Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Shanto Pramanik"'
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 8, Iss 9, Pp 3051-3053 (2019)
The effect of coexistence of the prothrombotic Factor V Leiden mutation on the phenotypical expression in hemophilia is still debatable. Six-year-old boy with severe hemophilia A had presented with large soft tissue hematoma, treated with Factor VIII
Externí odkaz:
https://doaj.org/article/e6830c6b1f2c42d19e4ee926683df786
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 8, Iss 9, Pp 3051-3053 (2019)
Journal of Family Medicine and Primary Care
Journal of Family Medicine and Primary Care
The effect of coexistence of the prothrombotic Factor V Leiden mutation on the phenotypical expression in hemophilia is still debatable. Six-year-old boy with severe hemophilia A had presented with large soft tissue hematoma, treated with Factor VIII
Autor:
Piw Das, Priyankar Pal, Shanto Pramanik, Sushmita Banerjee, Arpita Bhattacharya, Subroto Chakrabarty
Publikováno v:
Indian journal of pediatrics. 76(6)
We present a series of five cases diagnosed and treated as reactive haemophagocytic lymphohistiocytosis (HLH) in three tertiary referral centers of Kolkata, within a time frame of 3 months. The initial presentations were very variable, the most promi
Publikováno v:
Pediatric dermatology. 24(6)
We describe an occurrence of Kawasaki disease presenting in the neonatal period with multiple coronary aneurysms. Very few such presentations of this entity have been described in the literature and this is probably the youngest patient reported from
Autor:
Shanto, Pramanik, Sushmita, Banerjee
Publikováno v:
Indian pediatrics. 44(10)
The insect order of Hymenoptera includes bees, hornets, wasps and fire-ants. Their stings are not usually life threatening, causing mainly local reactions and rarely anaphylaxis. This is a report of an 18 month old child who survived after an unusual
Publikováno v:
Journal of paediatrics and child health. 43(1-2)
Publikováno v:
Indian pediatrics. 43(8)
This study aims to highlight the difficulties faced in the clinical diagnosis of Kawasaki Disease (KD) presenting beyond the first week. This is a retrospective study of 25 cases of which only 36% met the criteria for classical and 8% was incomplete
Publikováno v:
Indian journal of pediatrics. 73(7)
Nager acrofacial dysostosis comprises defects of cranio facial region and limbs (mostly upper) with variable associated anomalies. The cranio- facial complex is indistinguishable from the mandibulo facial dysostosis (Treacher Collins syndrome). About
Publikováno v:
Journal of Pediatric Hematology/Oncology. 31:223-224