Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Sona, B."'
Autor:
Warrier, Sona B., Kharkar, Prashant S.
Publikováno v:
In Journal of Luminescence July 2018 199:407-415
Autor:
Nair, Sona B.1 (AUTHOR), Athalye, Arundhati S.1 (AUTHOR), Panphalia, Madhavi1 (AUTHOR), Parikh, Firuza R.1 (AUTHOR)
Publikováno v:
Hemoglobin. Sep2022, Vol. 46 Issue 5, p269-271. 3p.
Publikováno v:
Hemoglobin. 46:269-271
Publikováno v:
Applied Mathematics and Nonlinear Sciences, Vol 1, Iss 1, Pp 207-228 (2016)
We present here a case study for modelling the control of the Aujeszky disease, in a farm declared virus-free. The model is validated on the available data. Simulations are performed to assess different containment strategies for the epidemic. Final
Externí odkaz:
https://doaj.org/article/e0d1f9a26b944036ac1b490fdc49df76
Publikováno v:
Indian Journal of Neurosurgery, Vol 02, Iss 02, Pp 193-195 (2013)
The authors here describe a rare cranio-cerebral injury, which occurred due to a self-inflicted suicidal attempt by the patient, who hammered an 8 cm long nail into his skull. This patient was a known case of schizophrenia. The nail entered in the re
Externí odkaz:
https://doaj.org/article/73bc409436114fbfb2bbda1c9b2bd0aa
Autor:
Bipin P Kulkarni, Sona B Nair, Manasi Vijapurkar, Leenam Mota, Sharda Shanbhag, Shehnaz Ali, Shrimati D Shetty, Kanjaksha Ghosh
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e108683 (2014)
BackgroundThough rare in occurrence, patients with rare bleeding disorders (RBDs) are highly heterogeneous and may manifest with severe bleeding diathesis. Due to the high rate of consanguinity in many caste groups, these autosomal recessive bleeding
Externí odkaz:
https://doaj.org/article/e4d25ae4a78646f6a6fc35a903eaf86b
Autor:
Italia, Khushnooma Y., Jijina, Farah J., Merchant, Rashid, Panjwani, Sangeeta, Nadkarni, Anita H., Sawant, Pratibha M., Nair, Sona B., Ghosh, Kanjaksha, Colah, Roshan B.
Publikováno v:
In Clinica Chimica Acta 2009 407(1):10-15
Autor:
Sona B. Nair
Publikováno v:
Journal of Rare Diseases Research & Treatment. 3:9-12
Akademický článek
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Publikováno v:
Hemoglobin. 42(5-6)
We here report a case of a 23-year-old female from Mumbai, Maharashtra, India who was detected to carry the α chain variant Hb J-Norfolk [HBA2: c.173G>A (or HBA1]. She had no clinical symptoms and was referred to us for routine investigations and sc