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Volume 9 Number 1 Year 2020

9 articles in this issue 

Viraraghavan Vadakkencherry Ramaswamy,Gajanan Venkat Rao,Nori Suryanarayana,Sanghamitra Gummadapu

Umbilical vein catheterisation is a very common procedure in Neonatal Intensive Care Units. The tip of the umbilical vein catheter (UVC) should be located at the junction of inferior vena cava and right atrium, which is confirmed by an abdominal radiograp... see more

Pags. e090102  

Igne Kairiene,Vaidas Dirse,Ugnius Mickys,Audrone Muleviciene,Paresh Vyas,Jelena Rascon

Transient abnormal myelopoiesis (TAM) is a unique entity that usually occurs in children with Down syndrome (DS) or with trisomy 21 mosaicism. The somatic GATA1 mutation is a distinct feature of TAM. At presentation, TAM can resemble congenital leukemia (... see more

Pags. e090104  

Kamal Nain Rattan,Jasbir Singh,Poonam Dalal,Ravi Rohilla

Despite significant advances, the management of giant omphalocele (GO) still remains a challenging job for neonatologists and pediatric surgeons. Early surgical treatment of GO may not be undertaken in every patient due to the risk of fatal hemodynamic an... see more

Pags. e090105  

Doris Barcellona,Francesco Marongiu

The hemostatic system is a complex ancestral pathway physiologically dedicated to protect the individual from bleeding. It starts immediately after an endothelial injury. Platelets and blood coagulation act synergically to provide a strength clot able to ... see more

Pags. e090106  

Luís António Sousa Queirós,Maria Hercília Ferreira Guimarães Pereira Areias,Amélia Ricon Ferraz

The authors aim to describe the 35 years of history of the neonatal unit of the São João University Hospital Center (Centro Hospitalar Universitário São João), Porto, Portugal, a level III-C hospital, analyzing the evolution of its health care and academi... see more

Pags. e090108  

Allam Fayez Abuhamda,Aymen Mohammed Elsous

Sanjad-Sakati syndrome is an autosomal recessive disorder found mainly in people of Arabian origin. This is a report of a Palestinian premature (35 weeks gestation) newborn who was part of twins and had this rare disease. The syndrome comprises congenital... see more

Pags. e090123