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pro vyhledávání: '"Anshul Raja"'
Publikováno v:
Journal of Medical Sciences and Health, Vol 2, Iss 3, Pp 40-42 (2016)
Williams–Campbell syndrome is a rare congenital syndrome characterized by the absence of cartilage in subsegmental bronchi leading to formation of bronchiectasis distal to the affected bronchi. The syndrome is usually presented in childhood, with r
Externí odkaz:
https://doaj.org/article/3b503a61d54c443d85ad20e302f62857
Publikováno v:
International Journal of Contemporary Pediatrics. :1293-1296
Background: Necrotising enterocolitis (NEC) is primarily a disease of premature infants, but may also be present in 10% of term and near term babies. It is the most common gastrointestinal (GI) medical/surgical emergency occurring in neonates. The ob
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 4:9511-9514
Publikováno v:
Journal of Medical Sciences and Health, Vol 2, Iss 3, Pp 40-42 (2016)
Williams–Campbell syndrome is a rare congenital syndrome characterized by the absence of cartilage in subsegmental bronchi leading to formation of bronchiectasis distal to the affected bronchi. The syndrome is usually presented in childhood, with r
Publikováno v:
Pediatric Oncall. 14
Publikováno v:
Pediatric Oncall. 13
Publikováno v:
Journal of Clinical Imaging Science, Vol 5, Iss 1, Pp 9-9 (2015)
Journal of Clinical Imaging Science
Journal of Clinical Imaging Science
Twin reversed arterial perfusion (TRAP) sequence is an extremely rare complication of monochorionic multi-fetal pregnancy, occurring once in 35,000 births. This condition is characterized by a malformed fetus without a cardiac pump being perfused by
Publikováno v:
Tropical Journal of Medical Research. 18:51
Cystic lesions of the spleen are rare, and splenic hydatid cysts account for only 0.5-8% of all hydatidosis. The authors here report a case where a 50-year-old female presented to our hospital with the complaints of heaviness and pain over the left u