:
Pediatric Nephrology. 36:2033-2037
Autor:
Shrutiprajna Kar, Praneetha Mude, Usha Devi, Tapas Som, Pankaj Kumar Mohanty, Tanushree Sahoo, Prabodha Kumar Das
Publikováno v:
Indian Journal of Pediatrics. 90:415-415
Publikováno v:
Journal of Neonatology. :097321792211431
Edwards’ syndrome (trisomy 18) is a rare autosomal inherited disorder arising from the presence of an extra copy on chromosome 18. It is the second most common polymalformative genetic syndrome following Down syndrome. The most common characteristi
Autor:
Shrutiprajna Kar, Sriram Krishnamurthy, Pediredla Karunakar, Malini Maya, Abarna Thangaraj, Yamini Agarwal
Publikováno v:
Pediatric Nephrology. 36:2031-2032